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Cooperation of Sox4 with β-catenin/p300 complex in transcriptional regulation of the Slug gene during divergent sarcomatous differentiation in uterine carcinosarcoma
BMC Cancer volume 16, Article number: 53 (2016)
Uterine carcinosarcoma (UCS) represents a true example of cancer associated with epithelial-mesenchymal transition (EMT), which exhibits cancer stem cell (CSC)-like traits. Both Sox and β-catenin signal transductions play key roles in the regulation of EMT/CSC properties, but little is known about their involvement in UCS tumorigenesis. Herein, we focused on the functional roles of the Sox/β-catenin pathway in UCSs.
EMT/CSC tests and transfection experiments were carried out using three endometrial carcinoma (Em Ca) cell lines. Immunohistochemical investigation was also applied for a total of 32 UCSs.
Em Ca cells cultured in STK2, a serum-free medium for mesenchymal stem cells, underwent changes in morphology toward an EMT appearance through downregulation of E-cadherin, along with upregulation of Slug, known as a target gene of β-catenin. The cells also showed CSC properties with an increase in the aldehyde dehydrogenase (ALDH) 1high activity population and spheroid formation, as well as upregulation of Sox4, Sox7, and Sox9. Of these Sox factors, overexpression of Sox4 dramatically led to transactivation of the Slug promoter, and the effects were further enhanced by cotransfection of Sox7 or Sox9. Sox4 was also able to promote β-catenin-mediated transcription of the Slug gene through formation of transcriptional complexes with β-catenin and p300, independent of TCF4 status. In clinical samples, both nuclear β-catenin and Slug scores were significantly higher in the sarcomatous elements as compared to carcinomatous components in UCSs, and were positively correlated with Sox4, Sox7, and Sox9 scores.
These findings suggested that Sox4, as well as Sox7 and Sox9, may contribute to regulation of EMT/CSC properties to promote development of sarcomatous components in UCSs through transcriptional regulation of the Slug gene by cooperating with the β-catenin/p300 signal pathway.
Uterine carcinosarcomas (UCSs), previously referred to as malignant mixed mullerian tumors, are aggressive neoplasms that contain both carcinomatous and sarcomatous elements, and the incidence is only 2–5 % of all uterine carcinomas [1, 2]. Clinically, more than 40 % of patients with UCSs are categorized as advanced stage at diagnosis, and over 50 % of cases show recurrence of the disease . Histopathologically, the most common epithelial components are serous, followed by endometrioid type, while the sarcomatous components are composed of homologous (composed of tissues normally found in the uterus) or heterologous tissues (containing tissues not normally found in the uterus, most commonly malignant cartilage and skeletal muscle) [4, 5].
Epithelial-mesenchymal transition (EMT) plays a central role in converting both normal and neoplastic epithelial cells into derivatives with a more mesenchymal phenotype [6, 7]. A hallmark of EMT is loss of cell-cell adhesion molecules, down-regulation of epithelial differentiation markers, and transcriptional induction of mesenchymal markers, along with nuclear localization of β-catenin . Snail, Slug, and Twist, all repressors of the E-cadherin gene, are also involved in the process [9–12]. Given that UCSs are regarded as metaplastic carcinomas when the sarcomatous component is derived from the carcinoma, it is suggested that EMT may play an important role in tumorigenesis of UCSs.
A growing body of evidence shows that tumors contain a very small subpopulation of cancer stem cells (CSCs) or tumor-initiating cells . CSCs, similar to somatic stem cells, are defined as cells within a tumor that possess the capacity to self-renew and to differentiate into the heterogeneous lineages of cancer cells that comprise the tumors . Interestingly, a relationship between EMT and CSCs has been proposed with evidence demonstrating that EMT cells exhibit stem cell-like traits and CSCs acquire mesenchymal-like characteristics,  pointing to the possibility that sarcomatous stem-like cells derived from carcinoma cells may also be present and act as progenitors for divergent sarcomatous differentiation.
Both Sox and β-catenin signal transductions display a broad spectrum of biological function in the regulation of EMT/CSC properties in a wide variety of cells [15–17]. We therefore hypothesize that this signal pathway may contribute to the determination of phenotypic characteristics through modulation of EMT/CSC properties in UCSs. To test this, we hereby investigated the expression of several Sox factors, β-catenin, and Slug, with reference to EMT/CSC properties, using endometrial carcinoma (EmCa) cell lines and clinical UCS samples.
Plasmids and cell lines
The pGL3B-Slug luc constructs, including −2125/−235 bp, −1859/−235 bp, −1587/−235 bp, and −813/−235 bp fragments, pcDNA3.1-HA-β-cateninΔS45, pcDNA3.1-Sox4, pcDNA3.1-Sox7, pcDNA3.1-Sox9, pcDNA3.1-HA-Slug, PCI-Flag-p300, pcDNA3.1-TCF4ΔN30 (dominant-negative form of TCF4), pG5 luc, and pM-β-cateninΔS45 were used as described previously [18–21]. pM-Sox4 was constructed by inserting the Sox4 cDNA fragment into the pM DNA-BD vector (BD Biosciences Clontech, Worcester, MA, USA). Site-directed mutagenesis of putative Sox4 binding sites in the Slug promoter was performed using the PrimeSTAR Mutagenesis Basal kit (Takara Bio, Shiga, Japan).
The Em Ca cell lines, Ishikawa, Hec251, and Hec6 cells, were maintained in Eagle’s MEM with 10 % bovine calf serum. To establish cells stably overexpressing HA-Slug, the expression plasmids or empty vectors were transfected into Hec6 cells, and stable clones were established as described previously .
Antibodies and reagents
Anti-β-catenin and anti-p27kip1 antibodies were purchased from BD Biosciences (San Jose, CA, USA). Anti-Sox4, anti-Sox6, anti-Sox7, anti-Sox9, anti-Sox11, and β-actin antibodies were obtained from Sigma-Aldrich Chemicals (St. Louis, MO, USA). Anti-Snail and anti-Slug antibodies were from Cell Signaling (Danvers, MA, USA). Anti-p21waf1, anti-cyclin D1, and anti-CD44s antibodies were purchased from Dako (Copenhagen, Denmark). Anti-Sox2 and anti-cyclin A antibodies were from Abcam (Cambridge, MA, USA) and Novocastra (Newcastle, UK), respectively. Anti-HA and anti-E-cadherin antibodies were obtained from Santa Cruz Biotechnology (Santa Cruz, CA, USA) and Takara (Shiga, Japan) respectively. Anti-CD133 antibody was from Miltenyi Biotechnology (Bergisch Gladbach, Germany).
STK2, which is a serum-free culture medium for mesenchymal stem cells,  was obtained from DS Pharma Biomedical (Osaka, Japan).
Transfection was carried out using LipofectAMINE PLUS (Invitrogen, Carlsbad, CA, USA) in duplicate or triplicate as described previously [18–21]. Luciferase activity was assayed as described previously [18–21].
Real-time reverse-transcription polymerase chain reaction (RT-PCR)
cDNA was synthesized from 2 μg of total RNA. For quantitative analysis, real-time RT-PCR was carried out using a Power SYBR Green PCR Master Mix (Applied Biosystems, Foster City, CA, USA) with specific primers (Table 1). Fluorescent signals were detected using the ABI 7500 real-time PCR System, and data were analyzed using the associated ABI 7500 System SDS Software (Applied Biosystems). Primers for the GAPDH gene were also applied, as described previously [18–21].
Western blot assay and immunoprecipitation
Total cellular proteins were isolated using RIPA buffer [20 mM Tris–HCl (pH7.2), 1 % Nonidet P-40, 0.5 % sodium deoxycholate, 0.1 % sodium dodecyl sulfate]. Aliquots of the proteins were resolved by SDS-PAGE, transferred to membranes, and probed with primary antibodies, coupled with the ECL detection system (Amersham Pharmacia Biotechnology, Tokyo, Japan).
For immunoprecipitation, cells cultured in STK2 were lysed with TNE buffer [10 mM Tris–HCl (pH7.6), 150 mM NaCl, 1 % NP-40, 1 mM EDTA]. Cell lysates were cleared and incubated with anti-Sox4 antibody, followed by incubation with Protein G-Sepharose (Amersham Pharmacia Biotechnology). Western blot assay was subsequently performed with anti-β-catenin and anti-Sox4 antibodies.
Flow cytometry and Aldefluor assay
Cells were fixed using 70 % alcohol and stained with propidium iodide (Sigma) for cell cycle analysis. ALDH 1 enzyme activity in viable cells was determined using a fluorogenic dye based Aldefluor assay (Stem Cell Technologies, Grenoble, France) according to the manufacturer’s instructions. The prepared cells were analyzed by flow cytometry using BD FACS Calibur (BD Biosciences) and CellQuest Pro software version 3.3 (BD Biosciences).
Cells (x103) were plated in low cell binding plates (Thermo Fisher Scientific, Yokohama, Japan) in STK2 or Eagle’s MEM with 10 % bovine calf serum. Uniform spheroids of at least 50 μm in size were counted approximately 2 weeks after plating.
Chromatin immunoprecipitation (ChlP) assay
ChIP analysis was performed using an EpiXplore ChIP assay kit (Clontech Laboratory, Mountain View, CA, USA). Briefly, after culture in STK2 for 1 week, cells were cross-linked with formaldehyde. Cell lysates were sonicated to shear DNA to lengths between 200 and 1000 bp, and then precipitated overnight using anti-Sox4 antibody or rabbit IgG as negative control, along with magnetic beads. After proteinase K digestion, DNA was extracted and analyzed by PCR. ChIP analysis was conducted with a reduction in the number of cycles from 30 to 25, using four specific primer sets.
We reviewed cases of comprehensively staged high-grade endometrial adenocarcinomas from the patient records of Kitasato University Hospital in the period from 1997 to 2012. According to the criteria of the 2014 World Health Organization classification,  tumors were designated as UCS if they had evidence of both malignant epithelial (endometrioid, serous, or clear cell) components and mesenchymal (homologous or heterologous) elements. Endometrioid adenocarcinomas with spindle elements and hyalinized stroma were specifically excluded. Finally, a total of 32 UCSs were investigated. Of these, 9 cases had endometrioid and 23 cases had non-endometrioid epithelial components, while 25 and 8 cases showed homologous and heterologous mesenchymal elements, respectively. All tissues were routinely fixed in 10 % formalin and processed for embedding in paraffin wax. Approval for this study was given by the Ethics Committee of the Kitasato University School of Medicine (B14-35). Signed informed consent forms were not required from the participants due to the retrospective approach of the study, which did not impact on their treatment.
IHC was performed using a combination of the microwave-oven heating and polymer immunocomplex (Envision, Dako) methods, as described previously [18–21]. The immunoreactions were visualized with DAB (3,3′ diaminobenzidine), and the nuclei were counterstained with methyl green.
For evaluation of IHC findings, scoring of nuclear immunoreactivity was performed, on the basis of the percentage of immunopositive cells and the immunointensity, with multiplication of values of the two parameters, as described previously [18–21].
Comparative data were analyzed using the Mann–Whitney U-test, and the Spearman’s correlation coefficient. The cutoff for statistical significance was set as p < 0.05.
Changes in expression of Sox factors during the EMT process in Em Ca cells
To induce EMT in Em Ca cells, the three cell lines, including Ishikawa, Hec251, and Hec6 cells, were cultured in STK2, a serum-free medium for mesenchymal stem cells . As shown in Fig. 1a, cells cultured in STK2 demonstrated a dramatically altered morphology toward a fibroblast-like appearance after 73 h, along with decreased E-cadherin and increased Slug expression at both mRNA and protein levels (Fig. 1b and c). In contrast, changes in Snail expression at the protein level (Fig. 1b), as well as the mRNA level, were relatively weak (data not shown).
Next, we examined whether Sox factors are directly involved in regulation of the EMT process observed in cells cultured in STK2, since some molecules are involved in the promotion of EMT . The Ishikawa, Hec251, and Hec6 cells cultured in STK2 showed increased expression of Sox4, Sox7, and Sox9, but not Sox6 and Sox11, at both protein and mRNA levels (Fig. 1d and e). In addition, the Sox4 promoter activity was increased by 20–50 folds following transfection of Sox7, while changes in the promoter activity of both Sox7 and Sox9 in response to other Sox factors were relatively minor (Fig. 1f and Additional file 1: Figure S1A). These findings suggested that culturing Em Ca cells in STK2 was sufficient to induce EMT, along with downregulation of E-cadherin and upregulation of Slug. In addition, upregulation of some Sox factors through formation of complex transcriptional regulatory loops occurs during the EMT process in Em Ca cells.
Relationship between EMT and CSC properties in Em Ca cells
To examine whether EMT is linked to CSC properties, Hec6 cells were selected since they showed higher Slug expression as compared to those in Ishikawa and Hecc251 cells after culturing in STK2 (Fig. 1b). Cultured Hec6 cells had a low cell proliferation rate, particularly in the exponential growth phase, which correlated with increased p21waf1 but not p27Kip1 expression, and a decreased S-fraction during cell cycle progression (Fig. 2a). The inhibitory effects were also observed in Ishikawa and Hec251 cells (data not shown). Aldefluor assay revealed an increase in the ALDH1high activity population (Fig. 2b), in line with the significantly increased number of well-defined, round spheroids that were over 50 um in size (Fig. 2c). In addition, expression of other CSC markers, including CD44s and Sox2, but not CD133, was also increased in Hec6 cells as well as Ishikawa and Hec251 cells cultured in STK2 (Additional file 1: Figure S1B). These findings indicated that the Em Ca cells cultured in STK2 exhibited EMT/CSC properties.
Slug is associated with EMT/CSC properties in Em Ca cells
To examine whether Slug is directly linked to induction of EMT/CSC properties, two independent Hec6 cell lines stably overexpressing Slug (H6SL#8 and #21) were established. The stable cells underwent a dramatic change in morphology to fibroblast-like mesenchymal features with decreased E-cadherin expression, independent of Snail status (Fig. 2d). In H6SL#8 cells, the proliferative activity was extremely low, along with an inhibition of the S- to G2/M-phase during cell cycle progression (Fig. 2e). In addition, the ALDH1high activity population was increased in the stable cells (Fig. 2f). However, changes in expression of Sox4, Sox7, and Sox9 were relatively minor in H6SL#8 cells as compared to the mock (Additional file 1: Figure S1C). These findings suggested that exogenous overexpression of Slug is sufficient in induction of EMT/CSC properties in Em Ca cells, independent of Sox factors.
Transcriptional regulation of the Slug gene by Sox factors in Em Ca cells
To examine whether Sox factors are directly involved in transcription of the Slug gene, the three Sox factors, whose expression was differentially regulated by culturing in STK2, were transfected into three Em Ca cell lines. Transient transfection of Sox4 resulted in increased activity of the Slug promoter, along with increased mRNA levels, which were further enhanced by cotransfection of Sox7 or Sox9. In contrast, such effects were relatively minor when only Sox7 and/or Sox9 were transfected (Fig. 3a and Additional file 2: Figure S2A and B).
Analysis of an approximately 2000 bp fragment upstream of the translation start site in the Slug gene (AF084243) revealed four potential Sox4-binding elements (BE) (A/T A/T CAA A/T G) (Fig. 3b). Using a series of 5′-truncated promoter constructs, we found that deletion from −2125 to −1587 bp had little effect on induction of the promoter activity by Sox4, as well as Sox7 and Sox9, whereas the -813/-235 bp deletion appeared to have prevented binding of the Sox factors and reduced the promoter activity to a very low level (Fig. 3c and Additional file 2: Figure S2C). This indicated that the region involved in the response to Sox4 is present between −2125 to −813 bp. Additional promoter constructs carrying four nucleotide alterations in all of the putative Sox4-binding sites, including Sox4-1, Sox4-2, Sox4-3, and Sox4-4 (Fig. 3b), resulted in considerable reduction of response to Sox4 (Fig. 3d). ChIP assays revealed that increased amount of Sox4 by STK2 culture caused its recruitment to these four Sox4-BEs within the promoter (Fig. 3e). These findings suggest that Slug is a target gene of Sox4.
Association between β-catenin and Sox4 on transcriptional regulation of the Slug gene in Em Ca cells
Since it has been reported that β-catenin is a positive regulator of Slug expression,  we examined for an association between Sox4 and β-catenin in regulation of the Slug promoter. The promoter activity was increased by a combination of β-catenin and Sox4, and the effect was further enhanced by cotransfection of the multifunctional coactivator p300, but not by dominant-negative TCF4 (Fig. 4a and Additional file 3: Figure S3A). Cotransfection of GFP-Sox4, HA-β-cateninΔS45, and Flag-p300 resulted in formation of several enlarged dots in the nuclei (Fig. 4b), whereas such nuclear aggregates were not observed after cotransfection of GFP-Sox4 and HA-β-cateninΔS45 alone (Additional file 3: Figure S3B). One-hybrid assays revealed that the pG5 luc reporter activity was raised by 3–12 folds following cotransfection of either DNA-BD-fused full-length β-catenin or Sox4 fragment (pM-β-cat or pM-Sox4) and p300, but such effects were relatively minor with cotransfection of only pM-β-catenin and Sox4, Sox7 or Sox9 (Fig. 4c and Additional file 3: Figure S3C and D). Finally, coimmunoprecipitation using lysates of cells cultured in STK2 revealed a weak interaction between β-catenin and Sox4 (Fig. 4d). These findings suggested that Sox4 cooperates with β-catenin/p300 complexes in the transcriptional regulation of the Slug gene.
Immunohistochemical (IHC) findings in UCSs
Representative images of IHC findings for Slug, β-catenin, and Sox factors are illustrated in Fig. 5a. Distinct nuclear immunostaining for Slug, Sox4, Sox7, and Sox9, and nuclear and cytoplasmic/membranous immunoreaction for β-catenin were observed in both the carcinomatous and sarcomatous components of UCSs. Average nuclear β-catenin and Slug scores were significantly higher in the sarcomatous elements than those in the carcinomatous components, in contrast to no significant differences in the scores of Sox4, Sox7, and Sox9 (Fig. 5b). The average Slug score was positively correlated with nuclear β-catenin score and combinations of the three Sox factors, including Sox4/Sox9, Sox7/Sox9, and Sox4/Sox7/Sox9. The nuclear β-catenin score also showed a positive correlation with combinations of the three Sox factors (Table 2).
The present study clearly provided evidence for a close link between EMT and CSC properties in Em Ca cells. We found that culturing Em Ca cells in STK2 was sufficient to induce EMT, as demonstrated by the acquirement of a spindle-like morphology as well as decreased E-cadherin and increased Slug expression. The IHC data also demonstrated a significantly higher Slug score in sarcomatous elements relative to carcinomatous components of UCSs. Further, the cell proliferation rates were significantly decreased during the process, in line with the report showing that Snail-expressing epithelial cells undergoing EMT have a low proliferation potential . The cells cultured in STK2 also showed stem cell properties as evidenced by an increase in the ALDH1high cell population and the number of spheroid formation. Given that EMT leads to a greater number of self-renewing cells that can initiate the seeding of spheroids with enriched stem cells,  it is likely that mesenchymal stem-like cells derived from carcinoma cells may be necessary for establishment of the sarcomatous components in UCSs.
In addition to EMT/CSC properties, the Em Ca cells cultured in STK2 also exhibited simultaneous upregulation of Sox4, Sox7, and Sox9. Interestingly, the Sox4 promoter activity was drastically increased by transfection of Sox7, in line with the IHC data showing significant positive correlation between the two in UCS tissues. Although both Sox7 and Sox9 promoters were also weakly activated by either Sox4, Sox7, or Sox9 in Hec6 cells, such associations were absent in UCS tissues. Given the evidence that expression of Sox genes themselves is frequently subjected to auto-regulation or control by other Sox proteins,  it appeared that complex regulatory loops among these Sox factors including the Sox7/Sox4 axis may be activated during the EMT/CSC process.
Unexpectedly, we found that Hec6 cells stably overexpressing Slug did not show any changes in expression of Sox4, Sox7, and Sox9, although the cells displayed EMT/CSC properties. This may be because Sox factors are upstream of Slug and thus are no longer required for the process in cells exogenously overexpressing Slug. In addition, it is also unexpected that there were no significant differences in the Sox factor scores between sarcomatous and carcinomatous components in UCSs, although combinations of the Sox factors showed positive correlations with both Slug and nuclear β-catenin scores. At the present time, although we are unable to provide an appropriate explanation for the observation, one possible reason may be that various post-translational modifications modulate the activity, stability, and intracellular localization of some Sox proteins. For example, some Sox factors are subject to various covalent modifications such as phosphorylation, sumoylation, acetylation, methylation, and glycosylation [26–31]. Further studies to clarify these points are clearly warranted.
Several lines of evidence from the present study support the conclusion that Sox4 contributes to transcriptional control of the Slug gene. First, overexpression of both Slug and Sox4 occurred in Em Ca cells cultured in STK2. Second, transient transfection of Sox4 caused an increase in Slug mRNA expression, in line with activation of its promoter. Third, Sox4 could bind to the promoter region of the Slug gene from −2125 to −813 bp, probably through its interaction with four putative Sox4-BEs. The effects were further enhanced by cotransfection of Sox9 and/or Sox7. Interestingly, it has been recently reported that ectopic Sox4 expression in human mammary epithelial cells could induce a mesenchymal phenotype, which was associated with increased stem cell properties, cellular migration, and invasion in vitro .
Sox proteins generally exhibit gene regulatory functions only by forming complexes with partner transcription factors . Transcriptional activity and target gene specificity of Sox4 are also considered to be controlled through cooperative interactions with distinct transcription factors and cofactors . In this study, Sox4 was able to enhance β-catenin-mediated transcription of the Slug gene through formation of transcriptional complexes including β-catenin, Sox4, and p300. Although Sox4 has been demonstrated to directly interact with TCF4 via their respective HMG domain by in vitro protein-binding assay,  our present data revealed that activation of the Slug promoter by Sox4, as well as β-catenin, was not abrogated by dominant-negative TCF4, indicating that the observed activation did not require TCF4-binding sites in the promoter.
Our observations suggest a mode of molecular mechanism for establishment of sarcomatous components with EMT/CSC properties in UCSs (Fig. 6). Upregulation of Slug by Sox4, as well as β-catenin and p300 complexes, induces EMT and associated CSC properties, which in turn results in the promotion of homologus and heterologous sarcomatous components in UCSs. Increased expression of Sox7 and Sox9, as well as cooperation between Sox7 and Sox4, also participate in the process. Thus, the present study clearly provided evidence of a functional role for Sox4 through its association with β-catenin and p300 in regulation of the Slug gene during development of the sarcomatous component in UCSs.
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This study was supported by a grant from JSPS KAKENHI Grant Number 26460427.
The authors declare that they have no competing interests.
HI and MS carried out the majority of the experiments, analyzed the data, and wrote the manuscript. They were helped by HT, MH and AM. KE and TM were involved in the study design and data collection. All authors reviewed and approved the final manuscript.
(A) Ishikawa (Ish) cells were transfected with Sox4, Sox7, and Sox9 reporter constructs, together with either Sox4, Sox7, or Sox9. Relative activity was determined based on arbitrary light units of luciferase activity normalized to pRL-TK activity. The activities of the reporter plus the effector relative to that of the reporter plus empty vector are shown as means ± SDs. The experiment was performed in duplicate. (B) Western blot analysis for the indicated proteins from Ishikawa, Hec251, and Hec6 cells cultured in STK2. (C) Western blot analysis for the indicated proteins from H6SL#8 and mock cells. (TIF 2816 kb)
(A) Ishikawa (left) and Hec251 cells (right) were transfected with Slug reporter constructs, together with Sox4, Sox7, and Sox9. Relative activity was determined based on arbitrary light units of luciferase activity normalized to pRL-TK activity. The activities of the reporter plus the effector relative to that of the reporter plus empty vector are shown as means ± SDs. (B) Analysis of mRNA levels for the Slug gene with total RNA extracted from Hec251 cells after transfection of Sox4, Sox7, and Sox9 using real time RT-PCR assays. The experiment was performed in triplicate. (C) Various promoter constructs were used for evaluating transcriptional regulation of the Slug promoter by Sox4, Sox7, and Sox9 in Ishikawa (left) and Hec251 cells (right). The experiment was performed in triplicate. (TIF 1198 kb)
(A) Hec251 (left) and Hec6 cells (right) were transfected with Slug reporter constructs, together with β-cateninΔS45 (β-cat), Sox4, and p300. Relative activity was determined based on arbitrary light units of luciferase activity normalized to pRL-TK activity. The activities of the reporter plus the effector relative to that of the reporter plus empty vector are shown as means ± SDs. The experiment was performed in duplicate. (B) After transfection of HA-β-cateninΔS45 and GFP-Sox4, cells were stained with anti-HA antibody. Immunopositive cell is indicated by arrow. Nuclei were stained by DAPI. (C,D) Hec251 (C) and Hec6 (D) cells were transfected with pM-β-catenin (left) or pM-Sox4 (right), along with pGL5 luc, Sox4, Sox7, Sox9, and p300. The experiment was performed in duplicate. (TIF 2017 kb)
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Inoue, H., Takahashi, H., Hashimura, M. et al. Cooperation of Sox4 with β-catenin/p300 complex in transcriptional regulation of the Slug gene during divergent sarcomatous differentiation in uterine carcinosarcoma. BMC Cancer 16, 53 (2016) doi:10.1186/s12885-016-2090-y
- Uterine carcinosarcoma