Cancer stem cell (CSC)-dictated intratumor heterogeneity accounts for the majority of drug-resistance and distant metastases of breast cancers. Here, we identify a SIRT1-PRRX1-KLF4-ALDH1 circuitry, which couples CSCs, chemo-resistance, metastasis and aging. Pro-longevity protein SIRT1 deacetylates and stabilizes the epithelial-to-mesenchymal-transition (EMT) inducer PRRX1, which inhibits the transcription of core stemness factor KLF4. Loss of SIRT1 destabilizes PRRX1, disinhibits KLF4, and activates the transcription of ALDH1, which induces and functionally marks CSCs, resulting in chemo-resistance and metastatic relapse. Clinically, the level of PRRX1 is positively linked to SIRT1, whereas KLF4 is reversely correlated. Importantly, KLF4 inhibitor Kenpaullone sensitizes breast cancer cells and xenograft tumors to Paclitaxel and improves therapeutic effects. Our findings delineate a SIRT1-centered circuitry that regulates CSC origination, and targeting this pathway might be a promising therapeutic strategy.
Tumor is composed of heterogeneous cell populations including those capable of self-renewal and multi-lineage differentiation, termed tumor-initiating cells or cancer stem cells (CSCs) . Accumulating evidence suggests that cancer stemness underlies the majority of drug-/radiation-resistance and recurrent metastases, accounting for more than 90% mortality . CSCs are identified with specific markers, such as CD44 and CD24 (breast CSCs), SSEA-1, ALDH1, and CD133 (lung CSCs) [3,4,5,6], the ability to expel DNA dyes, the formation of spheroids, and xenograft tumors . Where and how CSCs are originated has been a focus of cancer research, however, important questions remain . One hypothesis proposes that CSCs are transformed tissue stem cells , while others believes that cancer cells acquire stemness via dedifferentiation, sharing the same concept of induced pluripotency . Indeed, key stemness factor OCT3/4, SOX2, KLF4, and NANOG are active in certain tumors . Among the four factors, KLF4 serves in part as an upstream enforcer of feed-forward circuits involving OCT3/4 and SOX2, as well as downstream NANOG. Ectopic expression of KLF4 together with OCT3/4 and SOX2 is sufficient to reprogram somatic cells to pluripotent stem cells (iPSCs). Indeed, KLF4 is activated in diverse human cancers and predictive of mortality [12, 13]; however, the molecular mechanisms by which KLF4 is driven to induce CSCs remain less well documented.
Besides the intratumor genetic and phenotypic heterogeneity, CSCs maintain the plasticity of transition between epithelial and mesenchymal states via a process of epithelial-to-mesenchymal transition (EMT) and the reverse MET during metastasis . Indeed, the restoration of classical EMT transcription factors, such as SNAIL1/2, TWIST1/2, and ZEB1/2, serves as a main mechanism for induced CSCs [15, 16]. However, the relationship between EMT and CSC origination is seemingly controversial. For instance, some studies found EMT rather suppresses tumor-initiating abilities , i.e., suppression of PRRX1 promotes MET to enhance stemness and metastatic potential of breast cancers . The mechanisms involved in PRRX1-mediated acquisition of CSC properties remain unknown.
Aging is one major driver of human malignancy . Stem cell number and function drop with aging . However, the molecular mechanisms of such stem cell decline and their relevance to CSC initiation are still puzzled. NAD+-dependent deacetylase SIRT1 belongs to the most conserved longevity genes that link metabolism to stress response, endocrine mechanism, aging, and cancer . Here we did two round screens of aging-related genes  and identified SIRT1 as a central element regulating age-related CSCs in breast cancer. Depletion of SIRT1 remarkably increases the number of ALDH1+ CSCs, elicits partial MET, and promotes lung metastasis by upregulating KLF4 in human and mouse breast cancer cells. Molecularly, SIRT1 deacetylates and stabilizes PRRX1, an EMT inducer, whose destabilization promotes KLF4 transcription. KLF4 upregulates ALDH1 transcription and thus induces CSCs. KLF4 inhibitor Kenpaullone overcomes Paclitaxel (PTX) resistance imposed by SIRT1 deficiency and reduces lung metastasis in mouse models. Our data identify a SIRT1-PRRX1-KLF4-ALDH1 circuitry as a central regulator of CSCs and highlight its therapeutic potential in targeting the progression and metastasis of breast cancer.
A SIRT1-centered circuitry underlies age-related CSC induction
To understand potential links between aging and breast cancer stemness, we employed the GenAge Human Genes list to screen for genes that are correlated with core stemness factor OCT4, SOX2, NANOG, and KLF4 in a cohort of breast cancer cell lines collected from the TCGA database [11, 22, 23]. ALDH1A1/3 and CD44 were included as CSC markers in the analysis. As shown, 75 out of 300 genes are negatively correlated with the core “stemness” program, and 8 of the 75 are reversely correlated with ALDH1A1/3 or CD44 (Table S1). Interestingly, the top enrichment list includes SIRT1, which is centered in a KLF4-ALDH1A1-ALDH1A3 triangle of functionally interacting network (Fig. 1a). Further, nine genes in the OCT4-SOX2-NANOG-KLF4 circuitry and breast cancer CSC markers were analyzed and the correlation was assessed in breast cancer cell lines . A strong reverse correlation between SIRT1 and KLF4 was obtained (Fig. 1c and Table S2, R = −0.304, P = 0.026, determined by non-parametric Mann–Whitney t-test). Of note, a decline of SIRT7 was associated with high CD44 (Fig. 1a, b and Table S1, R = −0.2604, P = 0.0385). We recently demonstrated that SIRT7 deficiency activates TGF-β signaling, enhances EMT and promotes lung metastasis , and induces mesenchymal-like CSCs marked with CD44+CD24- in breast cancers (Figure S1), providing a proof of concept of aging-promoted CSC induction. To confirm the findings, we did pathway enrichment analysis via STRING v10 . The KEGG analysis showed an enrichment of pathways that safeguard genome integrity, wherein KLF4 and ALDH1A1/3 are the most correlated, followed by NANOG, then SOX2, and CD44 and OCT3/4 are the least and even lack of correlation (Fig. 1b and Table S3). Interestingly, EMT-type CSCs (CD44+) are associated with low SIRT7 and share similar set of genes with OCT3/4, suggesting differential roles of Sirtuins on breast cancer stemness: SIRT1 is related to MET-type CSCs (ALDH1+), whereas SIRT7 is correlated with EMT-type (CD44+). Together, the data points to a SIRT1-KLF4-ALDH1 circuitry, which couples aging and CSCs.
Genetic ablation of SIRT1 induces ALDH1+ CSCs via upregulating KLF4
CSCs are largely responsible for the recurrence and distant metastasis of breast cancer. To investigate the clinical relevance of these CSC-related genes, we analyzed their mRNA levels in cohorts of invasive breast carcinoma (IBC) collected from the Kaplan–Meier database . Significantly, two of them, i.e., SIRT1 and SIN3A, are positively correlated with relapse free survival (RFS) and distant metastasis free survival (DMFS) in IBCs (Figure S2A). Further, low SIRT1 level predicts poor survival, chemotherapy-resistance and metastasis of breast cancer (Figure S2B). We are particularly interested in SIRT1, whose precise function in CSCs remains less well documented.
To determine its molecular function in CSCs, SIRT1 was knocked out in triple-negative basal-like breast cancer BT-549 cells via a CRISPR/Cas9 procedure. As predicted, loss of SIRT1 increased the mammosphere-forming capacity by more than 3 folds (Fig. 2a–c). Similarly, knocking down Sirt1 in a murine triple-negative basal-like breast cancer cell line 4T1 significantly promoted mammosphere-formation (Figure S3A–C). We next did RNAseq and gene set enrichment analysis (GSEA) in SIRT1-deficient and control BT549 cells. As shown, cancer cells with SIRT1 depletion were positively associated with poor tumor differentiation (NES = −1.61, P<0.007) (Fig. 2d). These data implicate that SIRT1 deficiency promotes CSC-like phenotypes in breast cancer cells.
Having uncovered the role of SIRT1 deficiency in promoting breast cancer stemness, we then sought to identify its downstream effectors. Consistent with the predicted data (Fig. 1), SIRT1 KO BT549 cells exhibited increased expression of stemness factor KLF4, coupled with MET-type CSC marker ALDH1A1 (Figure S4A). In contrast, the expression of EMT-type CSC marker CD44 was far from pronounced. Quantitative RT-PCR confirmed that SIRT1 deficiency increased expression of KLF4 and ALDH1A1 in both human BT549 cells and mouse 4T1 cells (Fig. 2e and S3D).
The predicted and experimentally validated co-expression suggest potential molecular crosstalk between KLF4 and ALDH1A1. To test the hypothesis, we first compared the expression of KLF4, ALDH1A1, ALDH1A3, CD44, and CD24 in human breast cancer samples available in TCGA database . Indeed, the mRNA levels of KLF4 and ALDH1A1 are significantly correlated across all samples by Pearson correlation analysis (Figure S4B, R = 0.3014, P<0.0001). The mRNA level of KLF4 from all 683 samples was also correlated with that of ALDH1A3 (R = 0.0915, P = 0.0168), but not CD44 or CD24. We further analyzed microarray dataset GSE52262 and GSE52327  and found that the mRNA level of SIRT1 was decreased but that of KLF4 was elevated in ALDH1+ population isolated from human breast cancers (Fig. 2f). In contrast, the negative correlation was not observed in CD44+CD24- population. To understand the precise function of KLF4 on ALDH1, we performed online data analysis and found four putative binding sites of KLF4 in the promoter region of ALDH1A1/3 (Figure S4C). We cloned the promoter regions of ALDH1A1 and ALDH1A3 for luciferase assay. As shown, the activity of luciferase driven by both promoters was significantly increased upon HA-KLF4 overexpression (Figure S4D). We further performed quantitative RT-PCR and Western blotting analysis. Knocking down KLF4 by shRNA in SIRT1 KO BT549 cells (SKO) downregulated both mRNA and protein levels of ALDH1, which were, however, elevated upon ectopic expression of HA-KLF4 (Fig. 2g, h). Consistently, as assessed by ALDEFLUOR assay, the induction of ALDH1+ breast CSCs by SIRT1 deficiency is significantly correlated with KLF4 level (Fig. 2i, j).
Previous reports identified that ALDH1+ population has high proliferative capacity and enhanced mammosphere-forming capacity . Indeed, we found that silencing KLF4 in SKO cells inhibited both number and size of mammospheres (Fig. 2k, l). On the other hand, KLF4 restoration rescued the proliferative phenotype and mammosphere formation in parental cells (Fig. 2k, l and S4E). Thus, the data support KLF4 as a key CSC-related transcription factor, reversely regulated by SIRT1 in breast tumors.
KLF4 upregulation is likely owing to elevated histone H3 lysine 9 acetylation (H3K9ac) in promoter region caused by SIRT1 removal (Figure S5A). To test the hypothesis, we performed chromatin immunoprecipitation (ChIP) assay in BT549 cells overexpressing SIRT1. However, neither direct binding of SIRT1 or enrichment of H3K9ac was found at the KLF4 promoter region in SKO cells (Figure S5B–C). Therefore, KLF4 is unlikely to be a direct SIRT1 target in our experimental context.
PRRX1 underlies SIRT1 deficiency-induced CSCs
In initial stage of somatic reprogramming, KLF4 activates MET. Moreover, silencing SIRT1 induces epithelial-like ALDH1+ CSCs in BT549 breast cancer cells, which are basal-like and originally enriched with mesenchymal traits. Therefore, we reasoned that the EMT-MET program might be involved in SIRT1 deficiency-induced CSCs. To test the hypothesis, we compared the RNAseq data (GSE112365) of control and SKO cells, and found a significant downregulation of EMT program in SKO cells (Fig. 3a). Further, a partial MET was evidenced by the restoration of membranous E-Cadherin and the reduction of Fibronectin in SIRT1 KO BT549 cells (Fig. 3b). EMT-MET program is regulated by a group of transcription factor ZEB1/2, TWIST1, SNAIL1, SLUG, and PRRX1. However, quantitative RT-PCR analysis in BT549 and 4T1 cells revealed that silencing SIRT1 by either CRISPR/Cas9 or shRNA barely altered the mRNA levels of these EMT transcription factors (Figure S6 and S3E). Instead, the protein level of PRRX1 was found decreased in SKO cells (Fig. 3c). Knocking down SIRT1 downregulated the level of PRRX1 but upregulated that of E-Cadherin, KLF4 and ALDH1A1 in mouse 4T1 cells (Fig. 3d).
We then asked whether PRRX1 regulates CSCs via the SIRT1-KLF4-ALDH1 axis. To this end, TRANSFAC and JASPAR databases were employed to search for potential transcriptional regulatory elements in KLF4 promoter. Interestingly, a PRRX1-binding motif was identified (Figure S7A), suggesting that the decline of PRRX1 most likely underlines the MET transition and CSC phenotypes induced by SIRT1 deficiency. We thus generated PRRX1 KO (PKO) BT549 cells via CRISPR/Cas9 system and examined the mesenchymal and epithelial traits. Similar to SKO, depletion of PRRX1 induced an epithelial shift, abrogated mesenchymal traits and inhibited cell invasion in PKO cells (Fig. 3e, f).
PRRX1 has two isoforms, PRRX1A and PRRX1B, which share identical N-terminus (a.a. 1–199) but different C-terminus (Figure S7B). We found that PRRX1B was much more highly expressed than PRRX1A in BT549 cells (Figure S7C). Further determined by ChIP-qPCR analysis, FLAG-PRRX1B rather than FLAG-PRRX1A was enriched at a −100 to +223 region of KLF4 promoter, suggesting potential binding motifs (Fig. 3g). Next, the ~1.3 kb KLF4 promoter region containing the predicted PRRX1-binding core sequence TCGGCCAATTT was cloned and subjected for luciferase reporter assay. As shown, the activity of KLF4 promoter-driven luciferase was significantly reduced upon FLAG-PRRX1 transfection (Fig. 3h). In addition, a 4-bp mutation (AATT to GGCC) in the seed sequence restored PRRX1-suppressed luciferase activity. These data suggest that PRRX1 binds to the TCGGCCAATTT motif locating in the downstream of KLF4 transcription start site, and block its transcription.
To determine whether PRRX1 regulates KLF4 transcriptipn in vivo, we re-introduced the abundant isoform PRRX1B into SKO cells and compared KLF4 mRNA transcripts. A quantitative assessment revealed that loss of SIRT1 or PRRX1 markedly increased the mRNA level of KLF4, and re-introduction of PRRX1B completely restored KLF4 transcripts to levels close to those in parental cells (Fig. 3i). Next, we examined the correlation of SIRT1, KLF4, and PRRX1 in EMT transition and sphere forming abilities. Depletion of SIRT1 or PRRX1 induced distinct morphological change from spindle-like to cobblestone-like appearance, which was completely reversed by ectopic PRRX1B (Fig. 3j). Both SKO and PKO cells showed mixed epithelial/mesenchymal traits, i.e., a partial MET. Restoration of PRRX1 in SKO cells reversed MET, i.e., upregulation of N-Cadherin but loss of E-Cadherin, accompanied with a reduction of KLF4 (Fig. 3k). Compared with control BT549 cells, we observed 3.4-fold increase and 4.9-fold increase in the number of mammospheres in SIRT1-depleted and PRRX1-depleted cells, respectively (Fig. 3l). Notably, the mammosphere-forming capability of SKO cells with ectopic PRRX1B was comparable to that of parental controls, likely due to direct suppression of KLF4 transcription. Together, the data implicate that PRRX1 underlies SIRT1 deficiency-induced CSCs.
SIRT1 deacetylates PRRX1
SIRT1 is a NAD+-dependent deacetylase regulating various proteins. We hypothesized that SIRT1 might deacetylate PRRX1. As determined by co-immunoprecipitation (Co-IP), the binding between SIRT1 and PRRX1 was consistently observed (Fig. 4a, b). The interaction was confirmed by fluorescence microscopy displaying co-localization of SIRT1 and PRRX1 in MEFs (Fig. 4c), and co-localized GFP-SIRT1 and DsRed-PRRX1 in HEK293 cells (Figure S8). To determine specific domains that mediate such interaction, GST-tagged full-length SIRT1 (GST-SIRT1FL), N-terminal SIRT1 (GST-SIRT1 1–244), enzymatic domain of SIRT1 (GST-SIRT1245–498), and C-terminal SIRT1 (GST-SIRT1499–747) were expressed in bacteria, purified and incubated with Myc-PRRX1. Myc-PRRX1 was pull down by GST-SIRT1FL and GST-SIRT1245–498 but not GST-SIRT11–244, GST-SIRT1499–747 or GST (Fig. 4d), supporting a direct interaction between PRRX1 and SIRT1.
We next examined whether SIRT1 deacetylates PRRX1. As shown, the acetylation level of PRRX1 was inhibited by a pan-sirtuin inhibitor nicotinamide (NAM) and a SIRT1-specific inhibitor EX527, but not class I/II histone deacetylase (HDAC) inhibitor TSA (Figure S9A). To test whether SIRT1 deacetylates PRRX1, FLAG-PRRX1 constructs were transfected into Sirt1+/+ and Sirt1-/- MEFs, followed by immunoprecipitation using antibody against FLAG to determine acetylation level of FLAG-PRRX1. As expected, SIRT1 depletion led to a significant increase in acetylated FLAG-PRRX1 (Fig. 4e). Cells treated with specific siRNA against SIRT1 showed a significant increase in the acetylation level of FLAG-PRRX1 compared with scramble (Figure S9B). Direct deacetylation of PRXX1 by SIRT1 was evaluated using an in vitro deacetylation assay, wherein purified protein FLAG-PRRX1 was incubated with recombinant human SIRT1 (rhSIRT1) and its acetylation level was determined. As shown, SIRT1 deacetylated PRRX1 in an NAD+-dependent manner, and that was abolished by NAM, a pan-Sirtuin inhibitor (Fig. 4f). To determine the lysine residues that are deacetylated by SIRT1, we performed site-directed mutagenesis, mutating lysine (K) to arginine (R) to mimic nonacetylated form, i.e., K31/32R, K89/90/91/93R, K148R, K160R, and K166R. As shown, the acetylation of FLAG-PRRX1 was completely abolished in K160R mutant, while others were barely affected (Fig. 4g). Overexpression of SIRT1 decreased the acetylation level of Myc-PRRX1, but enzyme-dead mutant H355A loosed such ability (Fig. 4h). In addition, neither WT nor H355 A SIRT1affected the acetylation level of K160R mutant. These results suggest that K160 is a deacetylation site directly regulated by SIRT1.
SIRT1-mediated deacetylation prevents proteasomal degradation of PRRX1
Given only protein level was affected, it is most likely that SIRT1 deficiency-mediated PRRX1 decline is attributable to accelerated protein degradation. Indeed, the treatment with proteasome inhibitor MG132 reversed the degradation of endogenous PRRX1 in the presence of protein synthesis inhibitor cycloheximide (CHX) (Figure S9C), suggesting that SIRT1 regulates PRRX1 protein stability via ubiquitination-proteasome system. To test it, FLAG-PRRX1-expressing HEK293 cells were treated with EX527, NAM, or TSA, and the protein levels were examined. In the presence of CHX, both EX-527 and NAM destabilize FLAG-PRRX1, whereas TSA merely affected it (Figure S9D). To determine whether SIRT1 activity is essential for PRRX1 stability, we co-transfected wild-type and enzyme-dead H355A SIRT1 with Myc-PRRX1 construct to HEK293 cells, treated the cells with CHX, and then monitored the decline of Myc-PRRX1 by Western blotting. As shown, the degradation rate of Myc-PRRX1 was reduced in the presence of SIRT1 instead of H355A (Fig. 5a), suggesting that SIRT1-mediated deacetylation prevents the proteasome degradation of PRRX1.
To address how SIRT1 increases PRRX1 protein stability, we examined ubiquitination of WT, K160R and K160Q PRRX1. SIRT1 might deacetylate PRRX1 at K160 to inhibit preferential attachment for ubiquitin. As shown, poly-ubiquitination of PRRX1 K160R was largely impaired, whereas that of K160Q was enhanced (Fig. 5b). Consistently, K160R inhibited but K160Q accelerated the protein degradation of Myc-PRRX1. The degradation of Myc-PRRX1 was rescued by MG132, indicating that it is, at least partially, subjected to proteasomal degradation (Fig. 5c). The half-life of Myc-PRRX1 WT, K160R, and K160Q are around 5.4 ± 0.3, 14.7 ± 3.0 and 4.9 ± 0.3 h, respectively (Fig. 5d). Together, the data implicate that SIRT1 deacetylates PPRX1 to inhibit its polyubiquitination and proteasomal degradation.
Given that PRRX1 deficiency promotes MET and CSCs in breast cancer , we reasoned that re-introduction of PRRX1 would reverse MET and CSC-like phenotypes in SIRT1-depleted cells. To test it, WT and K160R PRRX1 were reconstituted in SKO cells. As shown, reconstitution of K160R suppresses KLF4 and ALDH1 expression (Fig. 5e), and abolished the mammosphere formation (Fig. 5f), accompanied with deceased ALDH activity (Fig. 5g). To evaluate the in vivo relevance, we explored a MMTV-PyMT transgenic model of breast cancer and isolated primary mammary tumors for Western blotting analysis (Fig. 5h). Quantitative data confirmed a strong positive correlation between endogenous SIRT1 and PRRX1 levels in breast tumors (R = 0.867, P = 0.001). Collectively, our data support the notion that PRRX1 instability, at least partially, underlies SIRT1 deficiency-induced epithelial plasticity and CSC properties of breast cancers.
Suppressing KLF4 sensitizes breast cancer cells to chemotherapy
CSCs accounts for the majority of drug-resistance of breast cancer; the SIRT1-PRRX1-KLF4 core circuitry might regulate such chemo-resistance. We evaluated the impact of SIRT1 deficiency or KLF4 overexpression on apoptosis or cell survival in response to Paclitaxel (PTX), which belongs to the most frequently applied cytotoxics. However, almost half of subjects develop resistance after first treatment . Here, log-dose curves and IC50 values of control and various mutant cells were determined by MTT assay. Depletion of SIRT1, PRRX1 or re-introduction of KLF4 in BT549 cells rendered the cells more resistant to apoptosis; the PTX resistance caused by SIRT1 deficiency was reversed by ectopic expression of PRRX1 K160R or silencing KLF4 (KKD) (Fig. 6a). This is consistent with the apoptotic data as adjudged by Annexin V/PI staining (Fig. 6b).
We reasoned that combination of chemotherapy and KLF4 inhibitors like Kenpaullone (KEN) might have a synergetic effect on killing breast cancer cells. In particular, log-dose response analysis showed a KLF4-dependent cytotoxicity of KEN in BT549 cells (Fig. 6c). Adding non-cytotoxic concentration of KEN significantly sensitized breast cancer cells to PTX with minimal IC50 (Fig. 6d). Given the excellent tolerability of KEN, we assessed the effect of combined treatment with PTX and KEN on the highly aggressive and multidrug-resistant murine 4T1 cells. As shown, PTX alone decreased the tumor size, while PTX plus KEN almost abrogated the tumor formation (Fig. 6e). Consistent with in vitro cultured BT549 cells, co-treatment with PTX and KEN not only downregulated KLF4 level but also induced cell death (1.8-fold increase of TUNEL-positive cells relative to PTX only group) in 4T1 xenografts (Fig. 6f–h). Histological examination revealed that lung metastatic lesions derived from KEN-treated mice was smaller than those received vehicle (Fig. 6i), with strong membranous staining of E-cadherin. Further, while PTX alone had a modest effect on the survival of 4T1 and SKO BT549-bearing mice, PTX plus KEN administration resulted in significantly improved survival (Fig. 6j and S10A). Mice treated with vehicle or PTX alone often died from lung metastases (Fig. 6i and S10B-C). Together, pharmacological intervention of KLF4 elicits strong therapeutic effect on chemo-resistance induced by SIRT1 or PRRX1 deficiency.
The SIRT1-PRRX1-KLF4 core circuitry controls breast cancer metastasis
Spatiotemporal heterogeneity caused by EMT-MET transition and CSCs also underlies cancer metastasis . The partial MET and cancer stemness induced by SIRT1 deficiency, and the correlation between SIRT1 and DMFS prompted us to investigate the function of SIRT1-PRRX1-KLF4 axis in breast cancer metastasis. To this end, 5 × 106 parental and various mutant BT549 cells were injected intravenously into nude mice. As shown, the lungs of all five mice were colonized by SKO cells within 60 days, and PKO and KLF4-overexpressing BT549 cells formed micro-metastases within 30 days (Fig. 7a). Significantly, overexpression of PRRX1 K160R suppressed lung metastasis in SKO cells: only 1 out of 5 mice formed metastatic lesions. Almost no metastatic lesions were detected in all mice injected with unmodified BT549 cells, supporting an essential role of the SIRT1-PRRX1-KLF4 axis in regulating breast cancer metastasis. Further, Immunofluorescence staining demonstrated that these metastases were positive for E-Cadherin and ALDH1 (Fig. 7b), highlighting the significance of MET-type CSCs in breast cancer metastasis. Interestingly, while some tumor cells in the metastatic lesions of SKO cells still retained keratin 5 (CK5), an undifferentiated marker of basal lineage, some cells in these lesions activated expression of keratin 8 (CK8), a marker of luminal cells. These results suggest that loss of SIRT1 induces dedifferentiation and increases cellular heterogeneity. In the metastatic lesions of PKO or KOE cells, keratins 5 and 8 were co-expressed (Fig. 7b), indicating that these cells are immediate progenitors.
To further investigate the clinical relevance of the SIRT1-PRRX1-KLF4 axis, human breast cancer arrays were subjected for immunohistochemical microscopy analysis. The overall clinicopathologic parameters were summarized in Figure S11A-C. While SIRT1 was found in both nucleus and cytoplasm, PRRX1 was predominantly nuclear (Fig. 7c). A significant positive correlation (R = 0.38, P = 0.0012) between nuclear SIRT1 and PRRX1 was observed in breast carcinomas (Fig. 7d). Considering the nuclear proportion of SIRT1 might be more relevant in regulating PRRX1, we evaluated the correlation between nuclear SIRT1 and breast malignancy. In this case, 50% (60 of 120) malignant tissues and 94% (30 of 32) metastases were nuclear SIRT1 negative/low (Fig. 7e), suggesting a reverse correlation between nuclear SIRT1 and breast cancer progression. Likewise, 40% (27 of 68) invasive ductal carcinoma, 68% (15 of 22) invasive lobular carcinoma and more than 94% (30 of 32) metastases were completely negative for PRRX1 (Fig. 7f), whereas 90% (27 of 30) ductal/lobular carcinoma in situ and fibroadenoma were positive. Importantly, the nuclear proportion of SIRT1 and PRRX1 are significantly correlated with each other, i.e., more than 90% metastases were nuclear SIRT1-PRRX1 double negative/low (Fig. 7g, P<0.001), supporting a SIRT1-PRRX1 axis in regulating breast cancer metastasis.
We next did immunohistochemical analysis of KLF4 on 122 subjects of breast cancer to validate the association between KLF4 and SIRT1 and to elucidate the clinical relevance of KLF4 overexpression in patients with distal metastases. As shown, a significant reverse correlation (R = −0.18, P<1 × 10−4) between KLF4 and SIRT1 was observed in these specimens, wherein 79% (42 of 53) of the tumors with low SIRT1 exhibited high KLF4 expression, and 75% (52 of 69) of the tumors with high SIRT1 exhibited low KLF4 (Fig. 7h). In breast cancer patients, decrease of SIRT1 was associated with reduced PRRX1 but increased KLF4 (Figure S11D), and the latter was positively correlated with distal metastases (P<0.001, χ2 test) (Fig. 7i).
Collectively, the data suggest that SIRT1 blocks the transition between epithelial and mesenchymal state of breast cancer cells. It elicits such function via deacetylating and stabilizing the EMT inducer PRRX1, which inhibits the transcription of core stemness factor KLF4. Loss of SIRT1 destabilizes PRRX1 and leads to upregulation of KLF4, accompanied with partial MET. KLF4 subsequently promotes transcription of ALDH1, which induces and marks CSCs, and clinically leads to chemo-resistance and metastatic relapse (Fig. 7j).
Independent studies found that the reprogramming factor OCT3/4, SOX2, NANOG, and KLF4 induce CSCs in human mammary epithelial cells and promote carcinogenesis in vivo [31, 32]. Among these factors, KLF4 functions to enhance OCT3/4 and SOX2. Here, we performed a bioinformatics screening in a list of aging-related genes and identified a SIRT1-KLF4-ALDH1 circuitry driving CSC origination. This process is mediated by an EMT inducer PRRX1 and accompanied with partial MET. Indeed, the sequential activation of EMT-MET enhances efficiency of somatic reprogramming [33, 34], and is also critical for tumor initiation, progression, and metastasis . In breast cancer, EMT-type CSCs with high CD44 but low CD24 in the invasive front and MET-type CSCs expressing high level of ALDH1 in the tumor interior co-exist . Dynamic epithelial and mesenchymal transition might dictate different pluripotent stages of CSCs, which are coordinated by a series of EMT inducers. Several types of carcinoma cells have been found to gain tumor-initiating capability, usually depicted as the defining trait of CSCs, after induction of EMT [16, 35]. Yet other studies report the presence of proposed MET-type CSCs via downregulating PRRX1, rather than carcinoma cells that undergo an EMT [14, 18]. The roles and underlying mechanism for PRRX1 in cancer pathogenesis and the origination of MET-type CSCs remain unknown.
In this study, we revealed a novel SIRT1-PRRX1-KLF4 circuitry, whereby SIRT1 deacetylates and thus prevents the proteasomal degradation of PRRX1.We demonstrate that PRRX1 exerts its stemness-promoting effect on breast cancer cells by orchestrating the crosstalk between epithelial and proliferative states via transcriptional regulation of KLF4. Loss of PRRX1 disinhibits KLF4 transcription, which activates functional breast CSC marker ALDH1A1 and ALDH1A3. SIRT1 depletion enhances epithelial plasticity in basal-like breast cancer cells, induces highly proliferative MET-type ALDH1+ CSCs, confers cellular resistance to chemotherapy and promotes distant metastases.
Increasing proofs support a partial MET or hybrid EMT/MET in cancer metastasis . Here, an upregulation of epithelial E-Cadherin but reduced mesenchymal Fibronectin were shown, while other mesenchymal traits like N-Cadherin and Vimentin remained unchanged. Only epithelial like ALDH1-positive cells were present in lung metastases, suggesting the contributing role of epithelial plasticity in metastatic localization in the context of SIRT1 or PRRX1 deficiency or KLF4 overexpression. This is consistent with a recent report revealing the coexistence of epithelial and mesenchymal traits in primary breast tumors, but only epithelial cells metastasize to murine lung .
The role of SIRT1 in breast malignancy and metastasis has been controversial . SIRT1 was found elevated in leukemia, skin cancer, prostate cancer, and colon cancer [39,40,41,42], but decreased in colorectal adenocarcinoma . In contrast, most studies in transgenic models support a tumor-suppressing role of SIRT1 as no increased tumor formation has been documented so far [44, 45]. In this study, if nuclear and cytoplasmic proportions are considered, 52% cases of malignant or metastatic breast cancers were SIRT1 negative or low. This is indeed consistent with the public data that 20–50% cases were SIRT1 negative/low [46,47,48,49]. As a transcription factor, PRRX1 is predominantly localized in the nucleus. Given that PRRX1 directly interacts with SIRT1, the nuclear proportion of SIRT1 seems more relevant in the SIRT1-PRRX1 axis. Remarkably, nuclear staining of the SIRT1-PRRX1 axis were absent/low in more than 45% cases of IBC and 90% lymph node metastases, thus providing potential diagnostic and therapeutic targets for human breast malignancies. In line with our data, a predominant cytoplasmic localization of SIRT1 has been reported in a group of cancer cells, owing to aberrant PI3K/IGF-1R signaling . It would be worthwhile to investigate whether PI3K/IGF-1R signaling is affected in human breast cancers in future study, especially those showing increased cytoplasmic but reduced nuclear level of SIRT1. Nonetheless, our findings emphasize the significance of protein subcellular distribution in cancer biology, diagnosis and targeted therapy, and explain the seeming discordance between SIRT1 and human breast cancer in the literature. Further, as it works as key regulator in the SIRT1-PRRX1-KLF4 axis, PRRX1 likely plays a more dominant role in breast cancers. Indeed, we found that PRRX1 declines along tumor progression and is stained negative in 78% metastases, making it alone a potential diagnostic biomarker for breast cancer. Collectively, we propose that depleting SIRT1 accelerates the degradation of PRRX1 and disinhibits KLF4 transcription, leading to a partial MET, ALDH1-positive CSCs, and distant metastases. Reduced nuclear level of SIRT1-PRRX1 axis is positively correlated with lung metastasis of breast cancer. The findings not only shed light on the understanding of roles for SIRT1 in regulating breast malignancy, but also indicate a unique mechanism of CSC origination, malignant transformation, and metastasis.
Materials and Methods
Cell lines, constructs and oligos
Human BT-549 breast cancer cell line was obtained from American Type Culture Collection (ATCC), and is free of mycoplasma contamination. HEK293T cells and mouse embryonic fibroblasts (MEFs) were maintained in Gibco® DMEM (Life Technologies) supplemented with 10% FBS (Biosera America), 1% non-essential amino acid (Life Technologies) and 0.1 mM 2-mercaptoethanol (Sigma-Aldrich). BT549 cells were cultured in Gibco® RPMI 1640 (Life Technologies) supplemented with 10% FBS. For mammosphere formation, single BT-549 cells were plated in MammoCult® Medium (Stem Cell Technologies), at a density of 2 × 103 cells/cm2. After a 10-day culture, mammospheres larger than 150 μm in diameter were photographed and counted. Cells were treated with MG132 (Sigma-Aldrich), Cycloheximide (CHX) (Sigma-Aldrich), Trichostatin A (TSA) (Sigma-Aldrich), Nicotinamide (NAM) (Sigma-Aldrich), Ex-527 (Sigma-Aldrich), Paclitaxel (PTX) (Sigma-Aldrich), or Kenpaullone (KEN) (Sigma-Aldrich) for the indicated time at various concentration.
SIRT1 (h) and Sirt1 (m) siRNA oligos were purchased from Life Technologies. EGFP-SIRT1 construct was a gift from Dr Qiwei Zhai (Shanghai Institutes for Biological Sciences, China). FLAG-SIRT1 construct was from Dr. Zhenkun Lou (Mayo Clinic College of Medicine, USA). pcDNA3.1-HA-KLF4 full length construct was purchased from Addgene (Plasmid #34593). Full-length PRRX1A and PRRX1B were amplified from human cDNA using PrimeSTAR® GXL DNA Polymerase (Takara) and cloned into pDsRed1-Express-C1 and pET28a (+) (Clontech®). Full-length PRRX1 ORF with 3 × FLAGs was cloned into pcDNA3.1 (+)/Myc-his (Life Technologies) through NheI and HindIII cutting sites. The K31/32 R, K89/90/91/93 R, K148R, K160R, K160Q, and K166R mutants were introduced into full-length PRRX1B by PCR-driven overlap extension using the two PCR primer pairs shown in Table S4. ~1.2 kb KLF4 promoter region (WT and mutant) were amplified from BT549 genomic DNA using PrimeSTAR® GXL DNA Polymerase (Takara) and cloned into pDsRed1-Express-C1 and pET28a (+) (Clontech®). F Digestion enzymes were from New England Biolabs.
Normal transfection was performed with FuGENE® 6 Transfection Reagent (Promega) and Opti-MEM® medium (Life Technologies) according to the manufacturer’s instructions. siRNA transfection was performed with Lipofectamine® RNAiMAX Transfection Reagent (Life Technologies). Drug-resistant colonies were picked and expanded to establish stable cell lines.
Six-week-old female athymic nu/nu mice were purchased from Vital River Company. Animals were randomly assigned to the treatment group by simple randomization, and investigator was single blinded during group allocation. Mice were housed and handled in accordance with protocols approved by the Committee on the Use of Live Animals in Teaching and Research of Shenzhen University.
CRISPR/Cas9-mediated genome editing
The CRISPR/Cas9-mediated gene mutagenesis was conducted as described . Briefly, pX459 vector (Addgene#48139) was digested with BbsI and ligated with annealed oligonucleotides. BT-549 cells were transfected with pX459-gSIRT1 or pX459-gPRRX1 using Lipofetamine® 3000 Transfection Reagent according to manufacturer’s introductions. After transfection, cells were selected with 1 μg/ml puromycin (Invitrogen). The targeted mutation(s) were confirmed by DNA sequencing (BGI) and western blot analysis.
After sample preparation by fixation, permeabilization, and blocking, the slides were incubated with primary antibody diluted in 1% BSA/PBST at 4 °C overnight. Following primary antibody incubation, the slides were then washed twice with PBST and incubated with conjugated secondary antibodies (Life Technologies) for 1 h at room temperature. Following secondary antibody incubation, the slides were washed three times with PBST and cover-slipped with SlowFade® Gold antifade reagent with DAPI (Life Technologies). Immunostained samples were imaged using Zeiss LSM710 confocal microscopes and analyzed with the Zen software. Photos were processed with Photoshop CS®.
Cell viability and apoptosis assays
Cell viability assays were performed using MTT dye (3-(4, 5-Dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide) method. Relative cell numbers were determined by staining with MTT dye at indicated time point, dissolving the stained cell with SDS-Dimethylformamide solution, and measuring with a spectrometer (OD590). Apoptosis was measured by flow cytometry with the FITC Annexin-V Apoptois Detection Kit (BioVision) according to the manufacturer’s instruction. Annexin V+PI– and Annexin V+PI+ cells were considered early and late apoptotic cells, respectively.
ALDEFLUOR Kit (Stem Cell Technologies) was used for the identification of ALDH high and low expression cells according to manufacturer’s protocol.
Protein extraction, Western blotting, and Co-immunoprecipitation
Lysates from cells in culture were prepared by suspending in suspension buffer (0.1 M NaCl, 10 mM Tris-HCl [pH 7.5], 1 mM EDTA [pH 8.0], 1 mM DTT and protease inhibitors) and a same volume of Laemmli buffer (0.1 M Tris-HCl [pH 7.0], 4% SDS, 20% glycerol, 1 mM DTT and protease inhibitors), and boiled for 10 min. Western blotting was performed according to standard procedures and quantified by Image J®. For statistical analysis, at least three independent immunoblots were analyzed. For co-immunoprecipitation, cells were lysed into cold RIPA 250 buffer (50 mM Tris-HCl [pH 7.4], 250 mM NaCl, 0.5% NonidetP-40, 1 mM EDTA, 1 mM DTT, 10 mM NAM and protease inhibitor cocktail). 2 μg primary antibodies or appropriate control IgGs (Santa Cruz) were added to the lysates and incubated for 2 h on a rocking platform at 4oC, following incubation with Protein G Agarose beads (Life Technologies) for overnight. The beads were then washed twice with lysis buffer and boiled in SDS sample buffer. Subsequently, the protein suspension was collected and detected by western blotting.
Glutathione S-Transferase (GST) pull-down assay
GST or GST fusion proteins was expressed in Rosetta (DE3) induced by 0.4 mM isopropyl-β-D-thio-galactoside. The pellet of bacteria was resuspended in TEN buffer (20 mM Tris-HCl [pH 7.4], 0.1 mM EDTA, and 100 mM NaCl) supplemented with 1 mM DTT and protease inhibitor cocktail and sonicated. The resulting soluble fractions were incubated with Glutathione Sepharose® 4 fast flow (GE Healthcare) and then washed twice. Purified Myc/His-Prrx1 protein was expressed in bacteria, purified and incubated with GST or GST fusion proteins. After incubation at 4℃ for 4 h with rotation, the beads were washed four times with TENT buffer (0.5% Nonidet P-40, 20 mM Tris-HCl [pH 7.4], 0.1 mM EDTA, and 300 mM NaCl) and analyzed by western blotting with anti-Myc or anti-GST antibody.
RNA isolation, reverse transcription, and quantitative PCR analysis
Total RNA was extracted using TRIZOL® reagent (Life Technologies). Complementary DNA was synthesized with 2 μg of total RNA by using SuperScript® III First-Strand Synthesis System (Life Technologies). Quantitative PCR was performed with SYBR® Ex Taq Premixes from Takara on an ABI StepOne plus system (Applied BioSystems). Gene specific primers used in the study are listed in Table S4. The quality of the amplified fragments was controlled by the melting curve. Transcipt levels were normalized with GAPDH and relative mRNA levels in experimental samples were normalized to controls.
Cells were grown to 80% confluence and cells were then crosslinked with 1% formaldehyde and processed. The crosslinking, immunoprecipitation, washing, elution, reverse crosslinking, and proteinase K treatment were performed according to the manufacturer’s directions described in the Magna ChIP G Chromatin Immunoprecipitation Kit from Millipore. Purified immunoprecipitated DNA was used for quantitative RT-PCR.
Luciferase reporter assay
HEK293T cells were seeded in 12-well plates 24 h before transfection. The following day, various plasmids together with reporter plasmid and Renilla-luciferase control vector was co-transfected. Cells were collected 48 h post-transfection and assayed for luciferase activity by using a Varioskan Flash spectral scanning multimode reader (Thermo Scientific).
In vitro deacetylation assay
Constructs encoding FLAG-tagged PRRX1 and PRRX1K160R were separately transfected in HEK293T cells. The lysates were immunoprecipitated by anti-FLAG® M2 Agarose (Sigma-Aldrich). The bound proteins were eluted by competition with a large excess of free FLAG peptides. Purified proteins were incubated with 1 µg GST-SIRT1 protein in the deacetylation buffer (50 mM Tris–HCl [pH 8.0], 0.8 mM MgCl2, and/or 1 mM NAD+. Meanwhile, 10 mM NAM) at 30 °C for 15 min with constant agitation. Meanwhile, 10 mM NAM was added in one reaction to inhibit SIRT1 deacetylase activity. The reactions were then stopped and the acetylation level was determined by western blotting with anti-acetyl lysine antibody.
Tumorigenesis and metastasis assay
105 4T1 cells were subcutaneously injected into the inguinal mammary gland. Tumor volume (mm3) was determined by measuring length (l) and width (w) and calculating volumes (V = lw2/2). Control and mutant BT-549 cells were propagated as monolayers and trypsinized. For tail injection, cells were resuspended in PBS at a concentration of 5 × 106 cells/ml. 100 μl cell suspension was injected into tail veins. At the endpoint, all of the mice were sacrificed and the tissues were removed, fixed in 4% Paraformaldehyde (PFA), paraffin-embedded and sectioned. The TUNEL working procedure was carried out following the producer’s directions (Roche).
Paraffin-embedded sections of PFA-fixed tumors were stained with anti-E-Cadherin monoclonal antibody. HRP-conjugated anti-mouse secondary antibody was added and detected according to the manufacturer’s protocol (Daco).
Human breast cancer array
The human tissue array (catalog# BR2082a and BR2082b) was bought from Cybrdi Shanxi ChaoYing Biotechnology, China. All the pathologic diagnosis was supplied in the manufacturer’s instructions of the product. Tissue staining was classified as negative, low, medium, and high according to the staining intensity and the percentage of positive cells. A χ2 test was used to evaluate where there is a significant association between SIRT1 and Prrx1 or KLF4 expression.
Data were analyzed using Prism 5.0 (GraphPad Software). The correlations were determined by a Pearson’s coefficient of correlation (r). Statistical comparisons between two groups were accessed by two-tailed student’s t-tests. Error bar represents standard error of the mean (SEM). The use of statistical tests was chosen according to the nature of the data. Statistical significance was defined as P values of<0.05.
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The authors thank Dr Qi-Wei Zhai (Shanghai Institutes for Biological Sciences, China) for EGFP-SIRT1 construct and Dr Zhen-Kun Lou (Mayo Clinic College of Medicine, USA) for FLAG-SIRT1 construct. This project is supported by research grants from National Natural Science Foundation of China (81422016, 91439133, 81571374, 81501206 and 81702909), National Key R&D Program of China (2017YFA0503900 and 2016YFC0904600), Research Grant Council of Hong Kong (773313 and HKU2/CRF/13G), Natural Science Foundation of Guangdong Province (2014A030308011 and 2015A030308007), Shenzhen Science and Technology Innovation Commission (CXZZ20140903103747568, JCYJ20160226191451487 and JCYJ20130329104732074), Discipline Construction Funding of Shenzhen (2016) and China Postdoctoral Science Foundation (2015M582419).
Conflict of interest
The authors declare that they have no conflict of interest.
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Shi, L., Tang, X., Qian, M. et al. A SIRT1-centered circuitry regulates breast cancer stemness and metastasis. Oncogene 37, 6299–6315 (2018). https://doi.org/10.1038/s41388-018-0370-5
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