|
Comparison of gene expression of SOX2 and OCT4 in normal tissue, polyps, and colon adenocarcinoma using immunohistochemical staining
Ardeshir Talebi, Kianoosh Kianersi, Mozhdeh Beiraghdar
Department of Pathology, Isfahan University of Medical Sciences, Isfahan, Iran
| Date of Submission | 09-May-2015 |
| Date of Acceptance | 29-Jul-2015 |
| Date of Web Publication | 22-Oct-2015 |
Correspondence Address:
Mozhdeh Beiraghdar
Department of Pathology, Isfahan University of Medical Sciences, Isfahan
Iran
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/2277-9175.167958
Background: Cancer stem cells have been isolated and characterized in all common cancers. SOX2 and OCT4 are important genes to enhance the self-renewal ability as activate stem cells and inhibit the genes that start differentiation and thus maintain the self-renewal ability of stem cells. Also, the aim of this study is "Comparison of gene expression of SOX2 and OCT4 in normal tissue, polyps, and colon adenocarcinoma using immunohistochemical staining."
Materials and Methods: This cross-sectional study conducted on 20 patients so that for each patient, a sample of healthy tissue, dysplastic polyp tissue, and colon adenocarcinoma were provided as microscopic sections and staining on each tissue was performed through immunohistochemistry method by markers OCT4 and SOX2. The collected data were interred into SPSS version 18.0, (SPSS Inc., Chicago, IL, USA) software and the level of significance were considered as <0.05.
Results: The study sample consisted of 20 patients including 11 men (55%) and 9 women (45%) with a mean age of 55.6 ± 9.88 years. There was no association between Oct4 and colorectal cancer (CRC) patients (P > 0.05), but there was a significant correlation between Sox2 expression and CRC (P < 0.05). Patients in many aspects such as race, type of polyp, presence of lymph node, grade and intensity of Sox2 in different types of patients' tissues (P < 0.05).
Conclusion: Regarding our findings, the expression of Sox2 would be a liable marker for evaluating of cancer progression and could be a treatment target of CRC cells. Keywords: Colon adenocarcinoma, colorectal cancer, dysplastic polyp, immunohistochemical, OCT4, SOX2
How to cite this article:
Talebi A, Kianersi K, Beiraghdar M. Comparison of gene expression of SOX2 and OCT4 in normal tissue, polyps, and colon adenocarcinoma using immunohistochemical staining. Adv Biomed Res 2015;4:234 |
How to cite this URL:
Talebi A, Kianersi K, Beiraghdar M. Comparison of gene expression of SOX2 and OCT4 in normal tissue, polyps, and colon adenocarcinoma using immunohistochemical staining. Adv Biomed Res [serial online] 2015 [cited 2023 Mar 26];4:234. Available from: https://www.advbiores.net/text.asp?2015/4/1/234/167958 |
| Introduction | |  |
Colon cancer after lung cancer is the most important cause of cancer-related deaths in the world. [1] According to the new theory of stem cell origin of cancer, most tumors originate from cancer stem cells. According to this theory, nowadays the factors that cause inhibiting the process of the differentiation and uncontrolled proliferation of tissue stem cells are the most important factors in the carcinogenesis process. [2],[3]
SOX2 (a member of the Sox [SRY-Related HMG box] gene family) and OCT4 (a member of the POU family) are important genes to enhance the self-renewal ability as activate stem cells and inhibit the genes that start differentiation and thus maintain self-renewal ability of stem cells. [4],[5] So these markers have a nuclear pattern in immunohistochemistry (IHC). The level of Oct4 and Sox2 mRNA in peripheral blood of patients with metastatic colorectal cancer (CRC) was found to be higher than in healthy controls by quantitative real-time-polymerase chain reaction (RT-PCR). [6] Also, in rectal cancer, higher mRNA levels of Oct4 and Sox2 in residual tumors after preoperative chemoradiotherapy were associated with higher rates of metastatic relapse. [7]
Cancer stem cells with metastatic potential represent poor resistance to treatment and prognosis. Recurrence of the tumor is one of the major causes of morbidity and mortality in patients with rectal cancer undergoing chemoradiotherapy. Therefore, the study of markers of stem cell (OCT4, SOX2) in colon cancer and the relationship between the expression of these genes and their clinical outcomes have particular importance. Patients with tumor recurrence after the chemotherapy for CRC show a higher level of expression of these genes (SOX2, OCT4) rather than those who do not have. The increased levels of these genes are clearly associated with poor prognosis. Gene expression of OCT4 and SOX2 can predict recurrence of the tumor and improve the prognosis of patients with rectal cancer treated with preoperative chemoradiotherapy. These genes together could be associated with recurrence and metastasis after chemotherapy. [8]
RT-PCR analysis of cells engaged in colon cancer showed gene expression of OCT4 and SOX2 and also IHC analysis confirmed the nuclear and cytoplasmic expression of OCT4. The role of OCT4 and SOX2 in colon cancer has been confirmed and suggested the level of gene expression could be defined as tumor markers in diagnosis and prognosis of colon tumors. These results are also confirming the role of the theory of cancer stem cell in cancer. [9]
Moreover, SOX2 is involved in metastases of lymph nodes. Also, these findings show the importance of markers associated with stemness in detecting the high risk colon cancer for distant metastases. [10]
Gene expression of OCT4 and SOX2 as self-renewal genes in colorectal adenocarcinoma HT-29 and CaCO 2 as cancer cells is confirmed that it helps to confirm the cancer stem cell theory. However, further studies are needed to find the cause of the existence of such localization. [11]
Given that, it is clinically proven that colon polyps can be converted to adenocarcinoma but in the case of pathogenesis of adenocarcinoma, a variety of content has been mentioned. But one of the causes of cancer could be related to the gene expression of stemness in cells, and studies about the role of SOX2 and OCT4 gene on polyps has been rare so far.
Therefore, this study, in the first stage, determine the relationship between these genes and cancer and in the second stage responds to this question of whether the emergence of dysplasia in colorectal polyps compared with healthy tissue, is related to these genes or not; In other words, whether the neoplastic and stepped progress of tumor from healthy to dysplasia and from dysplasia to cancer which is provable by morphological method, is compliant with to the level of gene expression of these genes in terms of quality and quantity or not?
| Materials and methods | | |
This is a cross-sectional study. In order to prepare the colon tissue sample, 20 patients with symptoms such as bleeding or severe anemia and the result of colonoscopy and biopsy reported as adenocarcinoma undergoing colectomy and had simultaneous polyps and cancer in their macroscopic examination in the laboratory have been participated. It should be noted that where microscopic polyps had dysplasia, they were included in the study. No limitation has been considered with regard to the stage of the disease. For each patient, a sample of healthy tissue, dysplastic polyp tissue (tubular, villous, or tubulovillous), and colon adenocarcinoma were provided as microscopic sections and staining on each tissue was performed through IHC method by markers OCT4 (mouse monoclonal anti-OCT4, Diagnostic BioSystem, Clone ≥ NRG1.1) and SOX2 (mouse monoclonal anti-SOX2, Diagnostic BioSystem, Clone ≥ NRG5.6) as follows. First, the slides were put in tumor at 74°C for 50 min to embed paraffin, and then they were put in two containers with xylenol (5 min), absolute alcohol (5 min), and 96% alcohol (2 min), respectively. For antigen retrieval, the slides were put on citrate buffer with pH = 6 in boiling water bath for 1 h. Then, the slides were put in phosphate buffer and then in 3% hydrogen peroxide for 10 min and were re-washed with phosphate buffered saline (PBS). Primary antibodies were poured on slides for 60 min, and the slides were placed in PBS and then put in EnVision Dual Link System Peroxidase for 1 h. The slides were washed again in phosphate buffer and put in 3, 3'-diaminobenzidine slides for 3-5 min (corrosion) and then, washed with distilled water. Finally, the slides were put into hematoxylin and dewatering process (taking on alcohol) was performed. By putting a cover slip and pasting slides by special IHC, staining was performed [Figure 1] and [Figure 2]. The percentage of stained cells with nuclear pattern (with ranking of Grade 0: Negative, Grade: 1-25%, Grade II: 26-50%, Grade III: 51-75%, and Grade IV: 76-100%) in each healthy sample, polyp, adenocarcinoma per high power field (averagely) and the intensity of their staining (with ranking of 0: Negative, 1: Weakly positive, 2: Mod (inter) positive, 3: Strongly positive) were recorded. (Note: In each cycle of doing IHC, positive control [seminoma for OCT4 and squamous cell carcinoma larynx for SOX2] and for both marker and the negative control, all conditions were kept the same, except that the primary antibody was omitted). The collected data were interred into SPSS version 18.0, (SPSS Inc., Chicago, IL, USA) software and for analysis, Chi-square test, independent t-test, and linear regression test were run and the level of significance was considered as <0.05. | Figure 1: Immunohistochemical staining of SOX2; (a) Positive control sox2 squamous cell carcinoma, (b) Sox2 immunohistochemistry in normal, (c) Sox2 immunohistochemistry in adenocarcinoma of colon, (d) Sox2 immunohistochemistry in villus polyp
Click here to view |
 | Figure 2: Immunohistochemical staining of OCT4; (a) Positive control of OCT4 (seminoma), (b) negative immunohistochemistry staining for oct4 in adenocarcinoma of colon, (c) OCT4 immunohistochemistry staining in normal epithelium of colon, (d) OCT4 immunohistochemistry staining in villus polyp
Click here to view |
| Results | | |
The study sample consisted of 20 patients including 11 men (55%) and 9 women (45%) with a mean age of 55.6 ± 9.88 among which 3 of them (15%) were from Afghanistan. Pathology results showed that tubular polyp was the most common types of polyps (60%) and the most common site of polyps was sigmoid with 8 cases (40%) and the maximum size of 1.83 ± 0.81 mm and the number was at least 1 and a maximum of 4. On the other hand, the cancer location in 9 patients (45%) had the highest prevalence in sigmoid with the cancer stages of I to IV. Metastatic lymph nodes were eventually positive in 11 cases (55%) [Table 1].
In order to detect the relation between these genes and development of colon cancer, SOX2 and OCT4 gene expression study in development of dysplasia in the colon polyps and cancer showed that in SOX2 marker, the percentage of stained cells and color ability of normal tissue to dysplasia and from dysplasia to carcinoma increased significantly so that the degree of expression and staining intensity had the lowest and the highest levels in normal and cancer tissues respectively (P < 0.05). But OCT4 marker had no expression in the three studied tissue samples and therefore it can say the diagnostic power of the gene is not enough to identify cancer. So in general, the SOX2 gene expression power is more than OCT4 that this difference was significant only in normal tissue ( P = 0.035) [Table 2]. | Table 2: Frequency distribution of the percentage and intensity of stained cells in Sox2 and Oct4 markers
Click here to view |
Also, expressed by markers SOX2 in comparison with the intensity of staining in tissue showed that in normal tissue from 4 cases have been 3 cases of intensity 1 and 1 cases of intensity 2. Against in polyp tissue, frequency in intensity 2 has 3. And eventually cancer tissue from 6 expressions observed in 5 cases were with the highest intensity (intensity 3), in fact, the progress of the disease, the staining intensity of marker been effective ( P < 0.05) [Table 3]. | Table 3: Comparison the frequency distribution of percentage of stained cells and the intensity of staining in the three tissues studied
Click here to view |
On the other hand, according to the performed regression analysis, no factor played an effective role in the expression of SOX2 in normal tissue; but polyp tissue the polyp type had a significant effect on the percentage of stained cells and in the cancer tissue, the role of race and lymph node with the impact factor of 2.589 and 0.318 were effective in the gene expression so that the percentage of stained cells and the intensity of staining in an Afghanistan patients and someone who had lymph node were significantly stronger than that in Iranian patient and without lymph node ( P < 0.05); also, as it can be seen in [Figure 2], the rate of expression in villous polyps with two cases was more which is statistically was significant. On the other hand all observed expression in third stages of C and A was cancer; however, these factors and others had statistically no significant role in the expression and incidence of gene [Table 4] and [Figure 3]. | Figure 3: The comparative investigation of the mean expression of gene in terms of type, number, polyp site, and cancer stage
Click here to view |
 | Table 4: Regression analysis of the role of factors affecting the percentage of cells stained in markers Sox2
Click here to view |
| Discussion | | |
CRC is one of the fastest worldwide growing and the most common causes of death cancers in which the life expectancy is slightly reduce, especially in young adults, [12] and has two major subtypes including high-under graded B-catenin cells caused by lesion in the Wnt/adenomatous polyposis coli/B-catenin pathway and microsatellite instability cells, leading to disrupt of from stem cells to normal colorectal epithelial cells transformation. [13] Both of these pathways are in association with pluripotency transcription factors such as Sox2, and Oct4. Furthermore, CRC stem cells have several markers such as CD133 and CD44, which are very important in order to distinct from other normal cell phenotypes. [14] CD133 expresses co-related with an expression of Sox2 and Oct4. [12] CD44 also promotes pluripotency by co-operating with Sox2 and Oct4. [15]
In the present study, we investigated about the potential tumor markers in the prognosis of CRC. We couldn't find any significant association between the expression of Oct4 and kinds of tissues (normal, polyp, and cancer) for both intensity and number of stained tissue cells. In the normal adult cells, Oct4 is not expressing normally, [16] but with not presence of expression in polyp or tumor tissues, we think that due to the limitation of our study population, we couldn't find any expression of Oct4 protein. In the previous study, it has been found that inhibition of Oct4 in colon cancer cells was beneficial for preventing them from metastasis. [17]
Moreover, Oct4 could regulate epithelial-mesenchymal transition, and lack of its expression might inhibit the epithelial to mesenchymal transition pathway, which consequently impedes from migration and invasion of CRC cells. [17] As the result, we presumed that our patients were not in metastasis phase, but our result indicated that more than 50% of our population had metastatic lymph node. It might be due to the lack of other markers' assessment such as EpCAM, because of its interaction with β-catenin in c-myc transcription, [18] or prevent p53 activity [19] and Lgr5 (since promoting Wnt signaling pathway to transcription of β-catenin), [20] which leads to undistinguishing reason for not having expression of Oct4; therefore, we could not find the alternating tumor initiation pathways to express the persuasive explanation. Also, according to the previous investigations, Oct4 is good marker for prognosis of CRC, [21] and expression of Oct4 informed the adverse prognosis of CRC patients, [14] but we could not find Oct4 expression in different patients' tissues and would not discuss it as well.
Despite not having Oct4 expression in our population, our assessment in accordance with previous study [22] revealed that the percentage of cells expressing Sox2 from normal tissues of patients to cancer tissues increased ( P = 0.040). Meanwhile, the intensity of IHC stain from normal to cancer tissues significantly increased ( P = 0.018). Sox2 is contributing to the cancer progress through its functional control of the pluripotent state and cell self-renewal. [23],[24] Besides, expression of Sox2 is contributing to keep stemness features of tumor-initiated cells, which has a pivotal role, in tumorigenic properties. [25],[26] In addition, evaluating of Sox2 expression in both nuclear and cytoplasm of CRC cells have demonstrated the enhanced level of protein, of which enhances the ability to colony formation, tumor development, and migration features. [27]
Another point we have found was that expression of Sox2 increased from normal to cancer tissue (P = 0.046). Other studies have shown that expression of Sox2 protein was dramatically increased in cancer cells compared to normal tissues, [27] and it was occurred because of inducing cancer stemness in CRC cells, [28] and controlling many receptor mediating signaling pathways participates in CRC progress such as epidermal growth factor receptor, which is one of the most important therapeutic targets of CRCs. [29],[30]
Interestingly, Grade of Sox2 expression was been in association with the type of polyp. One the other word, grade of Sox2 expression in villous polyp was higher than that of in Tubular polyp. It has been found that villous polyp due to the vast surface area and its expansion into the lumen has the highest potential for being malignant. [31] Furthermore, according to our study, the race had a significant correlation with Sox2 expression (P < 0.001). Also, in accordance with the previous investigation, [32] the expression of Sox2 in the patients with metastatic lymph node was significantly higher than those who not had any infected lymph node. Another study showed that patients with tumors with higher Sox2 staining by IHC developed more often metastases to lymph nodes and liver. [33]
| Conclusion | | |
This study demonstrated the noticeable insight for the current study. We could not find any association between Oct4 and CRC patients but as it illustrated, there was a significant correlation between Sox2 expression and CRC patients in many aspects such as race, type of polyp, presence of lymph node, grade and intensity of Sox2 in different types of patients' tissues. Regarding our findings, the expression of Sox2 would be a liable marker for evaluating of cancer progression and could be a treatment target of CRC cells.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
| References | | |
| 1. | Leong AF, Seow-Choen F, Tang CL. Diminutive cancers of the colon and rectum: Comparison between flat and polypoid cancers. Int J Colorectal Dis 1998;13:151-3.  |
| 2. | Gostjeva EV, Thilly WG. Stem cell stages and the origins of colon cancer: A multidisciplinary perspective. Stem Cell Rev 2005;1:243-51. |
| 3. | Clarke MF, Fuller M. Stem cells and cancer: Two faces of eve. Cell 2006;124:1111-5. |
| 4. | Avery S, Inniss K, Moore H. The regulation of self-renewal in human embryonic stem cells. Stem Cells Dev 2006;15:729-40. |
| 5. | Rodda DJ, Chew JL, Lim LH, Loh YH, Wang B, Ng HH, et al. Transcriptional regulation of nanog by OCT4 and SOX2. J Biol Chem 2005;280:24731-7. |
| 6. | Padín-Iruegas ME, Herranz-Carnero M, Aguin-Losada S, Brozos-Vazquez E, Anido-Herranz U, Antunez-Lopez JR, et al. Prognostic value of changes in the expression of stem cell markers in the peripheral blood of patients with colon cancer. Oncol Rep 2013;29:2467-72. |
| 7. | Saigusa S, Tanaka K, Toiyama Y, Yokoe T, Okugawa Y, Ioue Y, et al. Correlation of CD133, OCT4, and SOX2 in rectal cancer and their association with distant recurrence after chemoradiotherapy. Ann Surg Oncol 2009;16:3488-98. |
| 8. | Saigusa S, Tanaka K, Toiyama Y, Yokoe T, Okugawa Y, Ioue Y, et al. Correlation of CD133, OCT4, SOX2 in rectal cancer and their association with distant recurrence after chemoradiotherapy. Ann Surg Oncol 2009;16:3488-3498. |
| 9. | Amini S, Fathi F, Parivar K, Mohseni H. Evaluating the Expression of OCT-4, Nanog, SOX2 and Nucleostemin in Colon Cancer Cell Lines (CaCO-2 and HT-29). Cell J 2010;12:223-230. |
| 10. | Neumann J, Bahr F, Horst D, Kriegl L, Engel J, Luque RM, et al. SOX2 expression correlates with lymph-node metastases and distant spread in right-sided colon cancer. BMC Cancer 2011;11:518. |
| 11. | Liu RL, Zhang ZH, Zhao WM, Wang M, Qi SY, Li J, et al. Expression of nucleostemin in prostate cancer and its effect on the proliferation of PC-3 cells. Chin Med J (Engl) 2008;121:299-304. |
| 12. | Capocaccia R, Gatta G, Dal Maso L. Life expectancy of colon, breast, and testicular cancer patients: An analysis of US-SEER population-based data. Ann Oncol 2015;26:1263-8. |
| 13. | Kheirelseid EA, Miller N, Chang KH, Curran C, Hennessey E, Sheehan M, et al. Mismatch repair protein expression in colorectal cancer. J Gastrointest Oncol 2013;4:397-408. |
| 14. | Voutsadakis IA. Pluripotency transcription factors in the pathogenesis of colorectal cancer and implications for prognosis. Biomark Med 2015;9:349-61. [ PUBMED] |
| 15. | Bourguignon LY, Wong G, Earle C, Chen L. Hyaluronan-CD44v3 interaction with Oct4-Sox2-Nanog promotes miR-302 expression leading to self-renewal, clonal formation, and cisplatin resistance in cancer stem cells from head and neck squamous cell carcinoma. J Biol Chem 2012;287:32800-24. |
| 16. | Hochedlinger K, Yamada Y, Beard C, Jaenisch R. Ectopic expression of Oct-4 blocks progenitor-cell differentiation and causes dysplasia in epithelial tissues. Cell 2005;121:465-77. |
| 17. | Dai X, Ge J, Wang X, Qian X, Zhang C, Li X. OCT4 regulates epithelial-mesenchymal transition and its knockdown inhibits colorectal cancer cell migration and invasion. Oncol Rep 2013;29:155-60. |
| 18. | Jachin S, Bae JS, Sung JJ, Park HS, Jang KY, Chung MJ, et al. The role of nuclear EpICD in extrahepatic cholangiocarcinoma: Association with ß-catenin. Int J Oncol 2014;45:691-8. |
| 19. | Huang HP, Chen PH, Yu CY, Chuang CY, Stone L, Hsiao WC, et al. Epithelial cell adhesion molecule (EpCAM) complex proteins promote transcription factor-mediated pluripotency reprogramming. J Biol Chem 2011;286:33520-32. |
| 20. | Hao HX, Xie Y, Zhang Y, Charlat O, Oster E, Avello M, et al. ZNRF3 promotes Wnt receptor turnover in an R-spondin-sensitive manner. Nature 2012;485:195-200. |
| 21. | Amini S, Fathi F, Mobalegi J, Sofimajidpour H, Ghadimi T. The expressions of stem cell markers: Oct4, Nanog, Sox2, nucleostemin, Bmi, Zfx, Tcl1, Tbx3, Dppa4, and Esrrb in bladder, colon, and prostate cancer, and certain cancer cell lines. Anat Cell Biol 2014;47:1-11. |
| 22. | Papailiou J, Bramis KJ, Gazouli M, Theodoropoulos G. Stem cells in colon cancer. A new era in cancer theory begins. Int J Colorectal Dis 2011;26:1-11. |
| 23. | Sarkar A, Hochedlinger K. The sox family of transcription factors: Versatile regulators of stem and progenitor cell fate. Cell Stem Cell 2013;12:15-30. |
| 24. | Fong YW, Inouye C, Yamaguchi T, Cattoglio C, Grubisic I, Tjian R. A DNA repair complex functions as an Oct4/Sox2 coactivator in embryonic stem cells. Cell 2011;147:120-31. |
| 25. | Jeter CR, Badeaux M, Choy G, Chandra D, Patrawala L, Liu C, et al. Functional evidence that the self-renewal gene NANOG regulates human tumor development. Stem Cells 2009;27:993-1005. |
| 26. | Leis O, Eguiara A, Lopez-Arribillaga E, Alberdi MJ, Hernandez-Garcia S, Elorriaga K, et al. Sox2 expression in breast tumours and activation in breast cancer stem cells. Oncogene 2012;31:1354-65. |
| 27. | Fang X, Yu W, Li L, Shao J, Zhao N, Chen Q, et al. ChIP-seq and functional analysis of the SOX2 gene in colorectal cancers. OMICS 2010;14:369-84. |
| 28. | Pang R, Law WL, Chu AC, Poon JT, Lam CS, Chow AK, et al. A subpopulation of CD26+cancer stem cells with metastatic capacity in human colorectal cancer. Cell Stem Cell 2010;6:603-15. |
| 29. | Sekharam M, Zhao H, Sun M, Fang Q, Zhang Q, Yuan Z, et al. Insulin-like growth factor 1 receptor enhances invasion and induces resistance to apoptosis of colon cancer cells through the Akt/Bcl-x(L) pathway. Cancer Res 2003;63:7708-16. |
| 30. | O'dwyer PJ, Benson AB 3 rd . Epidermal growth factor receptor-targeted therapy in colorectal cancer. Semin Oncol 2002;29 5 Suppl 14:10-7. |
| 31. | Kumar V. "17 - Polyps". Robbins and Cotran Pathologic Basis of Disease . 8 th ed. Philadelphia, PA: Saunders/Elsevier; 2010. |
| 32. | Neumann J, Bahr F, Horst D, Kriegl L, Engel J, Luque RM, et al. SOX2 expression correlates with lymph-node metastases and distant spread in right-sided colon cancer. BMC Cancer 2011;11:518. |
| 33. | Han X, Fang X, Lou X, Hua D, Ding W, Foltz G, et al. Silencing SOX2 induced mesenchymal-epithelial transition and its expression predicts liver and lymph node metastasis of CRC patients. PLoS One 2012;7:e41335. |
[Figure 1], [Figure 2], [Figure 3]
[Table 1], [Table 2], [Table 3], [Table 4]
|
Search Pubmed for