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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
 
Oncogene. Author manuscript; available in PMC 2013 December 24.
Published in final edited form as:
PMCID: PMC3871884
NIHMSID: NIHMS536815

Identification of pY654-β-catenin as a critical co-factor in hypoxia-inducible factor-1α signaling and tumor responses to hypoxia

Abstract

Hypoxia is linked to epithelial mesenchymal transition (EMT) and tumor progression in numerous carcinomas. Responses to hypoxia are thought to operate via hypoxia-inducible factors (HIFs), but the importance of co-factors that regulate HIF signaling within tumors is not well understood. Here we elucidate a signaling pathway that physically and functionally couples tyrosine phosphorylation of β-catenin to hypoxia-inducible factor-1α (HIF1α) signaling and HIF1α-mediated tumor EMT. Primary human lung adenocarcinomas accumulate pY654-β-catenin and HIF1α. All pY654-β-catenin, and only the tyrosine phosphorylated form, was found complexed with HIF1α and active Src, both within human tumors and in lung tumor cell lines exposed to hypoxia. Phosphorylation of Y654, generated by hypoxia mediated, reactive oxygen species (ROS)-dependent Src kinase activation, was required for β-catenin to interact with HIF1α and Src, to promote HIF1α transcriptional activity, and for hypoxia-induced EMT. Mice bearing hypoxic pancreatic islet adenomas, generated by treatment with anti-vascular endothelial growth factor antibodies, accumulate HIF1α/pY654-β-catenin complexes and develop an invasive phenotype. Concurrent administration of the ROS inhibitor N-acetylcysteine abrogated β-catenin/HIF pathway activity and restored adenoma architecture. Collectively, the findings implicate accumulation of pY654-β-catenin specifically complexed to HIF1α and Src kinase as critically involved in HIF1α signaling and tumor invasion. The findings also suggest that targeting ROS-dependent aspects of the pY654-β-catenin/ HIF1α pathway may attenuate untoward biological effects of anti-angiogenic agents and tumor hypoxia.

Keywords: hypoxia, signaling, transcription, tumor, epithelial

Introduction

The process of tumor metastasis is thought to involve EMT (1, 2). EMT involves transcriptional reprogramming whereby epithelial tumor cells lose cell polarity and cell junction proteins (such as E-cadherin) and at the same time acquire signal transduction activities associated with mesenchymal cells and mesenchymal cell markers, e.g. fibronectin (Fn), collagen I, and metalloproteinases. This reprogramming facilitates migration, survival, and ultimately metastasis at distal sites (3, 4). Both hypoxia and overexpression of hypoxia inducible factor (HIF)-1α and/or HIF-2α have been shown to promote EMT and metastatic phenotypes (5, 6). Indeed the presence of tumor hypoxia has long been associated with poor cancer outcome (7). This problem has received additional attention because of the recently observed untoward effects of anti-angiogenic therapies on tumor invasion, likely operating at least in part through the generation of hypoxia (8, 9). Mechanisms possibly connecting hypoxia with EMT include intracellular reactive oxygen species (ROS)-dependent HIF accumulation (10), Snail translocation (11) and HIF1α-dependent accumulation of the transcription factors Snail, Twist, ZEB1 and ZEB2, key regulators of EMT (12). HIF1α is reported to directly bind the Snail and Twist promoter (13, 14). Although HIF1α accumulation is a fundamental regulator of the cellular response to hypoxia, HIF1α transcriptional activity is dependent not only on binding to its canonical DNA hypoxia response element (HRE) but also on a complex array of co-factors that dictate which genes are preferentially activated in different cells exposed to hypoxia (15). One such co-factor previously reported to bind HIF1α and promote its transcriptional activity is β-catenin (16).

Signaling through Wnt/β-catenin has been implicated in EMT in breast cancer cells via upregulation of the Wnt target gene Axin2 followed by stabilization of nuclear Snail (17, 18). In other cells Wnt is reported to mainly influence tumor cell proliferation via induction of c-myc and cyclin D1 (19). Indeed the principal mechanism underlying the strong association between stabilizing mutations in β-catenin and tumor development is thought to be β-catenin driven-tumor cell proliferation (20). In addition, a number of tyrosine phosphorylations of β-catenin have been reported and these appear to function not simply by promoting canonical Wnt target genes but instead by modifying the repertoire of β-catenin binding partners. For example, Y654-β-catenin phosphorylation disrupts the association between β-catenin and E-cadherin, favoring its transcriptional activity (21). We have previously reported that pY654-β-catenin is found in complexes with p-Smad2 following transforming growth factor (TGF) β1 signaling and such complexes strongly correlate with TGFβ1-induced EMT in kidney and lung alveolar epithelial cells both ex vivo and in vivo (22, 23). Accumulation of pY654-β-catenin following TGFβ1 stimulation had little or no contribution to canonical Wnt pathway signaling (24). Whether hypoxia-induced EMT in tumor cells either generates or requires pY654-β-catenin and whether tyrosine phosphorylation of Y654 regulates β-catenin association with HIF1α is currently unknown.

Activation of several oncogenic tyrosine kinases including Src family kinases, epidermal growth factor receptor (EGFR) (25) and hepatocyte growth factor receptor c-Met (26) have been reported to lead to β-catenin phosphorylation. However, only Src kinase(s) has been shown to directly phosphorylate Y654. Though mechanisms remain undefined, over-expression of activated Src kinase has been found to promote HIF1α accumulation and its transcriptional activity (27, 28), raising the possibility of an intrinsic linkage between Src kinase activity and HIF1α signaling. Elevated Src activation has been reported in hypoxic regions of tumor xenografts, but whether Src kinase activity is promoted by hypoxia in human cancer is not reported (29). Hence it is also unknown whether hypoxia-regulated tyrosine kinases contribute to the phosphorylation of β-catenin and hypoxia-induced EMT in human carcinomas. This is an important point because tumor invasion and metastasis may depend as much or more on activation of pro-invasive pathways within developed tumors as on driver mutations implicated in tumor initiation(30, 31). In this study we explore the importance of pY654-β-catenin accumulation in tumor responses to hypoxia.

Results

pY654-β-catenin accumulates and associates with HIF1α and Src in human lung adenocarcinomas

To test for the presence of pY654-β-catenin in human lung cancers, protein extracts of flash frozen tumor tissues and matched contiguous normal lung tissues surgically dissected from lung adenocarcinoma patients were analyzed by immunoblotting. pY654-β-catenin was easily detected in all the tumor tissues but not in the contiguous normal tissues (Figure 1a, top) although total β-catenin varied among the samples (Figure 1a, bottom). As observed in prior studies of fibrosis (23), p-Smad2 co-precipitated with pY654-β-catenin in all of the tumor specimens (Figure 1a). Several tyrosine kinases that are known to promote Y654-β-catenin phosphorylation including activated Src and EGFR (25), as well as activated and total c-Met, were also upregulated in the tumor tissues compared to the matched normal controls (Figure 1b and 1c). Further, both the EMT markers Snail1 and Twist as well as the hypoxia marker HIF1α accumulated in these lung tumors (Figure 1b). To initially assess whether there is a functional link between active Src, pY654-β-catenin, and EMT markers, slices of fresh adenocarcinomas were cultured in vitro with or without Src kinase inhibitors and then immunoblotted. The presence of pY654-β-catenin, active Src, and Snail1/Twist in lysates from cultured fresh tumor slices (Figure S1) were all abrogated by the Src inhibitors PP2 and SU6656, suggesting that Src family kinases play an important role in phosphorylating β-catenin and the subsequent EMT.

Figure 1
Multiple activated tyrosine kinases in human lung adenocarcinomas associated with formation of pY654-β-catenin complexes with HIF1α and p-Smad2. (a) Human lung tumors (T) and contiguous normal tissues (N) were lysed and the lysates immunoprecipitated ...

Because hypoxia-induced HIF1α has been shown to promote EMT and bind β-catenin (16, 32), we tested whether the tyrosine phosphorylated form of β-catenin preferentially interacts with HIF1α. Indeed pY654-β-catenin immunoprecipitation co-precipitated HIF1α and Src whereas sequential total β-catenin precipitates did not contain detectable HIF1α or Src (Figure 1d), implying association with HIF1α and Src depends on pY654. Consistent with this conclusion, immuno-depletion of HIF1α removed virtually all pY654-β-catenin from tumor lysates (Figure 1e). To explore further the requirement for pY654 in the interaction of β-catenin with HIF1α and its functional importance in tumor EMT we turned to model systems.

Hypoxia induces pY654-β-catenin association with HIF1α/Src and increases EMT markers in lung adenocarcinoma cells in a Src-dependent manner

We used human lung adenocarcinoma cell lines H358 and A549 as ex vivo models to test the role of HIF1α/pY654-β-catenin in hypoxia-stimulated EMT. After 2 or 12 hours incubation under hypoxic conditions (1% O2), there was a robust increase of pY654-β-catenin and low levels of pY654-β-catenin/p-Smad2 complexes, reflecting the low basal levels of p-Smad2 in H358 cells that is not altered by hypoxia (Figure 2a and S2a).

Figure 2
Hypoxia induces Src kinase-dependent pY654-β-catenin/HIF1α complexes and EMT in human lung adenocarcinoma cells. (a) pY654-β-catenin immunoprecipitation of H358 cells incubated in normoxia (21% O2) (N) or hypoxia (1% O2) (H) for ...

Exposure of H358 cells to hypoxia increased HIF1α protein level (Figure 2b and S2b, right) and Src activity (Figure 2c). HIF1α and Src were detected in pY654-β-catenin IP from cells exposed to hypoxia but not from cells cultured under normoxia or from hypoxic cells treated with Src inhibitor SU6656 (Figure 2b and S2b, left). Again, there was no HIF1α and Src discernible in the subsequent total β-catenin immunoprecipitates (Figure 2b and S2b, middle) and HIF1α depletion removed all detectable pY654-β-catenin (Figure 2d and S2c), similar to observations in human lung adenocarcinomas.

To further test whether pY654 is required for HIF1α and Src association, we stably expressed Myc-tagged wt (W) or a non-phosphorylated Y654F mutant (F) β-catenin in H358 cells. Myc immunoprecipitates of these cells under hypoxic conditions confirmed that only the wt but not the Y654F β-catenin associates with HIF1α and Src (Figure 2e). In additional experiments we observed that over-expression of either wt or Y654F β-catenin in 293 fibroblastic cells resulted in comparable HIF1α/β-catenin interactions, consistent with direct in vitro binding observed in a prior report (16). But at endogenous levels of HIF1α and β-catenin, at least in epithelial cells where the bulk of β-catenin is bound to E-cadherin, the only species of β-catenin found in association with HIF1α is pY654-β-catenin. Generation of this β-catenin species requires active Src kinase and presumably Y654 subsequently acts as a binding site for Src SH2 domain, though we have not specifically addressed this point.

Active Src kinase(s) was also found to be required for hypoxia-induced EMT. Under normoxia, lung cancer cells strongly expressed the epithelial marker E-cadherin at cell:cell contacts and had little mesenchymal marker Fn staining, whereas cells cultured under hypoxic conditions for 56 hours underwent clear morphological changes (Figure 2f and S2d, top). This phenotype was reversed by SU6656 (Figure 2f and S2d, bottom). Immunoblotting showed both hypoxia-induced Src activation and Snail1 expression were inhibited by SU6656 (Figure 2c). While hypoxia-induced upregulation of HIF1α does not require Src activity (Figure 2c), knockdown of HIF1α completely blocked hypoxia-induced EMT in H358 cells (Figure S3), indicating a critical role for both Src and HIF1α.

pY654-β-catenin and HIF1α act as a functional unit

To address the functional importance of pY654-β-catenin in hypoxia-induced EMT we utilized a T antigen-immortalized alveolar epithelial cell line homozygous for a floxed β-catenin allele, termed AECT. When plated onto Fn for 3 days AECTs activate latent TGFβ1 and undergo EMT as indicated by the induction of p-Smad2, loss of intact adherens junctions, and induction of mesenchymal genes (24). To test whether TGFβ1 signaling is required for hypoxia-induced EMT we treated cells with ALK5 inhibitor SB431542. As expected, when these cells were exposed to hypoxia there was induction of HIF1α (Figure 3a) and pY654-β-catenin that was not blocked by ALK5 inhibitor (Figure S4a). All pY654-β-catenin was again associated with HIF1α and this association was Src kinase dependent (Figure 3a). Cells null for β-catenin were generated upon adenovirus-Cre exposure (Ad-Cre). Under hypoxia, AECTs treated with Ad-Cre maintained an epithelial phenotype with strong cell border staining of E-cadherin (green) whereas AECTs treated with control adenovirus-GFP (Ad-GFP) completely lost cell:cell contact and border staining of E-cadherin (green) and β-catenin (red) (Figure 3b). The deletion of β-catenin also blocked hypoxia-induced EMT biomarkers collagen I (Figure 3c), Twist (Figure 3d), as well as the invasive metalloproteinase, MMP-2 (33), which was Src kinase dependent (Figure 3e). Depletion of either β-catenin (Figure 3f) or HIF1α (Figure 3g) blocked collagen I and Snail 1 mRNA induction by hypoxia, indicating both β-catenin and HIF1α are functionally important for hypoxia-induced EMT.

Figure 3
Hypoxia-induced EMT requires both HIF1α and β-catenin expression. (a) HIF1α and pY654-β-catenin sequential immunoprecipitation of AECTs under normoxia or hypoxia ± Src inhibitor for 4 h. (b) Immortalized AECTs with ...

We next reconstituted the β-catenin null AECTs with wild-type or specific point mutants of β-catenin to specifically assess the role of Y654. A Y654E mutation mimics its phosphorylated form, while a Y654F mutation mimics the non-phosphorylated form of β-catenin (21). We verified that the Y654E mutant β-catenin was recognized by the pY654-β-catenin antibody (Figure S4b). Interestingly, Y654E mutant cells already show a mesenchymal phenotype under normoxia as judged by disrupted border staining of E-cadherin (green) and strong staining of EMT marker, α-SMA (orange) while Y654F mutant cells maintain an epithelial phenotype (Figure 4a). When AECTs with β-catenin deletion (Cre), wt β-catenin (W), and Y654E (E) or Y654F (F) mutant β-catenin were exposed to hypoxia, Y654E mutant cells showed high levels of collagen I, left angle bracket-SMA, Twist (Figure 4b) as well as MMP-2 (Figure 4c) under both normoxia and hypoxia. While these markers were significantly induced by hypoxia in WT cells, Y654F mutant cells failed to respond to hypoxia, similar to the AECTs with ®-catenin deletion (Figure 4b–4d). Y654E-®-catenin proved to be most efficient in EMT induction among different ®-catenin forms, as illustrated by the EMT marker/®-catenin protein expression ratio quantified and pooled from 3 independent experiments (Figure 4d).

Figure 4
Y654-β-catenin phosphorylation is required for hypoxia-induced EMT and β-catenin promotion of HIF1α transcriptional activity. (a) E-cadherin (green) and α-SMA (orange) staining of AECTs expressing Y654E or Y654F-β-catenin. ...

To examine whether hypoxia-induced HIF1α transcriptional activity is regulated by the phosphorylation status of Y654, we transfected a HRE reporter construct into 293 cells expressing either wt (W), Y654E (E) or Y654F (F) mutant ®-catenin (Figure 4e, left). Under hypoxia, non-transfected cells expressing only endogenous ®-catenin had ~10-fold increase in luciferase activity. The ratio of hypoxia/normoxia for these cells was assigned a value of 1. Either wt or Y654E mutant cells showed 3–4-fold higher HRE activity over non-transfected cells whereas the HRE activity of Y654F mutant cells (Figure 4e, right) were no different than non-transfected controls. These findings demonstrate that Y654 phosphorylation directly promotes HIF1α transcriptional activity, consistent with our findings of ®-catenin/HIF1α-dependent induction of mRNA for EMT genes (Figure 3). Interestingly, in addition to EMT genes, a number of other classical HIF1α responsive genes (Figure S5a) were also found to be sensitive to Src activity (Figure S5b) and β-catenin expression (Figure S5c). Taken together, these data indicate that tumor cell responses to hypoxia that depend on upregulated HIF1α activity also require association of HIF1α with pY654-®-catenin for a full transcriptional response.

ROS activity is required for hypoxia-induced tyrosine kinase activation, β-catenin phosphorylation, and subsequent EMT

In some cell systems hypoxia is reported to generate ROS that can then lead to Src activation and EMT (32, 34). Indeed hypoxia significantly increased ROS activity in H358 cells (Figure 5a) and A549 cells (Figure S6a) as measured by fluorescence response of 3’-(p-aminophenyl) fluorescein (APF) (35). Both ROS inhibitors EUK-134 and/or N-acetyl-cysteine (NAC) inhibited hypoxia-induced Src activation and pY654-β-catenin formation in H358 cells (Figure 5b) and A549 cells (Figure S6b). In contrast, Src activation and pY654-β-catenin formation initiated by TGFβ1 signaling (24) were unaffected by ROS inhibitors (Figure 5b and S6b). Notably, HIF1α expression levels were suppressed by ROS inhibitor(s) in H358 cells (Figure 5b) but not in A549 cells (Figure S6b) indicating that pY654-β-catenin/HIF1α complexes rather than HIF1α levels alone track with EMT and its suppression by ROS inhibitors.

Figure 5
Hypoxia-induced pY654-β-catenin formation and EMT are dependent on ROS. (a) H358 cells were cultured in normoxia or hypoxia for 2 h ± ROS scavenger NAC (10 mM). APF signal (green) indicates ROS activity and the fluorescence intensity was ...

Hypoxia-induced activation of EGFR and c-Met was blocked by ROS inhibitors (Figure S7a and S7b) as well as Src inhibition (Figure S7c and S7d), implying that the activation of these receptor tyrosine kinases is triggered by hypoxia-increased ROS activity, but is also downstream of Src activation. Longer exposure of H358 cells to hypoxia confirmed that hypoxia-induced Snail1 (Figure 5c), the invasive marker MMP-9 (Figure 5d), and wound closure (Figure S8) were all dependent on ROS activity. Collectively, these findings indicate that hypoxia-induced ROS leads to activation of Src kinase(s) and then EGFR and c-Met activation that in turn further promotes Src activation and pY654-β-catenin accumulation. These co-factors then cooperate with HIF1α to drive an invasive EMT program. We next asked whether these ex vivo observations operate in vivo.

Anti-VEGF neutralizing antibodies induce tumor hypoxia, pY654-β-catenin/HIF1α/Src accumulation, and EMT in vivo

In a mouse model of pancreatic islet carcinogenesis (RIP-Tag2), Casanovas and colleagues reported that VEGF blockade in late-stage tumors resulted in hypoxia-mediated induction of VEGF-independent proangiogenic factors (36). Sennino and colleagues recently reported that anti-VEGF antibodies in this model led to both tumor EMT and marked tumor invasiveness, including metastasis (37). We therefore addressed our ex vivo findings in the RIP-Tag2 model. When 14-week old RIP-Tag2 mice were treated with a goat anti-VEGF antibody or control IgG daily for a week, there was marked pY654-β-catenin as well as HIF1α accumulation with the anti-VEGF antibody but not the controls (Figure 6a–6c). We also noted that p-Smad2 was associated with pY654-β-catenin in the tumor lysates, similar to human lung tumors (Figure 1), but anti-VEGF antibodies had no discernible effect on p-Smad2 levels (Figure 6a). All or virtually all pY654-β-catenin induced by anti-VEGF in these tumors was complexed with HIF1α and Src (Figure 6b). Western blot analysis confirmed upregulation of active Src, N-cadherin, vimentin, Snail1, and Twist by anti-VEGF antibody treatment (Figure 6c), indicating activation of an EMT program. Thus there is a strong correlation between anti-VEGF induced-hypoxia, pY654-β-catenin/HIF1α generation, and EMT reprogramming in the RIP-Tag2 tumor model.

Figure 6
pY654-β-catenin/HIF1α/Src complexes and EMT markers are increased in anti-VEGF antibody treated pancreatic tumors. (a) RIP-Tag2 tumor lysates from anti-VEGF- or control IgG-treated mice were immunoprecipitated for pY654-β-catenin ...

Finally we asked whether anti-VEGF induced pY654-β-catenin/HIF1α/Src activation and EMT in this model require ROS. Fourteen-week old RIP-Tag2 mice were concurrently treated with goat anti-VEGF antibody and the antioxidant NAC or control buffer daily for 4–5 days. Co-immunostaining of E-cadherin (red) and the RIP-Tag2 tumor cell marker insulin (green) revealed marked diminution of E-cadherin staining by antibody treatment and the antibody effect was reversed by NAC treatment (Figure 7a). Consistent with abrogation of the EMT program, pancreatic tumors in mice concurrently given NAC had sharp borders (Figure 7a and S9), typical of the adenomas prior to acquiring an invasive phenotype. Concurrent immunoblotting indicated that overall protein levels of E-cadherin did not decrease in the tumor specimens (Figure 6c) only the intensity of staining which reflects the loss of integrity of adherens junctions (37). Consistent with this finding, the margins of the tumors were more irregular and interlaced with pancreatic tissue in anti-VEGF treated mice (Figure 7a). We cannot exclude the possibility that some of the total E-cadherin protein in tumors of the anti-VEGF treated mice derives from normal pancreatic tissue infiltrated by the tumors. In contrast, the anti-VEGF antibody-enhanced pY654-β-catenin/HIF1α, EMT markers, Src activity and phospho-c-Met (Figure 7b–7e) were all reversed by NAC treatment. Reduced HIF1α is consistent with its reported stabilization by ROS (10).

Figure 7
pY654-β-catenin/HIF1α and p-c-Met accumulation, EMT markers, and tumor invasiveness induced by anti-VEGF are blocked by ROS inhibition. (a) Confocal images of anti-VEGF treated-RIP-Tag2 tumors ± NAC for 5 days stained for insulin ...

Discussion

In this study we identify a transcriptional complex that coordinates HIF1α and β-catenin signaling as a function of hypoxia-induced ROS and Src kinase activation. The data reported here indicate that activity of the HIF1α/pY654-β-catenin complex, over either element alone, promotes tumor cell acquisition of a mesenchymal phenotype both in vitro and in vivo. These findings provide a conceptual paradigm that extends prior studies of HIF1α, β-catenin, and Src kinase in tumor invasion and metastasis by linking the function of each element, and the complex as a whole, to the presence of hypoxia-induced ROS (Figure 8). Whereas β-catenin transcriptional activity as a function of Wnt-induced or mutation-based cytoplasmic stabilization mainly promotes epithelial proliferation (20), tyrosine phosphorylation of β-catenin switches β-catenin to an interaction with HIF1α that promotes mesenchymal transition. Interestingly, the interaction of pY654-β-catenin with HIF1α is required for a full transcriptional response of multiple HIF1α responsive genes to hypoxia (Figure S5). The levels of pY654-β-catenin, and therefore HIF1α/pY654-β-catenin complexes, could be expected to rise if Wnt signaling is superimposed on hypoxia(24), though hypoxia per se has little or no impact on Wnt activity in human lung adenocarcinoma cell lines (Figure S10a). The failure of β-catenin complexed with HIF1α to signal via the classical Wnt pathway has been previously noted (16), though the requirement and consequences of tyrosine phosphorylation were not evaluated. Overall, β-catenin appears to be at the center of intersecting signaling pathways that collectively determine the response of tumor cells to a hypoxic microenvironment. These findings provide further mechanistic insight into the established association between hypoxia and tumor invasion and highlight a pathway of acquisition of tumor invasiveness that, while involving activation of tyrosine kinases, operates through common features of a solid tumor without invoking acquisition of new driver mutations. This conclusion is consistent with the lack of evidence for metastasis as representing simply a genetic evolution of the primary tumor (31, 38).

Figure 8
Schematic diagram illustrating central role for ROS and Src in hypoxia-induced pY654-β-catenin/HIF1α formation and tumor EMT. Hypoxia exposure generates reactive oxygen species (ROS) and stabilizes HIF1α (10). Increased ROS activity ...

Prior studies demonstrate that HIF1α can directly promote EMT, at least in part through binding HIF response elements in the Twist and Snail1 promoters (14). Expression of HIF2α promotes lung tumorigenesis and EMT in a mutant K-Ras mouse model (39) and HIF1α expression levels correlate with tumor progression in several human cancers, including NSCLC (6). As reported here, HIF1α accumulation is prominent both in primary human lung adenocarcinomas and in experimentally induced tumor hypoxia (Figure 1 and and6),6), co-existing with markers of EMT including up-regulation of Twist and Snail1. However our analysis of hypoxia- and HIF1α-dependent EMT in three independent cell systems indicate the promoting effects of HIF1α on EMT require association with pY654-β-catenin. Expression of a phosphorylation mimic of β-catenin enhanced HIF1α promoter activity 3–4-fold over that of native β-catenin whereas a non-phosphorylatible form of β-catenin was without effect. In vivo, accumulation of HIF1α and pY654-β-catenin developed in parallel in mice bearing pancreatic tumors and exposed to anti-VEGF antibodies. Accumulation of both proteins, along with evidence of EMT, abated in response to ROS inhibitors. Collectively our findings invite the view that at least in epithelial cells HIF1α and pY654-β-catenin act as a functional signaling unit. If so, this concept implies determinants of Src kinase activity are also intrinsically linked to HIF1α signaling.

Of particular interest is the activation state of c-Met in the RIP-Tag2 tumors from mice treated with anti-VEGF antibodies. Activation of c-Met was recently reported to be crucial to anti-VEGF antibody-induced EMT and metastasis in the RIP-Tag2 tumor model (37). In our studies c-Met activation was ROS and Src kinase dependent both ex vivo and in vivo (Figure 5 and and7).7). An alternative mechanism for anti-VEGF mediated c-Met activation was recently reported in neuroblastoma cells. VEGF-dependent accumulation of the tyrosine phosphatase PTP1B in complexes of c-Met and VEGF receptors acts as a brake on c-Met activation. Anti-VEGF antibodies enhanced c-Met activation by attenuating phosphatase activity near the c-Met receptors (40). These mechanisms may not be mutually exclusive as the active site cysteines in a number of tyrosine phosphatases, including PTP1B, are known to be targeted by ROS (41). We speculate that hypoxia induced ROS may effect c-Met activation both by activation of Src leading to ligand independent activation of c-Met and ROS-dependent PTP1B phosphatase inhibition, further supporting c-Met activation.

Prior studies have identified Wnt-independent signaling events operating through tyrosine phosphorylation of β-catenin. For example, EGFR-dependent Src kinase activation leads to pY333-β-catenin that promotes its association with the glycolytic enzyme, pyruvate kinase M2. This β-catenin complex was shown to translocate to the nucleus and promote proliferation through a classical Wnt target gene, cyclin D1 (42). Whether Y654-β-catenin is phosphorylated in this signaling cascade is unclear. We have previously reported TGFβ1-dependent Src kinase activation leading to pY654-β-catenin and its association with p-Smad2. Formation of pY654-β-catenin/p-Smad2 complexes promoted EMT of kidney and lung alveolar epithelial cells (22, 23). Activation of Src kinase through hypoxia and TGFβ1 signaling is distinct because the former is critically dependent on ROS whereas TGFβ1-mediated Src activation is not affected by ROS inhibitors (Figure 5b). In vivo, as judged by co-immunoprecipitation experiments in extracts of human lung adenocarcinomas (Figure 1), both p-Smad2 and HIF1α are found in association with pY654-β-catenin, indicating both pathways likely contribute to EMT within lung cancers. This conclusion is supported by experiments in vitro with H358 cells that indicate although ROS-dependent pY654-β-catenin formation is critical to an EMT response under hypoxic conditions, activation of TGFβ1 signaling further promotes the response (Figure S10b).

Hypoxia and overexpression of HIF-1α have been associated with radiation therapy and chemotherapy resistance, an increased risk of invasion and metastasis, and a poor clinical prognosis of solid tumors (7). Similarly, a hypoxia-induced invasive phenotype and increased metastasis has been reported to result from anti-angiogenic treatment in preclinical models (8, 9) (5). The administration of anti-VEGF antibodies to mice bearing RIP-Tag2 pancreatic tumors was recently reported to result in both hypoxia-induced tumor EMT and enhanced hepatic metastases (37). Here we demonstrate activation of the HIF1α/pY654-β-catenin pathway in this model, the presence of EMT, and its dependence on ROS generation. This problem is also potentially a complication of anti-angiogenic therapy in humans and may contribute to the marginal survival benefits reported for such therapy in colon, breast, and lung cancer treatments (43). Neuroblastomas appear particular prone to acquire invasive properties in the presence of anti-VEGF induced tumor hypoxia (44). Indeed in preliminary studies we have observed marked activation of pY654-β-catenin in brain biopsies of patients progressing on Avastin when compared with the initial tumors (44) (Figure S11). Our data thus provide new information that is potentially clinically relevant. The finding that hypoxia-induced invasiveness in vivo can be markedly attenuated by concurrent administration of the anti-oxidant N-acetylcysteine (Figure 7) raises the possibility that blockade of hypoxia induced ROS accumulation, likely from mitochondrial sources (34) or administration of this or other anti-oxidants could attenuate the invasive switch that is apparently experienced by some patients receiving anti-angiogenic adjunctive therapy.

Materials and methods

Cells and cell culture

Human lung adenocarcinoma cell line H358 and human embryonic kidney 293 cells were purchased from ATCC (Manassas, VA) and grown in RPMI1640 medium or DMEM supplemented with L-glutamine, 10% FBS (Hyclone). Stable cell line of H358 that express wt or Y654F β-catenin were established by infection of lentivirus and selected by puromycin. T antigen immortalized mouse lung alveolar epithelial cells (AECTs) were generated as previously described (24) and were maintained on Matrigel (BD Biosciences) in small airway growth medium (SAGM, Lonza, Wakersville, MD) supplemented with 5% FBS and keratinocyte growth factor (KGF). For experiments, cells were incubated with Adenovirus-Cre (50 pfu/cell) to delete β-catenin or with control Adenovirus-GFP. AECTs expressing various forms of β-catenin were generated as previously described (24).

Tissue samples

Fresh or frozen tumor and adjacent normal tissues were obtained from patients with lung adenocarcinomas who were undergoing surgical resection of the primary tumor. The study was approved by the University of California San Francisco, Institutional Review Board (IRB#: 10-00959).

Animals and treatment

Tumor-bearing RIP-Tag2 transgenic mice (C57BL/6 background) (14 weeks old) were treated for 1 week with normal goat IgG or function-blocking goat anti-mouse VEGF antibody (150 µg in 50 µL sterile PBS) injected ip three times. Some mice were concurrently treated with NAC (1g/kg/day by gavage) for 4–5 days. Body weight and survival were recorded during the treatment period. All animal procedures were approved by the Institutional Animal Care and Use Committee of UCSF.

Additional methods

Detailed reagents list and all other experimental procedures are available in Supplementary Materials and Methods.

Supplementary Material

Supplementary Data

Acknowledgements

The authors thank Roshni Ray, Mazen Sidani, Toshina Ishiguro-Oonuma, Casey W. Williamson, Thomas Kim, Yonghyun Kim, Yang Gao, and Ronald Tsang for technical assistance; and Drs. Miguel Ramalho Santos and Martin Brown for generous gifts of reagents.

Grant Support: This work was supported by NIH grants to HL-44712 and CA-125564 (HAC).

Footnotes

Conflicts of Interest

No conflicts of interest.

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