Targeting lysyl oxidase (LOX) overcomes chemotherapy resistance in triple negative breast cancer

Saatci, Ozge; Kaymak, Aysegul; Raza, Umar; Ersan, Pelin G.; Akbulut, Ozge; Banister, Carolyn E.; Sikirzhytski, Vitali; Tokat, Unal Metin; Aykut, Gamze; Ansari, Suhail A.; Dogan, Hayriye Tatli; Dogan, Mehmet; Jandaghi, Pouria; Isik, Aynur; Gundogdu, Fatma; Kosemehmetoglu, Kemal; Dizdar, Omer; Aksoy, Sercan; Akyol, Aytekin; Uner, Aysegul; Buckhaults, Phillip J.; Riazalhosseini, Yasser; Sahin, Ozgur

doi:10.1038/s41467-020-16199-4

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Published: 15 May 2020

Targeting lysyl oxidase (LOX) overcomes chemotherapy resistance in triple negative breast cancer

Nature Communications volume 11, Article number: 2416 (2020) Cite this article

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Abstract

Chemoresistance is a major obstacle in triple negative breast cancer (TNBC), the most aggressive breast cancer subtype. Here we identify hypoxia-induced ECM re-modeler, lysyl oxidase (LOX) as a key inducer of chemoresistance by developing chemoresistant TNBC tumors in vivo and characterizing their transcriptomes by RNA-sequencing. Inhibiting LOX reduces collagen cross-linking and fibronectin assembly, increases drug penetration, and downregulates ITGA5/FN1 expression, resulting in inhibition of FAK/Src signaling, induction of apoptosis and re-sensitization to chemotherapy. Similarly, inhibiting FAK/Src results in chemosensitization. These effects are observed in 3D-cultured cell lines, tumor organoids, chemoresistant xenografts, syngeneic tumors and PDX models. Re-expressing the hypoxia-repressed miR-142-3p, which targets HIF1A, LOX and ITGA5, causes further suppression of the HIF-1α/LOX/ITGA5/FN1 axis. Notably, higher LOX, ITGA5, or FN1, or lower miR-142-3p levels are associated with shorter survival in chemotherapy-treated TNBC patients. These results provide strong pre-clinical rationale for developing and testing LOX inhibitors to overcome chemoresistance in TNBC patients.

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Introduction

Triple negative breast cancer (TNBC) is the most aggressive subtype of breast cancer. It accounts for 10–20% of all patients, yet is responsible for 30% of all breast cancer deaths¹. At the molecular level, TNBC is characterized by the lack of estrogen receptor alpha (ERα), progesterone receptor (PR) and epidermal growth factor receptor 2 (HER2/ErbB2)^2,3 expression. TNBC patients mostly rely on chemotherapy unlike other subtypes that can be treated with targeted therapies. Anthracyclines and taxane-based chemotherapy agents are among the most commonly used chemotherapeutics in both neo-adjuvant and adjuvant settings⁴. As compared to other subtypes, TNBC patients show low risk of recurrence if pathological complete response (pCR) is achieved⁵. However, while only 30–40% of TNBC patients show pCR towards treatment, the majority have <60% 5-year survival due to aggressive relapse⁶. Recently, the first immunotherapy for breast cancer was approved by the Food and Drug Administration (FDA) to treat locally advanced or metastatic TNBC patients. However, immunotherapy combined with chemotherapy produced only a 3 month improvement in progression-free survival, and improvement in overall survival was observed only in patients with PD-L1 positive tumors⁷. Therefore, there is still a dire need to identify novel molecular targets to improve the therapeutic benefit of chemotherapy given in first-line settings, as well as in patients with advanced, chemotherapy resistant TNBC. This will have immediate translational impact on improving the pCR rate to standard chemotherapy and will improve patient outcome for the most-aggressive breast cancer subtype.

Deregulation of distinct cell intrinsic processes, such as apoptosis⁸, growth factor signaling⁹, DNA repair¹⁰ as well as alterations in the levels of drug transporter proteins¹¹ have previously been associated with chemoresistance. In addition, accumulating evidence suggest that the tumor extracellular matrix (ECM) may also confer resistance to therapy, either by providing a protective barrier that hinders access of anti-cancer drugs to tumors^12,13,14 or by activating survival signaling or blocking apoptosis upon interacting with the integrin type transmembrane receptors^15,16. Integrins are heterodimeric cell surface receptors that control cell adhesion, cytoskeletal organization, signal transduction and cell migration via establishing focal adhesion complexes that serve as mechanical links that convey signals between ECM and the intracellular compartment of the interacting cell^17,18. Activation of integrin signaling may lead to resistance to therapy^15,19,20 and acquisition of metastatic traits²¹. Notably, increased expression of several integrin subunits have previously been associated with poor patient outcome^19,22,23.

The ECM is a highly dynamic structure that is constantly remodeled by cells through altered synthesis, degradation, reassembly and chemical modifications²⁴. While normal epithelial cells produce small amounts of ECM, fibroblasts and tumors cells produce large quantities of ECM molecules, such as collagen and fibronectin^25,26. In addition, overexpression of ECM remodeling enzymes such as matrix metalloproteases (ECM degraders) and lysyl oxidases (ECM stiffeners) have previously been associated with tumor aggressiveness²⁴. The lysyl oxidase (LOX) family proteins mediate the conversion of lysine residues in collagen and elastin precursors into highly reactive aldehydes thereby triggering cross-linking and stabilization of ECM proteins, specifically the type I collagen and elastin, and regulate cell adhesion, motility and invasion²⁷. In preclinical breast cancer models, LOX secretion from breast cancer cells was shown to induce the pre-metastatic niche formation²⁸, and LOX inhibition suppressed lung metastasis²⁹. LOX inhibition was also shown to sensitize pancreatic cancer to chemotherapy^30,31. Furthermore, novel intracellular functions of the LOX family proteins have been reported, such as the stabilization of transcription factors and maintenance of chromosome stability³². Despite the relatively well-established roles of LOX in stimulating cancer metastasis, its contribution to chemoresistance in TNBCs has not yet been reported.

In this study, we combine in vivo-developed chemoresistant xenograft models with an unbiased, genome-wide transcriptomic approach, 3D cell culture systems, primary breast cancer organoids, syngeneic and patient-derived xenograft (PDX) models and patient data/tissue analyses to identify mechanisms of chemotherapy resistance in TNBCs. We show that chemoresistance is driven by the HIF-1α/miR-142-3p/LOX/ITGA5/FN1 axis and targeting either LOX or its downstream FAK/Src signaling pathway, or overexpressing miR-142-3p can overcome chemoresistance in TNBC.

Results

Integrin signaling is a key mediator of chemoresistance in TNBCs

To elucidate the underlying mechanisms of chemoresistance in TNBCs, we modelled the clinical acquired resistance by using xenografts of the well-established TNBC cell line, MDA-MB-231^33,34. Tumor-bearing mice were continuously treated with either vehicle or doxorubicin, and the fast-growing vehicle-treated mice were sacrificed, and tumors were denoted as vehicle. When tumors from the doxorubicin-treated group exhibited initial response to therapy and shrunk, tumors from some of the mice were collected and denoted as sensitive. The rest of the mice were kept under doxorubicin treatment until their tumors exhibited re-growth at rates comparable to vehicle-treated tumors, and those tumors were classified as resistant (Fig. 1a). The average growth curves and the Waterfall plot showing tumor volume fold change over time for vehicle-treated, doxorubicin-sensitive and -resistant tumors are depicted in Fig. 1b, c, respectively.

We performed RNA-sequencing (RNA-seq) on bulk tumors (four tumors from each group) to identify transcripts differentially expressed between doxorubicin-sensitive and -resistant tumors. We used the 441 most differentially expressed genes (fold change (FC) cut-off = 1.75, p-value < 0.05, Supplementary Data 1) to create a doxorubicin resistance gene signature (DoxoR-GS). We then tested its clinical relevance using gene expression profiling datasets of chemotherapy-treated TNBC patients (for details, see “Methods” section)³⁵. Chemotherapy-treated TNBC patients from GSE58812³⁶ that have high DoxoR-GS scores exhibit poor overall survival (OS) as compared to those with low DoxoR-GS scores (Fig. 1d). These results were further confirmed using METABRIC dataset³⁷ (Supplementary Fig. 1a) and in another dataset (GSE31519) where we showed that expression of DoxoR-GS is significantly higher in patients who exhibit an event, described as either relapse- or distant metastasis (Supplementary Fig. 1b).

Having validated the clinical relevance of our in vivo-derived DoxoR-GS, we sought to identify the pathways that were most significantly represented among the differentially expressed genes. Ingenuity Pathway Analysis (IPA) revealed that integrin-linked kinase (ILK) signaling was the top deregulated pathway (Fig. 1e). Gene set enrichment analysis (GSEA) in chemotherapy-treated TNBC patients demonstrated that genes involved in focal adhesion signaling were significantly enriched in high DoxoR-GS scorers (Fig. 1f), underlining the importance of integrins and downstream focal adhesion in doxorubicin resistance.

Based on the RNA-seq analysis of our doxorubicin-resistant models, three integrin genes, ITGA5, ITGA10 and ITGB5 were significantly (FC cut-off = 1.5, p-value < 0.05) upregulated in resistant tumors (Fig. 1g and Supplementary Fig. 1c). We found that higher expression of only the integrin alpha 5 (ITGA5), but not that of ITGA10 or ITGB5, is associated with shorter relapse-free survival (RFS) in chemotherapy-treated basal patients (Fig. 1h, i and Supplementary Fig. 1d, e). No such relationship was observed in patients with basal subtype of breast cancer who were not treated with chemotherapy or in patients with other subtypes (Fig. 1i). As around 70% of TNBCs are basal subtype, and 76% of basal subtype are TNBCs³⁸, we classified patients also as TNBC using ERα, PR, and HER2 expression and again observed a strong association between ITGA5 expression and RFS in chemotherapy-treated TNBC patients (Supplementary Fig. 2a). Importantly, we also detected a significant upregulation of fibronectin (FN1), the main ligand for ITGA5, in doxorubicin-resistant tumors (Fig. 1j) and a significant association between high FN1 expression and poorer RFS in chemotherapy-treated basal patients (Fig. 1k, l). These results were further validated with another TNBC patient dataset (GSE58812) in which higher expression of either ITGA5 or FN1 is significantly associated with worse overall survival for the chemotherapy-treated TNBC patients (Supplementary Fig. 2b). Notably, when the patients are stratified based on ITGA5 and FN1 expressions in combination, a stronger separation of overall survival was achieved (Supplementary Fig. 2c, p = 0.0008; HR = 5.28). Altogether, these data suggest that deregulation of FN1-ITGA5 signaling could be a major driver of chemoresistance in TNBC.

Hypoxia-induced LOX hyperactivates ITGA5/FN1/FAK/Src axis

Hypoxia inducible factor-1 alpha (HIF-1α), encoded by the HIF1A gene, activates the transcription of several ECM-remodeling enzymes, including collagen prolyl and lysyl hydroxylases and lysyl oxidases thereby modulating ECM stiffness^39,40. Importantly, our IPA analysis revealed a significant enrichment of HIF1A signaling in the doxorubicin-resistant tumors (Fig. 1e). Given the involvement of hypoxia in ECM remodeling^41,42, we hypothesized that HIF-1α could activate integrin and focal adhesion signaling. We first validated activation of the hypoxic response in chemoresistant tumors by demonstrating upregulation of the CA9 gene, which is a direct HIF-1α target gene and a well-established hypoxia marker⁴³. CA9 mRNA and protein levels were significantly higher in resistant tumors (Fig. 2a). The induction of hypoxia signaling in the resistant tumors was not simply a result of an increase in tumor size, as there was no enrichment of hypoxia signaling in vehicle-treated tumors that are the largest in size vs. sensitive tumors (Supplementary Table 1). Furthermore, patients having high DoxoR-GS score also express high levels of hypoxia-related genes (Fig. 2b).

To experimentally demonstrate the acquisition of doxorubicin resistance under hypoxic conditions, we cultured MDA-MB-231 and MDA-MB-157 cells in normoxic vs. hypoxic conditions in the presence of increasing concentrations of doxorubicin. As shown in Fig. 2c, d, cells became less sensitive to growth inhibition induced by doxorubicin when grown under hypoxic conditions. Next, we performed Upstream Regulator analysis in IPA and found that 28 of 39 HIF-1α target genes had an expression direction consistent with the activation of HIF-1α (Supplementary Table 2). Among the actively transcribed genes upon HIF-1α activation during chemoresistance, we identified LOX, which is known to modulate ECM stiffness via collagen cross-linking and promote metastasis⁴⁴. Upregulation of LOX in doxorubicin-resistant xenografts was validated by qRT-PCR and immunohistochemistry (Fig. 2e). While LOX, ITGA5, and FN1 mRNAs were upregulated between sensitive and resistant tumors under doxorubicin treatment, the fast-growing vehicle-treated tumors showed no upregulation of these genes, suggesting that their upregulation is specific to chemotherapy resistance (Supplementary Fig. 3a). Importantly, we demonstrated increased fibrillar collagen in resistant tumors compared to sensitive counterparts by picrosirius red staining (Fig. 2f, g). We then examined gene expression from 9 different breast cancer datasets and found correlation between HIF1A and LOX, ITGA5, and FN1 mRNAs (Fig. 2h), supporting the upstream regulatory role of HIF1A in their transcription. Strikingly, the correlation of LOX with ITGA5 and FN1 mRNAs was the strongest among all pairs, even stronger than the correlation of these three genes with HIF1A. This suggested that hypoxia-induced LOX might specifically be regulating ITGA5 and FN1 expression, and the subsequent activation of intracellular downstream signaling could be contributing to doxorubicin resistance. Consistent with this, we detected a significant enrichment of hypoxia and focal adhesion signaling gene sets in tumors with high LOX expression (GSE58812³⁶, Supplementary Fig. 4a, b).

To test whether hypoxia can induce both LOX expression and integrin signaling, we cultured MDA-MB-231 cells under hypoxia for different time points and observed a prominent increase in HIF-1α protein stability that was followed by a coordinated upregulation of LOX, ITGA5 and FN1 mRNAs and protein levels (Fig. 2i, j). Hypoxia also resulted in activation of integrin signaling as shown by incases in p-FAK (Y397) and p-Src (Y416) (Fig. 2j). Moreover, LOX enzymatic activity was higher under hypoxia as compared to normoxia, potentially due to increased LOX expression (Fig. 2k). Here, BAPN, a LOX family inhibitor, was used as a negative control. The induction of LOX/ITGA5/FN1 and downstream signaling under hypoxic conditions has also been validated in another TNBC cell line, MDA-MB-157 (Supplementary Fig. 4c). Silencing LOX expression using two different siRNA sequences caused a LOX expression-dependent decrease in both ITGA5 and FN1 mRNA (Fig. 2l) and protein levels (Fig. 2m) together with attenuated downstream signaling (Fig. 2m). Moreover, stable and inducible knockdown of LOX with shRNAs also validated the inhibition of downstream signaling (Fig. 2n). These data strongly support a model in which LOX-mediated upregulation of ITGA5 and its ligand, FN1 play a role in hypoxia-mediated hyperactivation of integrin signaling.

To determine the clinical relevance of LOX expression in chemotherapy-treated TNBCs, we performed survival analyses and observed that higher LOX mRNA expression predicts poor RFS only in chemotherapy-treated basal breast cancer patients, but not in other breast cancer subtypes or in untreated cases (Fig. 2o and Supplementary Fig. 2d). Furthermore, in the GSE31519 dataset we observed that more than half of the patients that exhibit event, described as either a relapse or distant metastasis, express higher LOX levels (p-value = 0.012) (Supplementary Fig. 5a). Similarly, in another dataset (GSE25066), we observed that a significantly higher proportion of chemotherapy-treated TNBC patients with residual disease (RD) express higher levels of LOX (p-value = 0.011) (Supplementary Fig. 5b). Furthermore, TNBC patients with RD express significantly higher levels of LOX, ITGA5 and FN1 (Supplementary Fig. 5c–e). Importantly, we stained for LOX protein expression in tissues (Fig. 2p, Supplementary Table 3). In 77 TNBC patients treated with chemotherapy, we showed that higher LOX protein levels were significantly associated with worse disease-free survival (DFS) (p-value = 0.019, Fig. 2q). Although other LOX family members (LOXL1-4) have also been reported to be regulated by HIF-1α⁴⁵, none of them were significantly altered in doxorubicin-resistant xenografts (Supplementary Fig. 3b). Altogether, these data are consistent with a model in which hypoxia-induced LOX activates integrin signaling by upregulating ITGA5 and FN1, leading to poor survival and chemoresistance in TNBC patients.

LOX inhibition remodels ECM to confer chemosensitization

To test the potential role of LOX in mediating chemoresistance in TNBCs and elucidating the underlying mechanisms, we first embedded TNBC cells into a matrix of type I collagen, the major substrate of LOX, and demonstrated acquisition of resistance to doxorubicin in two different cell lines (Fig. 3a and Supplementary Fig. 4d) which was accompanied by protection against apoptosis (Fig. 3b and Supplementary Fig. 6a–c) and sustained levels of p-FAK and p-Src (Fig. 3c). Western blot analysis also demonstrated a decrease in HIF-1α expression and subsequently LOX levels upon doxorubicin treatment but only in cells cultured in the absence of collagen (Fig. 3c). Overexpressing LOX in MDA-MB-231 cells that were embedded in type I collagen conferred resistance to doxorubicin (Fig. 3d). Overexpression of LOX also caused a modest increase in ITGA5 protein levels (Fig. 3e). Analysis of LOX expression in a panel of breast cancer cell lines demonstrated that TNBC cells express relatively higher levels of LOX (Supplementary Fig. 7a). Importantly, inhibiting LOX using a LOX family inhibitor, BAPN in combination with doxorubicin in three different collagen I-embedded TNBC cell lines re-sensitized them to doxorubicin (Fig. 3f, Supplementary Fig. 7b). As BAPN is known to inhibit other LOX family members as well, we further confirmed the doxorubicin sensitization with LOX inhibition using two different siRNA sequences against LOX (Fig. 3g). Importantly, doxorubicin sensitization by LOX inhibition was specific to TNBC models. ERα+ cells express relatively low levels of LOX, and LOX inhibition did not lead to chemosensitization (Supplementary Fig. 7a, c). Finally, LOX inhibition sensitizes cells to two other DNA-damaging chemotherapy agents, epirubicin and paclitaxel (Supplementary Fig. 7d), which are common therapeutic options for TNBC patients⁴⁶.

To elucidate the mechanistic details of how LOX inhibition sensitizes TNBC cells to doxorubicin, we first examined the changes in ECM remodeling upon LOX inhibition. It has been reported that there is a molecular co-dependence between collagen cross-linking and fibronectin fibril assembly that causes reciprocal activation of both processes to ultimately increase ECM stiffness^47,48. In addition, cell-mediated processes, such as binding of cell surface integrins to fibronectin dimers and subsequent recruitment of FAK to focal adhesion sites can trigger fibronectin fibrillogenesis^49,50,51. We observed that both ITGA5 and FN1 expression, and subsequent FAK phosphorylation were dependent on LOX expression (Fig. 2). We therefore hypothesized that both collagen cross-linking (by LOX) and fibronectin deposition and assembly would be hindered by LOX inhibition. To test this hypothesis, we performed immunofluorescence staining of collagen and fibronectin in type I collagen-embedded MDA-MB-231 cells with and without LOX inhibition, and observed that TNBC cells are able to deposit large amounts of fibronectin into an ECM that is rich in collagen type I (Fig. 3h), and that LOX inhibition with BAPN decreased the extracellular deposition and assembly of fibronectin fibrils (Fig. 3h) and decreased overall extracellular fibrillar collagen content (Fig. 3i). This was validated using a cell-derived ECM system produced by human foreskin fibroblast (HFF) cells, better recapitulating the dynamics of ECM formation and stabilization. Growing cancer cells on fibroblast-derived ECM induced the formation of thick, cross-linked collagen fibers, as opposed to non-fibrillar, immature collagen in the ECM deposited in the absence of cancer cells (Fig. 3j). When LOX was inhibited with BAPN, we detected a significant decrease in the immunofluorescence staining intensities of both collagen and fibronectin, suggesting that cancer cell-derived LOX is required for the cross-linking of extracellular collagen into thick fibers and the subsequent fibronectin assembly during ECM maturation (Fig. 3k). Co-localization analysis demonstrated that almost half of the collagen fibers were in contact with fibronectin (similar to previous reports^47,48), but co-localization was decreased by LOX inhibition (Supplementary Fig. 8a). Analysis of 3D images of vehicle and BAPN-treated cells cultured on top of HFF-derived ECM further demonstrated that cells are still in contact with the ECM even though LOX inhibition decreased the extracellular collagen and fibronectin content (Supplementary Fig. 8b, c). The decrease in collagen cross-linking and fibronectin assembly upon LOX inhibition was also validated by biochemical measurement of extracellular hydroxyproline content (Fig. 3l) and deoxycholate (DOC) lysis (Fig. 3m), respectively, which are standard methods used to assess the amount of collagen cross-linking and fibronectin deposition and assembly⁵².

It has been proposed that LOX may reduce drug penetration under hypoxic conditions and lessen the cytotoxicity of chemo-agents in 3D collagen cultured cells and tumor models⁵³. We showed that doxorubicin decreased the activation of FAK/Src signaling in 2D-cultured cells, but not in 3D collagen culture (Fig. 3c). Therefore, we tested if targeting LOX could increase doxorubicin penetration and decrease FAK/Src signaling, leading to apoptosis. To assess drug penetration, we quantified doxorubicin autofluorescence (ex: 495 nm, em: 595 nm⁵⁴) and observed a significant increase in intracellular doxorubicin in combination-treated cells (Fig. 3n). This was accompanied by a decrease in FAK/Src phosphorylation (Fig. 3o) and induction of apoptosis (Fig. 3p and Supplementary Fig. 6d–g). Finally, we treated collagen-embedded cells with doxorubicin with and without inhibitors specific for FAK (PF-562271) or Src (Saracatinib) and observed a synergistic increase in growth inhibition (Fig. 3q), decreased phosphorylation of FAK and Src (Supplementary Fig. 9a), and induced apoptotic cell death (Supplementary Fig. 9b, c).

Targeting LOX or FAK/Src overcomes chemoresistance in vivo

To test if inhibiting LOX could overcome doxorubicin resistance and enhance drug response in advanced, chemotherapy-refractory TNBCs, we re-derived doxorubicin resistance in vivo, using a protocol similar to our initial acquired resistance model (though with lower doxorubicin dose), by treating MDA-MB-231 xenografts with doxorubicin until an accelerated tumor growth was achieved despite the given therapy. At this point, some of the doxorubicin-resistant tumors were treated with the combination of doxorubicin and BAPN while the rest continued to receive doxorubicin alone. Strikingly, addition of LOX inhibitor to doxorubicin in these aggressive, fast-growing doxorubicin-resistant tumors led to a significant decrease in tumor growth rate (Fig. 4a, b) and improved survival (Fig. 4c) until experiment termination when the tumor volume cut-off was reached or due to almost a 20% decrease in body weight in BAPN-added treatment arm (Fig. 4d). We confirmed the reduction of LOX activity (Fig. 4e) and fibrillar collagen (Fig. 4f, g) upon addition of BAPN to doxorubicin. These results were further validated by performing biochemical collagen assay (Fig. 4h), suggesting that chemosensitization with LOX inhibition involves reduction in collagen cross-linking.

**Fig. 4: Targeting LOX or downstream FAK/Src overcomes TNBC chemoresistance in vivo.**

We also evaluated the effects of LOX inhibition on doxorubicin response in vivo in an immunocompetent setting using a syngeneic TNBC model. The 4T1 mouse mammary tumor cell line is a highly aggressive model that represents the TNBC subtype⁵⁵ and exhibits relatively low response to doxorubicin. We examined the expression of LOX in 4T1 cells grown in vitro as well as in tumors and found that they express LOX at a level similar to the high LOX-expressing MDA-MB-231 model (Supplementary Fig. 10a, b). We observed a strong inhibitory effect of the combination therapy on tumor growth in this immunocompetent tumor model (Fig. 4i and Supplementary Fig. 10c, d). The LOX activity assay and picrosirius red staining confirmed the suppression of LOX activity and collagen cross-linking, respectively in all BAPN-treated tumors (Fig. 4j–l). This was accompanied by increased penetration of doxorubicin (Fig. 4m, n) and inhibition of FAK/Src signaling in the combination-treated tumors (Fig. 4o). To test the effect of FAK or Src inhibition on doxorubicin response in vivo, we combined specific inhibitors of FAK (PF-562271) or Src (Saracatinib) with doxorubicin and observed a significant decrease in tumor growth (Fig. 4p–s) and tumor weight (Supplementary Fig. 10e, f) in combination-treated tumors, validating the key roles of FAK and Src in doxorubicin resistance.

Next, we tested combination of LOX inhibition with doxorubicin in a highly aggressive TNBC PDX model. We first analyzed the gene expression profiling and drug response data of 15 well-characterized TNBC PDX models (Jackson Lab) and observed a significant positive correlation between LOX expression and hypoxia and focal adhesion scores (Fig. 5a). Based on these analyses, we selected a TNBC PDX model (TM01278) that is resistant to doxorubicin (and several other chemotherapy agents) and expresses high levels of LOX, hypoxia and focal adhesion scores (Fig. 5a). Then, we generated organoid cultures of this doxorubicin-resistant PDX tumor and demonstrated that combination of LOX inhibitor with doxorubicin significantly decreased organoid size compared to single agent treatments after 9 days of treatment (Fig. 5b, c). In vivo testing also showed a significant decrease in tumor growth upon combination therapy in this chemoresistant PDX model expressing LOX (Fig. 5d–f). These results complement our in vitro and in vivo findings with established cell lines and increase the clinical relevance of LOX inhibition to overcome chemotherapy resistance in TNBC. Importantly, we demonstrated reduced LOX activity (Fig. 5g) and fibrillar collagen content upon LOX inhibition with BAPN (Fig. 5h, i), which was accompanied by enhanced drug penetration into tumors (Fig. 5j, k) and more effective downregulation of downstream FAK/Src signaling in combination-treated tumors (Fig. 5l). Overall, we demonstrated that targeting LOX or its downstream FAK/Src overcomes chemotherapy resistance in highly aggressive, chemoresistant TNBC models.

**Fig. 5: Targeting LOX overcomes chemoresistance in highly aggressive TNBC PDXs.**

Targeting LOX at the first-line potentiates chemoresponse

Having identified LOX as a determinant of chemoresistance in TNBC, we tested whether LOX is also a target in potentiating chemotherapy response in first-line settings in treatment-naïve models using our inducible shLOX expressing MDA-MB-231 derivatives (referred to 231.shLOX) (Supplementary Fig. 11a, b). Inhibiting LOX in combination with doxorubicin as a first-line therapy led to a stronger delay in tumor growth as compared to individual treatments (Fig. 6a–e). We confirmed LOX knockdown at mRNA (Fig. 6f) and protein levels (Fig. 6g, h) and the decrease in LOX activity (Supplementary Fig. 11c) together with downregulation of its downstream ITGA5 (Supplementary Fig. 11d) after tumors were collected. We also demonstrated that other LOX family members did not decrease upon LOX knockdown (Supplementary Fig. 11e, f), further supporting our hypothesis that LOX inhibition is specifically involved in mediating chemoresponse in TNBCs. In consistent with the reduction in tumor growth, there was also a significant reduction in the proliferation marker, Ki-67 (Fig. 6i, j) and an increase in the expression of an apoptosis marker, Cleaved Caspase-3 (Fig. 6k, l) in combination-treated group as compared to LOX inhibition or doxorubicin treatment alone. Furthermore, ITGA5 levels, phosphorylation of Src (p-Y416) and FAK (p-Y397) were reduced upon LOX knockdown in combination with doxorubicin (Fig. 6m–q).

**Fig. 6: Targeting LOX at the first-line settings potentiates chemoresponse in TNBCs.**

Next, we examined the effect of combination therapy on the growth of a primary organoid model developed from a treatment-naïve TNBC patient. Combination treatment with doxorubicin and BAPN led to a significant reduction in organoid size as compared to individual treatment groups after 9 days of treatment (Fig. 6r, s). Altogether, these data demonstrate that inhibition of LOX could be a potential therapeutic strategy in combination with first-line chemotherapy in TNBCs.

miR-142-3p is a chemosensitizer regulating HIF1A/LOX/ITGA5

To elucidate the underlying molecular mechanisms of the coordinated activation of the HIF1A/LOX/ITGA5 axis under hypoxia, we sought for a common modulator. As miRNAs tend to function in a pathway-centric manner by targeting multiple genes in the same cascade⁵⁶, we searched for a potential miRNA modulator of HIF1A/LOX/ITGA5-mediated chemotherapy resistance. We examined all conserved miRNAs targeting HIF1A, LOX, and ITGA5 and found eight common miRNAs having binding sites in the 3′-UTRs of these three genes (Fig. 7a). Out of these eight miRNAs, only two miRNAs, miR-142-3p, and miR-128-3p, showed an inverse correlation with HIF1A signature, and LOX and ITGA5 expression in basal subtype (Fig. 7b and Supplementary Fig. 12a–c). One of these two miRNAs, miR-142-3p, showed a significant association with OS specifically in chemotherapy-treated TNBC patients (Fig. 7c, d and Supplementary Fig. 12d). Furthermore, miR-142-3p was significantly downregulated in doxorubicin-resistant xenografts that we developed in vivo as compared to sensitive ones (Fig. 7e). Importantly, induction of hypoxia inhibited the expression of miR-142-3p (Fig. 7f), while silencing HIF1A upregulated miR-142-3p expression (Fig. 7g), suggesting that hypoxia-mediated downregulation of miR-142-3p potentially involves HIF1A.

**Fig. 7: miR-142-3p regulates HIF1A/LOX/ITGA5 axis to confer chemosensitization in TNBC.**

We next tested to see if miR-142-3p could inhibit the expression of HIF1A, LOX or ITGA5. We overexpressed miR-142-3p in MDA-MB-231 cells and observed a significant downregulation of all three genes both at mRNA and protein levels, and a reduction in phosphorylation of downstream FAK/Src kinases (Fig. 7h, i). Importantly, downregulation of HIF1A, LOX and ITGA5 protein levels as well as decreased phosphorylation of FAK and Src was also seen in MDA-MB-231 xenografts stably expressing miR-142-3p (Fig. 7j and Supplementary Fig. 12e). The direct binding of miR-142-3p to the predicted binding sites in the 3′-UTRs of HIF1A, LOX, and ITGA5 (Fig. 7k) was validated by a dual luciferase assay (Fig. 7l). Finally, ectopic expression of miR-142-3p in TNBC cells grown in type I collagen sensitized to doxorubicin-induced growth inhibition and apoptotic cell death (Fig. 7m–p). We interpret these results to indicate that HIF1A and miR-142-3p are involved in a double-negative feedback loop that further increases HIF1A, LOX and ITGA5 levels under hypoxic conditions, leading to chemoresistant tumors, and that overexpression of miR-142-3p overcomes chemoresistance by inhibiting HIF1A/LOX/ITGA5 axis.

Discussion

TNBC is the most aggressive subtype of breast cancer and is responsible for 30% of all breast cancer deaths. Chemotherapy is the mainstay treatment for TNBCs; however, resistance is common, significantly decreasing long-term survival⁶. Therefore, novel strategies are urgently needed to enhance the clinical benefit from chemotherapy. Here, we identified a mechanism of chemotherapy resistance that involves activation of the HIF1A/miR-142-3p/LOX/ITGA5/FN1 axis in TNBCs. We showed that inhibiting LOX reduces the expression of ITGA5 and FN1, decreases extracellular collagen cross-linking, fibronectin deposition/assembly and enhances drug penetration that ultimately result in inhibition of FAK/Src signaling, resulting in apoptosis and reversal of chemotherapy resistance in TNBC cells cultured in contact with ECM (Fig. 3). These results were validated in acquired resistant TNBC xenografts and de novo resistant 4T1 syngeneic TNBC model (Fig. 4) as well as in well-characterized chemoresistant TNBC PDXs (Fig. 5). We also showed that targeting LOX potentiates chemotherapy in first-line settings (Fig. 6). Importantly, targeting the signaling molecules downstream of LOX, FAK or Src, strongly sensitized cancer cells to chemotherapy when grown in collagen-embedded cultures or in vivo, showing the key role of these pro-survival signals in driving resistance (Fig. 4). Finally, we showed a double-negative feedback loop between HIF1A and miR-142-3p regulating HIF1A/LOX/ITGA5/FAK/Src axis and chemoresistance in TNBC (Fig. 7).

The ECM re-modeler, LOX is a well-known modulator of cancer metastasis^29,44. LOX secretion from hypoxic tumors leads to collagen cross-linking at the pre-metastatic site and increases lung metastasis in TNBC models²⁸. Moreover, higher LOX expression was observed in metastatic brain tumors of breast cancer patients⁵⁷. Furthermore, Baker et al. demonstrated that LOX increases cell proliferation and invasion in colorectal cancer via Src activation⁵⁸ and enhances matrix stiffness, activates FAK, leading to invasion in vitro and metastasis in vivo in colorectal cancer⁵⁹. In terms of the potential effects of LOX on drug response, a few studies have reported an involvement of LOX in drug resistance that primarily focused on altered distribution/penetration of chemotherapeutics, including paclitaxel and gemcitabine in tumors as a consequence of LOX-mediated ECM stiffness under hypoxic conditions^30,53. In addition to forming a physical barrier, LOX-mediated ECM stiffness can also confer resistance via activating integrin receptors and the downstream effectors, FAK and Src kinases, leading to increased cellular survival⁶⁰. For instance, Miller et al. demonstrated that combination of a LOX antibody with gemcitabine improved survival of a pancreatic ductal adenocarcinoma (PDAC) model via inhibiting key microenvironment-mediated pro-survival signals without any evidence of increased penetrance of gemcitabine into tumors upon LOX inhibition³¹ in contrast to the studies described above^30,53. Furthermore, it was recently shown that LOX might also be involved in transcriptional regulation of certain genes⁶¹. In our study, we showed that LOX overexpression upon acquisition of doxorubicin resistance, on one hand, leads to protection against doxorubicin-induced FAK/Src inhibition by increasing collagen cross-linking, fibronectin assembly and decreasing drug penetration, and on the other hand, increases ITGA5 and FN1 expression, ultimately leading to increased FAK/Src signaling and chemoresistance. Considering the known potential of inhibiting FAK/Src kinases to enhance response to different chemotherapy agents⁶² and our data on the effect of LOX inhibition on FAK/Src signaling in chemosensitization, we propose that LOX inhibition reduces both the ECM stiffness to enhance drug penetration and the ITGA5/FN1 expression, thus culminating in inhibition of FAK/Src signaling, induction of apoptosis and chemosensitization. Overall, these findings suggest that LOX, which has primarily been studied in the context of metastasis, may also confer resistance to chemotherapy, making it a highly attractive therapeutic target.

Given the functional contribution of ECM modulation on different aspects of tumorigenesis, several inhibitors against multiple ECM modulators, such as matrix metalloproteinases, or the ECM-sensing integrin receptors have so far been developed. However, none of them achieved clinical success due to context-dependent efficacy, low specificity or severe toxicity⁶³. Furthermore, inhibitors targeting the HIF pathway have so far been unable to enter clinics due to the complexity of the HIF pathway and the difficulty in targeting protein-protein interactions⁶⁴. Therefore, identification of the well-defined modulators of ECM that are specifically overexpressed in aggressive, chemoresistant tumors, such as LOX that stands out as an attractive target with strong translational profile will be beneficial towards achieving a superior clinical outcome^44,65. In this line, we demonstrated that more than half of the chemoresistant TNBC patients express high levels of LOX mRNA (Supplementary Fig. 5a, b) and are therefore expected to respond to LOX targeting therapies in combination with chemotherapy. In addition, we showed that high expression of LOX protein is significantly associated with survival in a cohort of chemotherapy-treated TNBC patients. Moreover, we also demonstrated a superior anti-tumorigenic effect of doxorubicin in vivo and in a TNBC organoid when combined with BAPN in the first-line settings (Fig. 6) that altogether supports the translational potential of targeting LOX with a potentially large target population in the clinic. Although BAPN is the most commonly used LOX inhibitor, it inhibits all LOX family members. In this line, there have been several recent efforts to identify novel and selective small molecule inhibitors against different family members, including LOX⁶⁶ and LOXL2⁶⁷ that can hopefully be tested in clinics to improve patient outcome in aggressive cancers, including the chemoresistant TNBCs. Moreover, our in vitro and in vivo data showing strong chemosensitization upon inhibiting FAK or Src kinases suggest that FAK/Src axis is critical for tumor cell survival in the presence of chemotherapy and targeting these proteins could also be an effective strategy to overcome chemoresistance in TNBCs in the future. Indeed, inhibitors of FAK and Src kinases are currently being tested in clinical trials and demonstrate promising results when combined with targeted therapies or chemotherapy (e.g. NCT03875820 and NCT02389309, respectively).

Signaling pathways need to be tightly regulated and are repressed in the absence of a stimulus. This ensures that target genes are activated only in the presence of a signal. miRNAs have been shown to be key regulators of this repression by inhibiting the expression of several transcripts⁶⁸. Furthermore, others and us have previously shown that expression of genes functioning in the same cascade can be co-regulated by the same miRNA to ensure its robustness^56,68. Therefore, we asked if miRNAs can inhibit the HIF1A/LOX/ITGA5 axis and confer chemosensitivity. We identified miR-142-3p to be significantly downregulated in chemoresistant tumors by HIF1A, and its overexpression inhibits HIF1A, LOX and ITGA5 in a robust double-negative feedback loop, thus sensitizes cells to chemotherapy. Although we have shown that miR-142-3p is significantly associated with survival specifically in chemotherapy-treated TNBC patients, future studies including miRNA profiling or in situ hybridization in large chemotherapy-treated patient cohorts are warranted to fully uncover the potential of this miRNA as a biomarker and a therapy sensitizer in TNBCs.

In summary, we uncovered a molecular mechanism of chemotherapy resistance in TNBC involving hypoxia-driven LOX expression, which on one hand, leads to increased collagen cross-linking, fibronectin assembly and decreased drug penetration, and on the other hand, increases ITGA5 and FN1 expression, collectively leading to increased FAK/Src signaling, decreased apoptosis and chemoresistance. Furthermore, hypoxia-driven repression of miR-142-3p increases HIF1A, LOX, and ITGA5 expression, leading to further activation of FAK/Src signaling (Fig. 8). Based on these results, we propose that targeting LOX or its downstream FAK or Src or restoring the hypoxia-inhibited miR-142-3p can overcome chemoresistance by effectively blocking FAK/Src signaling (Fig. 8). Overall, our results provide valuable insights into how chemoresistance can be modulated at multiple levels and a pre-clinical support for inhibiting a key ECM-remodeler, LOX in TNBCs to potentiate chemotherapy response.

**Fig. 8: Mechanistic summary and targeting approaches for overcoming chemoresistance.**

Methods

In vivo experiments

To develop doxorubicin-resistant xenografts, 6–8-weeks-old female athymic nu/nu mice were injected with 2 × 10⁶ MDA-MB-231 cells into mammary fat pads (MFP). Mice were randomly allocated into two groups, and vehicle or doxorubicin treatments (5 mg/kg, weekly, i.v.) were started when tumors became palpable. Vehicle-treated tumors were collected and designated as vehicle. Half of the doxorubicin-treated mice were sacrificed when they were responsive to treatment, and tumors were collected and designated as sensitive. The remaining mice continued to receive doxorubicin until their tumors started regrowth. Then, these mice were also sacrificed, and tumors were collected and designated as resistant.

To test the role of LOX or FAK or Src inhibition to overcome chemotherapy resistance in immunocompetent setting, 2 × 10⁵ 4T1 cells were injected into the MFPs of 6–8 weeks-old Balb/c mice. Mice were treated with vehicle, doxorubicin (2.5 mg/kg, once a week, i.v.), BAPN (100 mg/kg, daily, ip.), PF-562271 (15 mg/kg, daily, oral), Saracatinib (25 mg/kg, daily, oral), or their combinations with doxorubicin. Once the vehicle group reached at 800 mm³, all mice were sacrificed, and tumor weight was measured.

For shLOX induction experiments using the luciferase overexpressing MDA-MB-231.Luc2GFP cells, doxycycline was given to induce shLOX expression at 100 ug/ml in drinking water when the tumors reach at 100 mm³. All mice were sacrificed; tumors were collected and weighed once the vehicle-treated tumors reached at 1500 mm³. For bioluminescence imaging, mice were intraperitoneally injected with 150 mg/kg D-luciferin (Perkin Elmer, MA, USA), and images were acquired with Lumina III In Vivo Imaging System (Perkin Elmer, MA, USA). Analysis was performed with Living image software by measuring photon flux.

For PDX experiments, 2–3 mm³ pieces of frozen PDX tumors were placed into the flank region of NSG mice. When tumors become palpable, mice were distributed into treatment groups. Doxorubicin (2 mg/kg, once a week, i.v.) and BAPN (100 mg/kg, daily, i.p.) was given individually or in combination for 30 days after which mice were sacrificed and tumors were collected for downstream analysis.

Primary tumor growth was monitored by measuring the tumor volume at least twice a week with a caliper after tumors became palpable. Tumor volumes were calculated as length × width²/2. All mice used were of the same age and similar body weight. All animal experiments have been approved by the Animal Ethics Committee of Bilkent University or the Institutional Animal Care and Use Committee of University of South Carolina. All mice were maintained under a temperature-controlled environment with a 12-h light/dark cycle and received a standard diet and water ad libitum.

Patient tumor-derived and PDX-derived organoids

For the generation of patient organoids, breast cancer surgical patients were consented under an IRB approved protocol for the USC-Palmetto Health Biorepository. TNBC organoids were established from a fresh surgical tissue by cutting the tumor into small pieces and incubating in collagenase A solution with ROCK inhibitor on a shaker at 37 °C for 30 min. The collagenase activity was inhibited by adding FBS, and pipetting was done to ensure the formation of almost a single cell solution. After several washes with PBS, the cell pellet was dissolved in matrigel. Breast organoid media containing ROCK and GSK inhibitors was added after the matrigel solidified⁶⁹. For the PDX organoid, a small, 2–3 mm³ piece of the PDX tumor that was freshly excised from an NSG mouse was minced and separated into single cell suspension as previously described⁷⁰. For drug testing studies, organoids were disrupted to single cells by digesting at 37 °C for 30 min with TrypLE (A1217701, Gibco, NY, USA) in the presence of 10uM Rock inhibitor (s1049, Selleckchem, TX, USA). Organoids were plated into wells of 96-well plate (20,000 cells/well) on a collagen-coated surface with media containing 2% matrigel (356252, Corning, NY, USA). Drugs were added 72 h after plating (final concentration of doxorubicin at 40 nM and BAPN at 25 mM). Cells were grown in the presence of drug(s) or vehicle for 9 days, and the diameter of organoids were measured.

Whole-transcriptome sequencing (RNA-seq) and data analyses

rRNA-depleted stranded libraries for each condition (four biological replicates for each of vehicle, doxorubicin-sensitive tumors and doxorubicin-resistant tumors) were generated and multiplexed. Paired-end 100 bp sequencing was performed using the Illumina HiSeq 2000 platform at McGill University and Genome Quebec Innovation Centre. In all, 60–70 million sequencing reads were obtained for each sample. Raw sequence reads were aligned to the UCSC human reference genome (hg19) using TopHat. with default parameters. To count the mapped reads, HTSeq was used with the reference genome annotation (USCS, hg19). In order to determine differentially expressed genes between doxorubicin-sensitive and doxorubicin-resistant groups, Bioconductor package, edgeR, was utilized.

Patient data analyses

To analyze the effects of LOX expression on the survival of chemotherapy-treated TNBCs, we performed IHC staining of LOX in primary tumor samples from 77 TNBC patients that were diagnosed with breast cancer between 2006 and 2015 at Hacettepe University School of Medicine, Ankara, Turkey and treated with chemotherapy (35% adjuvant anthracycline-based therapy, 43% anthracyclines in combination with taxanes and 22% other chemotherapy agents). The study was approved by the Non‐Interventional Clinical Research Ethics Committee of Hacettepe University (approval no: 2020/02-40). To generate DoxoR-GS scores in patients from METABRIC, GSE31519 and GSE58812, we used the top 441 differentially (up or down-regulated) expressed mRNAs between doxorubicin-sensitive vs. -resistant xenografts with a fold change cut-off of 1.75 and p-value cut-off of 0.05 (Supplementary Data 1). First, expression of these 441 genes in patients were converted into z-scores. Then, the sum of z-scores of the downregulated genes in the DoxoR-GS was subtracted from the sum of z-scores of the upregulated genes for each patient³⁵ using the SPSS Statistics software. Chemotherapy-treated patient subgroup from the KM Plotter database (release version 2017) were created by selecting the adjuvant chemotherapy-treated patients and excluding the endocrine-treated ones. In GSE19783 dataset, patients are stratified based on the PAM50 subtyping (basal patients were selected) and ERα, PR and HER2 expression.

Statistics and reproducibility

The results are represented as mean ± standard deviation (SD) or mean ± standard error of the mean (SEM), as indicated in the figure legends. All statistical analyses were performed in GraphPad Prism Software using two-sided Student’s t-test for comparisons between two groups, one-way ANOVA followed by Dunnett multiple comparison test for comparing combination treatment group with single agent-treated groups, and two-way ANOVA for comparing tumor volume change over time among different treatment groups. Survival curves were generated based on median separation using Kaplan–Meier method, and significance between groups was calculated by Log-rank test. For correlation analysis, Pearson correlation coefficients were calculated. Experiments were repeated two to three times independently with similar results.

Methods for cell culturing, cell-based assays, transient and stable transfections, qRT-PCR and Western blot analysis, immunofluorescence, immunohistochemical and Picrosirius red staining, Annexin V/DAPI staining, hypoxia, cloning, dual luciferase, LOX activity, collagen and deoxycholate lysis assays, other animal experiments, measuring doxorubicin penetration in vitro and in vivo, and patient data and pathway analyses were provided in Supplementary Methods. The list of primers for qRT-PCR, antibodies for Western blotting, IF and IHC as well as the primer sequences for 3′-UTR cloning are provided in Supplementary Table 4.

Reporting summary

Further information on research design is available in the Nature Research Reporting Summary linked to this article.

Data availability

The RNA-Seq data has been uploaded to the Sequence Read Archive (SRA) of NCBI with the submission ID: SUB6918779 (https://www.ncbi.nlm.nih.gov/bioproject/PRJNA607780). Data presented on Figs. 1d, f, 2b and Supplementary Figs. 2b, c, 4a, b were generated by analyzing the data available under the accession number GSE58812 from GEO depository (https://www.ncbi.nlm.nih.gov/geo/). Data presented on Figs. 1h, i, k, l, 2o and Supplementary Figs. 1d, e, 2a, d were generated by analyzing the KM Plotter database (http://kmplot.com/analysis/). Data presented on Fig. 7c, d and Supplementary Figs. 1a, 12d were generated by analyzing the METABRIC data from EMBL European Genome–Phenome Archive (http://www.ebi.ac.uk/ega/) with an accession number EGAS00000000122. GSEA gene sets were downloaded from the GSEA MSigDB Collections website: https://www.gsea-msigdb.org/gsea/msigdb/collections.jsp. Data presented on Fig. 7b and Supplementary Fig. 12a, b, c were generated by analyzing the data available under the accession number GSE19783 from NCBI. Data presented on Supplementary Figs. 1b, 5a were generated by analyzing the data available under the accession number GSE31519 from NCBI. Data presented on Supplementary Fig. 5b–e were generated by analyzing the data available under the accession number GSE25066 from NCBI. Data presented on Fig. 2h was generated by analyzing the data available under the accession numbers GSE16446, GSE19783, GSE21653, GSE22219, GSE22226, GSE25066, GSE58644 from NCBI and under METABRIC datasets and The Cancer Genome Atlas (TCGA) data. The source data underlying Figs. 1a–h, j, k; 2a–e, g–o, q; 3a–g, i, k–q; 4a–e, g–j, l, n–p, r; 5a, c–e, g, i, k–l; 6a, c, e–f, h, i, k, m, o, q, s; 7b, c, e–j, l, m, p and Supplementary Figs. 1a–c; 2a–c; 3a–b; 4c, d; 5c–e; 6b, f; 7a–d; 8a, c; 9a, c; 10a–c, e, f; 11b–f; 12e are provided as a Source Data file. All the other data supporting the findings of this study are available within the article and its Supplementary Information files and from the corresponding author upon reasonable request. A reporting summary for this article is available as a Supplementary Information file.

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Acknowledgements

We thank Madeleine Arseneault and Ozlem Sener Sahin for technical and organizational support, and Jitao David Zhang for his help with the initial analysis of RNA-Seq data. We also thank the Center for Targeted Therapeutics (CTT) Microscopy and Flow Cytometry Core (Dr. Chang-uk Lim) of the University of South Carolina, for assistance with flow cytometry. This work was supported by National Institutes of Health Grant 2P20GM109091-06 (O.S.), and in part by European Commission FP7 Marie Curie Career Integration Grant PCIG14-GA-2013-631149 (O.S.), European Molecular Biology Organization (EMBO) Installation Grant 2791 (O.S.), the American Cancer Society Institutional Research Grant IRG-17-179-04 (O.S.), the American Cancer Society Research Scholar Grant RSG-19-194-01-CSM (O.S.), Susan G. Komen Interdisciplinary Graduate Training to Eliminate Cancer Disparities (IGniTE-CD) GTDR17500160 (Ozge S.), the scholarship from Higher Education Commission of Pakistan (U.R.), and research scholarship of the Fonds de recherche du Québec—Santé (FRQS) (Y.R.).

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Department of Drug Discovery and Biomedical Sciences, University of South Carolina, Columbia, SC, 29208, USA
Ozge Saatci, Aysegul Kaymak, Carolyn E. Banister, Vitali Sikirzhytski, Phillip J. Buckhaults & Ozgur Sahin
Faculty of Science, Department of Molecular Biology and Genetics, Bilkent University, 06800, Ankara, Turkey
Umar Raza, Pelin G. Ersan, Ozge Akbulut, Unal Metin Tokat, Gamze Aykut, Suhail A. Ansari & Ozgur Sahin
Department of Medical Pathology, Ankara Yildirim Beyazit University, 06800, Ankara, Turkey
Hayriye Tatli Dogan
Department of Medical Pathology, Ankara Oncology Education and Research Hospital, 06200, Ankara, Turkey
Mehmet Dogan
Department of Human Genetics, McGill University, Montreal, QC, H3A 1B1, Canada
Pouria Jandaghi & Yasser Riazalhosseini
McGill University and Genome Quebec Innovation Centre, Montreal, QC, H3A 0G1, Canada
Pouria Jandaghi & Yasser Riazalhosseini
Hacettepe University Transgenic Animal Technologies Research and Application Center, 06100, Ankara, Turkey
Aynur Isik & Aytekin Akyol
Faculty of Medicine, Department of Pathology, Hacettepe University, 06100, Ankara, Turkey
Fatma Gundogdu, Kemal Kosemehmetoglu, Aytekin Akyol & Aysegul Uner
Department of Medical Oncology, Hacettepe University Cancer Institute, 06100, Ankara, Turkey
Omer Dizdar & Sercan Aksoy
Hacettepe University Molecular Pathology Research and Application Center, 06100, Ankara, Turkey
Aysegul Uner

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Ozge Saatci
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Contributions

Ozge S., A.K., and U.R. designed and performed experiments, acquired and analyzed data, interpreted data, and prepared the paper; P.G.E. and O.A. contributed to in vivo experiments, IHC staining and data collection; C.E.B. generated TNBC patient organoids; V.S. contributed to confocal microscopy experiments and data analyses; S.A.A. performed cloning and luciferase reporter experiments; U.M.T. contributed to RNA-seq analyses; G.A. contributed to in vivo experiments; H.T.D., M.D., performed the IHC staining of xenografts and contributed to data interpretation; P.J. performed RNA-sequencing; A.I., F.G., K.K., A.A., and A.U. performed the IHC staining of TNBC patient tissues and contributed to data interpretation; O.D. and S.A. provided clinical information of TNBC patients and contributed to data analyses; P.J.B. contributed to TNBC tumor organoid experiments and critically read and edited the manuscript; Y.R. performed RNA-sequencing, and critically read and edited the manuscript; O.S. designed the study, oversaw experiments and data analyses, and prepared the paper. All authors reviewed and commented on the paper.

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Correspondence to Ozgur Sahin.

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Saatci, O., Kaymak, A., Raza, U. et al. Targeting lysyl oxidase (LOX) overcomes chemotherapy resistance in triple negative breast cancer. Nat Commun 11, 2416 (2020). https://doi.org/10.1038/s41467-020-16199-4

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Received: 19 August 2019
Accepted: 20 April 2020
Published: 15 May 2020
DOI: https://doi.org/10.1038/s41467-020-16199-4

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