The clinical and biological significance of STAT1 in esophageal squamous cell carcinoma
© Zhang et al.; licensee BioMed Central Ltd. 2014
Received: 14 July 2014
Accepted: 13 October 2014
Published: 29 October 2014
Loss of STAT1 (Signal Transducer and Activator of Transcription-1) has been implicated in the pathobiology of a number of cancer types. Nonetheless, the biological and clinical significance of STAT1 in esophageal squamous cell carcinomas (ESCC) has not been comprehensively studied.
Using immunohistochemistry, we detected the STAT1 expression in a cohort of ESCC patients; In-vitro experiments, we used enforced gene transfection of STAT1C into two STAT1- weak/negative ESCC cell lines and siRNA knockdown of STAT1 in two STAT1-strong ESCC cell lines to detect STAT1 function in ESCC.
We found that the expression of STAT1 was heterogeneous in ESCC, with 64 (49.0%) strongly positive cases, 59 (45.0%) weakly positive cases and 8 (6.1%) negative cases. STAT1 expression inversely correlated with the depth of tumor invasion and tumor size (p=0.047 and p=0.029, respectively, Chi square). Furthermore, patients with STAT1-strong/weak tumors had a significantly longer survival compared to those with STAT1-negative tumors (33.6 months versus 13.1 months, p=0.019). In patients carrying tumors of aggressive cytology (n=50), those with STAT1-strong tumors survived significantly longer than those with STAT1-weak/negative tumors (34.6 months versus 20.5 months, p=0.011). Our in-vitro experiments revealed that STAT1 is proapoptotic and inhibitory to cell-cycle progression and colony formation. Lastly, we found evidence that STAT1 signaling in ESCC cells down-regulated the expression and/or activity of NF-κB and STAT3, both of which are known to have oncogenic potential.
To conclude, our findings suggest that STAT1 is a tumor suppressor in ESCC. Loss of STAT1, which is frequent in ESCC, contributes to the pathogenesis of these tumors.
KeywordsSTAT1 Esophageal squamous cell carcinoma Prognosis NF-κB STAT3
Members of the STAT protein family are known to regulate various cellular processes involved in oncogenesis, including cell cycle progression, apoptosis, angiogenesis, invasion, metastasis, and evasion of the immune system . STAT1, as the first discovered member of the STAT family, serves as the principal mediator of both type I and type II interferon activation . Recent studies have revealed that the expression of STAT1 is frequently lost in various types of human cancer such as breast cancer, head and neck cancer, multiple myeloma and leukemia . Furthermore, it has been reported that STAT1 can inhibit the growth of benign and neoplastic cells by regulating the transcription and expression of a host of pro-apoptotic and anti-proliferative genes, such as caspases, BCL-xL and p21waf1. Overall, these observations suggest that STAT1 carries tumor suppressor functions.
Esophageal cancer is one of the leading causes of cancer-related deaths worldwide . This type of cancer is known to be highly frequent in specific geographic regions in China, such as the Chaoshan area. Specifically, the annual average age-standardized incidence rate of esophageal cancer in Chaoshan is 74.5 /100,000 people , as compared to 7.0/100,000 people worldwide. This finding suggests that various genetic and/or environmental factors may predispose the population in Chaoshan to esophageal cancer. Interestingly, esophageal cancer found in Chaoshan predominantly carries the histology of squamous cell carcinoma, in contrast with that in the Western world which predominantly carries the histology of adenocarcinoma . The pathogenesis of ESCC is incompletely understood. The overall survival of these patients remains to be relatively poor, with the overall 5-year survival rate being approximately 15% . In one previous study, it was found that γ-interferon can induce significant apoptosis in ESCC cell lines and this process correlates with STAT1 activation . In parallel with this observation, it was reported that the EGF-STAT1 signaling pathway, which is active in normal esophageal epithelial cells, is lost in a considerable fraction of esophageal cancer; furthermore, loss of EGF-STAT1 signaling was found to correlate with a worse clinical outcome . Nevertheless, the clinical and biological significance of STAT1 in ESCC has never been directly or comprehensively examined.
In the present study, we tested our hypothesis that STAT1 is a tumor suppressor in ESCC. First, using immunohistochemistry and Western blots, we comprehensively evaluated the expression of STAT1 in a large cohort of ESCC harvested from patients from Chaoshan. Second, we evaluated the clinical and prognostic significance of STAT1 in ESCC. Third, we used an in-vitro model to assess the biological functions of STAT1 in ESCC cells.
ESCC tumor samples and cell lines
We collected 131 consecutive ESCC tumors at the Shantou Tumor Hospital between 2005 and 2012. All patients underwent potentially curative surgery without preoperative chemotherapy or radiotherapy. In this cohort, 98 were men and 33 were women; the age was 36-78 years, with a median of 57 years. Follow-up data was available for 74 patients; most (58, 78.4%) died during the follow-up period (median, 31.4 months). The study was approved by the ethical review committees of the Medical College of Shantou University. All participants involved in our study were given written informed consents.
Four ESCC cell lines (EC1, EC109, KYESE150 and KYSE510) and 4 human esophageal immortalized epithelial cell lines (SHEE, NE2, NE3, and NE6) were included in this study. The ESCC cell lines were gifts from Shantou University Medical College and esophageal immortalized epithelial cell lines were gifts from University of Hong Kong. All of them were cultured in DMEM supplemented with 10% fetal bovine serum at 37°C under 5% CO2.
Antibodies, subcellular fractionation and western blotting
Western blot analysis was performed using standard techniques as previously described . The following antibodies were employed: anti-STAT1 (1:1000) and anti-p-STAT1 (Tyr-701) (1:1000), anti-FLAG (1:1000), anti-caspase 3 (1:1000), anti-survivin (1:1000), anti- BCL-2 (1:1000) anti-p21 (1:1000) and anti-cyclin D1 (1:1000), all of which were purchased from Cell Signaling (Danvers, MA, USA). Anti-STAT3 (1:1000), anti-p-STAT3 (Tyr-705) (1:1000), anti-BCL-xL (1:1000) and anti-ß-actin (1:1000) were obtained from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Densitometric analysis was performed using the ImageJ analysis system (Bethesda, WA, USA); the values for the STAT1 bands were normalized to those of the β-actin bands.
Immunohistochemistry to detect STAT1 expression was performed using a method similar to that described previously . Using the same antibody we employed for our Western blot studies, we performed immunohistochemistry and the staining results were independently evaluated by two pathologists who were blinded to the clinical data. For each case, the percentages of cells showing negative, weak or strong cytoplasmic STAT1 staining was recorded. Using our scoring system (the sum of % of cells strongly positive for STAT1 x 3 and % of cells weakly positive for STAT1 x 1), we determined that a cut-off of 80 points allowed us to achieve the lowest p-values in our statistical analysis. Thus, tumors with a score of <80 point were classified as STAT1-weak whereas those with a score of ≥80 points were classified as STAT1-strong.
A total of 2 μg of anti-STAT3 monoclonal antibody (Santa Cruz Biotechnology) was added to 500 μg of protein lysate isolated in cell lytic M (Sigma Aldrich, St Louis, MD, USA) and the samples were rotated overnight at 4°C. Subsequently, 30 μl of protein G Plus/A beads (Emdmillipore, Billerica, MA, USA) was added to the samples and rocked overnight at 4°C. The beads were then washed 3 times with cold phosphate-buffered saline followed by the final wash using cold cell lysis buffer. Western blot analysis was then performed using standard techniques as previously described .
Plasmids, cell transfection and NF-κB transcriptional activity
FLAG-tagged STAT1C cloned into the backbone of pcDNA3.1 was a gift from Dr. Ouchi (University of New York) . For each experiment, 1 × 106 ESCC cells were transiently transfected with 10 μg of STAT1C vector or the pcDNA3.1 empty vector (Invitrogen, Burlington, Ontario, CA) in 6-well plates using the lipofectamine 2000 reagent (Invitrogen) as per manufacturer’s suggested protocol. The NF-κB transcriptional activity analyses were performed as previously described .
Short interfering RNA and gene transfection
5 × 106 ESCC cells in 2 ml of culture medium were transfected with 100 pmol of SMARTpool-designed siRNA against STAT1 obtained from Dharmacon (Lafoyetle, CO, USA). Cells transfected with scrambled siRNA (Dharmacon) were used as the negative controls. Gene transfection was performed by using lipofectamine RNAiMax (Invitrogen) as per manufacturer’s suggested protocol.
Cell-cycle analysis by flow cytometry and assessment of cell growth
Flow cytometry analyses were performed at the University of Alberta flow cytometry core facility as previously described . All experiments were performed in triplicates.
To assess cell growth, ESCC cells were plated at a density of 20,000/ml of culture medium. Cell count, done daily for 4 days, was performed using trypan blue staining (Sigma-Aldrich) according to the manufacturer’s protocol. Triplicate experiments were performed.
Colony formation assay
After STAT1C transfection, 500 cells/well were plated in six-well plates and incubated 10 days at 37°C. The cells were fixed with 4% buffered formalin for 15 min and then stained with 1% crystal violet (Sigma Aldrich) for 30 min. The plates were gently washed with PBS and dried before microscopic evaluation. Cell clusters with >30 cells were considered as a colony.
Using the RNeasy Mini Kit (QINGEN, Valencia, CA, USA), total cellular RNA was extracted from cells following the manufacture’s protocol. Reverse transcription was performed using 1 μg of total RNA and superscript reverse transcriptase obtained from Invitrogen. Quantitative PCR was performed using SYBR green (Invitrogen), and the primer sets for STAT1 and GAPDH were purchased from Invitrogen. For both primer sets, the PCR conditions were as follows: 95°C for 10 minutes, followed by 40 cycles of 95°C for 15 seconds and 60°C for 1 minute. Samples were processed on an ABI 9700 HT system (Applied Biosystems Inc., Foster City, CA). Results were examined using the SDS 2.2 software, and the relative expression levels of STAT1 were calculated by normalizing with those of GAPDH.
Cell invasion assay
The invasion assays were done using basement membrane (Cell biolabs, NY). The ESCC cell treat with STAT1C or empty vector were prepared before the experiment. Then, 5 × 105 cells in 300 μL serum-free DMEM supplemented were seeded into the upper part of each chamber, whereas the lower compartments were filled with 500 μl of 10% fetal bovine serum media. Following incubation for 48 hours at 37°C, the insert was incubated in the cell detachment solution. The invasiveness was determined by fluorescence measurement, and the extent of invasion was expressed as an average number of cells per microscopic field.
Statistical analysis was performed with the SPSS15.0 software. The association between expression of STAT1 and survival was analyzed using the Kaplan–Meier’s. The correlation between STAT1 and other clinical parameters was evaluated using Chi square or Student’s t test. A value of p < 0.05 was considered as statistically significant.
Expression of STAT1 in esophageal squamous cell carcinoma (ESCC)
STAT1 expression in ESCC: significant correlation between IHC and Western blot data
STAT1 expression level by IHC
STAT1 expression level by western-blot
P = 0.0003
The clinical significance of STAT1 expression in ESCC
Correlations between STAT1 expression and various clinicopathologic parameters in ESCC
STAT1 expression by IHC
p = 0.337
p = 0.653
p = 0.572
p = 0.074
p = 0.029*
Depth of invasion
p = 0.047*
p = 0.286
p = 0.257
Clinical follow-up data was available for 74 of the 131 patients included in this study (median follow-up, 31.4 months; range 1-70 months). The survival data was analyzed using Kaplan-Meier’s. Approximately half of these tumors (34 of 74, 45.9%) were assessed strongly positive for STAT1 by IHC, and 40 (54.0%) were assessed weak/negative. The overall survival of patients with STAT1-strong tumors was found to be similar to that of patients with STAT1-weak/negative tumors (35.9 months versus 31.1 months, p > 0.05). In contrast, patients with STAT1-strong/weak tumors (n = 66) had a significantly longer survival compared to those with STAT1-negative tumors (n = 8) (33.6 months versus 13.1 months, p = 0.019). Furthermore, of the 74 patients for whom follow-up data was available, 50 carried poorly or intermediate-differentiated tumors. In this sub-group, patients with STAT1-strong tumors survived significantly longer than those with STAT1-weak/negative tumors (34.6 months versus 20.5 months, p = 0.011). Nuclear STAT1 expression again did not significantly correlate with the overall survival in this sub-group.
Roles of STAT1 in ESCC cell lines
STAT1 expression in ESCC cell lines
The biological impact of STAT1C in ESCC cell lines
The biological impact of siRNA knockdown of STAT1 in ESCC cell lines
STAT1 inhibits NF-κB
STAT1Ctransfection downregulates STAT3 expression and activation
STAT1 has been reported to regulate cellular differentiation and apoptosis through transcription-dependent as well as transcription-independent mechanisms . There is also evidence that STAT1 carries tumor suppressor functions [23–25]. Decreased or loss of STAT1 expression has been observed in many cancer types such as breast cancer, melanoma and leukemia [2, 26–28]; transfection of STAT1 or STAT1C into cancer cells can arrest their growth by inducing apoptosis and cell-cycle arrest [1, 9, 29]. STAT1 appears to exert its tumor suppressor functions via multiple mechanisms, including downregulation of caspases, Fas, FasL, TRAIL and p21waf1. The apoptosis-inducing function of STAT1 also has been linked to its inhibition of IFN-γ signaling and the subsequent downregulation of several pro-apoptotic proteins including Bak and Bax . Despite the fact that the tumor suppressor function of STAT1 is increasingly recognized, the significance of STAT1 in ESCC has not been clearly defined.
One of the key findings of this study is that the absence of STAT1 expression in ESCC significantly correlates with a worse clinical outcome. Of note, we would like to acknowledge that this observation was based on a comparison between 8 STAT1-negative and 66 STAT1-strong/weak tumors. This highly skewed pattern may have introduced some biases; thus, larger studies using other patient cohorts are needed to confirm this finding. Nonetheless, we do believe that STAT1 holds prognostic value, since we found prognostic significance when we compared STAT1-weak/negative cases and STAT1-strong cases in the cohort of poorly or intermediate-differentiated tumors (Figure 1C). Furthermore, STAT1 expression was also found to correlate with the depth of tumor invasion and tumor size. In this regard, tumor size is one of the determinants of the TNM clinical staging system for ESCC patients [30, 31]. To our knowledge, the prognostic significance of STAT1 in ESCC has never been previously described. Nevertheless, we are aware of a relatively small number of published studies that had found prognostic significance of STAT1 in other types of cancer, such as gastric cancer and melanoma [26, 32].
Correlating with our clinical observations, our in-vitro studies have provided further support that STAT1 carries tumor suppressor functions in ESCC. Specifically, we found that transfection of STAT1C into ESCC induced apoptosis and cell-cycle arrest, with the effect on apoptosis being more pronounced than that on cell proliferation (Figures 3 and 4). On the other hand, siRNA knock-down of STAT1 in ESCC cells results in opposite effects. In parallel to our findings, we have identified two in-vitro studies in the literature that may have implicated a role of STAT1 in the biology of ESCC [9, 33]. In one of these two studies, IFN-γ and EGF were found to induce apoptosis in KYSE 70 and KYSE 590, two ESCC cell lines . However, while the apoptosis induced by both cytokines was found to correlate with STAT1 activation, whether STAT1 activation is directly responsible for the occurrence of apoptosis in these cells was not clear. In this current study, the use of STAT1C and STAT1 siRNA allowed us to pinpoint STAT1 as a key mediator of the induction of apoptosis and cell-cycle arrest in ESCC.
We attempted to delineate the mechanisms by which STAT1 induces apoptosis in ESCC. We found that some of the mechanisms are similar to those previously reported for other cancer types . Thus, gene transfection of STAT1C in fibrosarcoma cell lines was found to induce caspase activation and caspase-dependent apoptosis . As we found that STAT1C-induced apoptosis in ESCC correlates with the down-regulation of several pro-survival proteins such as BCL-2 and BCL-xL, previous studies also have shown that STAT1 can promote apoptosis by down-regulating BCL-2 and BCL-xL in multiple myelomas .
We also have found evidence that STAT1 can modulate the expression of G1 cell-cycle regulatory proteins such as p21waf1 and cyclin D1 in ESCC. Upregulation of cyclin D1 has been shown to shorten the G1 phase and reported to link to the development and progression of many types of cancer, such as breast cancer , gastric cancer  and mantle cell lymphoma . In ESCC, cyclin D1 expression detectable by IHC is associated with a worse prognosis [38, 39]. Thus, down-regulation of cyclin D1 induced by STAT1 may partly explain our observation that high STAT1 expression in ESCC is associated with a better clinical outcome. As shown in Figure 4B, our observation that the down-regulation of cyclin D1 occurred as early as 6 hours after STAT1C gene transfection suggests that this biochemical change was a consequence of STAT1 up-regulation, rather than a ‘by-product’ of apoptosis.
In various cancer cell types, STAT1 has been previously reported to be an important mediator for NF-κB, which is known to play a critical role in carcinogenesis and chemoresistance in ESCC [40, 41]. The NF-κB signaling pathway was found to be constitutively activated in many ESCC cell lines; down-regulation of p65 has been shown to increase the sensitivity of ESCC cells to chemotherapeutic drugs [17, 18]. With this background, we tested if STAT1 is functionally linked to NF-κB in our experimental model. Our findings that modulation of STAT1 expression changed the expression level of phospho-p65, as well as the nuclear localization of p65/phospho-p65, and these findings support the concept that the STAT1 inhibits the growth of ESCC via its suppression of NF-κB signaling. Similar results have been described in cervical cancer, melanomas and fibrosarcomas [16, 42–44].
STAT3, another member of the STAT family, has been shown to exert opposing biological effects of STAT1 [20, 21, 45]. In contrast with STAT1, STAT3 promotes survival, proliferation and motility of cancer cells, and induces immune tolerance . Some of these opposing biological effects are likely related to the cross-talk between STAT1 and STAT3. For instance, it has been shown that STAT3 can block the activation and function of STAT1 in human monocytic cells . STAT3-knockout mouse embryonic fibroblasts exhibited prolonged IL-6-mediated STAT1 activation and induction of IFN-γ-inducible genes . In this study, we found evidence that STAT1 interferes with STAT3 signaling in ESCC cells using at least two mechanisms. First, STAT1 down-regulates STAT3 as well as phospho-STAT3. To our knowledge, this is a novel finding. Second, co-immunoprecipitation studies showed that STAT1C transfection in ESCC cells substantially increased STAT1:STAT3 heterodimer. Since the total STAT3 protein level was decreased after STAT1C transfection, it is logical to assume that STAT3:STAT3 homodimers were dramatically decreased at the same time. We believe that these findings are linked to the tumor suppressive effects of STAT1C in ESCC, as previous studies have shown that the relative proportions of STAT1 homodimers, STAT3 homodimers and STAT1:STAT3 heterodimers dictate the cell fate [21, 49, 50]. Based on the literature, other mechanisms where STAT1 inhibits STAT3 signaling may also exist. For instance, it has been shown that STAT1 can compete with STAT3 for the common receptor docking sites or target DNA sequences [2, 20]. Of note, most of these STAT1-mediated effects on STAT3 take place in the cytoplasm, and this may correlate with our observation that cytoplasmic STAT1, rather than nuclear STAT1, was prognostically important.
The role of STAT1 as a tumor suppressor is not without controversy. STAT1 overexpression has been demonstrated in several types of human cancer [51–55]. Some reports also have demonstrated that constitutive STAT1 signaling promotes tumor growth, increases resistance to chemotherapy and radiation, and carries a worse clinical outcome in patients with glioblastoma multiforme . The possible explanations for these rather contradictory findings may be related to the biological heterogeneity of cancer and STAT1 may function as a tumor suppressor or oncoprotein in a cell-type specific manner.
In conclusion, our findings suggest that STAT1 is a tumor suppressor in ESCC. Loss of STAT1, which is frequent in ESCC, contributes to the pathogenesis of these tumors. We have provided evidence that STAT1 attenuates the tumorigenicity of ESCC by inhibiting the STAT3 and NF-κB signaling pathway, and therefore that activation of STAT1 may be a useful approach to treat ESCC.
We thank the Professor Liyan Xu at the Shantou University Medical College for sharing SHEE, KYSE150 and KYSE510 cells with us. We also would like to thank Professor George Tsao from the University of Hong Kong for sharing NE2, NE3 and NE6 with us. ZY is a graduate student supported by the Li Ka Shing funding scholarship administered by the University of Alberta. This study was supported by NSFC-Guangdong joint fund key project (Certificates U1132004), NSFC (Certificates 31171226), Guangdong International Cooperative Technical Innovation Platform(Certificates gihz1106) and an operating research grant from the Canadian Institute of Health Research awarded to RL.
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