Abstract
In the tumor microenvironment, cancer cells experience hypoxia resulting in the accumulation of misfolded/unfolded proteins largely in the endoplasmic reticulum (ER). Consequently, ER proteotoxicity elicits unfolded protein response (UPR) as an adaptive mechanism to resolve ER stress. In addition to canonical UPR, proteotoxicity also stimulates the selective, autophagy-dependent, removal of discrete ER domains loaded with misfolded proteins to further alleviate ER stress. These mechanisms can favor cancer cell growth, metastasis, and long-term survival. Our investigations reveal that during hypoxia-induced ER stress, the ER-phagy receptor FAM134B targets damaged portions of ER into autophagosomes to restore ER homeostasis in cancer cells. Loss of FAM134B in breast cancer cells results in increased ER stress and reduced cell proliferation. Mechanistically, upon sensing hypoxia-induced proteotoxic stress, the ER chaperone BiP forms a complex with FAM134B and promotes ER-phagy. To prove the translational implication of our mechanistic findings, we identified vitexin as a pharmacological agent that disrupts FAM134B-BiP complex, inhibits ER-phagy, and potently suppresses breast cancer progression in vivo.
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Introduction
Cancers often encounter a characteristic microenvironment called tumor microenvironment (TME), which comprises of chemical (pH, hypoxia, metabolite concentration) and cellular milieu (blood vessels, immune suppressor cells, fibroblasts, extracellular matrix, stromal cells) that influences the growth of cancerous cells [1,2,3,4]. Hypoxic environment arises as a result of vascular insufficiency during the tumor expansion and progression [5]. It alters the cancer cell metabolism and contributes to therapy resistance by activating adaptive responses such as endoplasmic reticulum (ER) stress, anti-oxidative responses, and autophagy [6]. Therefore hypoxia is considered a major impediment for effective anti-cancer therapy [5, 7].
ER is a multifunctional organelle with a central role in protein synthesis, modifications, and transport. The disulfide bonds that are formed during protein synthesis are independent of oxygen availability whereas the bonds that are formed during the post-translational folding in the ER are oxygen-dependent [8]. This process is altered during hypoxia resulting in the accumulation of misfolded/unfolded proteins in the ER lumen, therefore perturbing its homeostasis. Thus, hypoxia directly impacts protein modifications in the ER leading to the activation of UPR to preserve ER homeostasis [9]. UPR is a signaling system which activates cellular responses coordinated via three key regulators—inositol-requiring enzyme 1 (IRE1), PKR-like ER kinase (PERK), and activating transcription factor 6 (ATF6) [10,11,12,13]. Binding immunoglobulin protein (BiP or glucose-regulatory protein 78—Grp78) is a chaperone abundantly present in the ER, which transiently binds to the luminal domain of UPR receptors—IRE1, PERK, and ATF6 [14]. When the misfolded/unfolded proteins begin to accumulate in the ER, BiP rapidly dissociates from the three UPR signaling sensors and binds the exposed hydrophobic regions of the nascent polypeptides to facilitate proper folding [13]. In addition, UPR also induces autophagy as a key response to the stress pathway activation in cancer cells which allows them to maintain metabolic homeostasis [15,16,17].
Autophagy involves the sequestration of cytoplasmic components into autophagosomes, which then fuse with lysosomes and degrade their contents [18]. Although autophagy is a constitutive homeostatic mechanism which regulates intracellular recycling, it is also a major stress responsive mechanism that facilitates the removal of damaged proteins and organelles [19]. Hence, autophagy bestows tolerance to stress and sustains cell viability under hostile conditions and is considered a “double-edged sword” because of its ability to suppress tumor yet promote tumor survival under stress [19]. Despite accumulating evidences suggesting that autophagy is critical in cancer, it is still a question of intense debate and remains complex [20]. For a long time autophagy was considered a non-selective degradation pathway; however, it can selectively degrade specific organelles including mitochondria (mitophagy), peroxisomes (pexophagy), ER (ER-phagy), nucleus (nucleophagy) [18], and aggregate-prone proteins (aggrephagy) [21].
ER-phagy was first described by Peter Walter’s group [22] where they demonstrated that selective engulfment of ER into autophagosomes utilize several autophagy proteins following UPR and this process is essential for the survival of cells exposed to severe ER stress. ER was originally considered only as the primary source of autophagosome membranes [23] and ER membranes observed in autophagosomes was viewed as a result of bulk engulfment of cytosol [23, 24]. After the identification and characterization of specific receptors that mediate the elimination of ER through autophagosomes, this type of selective autophagy was termed “ER-phagy or reticulophagy” [25]. To date, eight ER-resident proteins have been identified as selective ER-phagy receptors: FAM134A [26], FAM134B [27], FAM134C [26], RTN3 [28], SEC62 [29], CCPG1 [30], ATL3 [31], TEX264 [32,33,34], and the soluble ER-phagy receptors CALCOCO1 [35] and C53 [36].
Here we report that in cancer cells, hypoxia-induced ER stress activates ER-phagy through the ER-phagy receptor FAM134B. Upon hypoxic stress, FAM134B is included in a complex with the ER chaperone BiP to target discrete zone of ER for autophagic degradation. Inhibition of ER-phagy, by silencing FAM134B, or BiP reduces breast cancer cell proliferation. To prove concrete translational implications to these mechanistic aspects, we have identified vitexin as a pharmacological inhibitor of BiP complex regulated ER-phagy that potently limits the tumor burden in a breast cancer xenograft model.
Results
Hypoxia induces ER stress response and autophagy
Hypoxia is characterized by the stabilization of HIF-1α. Hence, we first investigated if HIF-1α is expressed and stabilized in our model of MCF-7 breast cancer cells upon hypoxic stress induced chemically using cobalt chloride (CoCl2) or growing cells in hypoxic environment (1% O2) for 24 h. Although CoCl2 has been widely used as a chemical inducer of hypoxia, reports indicate that CoCl2 activates a complex relationship between adaptive and cell death responses [37]. We observed HIF-1α expression was concentration dependent for CI-hypoxia (Supplementry Fig. 1a). We chose 500 µM of CoCl2 as an optimal concentration to induce HIF-1α (Fig. 1a). Exposing MCF7 cells to hypoxic environment (HE) also resulted in HIF-1α expression and stabilization (Supplementary Fig. 1b). Time-lapse imaging of MCF-7 cells treated with CoCl2 at 500 µM for 24 h showed more than twofold increase in cell proliferation compared to the untreated cells (normoxic cells) (Fig. 1b; Videos 1 and 2). Similar increase in cell proliferation was also observed when cells were cultured in 1% O2 environment (HE) (Fig. 1c).
Hypoxia results in the accumulation of unfolded/misfolded proteins in the ER causing ER-stress and cancer cells adapt by activating UPR mechanisms which enable them to survive and proliferate [4, 9]. Confocal microscopy of cells expressing mCherry-ER-3 (Calreticulin-KDEL) and grown in HE showed altered ER structure compared to cells under normoxic culture conditions (Fig. 1d). Furthermore, transmission electron microscopy (TEM) revealed discontinuous ER structures when MCF7 cells were subjected to CI-hypoxia (Fig. 1e) or HE (Fig. 1f) respectively. Consistently, UPR markers BiP, spliced XBP1 (XBP-1s), CREB-2/ATF4 and CHOP, monitored via quantitative real-time PCR (qRT-PCR) (Supplementary Fig. 1c–f) and western blot (Fig. 1g), showed significant upregulation upon CI-hypoxia. Increased expression of UPR target proteins was also confirmed in cells grown in HE (Fig. 1h).
These data suggest that hypoxia induced HIF-1α and ER-stress response correlates with increased cancer cell proliferation.
Hypoxia induces ER-phagy to maintain ER homeostasis
It is well-known that autophagy is required for the survival of hypoxic cancer cells [38] and it assists in the degradation of misfolded/unfolded proteins to reestablish ER homeostasis [4, 39]. To this end, we next investigated whether autophagy is induced in cancer cells under hypoxia. In cells subjected to CI-hypoxia (Fig. 2a and Supplementary Fig. 2a) and HE (Supplementary Fig. 2b, c), LC3B showed increased conversion to its lipidated form (LC3II) compared to the normoxic cells. Moreover, inhibition of lysosomal activity using concanamycin A led to further increase in the accumulation of LC3II in cells treated with CoCl2 (Fig. 2a and Supplementary Fig. 2a). Remarkably, MCF7 cells in CI or HE conditions, showed increased distribution of WIPI-1 compared to normoxic cells Fig. 2b and Supplementary Fig. 2d–f). Similarly, LC3B puncta were also observed in the hypoxic regions of MMTV-pyMT mouse breast cancer tissue characterized by HIF-1α in the nucleus (Fig. 2c). During autophagy induction, damaged organelles are selectively targeted into autophagosomes for degradation. TEM of MCF7 cells subjected to CI-hypoxia and HE showed accumulation of damaged ER within autophagosomes when lysosomes were inhibited using concanamycin A (Fig. 2d). WIPI-1 was also found to colocalize with calnexin in MCF7 cells subjected to CI-hypoxia (Fig. 2b and Supplementary Fig. 2d) and HE (Supplementary Fig. 2e, f). Consistent results were obtained from time-lapse imaging of CI-hypoxic cells (Videos 5 and 6). TEM and co-localization of WIPI-1 with the ER suggested that damaged ER is possibly engulfed by autophagosomes to mitigate ER-stress caused by hypoxia. Therefore, we questioned if the recently described ER-selective autophagy (ER-phagy) [40, 41], was involved in the removal of damaged ER. We investigated the steady-state levels of ER-phagy-specific receptors such as FAM134B, RTN3, SEC62, CCPG1 and the COPII subunit SEC24C, which have been shown to target ER for autophagosomal degradation [42]. We did not observe any change in the protein abundance of CCPG1, RTN3, and SEC24C except a modest increase in SEC62 (Supplementary Fig. 2g). In contrast, FAM134B significantly decreased upon CI-hypoxia and in cells grown in HE (Fig. 2e and Supplementary Fig. 2h). However, removal of hypoxic stress by replacing CoCl2 with medium without CoCl2 restored the steady-state levels of FAM134B levels (Fig. 2f and Supplementary Fig. 2i). We found that the decline in FAM134B was due to lysosomal degradation as inhibition of lysosomal activity using concanamycin A prevented FAM134B degradation during HE-hypoxia (Fig. 2g and Supplementary Fig. 2j) and CI-hypoxia (Supplementary Fig. 2k). We also observed a similar degradation of FAM134B in U251 glioblastoma cells (Supplementary Fig. 2l) and C32 melanoma cells (Supplementary Fig. 2m) indicating ER-phagy as a general mechanism that cancer cells exploit to counteract hypoxia-induced stress. In addition, we observed FAM134B degradation when ER-stress was induced using tunicamycin in MCF7 cells, but it did not occur when cells were starved by depleting serum in the culture medium (Supplementary Fig. 2n). This suggests that, in MCF7 cells, FAM134B degradation occurs only upon ER-stress but not specific to hypoxia induced ER-stress. Furthermore, we observed co-localization between LC3 and FAM134B in hypoxic cells expressing HA-tagged FAM134B (Fig. 2h and Supplementary Fig. 3a,b) and in MMTV-pyMT mouse breast cancer tissue sections (Fig. 2i and Supplementary Fig. 3c). Moreover, LC3B co-immunoprecipitated with endogenous FAM134B under hypoxic conditions while there was little interaction between FAM134B and LC3B in control cells, strongly supporting an increase in ER-phagy upon hypoxia (Fig. 2j). Having found that hypoxia induces ER-phagy, we next examined if FAM134B-dependent ER-phagy contributes to ER-stress and cell proliferation upon hypoxia. As previously shown, CI-hypoxia increased UPR but, knocking down FAM134B (Supplementary Fig. 3d) further enhanced the induction of UPR proteins (Fig. 2k and Supplementary Fig. 3e–g) and transcription of UPR genes BiP, XBP-1s, and ATF4/CREB2 (Supplementary Fig. 3h–j) meaning increased ER-stress. Silencing FAM134B modestly reduced cell proliferation under normoxic conditions but was highly reduced under hypoxic conditions (Fig. 2l).
These observations indicate that hypoxia induces ER-phagy to overcome ER-stress and that FAM134B-dependent ER-phagy is vital for cancer cells to proliferate under hypoxic stress.
Hypoxia induced ER-phagy is BiP dependent
Since we deciphered that hypoxia leads to activation of UPR and FAM134B-dependent ER-phagy, we asked whether this circuit is HIF-1α dependent. Although depletion of HIF-1α (Supplementary Fig. 4a) limited hypoxia-induced UPR (Fig. 3a–e), degradation of FAM134B was not affected in cells subjected to CI-hypoxia (Fig. 3f and Supplementary Fig. 4b) and HE (Fig. 3g and Supplementary Fig. 4c). This suggests that hypoxia-induced ER-phagy is independent of HIF-1α but, triggered by an alternative pathway most likely connected to the presence of misfolded ER proteins. FAM134B lacks an intraluminal domain therefore, we wondered if it indirectly senses the accumulation of unfolded/misfolded proteins likely through an ER stress chaperone. We observed that, silencing BiP prevented the degradation of FAM134B during hypoxia (Fig. 3h and Supplementary Fig. 4d) signifying that ER-phagy is BiP dependent during hypoxic stress in MCF7 cells. BiP was also found to colocalize with FAM134B when cells were subjected to HE (Fig. 3i and Supplementary Fig. 4e). Consistently, BiP co-localized with FAM134B in MMTV-pyMT mouse breast cancer tissue sections (Fig. 3j and Supplementary Fig. 4f) and in human breast cancer tissues (Fig. 3k and Supplementary Fig. 4g). Of note, BiP co-immunoprecipitated with endogenous FAM134B when MCF7 cells were subjected to hypoxia (Fig. 3l). In addition, silencing BiP significantly reduced the proliferation of MCF7 breast cancer cells under normoxic and hypoxic conditions (Fig. 3m).
Taken together, these data show that ER-phagy is a specific response to ER-stress and is coregulated by BiP and FAM134B.
In silico molecular docking studies identified Vitexin as a potential BiP inhibitor
Above shown results revealed that ER-phagy alleviates ER-Stress response and facilitates the survival and progression of hypoxic cancer cells. Hence, the selective disruption of this axis may have a tremendous clinical value. To this end, we retrieved the high-resolution X-ray crystal structure of the protein from the Protein Data Bank (PDB ID: 5F0X.pdb, Resolution: 1.6 Å). We next performed molecular docking studies using Schrödinger Suite 2015-3. A small set of small molecules library was docked onto the ATP/ADP-binding site, which is occupied by the subdomains Ia, Ib, and IIa of the protein [43] and identified an apigenin flavone glucoside, vitexin, as a potential molecule targeting BiP (docking scores are shown in Supplementary Table 1). Vitexin showed lowest glide score towards BiP, i.e., −8.3 kcal/mol (Supplement Table 1). The putative binding mode of vitexin and important residues in the binding site of the BiP are shown in Fig. 4a, b. The binding site comprises a higher number of charged and polar residues. Vitexin was bound inside the binding site by two strong hydrogen bonding interactions between OH of the glucoside and the side chain of amino acid residues N389 and R367. The keto group of the flavanone moiety forms hydrogen bond interaction with S300 and arene-hydrogen interaction with R297 (Fig. 4c). These predicted interactions of vitexin resulted in top rank based on the docking score meaning higher binding affinity when compared to the other molecules screened against BiP. As a next step, we performed molecular dynamics simulations of the BiP-vitexin complex for explaining the stability of the predicted binding pose in the binding site of the protein and compared with the simulations of the protein structure without the ligand inside the binding site. The calculated root mean square deviation (RMSD) values of the Cα atoms of the complex and the apo structure rapidly reached an equilibrium state with approximately 1 Å deviation from the first frame of 100 ns simulations (Fig. 4d). The visual analysis of the trajectories shows that vitexin was anchored inside the binding site with the interaction pattern identified from the docking studies (Supplementary Fig. 5a and Supplementary Video 7). It maintains the key hydrogen bond interaction with the three residues (N389, R367, and S300) and possible arene interactio7n with R297. The root mean square fluctuation (RMSF) value of the protein showed a profile with large fluctuations in the Cα atoms are more stabilized in the BiP in complex with vitexin when compared to the protein without the binding of vitexin in the binding site (Fig. 4e). Based on these findings using molecular docking and molecular dynamics approaches, we subjected vitexin for further in-vitro validation.
Vitexin prevents FAM134B-BiP interaction and inhibits ER-phagy
Since our in silico molecular dynamics studies deciphered vitexin as a potential inhibitor of BiP, we next examined BiP protein levels in hypoxic cells treated with vitexin. Consistently, vitexin treatment downregulated BiP during hypoxia (Fig. 5a, b). Indeed, treatment with vitexin also downregulated CI-hypoxia induced UPR at the mRNA (Supplementary Fig. 6a–d) and protein levels (Supplementary Fig. 6e). We then asked if treatment with vitexin prevented the interaction of FAM134B with BiP during hypoxia. Strikingly, BiP did not coimmunoprecipitate with FAM134B upon vitexin treatment in hypoxic cells (Fig. 5c) and was found to less colocalize with BiP (Fig. 5d and Supplementary Fig. 6d). Furthermore, immunoblot analysis revealed that vitexin prevents autophagosomal degradation of FAM134B during CI-hypoxia (Fig. 5e, f) and HE-hypoxia (Fig. 5g, h). Consistently, time-lapse imaging of vitexin-treated cells expressing GFP-WIPI-1 and mCherry-ER-3 exhibited accumulation of autophagosomes. Thus, autophagic flux and protein turnover were inhibited leading to cell death (Video 8 and 9).
Collectively, these data confirm that vitexin blocks ER-phagy by inhibiting BiP from forming a complex with FAM134B
Vitexin reduces cancer cell proliferation and tumor burden in breast cancer xenograft mouse model
Having shown that vitexin inhibits ER-phagy, we surmised that it could inhibit cancer cell proliferation under hypoxic stress. As expected, vitexin treatment effectively prevented the increase in cell proliferation upon hypoxic stimuli (Fig. 6a). As we propose that ER-phagy resolves ER-stress, we also explored if vitexin can synergistically inhibit cancer cell growth with an ER-stress inducer tunicamycin. We observed that vitexin and tunicamycin synergistically inhibited cancer cell growth (Fig. 6b). We next asked if vitexin can reduce tumor burden in female balb/c athymic (nuþ/nuþ) mice xenografted with MCF7 cells. We found that after 13, 17, and 21 days of vitexin treatment, tumor volume was significantly reduced compared to the vehicle-treated mice (Fig. 6c, d).
Taken together, we could conclude that vitexin shows a higher therapeutic potential in treating breast cancer.
Discussion
Identification of receptors that specifically target damaged organelles and proteins into autophagosomes for degradation assists in discriminating from functional organelles. Recently, specific receptors have been identified to target damaged or excess parts of ER into autophagosomes for elimination and this process has been termed ER-phagy [44]. Here, we report that cancer cells undergo ER-phagy regulated by a complex including FAM134B and BiP when they are subjected to hypoxic stress which helps the cells to mitigate ER-stress and promote cell proliferation (Fig. 6e).
Numerous studies have confirmed that the TME promotes cancer progression due to the ability of tumor cells to overcome stress and survive in the hostile microenvironment. Hallmark of TME is diminished levels of oxygen (<2%) which is essential for a cell to meet its bioenergetic needs [45]. Hypoxic conditions can be mimicked in the laboratory by either growing the cells in a hypoxic incubator with reduced levels of oxygen or treating cells with CoCl2 [46]. Cells undergoing hypoxic stress stabilize HIF-1α which we could observe in cells subjected to CoCl2 treatment and those grown in a reduced Oxygen environment. Oxygen is not only required to meet the metabolic needs of the cells but is also essential for protein disulfide bond formation during protein-folding in the ER [8]. However, hypoxia disrupts protein folding resulting in the accumulation of unfolded/misfolded proteins causing ER-stress and cell death [47]. Cancer cells alleviate ER-stress by activating UPR characterized by the expression of BiP, XBP1-s, CHOP, and ATF4 [48, 49]. Our data also suggest that UPR could be regulated by HIF-1α in hypoxic cells as depletion of HIF-1α abrogates the expression of UPR proteins while the molecular mechanism by which HIF-1α regulates UPR remains to be investigated.
UPR has been shown to induce autophagy which helps in the removal of misfolded proteins and damaged organelles, thus preventing DNA damage and cancer progression. On the contrary, when the cancer cells undergo nutrient starvation or hypoxia, autophagy acts as a quality control mechanism to overcome the stress and survive [19]. Consistently, autophagy is increased when cancer cells are subjected to hypoxic stress as determined by LC3I to II conversion. Autophagy encompasses autophagosome formation marked by LC3 conversion and degradation of the cargo by fusion with the lysosomes. During general/macroautophagy, LIR (LC3-interacting region) motif containing adaptor proteins recognize ubiquitinated substrates and target them for autophagic degradation by binding to LC3 [50, 51]. Mounting evidence suggest that autophagy selectively degrades damaged organelles to maintain cellular homeostasis. In line with this, hypoxia has been shown to target mitochondria (mitophagy) [52] and peroxisomes (pexophagy) [53] for autophagic degradation.
As hypoxia causes damage to ER, a failure to restore ER structure and homeostasis could be lethal to cells. Restoration of ER is achieved by the removal of excess and damaged ER caused by ER-stress. Recent evidences suggest that ER can be selectively targeted for lysosomal degradation by ER-phagy [54]. UPR has also been linked to the activation of ER-phagy; however, no direct evidence linking hypoxia and ER-phagy has been reported thus far. Our data show that ER is selectively targeted for degradation in autophagosomes during hypoxia. Several proteins containing LIR motif have been shown to function as ER-phagy receptors, which have been shown to recruit subregions of the ER into autophagosomes [42]. For instance, FAM134B is localized on the edges of the ER sheets where protein synthesis and folding occurs, and has a clear role in maintaining ER volume and proteostasis [27, 28]. The reticulon homology domain (RHD) of FAM134B aids in the fragmentation of ER and LIR motif sequesters the fragmented ER into autophagosomes [25]. Hypoxia resulted in the co-localization of FAM134B with autophagosomal marker LC3 and was subsequently degraded in lysosomes indicating that cancer cells remove damaged ER by activating FAM134B-dependent ER-phagy. In addition, silencing of FAM134B during UPR results in cell death [27]. Consistently, hypoxia stimulated ER-stress reduces the viability of FAM134B-depleted breast cancer cells. We also observed a modest increase in SEC62 which has been shown to specifically regulate the recovery of ER [29, 55] but was not targeted for autophagic degradation during hypoxia. However, we cannot exclude the involvement of other ER-phagy receptors, which will be explored in the future. Notably, hypoxia upregulates FAM134B expression in chronic myeloid leukemia (CML) cells and is correlated with pro-survival [56]. It is also speculated that its upregulation is HIF-1α dependent [57]. However, silencing of HIF-1α did not alter the relative steady-state levels of FAM134B neither during hypoxia compared to normoxia.
FAM134B lacks intraluminal domains hence the question that remains to be answered is, how does FAM134B detect ER-stress or physiological changes within the ER? It is likely that it cooperates with accessory proteins to detect ER stress [25]. BiP and Calnexin are the two major chaperone systems in the ER lumen [58, 59] and recently it has been reported that FAM134B cooperates with Calnexin which possesses a luminal chaperone domain to sense and remove misfolded procollagen [60]. BiP is a chaperone which senses accumulation of misfolded proteins in the ER resulting in the release of BiP from the UPR proteins and also chaperones the folding of accumulated proteins [13]. We noticed that BiP co-immunoprecipitated with FAM134B in hypoxic cells and colocalizes in the breast cancer tissues. Additionally, depletion of BiP prevented FAM134B-dependent ER-phagy and stalled the proliferation of cancer cells subjected to hypoxia. Even if FAM134B does not have an ER luminal domain and BiP is an ER luminal chaperone, the two proteins seem to be connected in a common complex. Future experiments will be addressed to fully clarify the biochemistry of this complex and what are the other proteins that likely bridge FAM134B and BiP during the hypoxia stress.
Though ER-phagy has been speculated to be involved in various pathologies including cancer [61], therapeutic options to target ER-phagy has not been exploited yet. Having found that depletion of BiP prevents ER-phagy and cancer cell proliferation, we explored to pharmacologically target BiP-dependent ER-phagy. In silico analysis identified vitexin, a plant-derived flavone C-glycoside (apigenin-8-C-β-d-glucopyranoside) [62,63,64] as an inhibitor of BiP. Although several studies have reported the therapeutic potential of vitexin in treating various medical disorders including cancer, the precise molecular target remains unresolved. We show that vitexin not only abrogates BiP-dependent UPR but also inhibits FAM134B-dependent ER-phagy assisted by BiP. Decrease in UPR downstream of IRE1 and PERK in vitexin-treated cells could suggest that ER-stress is mitigated by vitexin. However, vitexin induces UPR in normoxic cells and prevents the proliferation of cancer cells. This indicates that vitexin induces UPR as it inhibits ER-phagy, which could potentially relieve the ER-stress. It also suggests that vitexin not only prevents BiP from binding to FAM134B but also prevents the ability of BiP to chaperone unfolded/misfolded proteins. Furthermore, induction of ER-stress with tunicamycin combined with ER-phagy inhibition using vitexin synergistically stunted cell proliferation. Therefore, we surmise that unresolved ER-stress is detrimental to cell survival and proliferation.
Disruption of ER and ER homeostasis could lead to the death of cells and cause disease pathologies. However, during the late stages of cancer when cancer cells are under various metabolic stresses including hypoxia, they adapt mechanisms such as ER-selective autophagy to overcome the damage to ER and the associated cellular processes. Therefore, targeting such adaptive mechanisms is a potential way forward to treat cancer. Our data reported here unveils FAM134B-BiP complex-mediated ER-phagy as a novel mechanism by which cancer cells prevail over hypoxia-induced proteotoxic stress and targeting ER-phagy machinery as a prospective therapeutic strategy to treat cancer.
Materials and methods
Cell culture
MCF-7 cells were cultured in Dulbecco’s modified Eagle medium (DMEM), C32 cells and U251 cells were cultured in RPMI medium supplemented with 10% fetal bovine serum and incubated at 37 °C, 5% CO2. For hypoxia experiments, cells were incubated in the hypoxia incubator at low oxygen levels, i.e., 1% O2. MCF-7, C32, and U251 cells from ATCC collection were gifted by Profs Greg Goodall, Claudine Bonder and Stuart Pitson respectively and tested mycoplasma free.
Drugs and treatments
CoCl2 0.1 M readymade solution (Cat No. 15862) and vitexin (CAS No. 3681-93-4) were procured from Sigma-Aldrich. CoCl2 and vitexin were used at a concentration of 500 and 20 µM, respectively. Concanamycin A was purchased from Sigma-Aldrich and used at a concentration of 100 nM.
Immunoblotting
MCF-7 cells were lysed in radioimmunoprecipitation assay (RIPA) buffer supplemented with protease and phosphatase inhibitors. Protein concentrations were estimated using Pierce BCA Protein assay kit (Thermo Fisher Scientific), as per the instructions. Equal amounts of proteins were separated on either 10% SDS/PAGE gels or 4–20% Mini-PROTEAN TGX Stain-Free Gels (#4568094, Bio-Rad). Proteins were then transferred onto PVDF membranes and probed with the following antibodies: HIF-1α (D2U3T) (#14179; Cell Signaling Technology), BiP (C50B12) (#3177; Cell Signaling Technology), CREB-2 (SC-200; Santacruz), CHOP (#2895; Cell Signaling Technology), LC3B (#83506; Cell Signaling Technology), ER Stress Antibody Sampler Kit (#9956; Cell Signaling Technology), Sec24C (#14676; Cell Signaling Technology), Lamin B1 (#12586; Cell Signaling Technology), CCPG1 (ab150465; Abcam), Sec62 (ab137022; Abcam), FAM134B (#61011; Cell Signaling Technology) and anti-FAM134B polyclonal antibody (a kind gift from Ivan Dikic), RTN3 (# PA578316; Thermo Fisher Scientific), Normal Rabbit IgG (#2729; Cell Signaling Technology), XBP-1s (#12782; Cell Signaling Technology), SQSTM1/p62 (#5114; Cell Signaling Technology). Beta actin, calnexin (#2679; Cell Signaling Technology), or GAPDH (sc-32233; Santacruz) were used as loading controls. After incubation with secondary horseradish peroxidase (HRP)-conjugated antibodies, the blots were washed and developed using enhanced chemiluminescence reagent in the Chemidoc MP or ImageQuant LAS4000.
Immunofluorescence staining and confocal microscopy
MCF-7 cells grown on the glass coverslips were treated with CoCl2 and vitexin for 16–24 h and fixed with 4% formaldehyde in PBS for 15 min at RT. The cells were then permeabilized with 0.3% Triton X-100 in PBS for 5 min and blocked with 3% BSA for 1 h at RT. The cells were incubated overnight with primary antibody against HIF-1a, BiP, CREB-2, CHOP, LC3B, calnexin, and FAM134B at 4 °C. After overnight incubation, the cells were washed with PBS and incubated with either Alexa Fluor 594-conjugated goat anti-rabbit/anti-mouse or Alexa Fluor 488-conjugated goat anti-rabbit/anti-mouse secondary antibody for 1 h at RT in the dark. The cells were then washed, and coverslips were mounted using ProLong Diamond antifade containing DAPI to stain the nuclei. Staining of mouse and human breast cancer tissues was performed after antigen retrieval using 0.01 M Citrate buffer pH 6.0. The slides were imaged under Leica SP8 confocal or Leica THUNDER imager. Human breast cancer tissues were obtained with consent from the patients which was approved by the Ethical committee of the University of Campania “Luigi Vanvitelli” (Prot. 71-13/2/2129).
Quantitative real-time PCR
Total RNA from MCF-7 cells (1 × 106 cells/well) was isolated using RNeasy Mini kit (74106; Qiagen), and 500 ng cDNA was synthesized with random hexamers by reverse transcription (SuperScript III; 18080; Invitrogen). Twenty microliters of PCR reactions contained10 ng cDNA, 0.4 µmol/L of each forward and reverse primer, and master mix (SsoFast EvaGreen Supermix; 1725201; Bio-Rad). Real-time PCR was performed under the following conditions: initial denaturation step at 95 °C for 2 min and 40 cycles at 95 °C for 5 s and 60 °C for 15 s, followed by a denaturation step at 95°C for 60 s and a subsequent melt curve analysis to check amplification specificity. Results were analyzed by the comparative threshold cycle method with hypoxanthine-guanine phospho ribosyl transferase (HPRT) as the endogenous reference gene for all reactions. The relative mRNA levels of untreated samples were used as normalized controls for the CoCl2 and vitexin-treated samples. All reactions were performed in triplicate and a non-template control was included in all experiments to exclude DNA contamination. Primer sequences are listed in Table 1.
Time-lapse imaging for cell proliferation
MCF-7 cells were seeded (2 × 104 cells/well) in the ibidi µ slide 8 well (cat no.80827) suitable for live cell imaging in the CellVoyager CV1000 confocal imaging system (Yokogawa). A day after the cells were treated with appropriate concentrations of CoCl2 and vitexin and set up for time-lapse imaging over 24 h duration at an interval of 20 min.
Time-lapse imaging for ER-phagy
MCF-7 cells were transfected with mCherry-ER-3 and GFP-WIPI-1 plasmids and seeded (2 × 104 cells/well) in the Nunc™ Lab-Tek™ II Chamber Slide (cat no. 154526) suitable for live imaging. The next day, following treatment with CoCl2 and vitexin cells were set up for time-lapse imaging in the Leica SP8 confocal or Leica THUNDER imager over 24 h duration at an interval of 20 min. The data were processed and analyzed using imageJ software.
siRNA and plasmid transfection experiments
MCF-7 cells (0.5 × 106 cells/well) were incubated with either 100 nM nontargeting siRNA (SR-CL000-005; Silencer™ Select) or 100 nM siRNA specific for HIF-1a (HIF1a; L-004018-00-0005; Dharmacon), BiP (siRNA ID: s29012; Silencer™ Select)and FAM134B (siRNA ID: s29012, s29013; Silencer™ Select) together with the transfection reagent Lipofectamine 3000 (L3000-008; Invitrogen) for 48 h according to the manufacturer’s instructions. Knockdown efficiency was assessed by western blot analysis using antibodies against HIF-1a, BiP, and FAM134B respectively. mCherry-ER-3 was a gift from Michael Davidson (Addgene plasmid # 55041; http://n2t.net/addgene:55041; RRID: Addgene_55041) and pMXs-IPGFP-WIPI-1 [65] was a gift from Noboru Mizushima (Addgene plasmid # 38272; http://n2t.net/addgene:38272; RRID:Addgene_38272). Plasmids were transiently transfected into the MCF-7 cells for 48 h using Lipofectamine 3000.
Immunoprecipitation
MCF-7 cells (5.0 × 106 cells/well) were lysed with RIPA buffer containing protease and phosphatase inhibitors. After preclearing the cell lysate with protein A/G agarose magnetic beads (16-663; Millipore) for 1 h, beads were removed by placing the tube on a magnetic rack. The whole-cell lysate (∼1000 µg of protein) was incubated overnight at 4 °C with 4 µg of an antibody against FAM134B. Protein A/G agarose beads were added again and incubated for an additional 1 h at room temperature. The immunoprecipitated proteins along with the agarose beads were collected by placing the tube on a magnetic rack. The collected beads were washed three times with RIPA buffer. The washed samples were mixed with SDS-PAGE sample loading buffer, boiled, and resolved on a 10% SDS-polyacrylamide gel. The respective proteins precipitated were probed for specific antibodies for immunoblot analysis.
Crystal violet cell viability assay
MCF-7 cells were cultured in a 96-well plate at a density of 1 × 104 cells/well. Some wells were kept without cells to serve as control for non-specific binding of the crystal violet. After 16–24 h, medium was aspirated and added 100 µL of fresh medium supplemented with appropriate concentrations of drugs (CoCl2 and vitexin) and incubated for 24 h at 37 °C in standard culture conditions. After 24 h of incubation, wells were gently washed twice with water and incubated with 50 µL 0.5% crystal violet staining solution for 20 min at room temperature on a bench rocker at a frequency of 20 oscillations per minute. Then the plate was air-dried without the lid for 2 h at room temperature and incubated with 200 µL methanol for 20 min at room temperature on a bench rocker at a frequency of 20 oscillations per minute. Absorbance was measured at 595 nm using a microplate reader (Bio TekTM EPOCH).
In silico molecular docking studies
Ligand preparation
The 2D structures of the selected ligands were drawn using ChemSketch software (https://chemsketch.en.softonic.com/). The ligands were prepared using Ligprep of Schrödinger suite. Bond orders were refined, missing hydrogen atoms were added followed by generating three-dimensional (3D) structures with possible ligand ionization and tautomeric states at pH 7.0 ± 2.0 using Epik module. The generated low-energy conformers were finally energy minimized by using OPLS_2005 force field.
Protein preparation for in silico docking studies
The 3D X-ray structure of human GRP78 ATPase domain complexed with 2′-deoxy-ADP and inorganic phosphate (5F0X.pdb, Resolution: 1.6 Å) was retrieved from protein data bank and was further prepared using protein preparation wizard of Schrödinger suite 2015-3. The initial protein structure was a homo dimer, where the redundant chains have been removed with deleting waters, refining bond orders and addition of hydrogens. Prime module was used for adding missing side chains and loops followed by generating protonation and tautomeric states of acidic and basic residues at normal pH 7.0 by PROPKA. Next, protein hydrogen bond assignment was done along with side chain flipping of His, Asp and Glu with reorienting hydroxyl and thiol groups. Finally, protein minimization was performed using OPLS_2005 (Optimized Potentials for Liquid Simulations) molecular force field with RMSD of crystallographic heavy atoms kept at 0.30 Å. The quality of prepared protein was validated using Ramachandran plot.
Grid generation and molecular docking
A grid box was generated at the centroid of active site keeping receptor van der Waals scaling of 1.0 with partial charge cutoff at 0.25. The generated low-energy conformers were docked into the active site of 5F0X.pdb using extra precision mode (XP) docking of Glide (Glide v 6.8, Schrödinger 2015-3) keeping default parameters. The docked pose was selected based on terms of Glide g score, Glide model, and Glide energy values.
Cell viability assay and synergism with tunicamycin
Cell viability was measured by the colorimetric 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyltetrazolium bromide (MTT) assay. Cells were seeded in 96-well plates at a density of 104 cells per well and treated with vitexin and tunicamycin. One hundred microliters of 1 mg/mL MTT (Sigma) in DMEM medium containing 10% fetal bovine serum was added to treated cells for 4 h at 37 °C. The medium was replaced with 200 μL of DMSO and shaken for 15 min, and then absorbance at 540 nm was measured using a microplate ELISA reader with DMSO used as the blank. To quantify the synergistic or antagonist effect of the drugs combinations, Combenefit® software was used.
In vivo mouse xenograft and vitexin treatment
Four- to six-week-old female balb/c athymic (nuþ/nuþ) mice were purchased from The Charles River Laboratories. The research protocol was approved, and mice were maintained in accordance with the institutional guidelines of the Università degli Studi della Campania L. Vanvitelli Animal Care and Use Committee. Animal care was in compliance with Italian (Decree 116/92) and European Community (E.C. L358/1 18/12/86) guidelines on the use and protection of laboratory animals. Mice were acclimatized at Università degli Studi della Campania L. Vanvitelli Medical School Animal Facility for 1 week prior to being injected with cancer cells and then caged in groups of three. A total of 5 × 106 MCF-7 cells were resuspended in 200 μL of Matrigel (BD Biosciences) and PBS (1:1) and implanted subcutaneously into the right flank of 12 nude female mice. At week 2, once tumors reached a mean volume of 600 mm3, mice were randomized into the treatment group (6 mice) or the control group (6 mice) to receive treatment with vitexin 2 mg/kg or vehicle (dimethyl sulfoxide (DMSO)), respectively, via intraperitoneal injection, 5 days a week, for 3 weeks. Tumor size was evaluated twice a week by caliper measurements using the following formula: π/6 × larger diameter × (smaller diameter)2. Tumor response was assessed by using volume measurements and adapted clinical criteria.
Statistical analysis
Statistical analyses were performed using GraphPad Prism Software (Version 8.0). Unpaired Student’s t-test or two-way ANOVA with Bonferroni post hoc test was conducted for all the datasets as indicated in figure legends to determine statistical significance. All the data are represented as mean ± SEM. For all tests, a p value < 0.05 was considered statistically significant (*p < 0.05; **p < 0.01; ***p < 0.001; ****p < 0.0001).
Data availability
All data are presented within the manuscript and supplemental material. There is no data to deposit on a repository.
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Acknowledgments
We thank the Robinson laboratory members and Dr. Alexandra Stolz, Institute of Biochemistry 2, Goethe University School of Medicine, Frankfurt, Germany for helpful discussions and critical review of the manuscript; Dr. Valentina Poltavets and Prof. Michael Samuel, Centre for Cancer Biology for their help with tissue sections; Dr. Makoto Kamei, Imaging Facility, Centre for Cancer Biology, Adelaide. The imaging facility is supported by funding from Australian Cancer Research Foundation. Dr. Chia Chi, Centre for Cancer Biology for helping us to set up hypoxic conditions and Dr. Srikanth Jupudi, JSS College of Pharmacy for his help with the in silico docking studies. Work in the laboratory of NR is supported by funds from Centre for Cancer Biology and University of South Australia, Neurosurgical Research Foundation (NRF), Adelaide and from Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD; funded by the DFG within the Excellence Initiative by the German federal and state governments). We thank Dr. Elena Polishchuk and the Microscopy Core of TIGEM for electron microscopy analysis. We thank Dr. Luca Persano and Dr. Elena Mariotto for their help in hypoxia treatments. The authors acknowledge Department of Science and Technology, Government of India for financial support vide reference no SR/WOS-A/LS-21/2016 under Women Scientist Scheme to carry out research in this area to SC. SC was also supported with a short-term travel fellowship from European Association for Cancer Research. The authors acknowledge Telethon Foundation and AIRC (MFAG 24856). AR was supported by Fondazione Umberto Veronesi.
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SC and NR conceived and designed the research. SC, RG, GM, LM, AR, ME, and VN performed experiments. SC, VN, AR, EK, PG, VD, and NR analyzed data. SC, AR, VN, PG, VD, and NR interpreted the results. SC, RG, LM, AR, ME, VD, PG, and NR prepared figures. SC, VD, and NR drafted the paper. SC, AR, EK, PG, VD, and NR edited and revised the paper. All authors approved the final version of the paper.
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Chipurupalli, S., Ganesan, R., Martini, G. et al. Cancer cells adapt FAM134B/BiP mediated ER-phagy to survive hypoxic stress. Cell Death Dis 13, 357 (2022). https://doi.org/10.1038/s41419-022-04813-w
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DOI: https://doi.org/10.1038/s41419-022-04813-w
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