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Erschienen in: Tumor Biology 6/2014

01.06.2014 | Research Article

OCT-1 overexpression is associated with poor prognosis in patients with well-differentiated gastric cancer

verfasst von: Sang-Ho Jeong, Young-Joon Lee, Bok-Im Cho, Woo-Song Ha, Sang-Kyung Choi, Eun-Jung Jung, Young-Tae Ju, Chi-Young Jeong, Gyung Hyuck Ko, Jiyun Yoo, Soon-Chan Hong

Erschienen in: Tumor Biology | Ausgabe 6/2014

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Abstract

Octamer transcription factor-1 (OCT-1) is a well-known transcription factor that is reportedly overexpressed in intestinal metaplasia and gastric carcinoma in the intestine. In this study, we investigated OCT-1 overexpression as a prognostic factor for gastric cancer. The association between OCT-1 overexpression (detected using immunohistochemistry) and clinicopathological features including survival was evaluated. In vitro gain-of-function approaches were utilized to assess the function of OCT-1 in malignancy. Analysis of OCT-1 expression in patients with gastric cancer with well-differentiated carcinoma as per the World Health Organization classification showed that OCT-1 overexpression was correlated with advanced tumor invasion (58.8 % of patients with advanced tumor invasion vs. 21.2 % of patients with early tumor invasion; p < 0.01), lymph node metastasis (63.9 % of patients with metastasis vs. 24.1 % of those without; p = 0.015), and cancer recurrence (83.3 % of patients with recurrence vs. 25.4 % of those without; p < 0.01), as well as a lower survival rate (62.8 vs. 87.9 Mo; p < 0.01). However, there were no significant differences in the levels of OCT-1 expression in gastric cancer patients with other carcinoma types (p > 0.05). Furthermore, we found that the proliferation rate of OCT-1-overexpressing MKN-45 cells was higher than that of the control cells. OCT-1 overexpression may be a marker for poor prognosis in patients with well-differentiated gastric adenocarcinoma.
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Literatur
2.
Zurück zum Zitat Townscend CM. Sabiston textbook of surgery. Elservier Inc.: Philadelphia; 2008. Townscend CM. Sabiston textbook of surgery. Elservier Inc.: Philadelphia; 2008.
3.
Zurück zum Zitat Korean Surgical Society. Text book of surgery. Koonja, Seoul; 2011. Korean Surgical Society. Text book of surgery. Koonja, Seoul; 2011.
4.
Zurück zum Zitat Tamura G. Alterations of tumor suppressor and tumor-related genes in the development and progression of gastric cancer. World J Gastroenterol. 2006;12:192–8.PubMedCentralPubMed Tamura G. Alterations of tumor suppressor and tumor-related genes in the development and progression of gastric cancer. World J Gastroenterol. 2006;12:192–8.PubMedCentralPubMed
5.
Zurück zum Zitat Griffiths EA, Pritchard SA, Valentine HR, Whitchelo N, Bishop PW, Ebert MP, et al. Hypoxia-inducible factor-1alpha expression in the gastric carcinogenesis sequence and its prognostic role in gastric and gastro-oesophageal adenocarcinomas. Br J Cancer. 2007;96:95–103.PubMedCentralCrossRefPubMed Griffiths EA, Pritchard SA, Valentine HR, Whitchelo N, Bishop PW, Ebert MP, et al. Hypoxia-inducible factor-1alpha expression in the gastric carcinogenesis sequence and its prognostic role in gastric and gastro-oesophageal adenocarcinomas. Br J Cancer. 2007;96:95–103.PubMedCentralCrossRefPubMed
6.
Zurück zum Zitat Smith MG, Hold GL, Tahara E, El-Omar EM. Cellular and molecular aspects of gastric cancer. World J Gastroenterol. 2006;12:2979–90.PubMedCentralPubMed Smith MG, Hold GL, Tahara E, El-Omar EM. Cellular and molecular aspects of gastric cancer. World J Gastroenterol. 2006;12:2979–90.PubMedCentralPubMed
7.
Zurück zum Zitat Beswick EJ, Bland DA, Suarez G, Barrera CA, Fan X, Reyes VE. Helicobacter pylori binds to cd74 on gastric epithelial cells and stimulates interleukin-8 production. Infect Immun. 2005;73:2736–43.PubMedCentralCrossRefPubMed Beswick EJ, Bland DA, Suarez G, Barrera CA, Fan X, Reyes VE. Helicobacter pylori binds to cd74 on gastric epithelial cells and stimulates interleukin-8 production. Infect Immun. 2005;73:2736–43.PubMedCentralCrossRefPubMed
8.
Zurück zum Zitat Holmes K, Egan B, Swan N, O’Morain C. Genetic mechanisms and aberrant gene expression during the development of gastric intestinal metaplasia and adenocarcinoma. Curr Genomics. 2007;8:379–97.PubMedCentralCrossRefPubMed Holmes K, Egan B, Swan N, O’Morain C. Genetic mechanisms and aberrant gene expression during the development of gastric intestinal metaplasia and adenocarcinoma. Curr Genomics. 2007;8:379–97.PubMedCentralCrossRefPubMed
9.
Zurück zum Zitat Almeida R, Silva E, Santos-Silva F, Silberg DG, Wang J, De Bolos C, et al. Expression of intestine-specific transcription factors, cdx1 and cdx2, in intestinal metaplasia and gastric carcinomas. J Pathol. 2003;199:36–40.CrossRefPubMed Almeida R, Silva E, Santos-Silva F, Silberg DG, Wang J, De Bolos C, et al. Expression of intestine-specific transcription factors, cdx1 and cdx2, in intestinal metaplasia and gastric carcinomas. J Pathol. 2003;199:36–40.CrossRefPubMed
10.
Zurück zum Zitat Almeida R, Almeida J, Shoshkes M, Mendes N, Mesquita P, Silva E, et al. Oct-1 is over-expressed in intestinal metaplasia and intestinal gastric carcinomas and binds to, but does not transactivate, cdx2 in gastric cells. J Pathol. 2005;207:396–401.CrossRefPubMed Almeida R, Almeida J, Shoshkes M, Mendes N, Mesquita P, Silva E, et al. Oct-1 is over-expressed in intestinal metaplasia and intestinal gastric carcinomas and binds to, but does not transactivate, cdx2 in gastric cells. J Pathol. 2005;207:396–401.CrossRefPubMed
11.
Zurück zum Zitat Verrijzer CP, Van der Vliet PC. Pou domain transcription factors. Biochim Biophys Acta. 1993;1173:1–21.CrossRefPubMed Verrijzer CP, Van der Vliet PC. Pou domain transcription factors. Biochim Biophys Acta. 1993;1173:1–21.CrossRefPubMed
12.
Zurück zum Zitat Kimura M, Tsuda H, Morita D, Ichikura T, Ogata S, Aida S, et al. A proposal for diagnostically meaningful criteria to classify increased epidermal growth factor receptor and c-erbb-2 gene copy numbers in gastric carcinoma, based on correlation of fluorescence in situ hybridization and immunohistochemical measurements. Virchows Arch. 2004;445:255–62.CrossRefPubMed Kimura M, Tsuda H, Morita D, Ichikura T, Ogata S, Aida S, et al. A proposal for diagnostically meaningful criteria to classify increased epidermal growth factor receptor and c-erbb-2 gene copy numbers in gastric carcinoma, based on correlation of fluorescence in situ hybridization and immunohistochemical measurements. Virchows Arch. 2004;445:255–62.CrossRefPubMed
13.
Zurück zum Zitat Lorentz O, Duluc I, Arcangelis AD, Simon-Assmann P, Kedinger M, Freund JN. Key role of the cdx2 homeobox gene in extracellular matrix-mediated intestinal cell differentiation. J Cell Biol. 1997;139:1553–65.PubMedCentralCrossRefPubMed Lorentz O, Duluc I, Arcangelis AD, Simon-Assmann P, Kedinger M, Freund JN. Key role of the cdx2 homeobox gene in extracellular matrix-mediated intestinal cell differentiation. J Cell Biol. 1997;139:1553–65.PubMedCentralCrossRefPubMed
14.
Zurück zum Zitat Suh E, Traber PG. An intestine-specific homeobox gene regulates proliferation and differentiation. Mol Cell Biol. 1996;16:619–25.PubMedCentralPubMed Suh E, Traber PG. An intestine-specific homeobox gene regulates proliferation and differentiation. Mol Cell Biol. 1996;16:619–25.PubMedCentralPubMed
15.
Zurück zum Zitat Seno H, Oshima M, Taniguchi MA, Usami K, Ishikawa TO, Chiba T, et al. Cdx2 expression in the stomach with intestinal metaplasia and intestinal-type cancer: prognostic implications. Int J Oncol. 2002;21:769–74.PubMed Seno H, Oshima M, Taniguchi MA, Usami K, Ishikawa TO, Chiba T, et al. Cdx2 expression in the stomach with intestinal metaplasia and intestinal-type cancer: prognostic implications. Int J Oncol. 2002;21:769–74.PubMed
16.
Zurück zum Zitat Sebastiano V, Dalvai M, Gentile L, Schubart K, Sutter J, Wu GM, et al. Oct1 regulates trophoblast development during early mouse embryogenesis. Development. 2010;137:3551–60.CrossRefPubMed Sebastiano V, Dalvai M, Gentile L, Schubart K, Sutter J, Wu GM, et al. Oct1 regulates trophoblast development during early mouse embryogenesis. Development. 2010;137:3551–60.CrossRefPubMed
17.
Zurück zum Zitat Shakya A, Kang J, Chumley J, Williams MA, Tantin D. Oct1 is a switchable, bipotential stabilizer of repressed and inducible transcriptional states. J Biol Chem. 2011;286:450–9.PubMedCentralCrossRefPubMed Shakya A, Kang J, Chumley J, Williams MA, Tantin D. Oct1 is a switchable, bipotential stabilizer of repressed and inducible transcriptional states. J Biol Chem. 2011;286:450–9.PubMedCentralCrossRefPubMed
18.
Zurück zum Zitat Wang P, Wang Q, Sun J, Wu J, Li H, Zhang N, et al. Pou homeodomain protein oct-1 functions as a sensor for cyclic amp. J Biol Chem. 2009;284:26456–65.PubMedCentralCrossRefPubMed Wang P, Wang Q, Sun J, Wu J, Li H, Zhang N, et al. Pou homeodomain protein oct-1 functions as a sensor for cyclic amp. J Biol Chem. 2009;284:26456–65.PubMedCentralCrossRefPubMed
19.
Zurück zum Zitat Rhodes DR, Kalyana-Sundaram S, Mahavisno V, Varambally R, Yu J, Briggs BB, et al. Oncomine 3.0: genes, pathways, and networks in a collection of 18,000 cancer gene expression profiles. Neoplasia. 2007;9:166–80.PubMedCentralCrossRefPubMed Rhodes DR, Kalyana-Sundaram S, Mahavisno V, Varambally R, Yu J, Briggs BB, et al. Oncomine 3.0: genes, pathways, and networks in a collection of 18,000 cancer gene expression profiles. Neoplasia. 2007;9:166–80.PubMedCentralCrossRefPubMed
20.
Zurück zum Zitat Zhou C, Tong Y, Wawrowsky K, Bannykh S, Donangelo I, Melmed S. Oct-1 induces pituitary tumor transforming gene expression in endocrine tumors. Endocr Relat Cancer. 2008;15:817–31.PubMedCentralCrossRefPubMed Zhou C, Tong Y, Wawrowsky K, Bannykh S, Donangelo I, Melmed S. Oct-1 induces pituitary tumor transforming gene expression in endocrine tumors. Endocr Relat Cancer. 2008;15:817–31.PubMedCentralCrossRefPubMed
21.
Zurück zum Zitat Wang VE, Tantin D, Chen J, Sharp PA. B cell development and immunoglobulin transcription in oct-1-deficient mice. Proc Natl Acad Sci U S A. 2004;101:2005–10.PubMedCentralCrossRefPubMed Wang VE, Tantin D, Chen J, Sharp PA. B cell development and immunoglobulin transcription in oct-1-deficient mice. Proc Natl Acad Sci U S A. 2004;101:2005–10.PubMedCentralCrossRefPubMed
22.
Zurück zum Zitat Tantin D, Schild-Poulter C, Wang V, Hache RJ, Sharp PA. The octamer binding transcription factor oct-1 is a stress sensor. Cancer Res. 2005;65:10750–8.CrossRefPubMed Tantin D, Schild-Poulter C, Wang V, Hache RJ, Sharp PA. The octamer binding transcription factor oct-1 is a stress sensor. Cancer Res. 2005;65:10750–8.CrossRefPubMed
23.
Zurück zum Zitat Shakya A, Cooksey R, Cox JE, Wang V, McClain DA, Tantin D. Oct1 loss of function induces a coordinate metabolic shift that opposes tumorigenicity. Nat Cell Biol. 2009;11:320–7.CrossRefPubMed Shakya A, Cooksey R, Cox JE, Wang V, McClain DA, Tantin D. Oct1 loss of function induces a coordinate metabolic shift that opposes tumorigenicity. Nat Cell Biol. 2009;11:320–7.CrossRefPubMed
24.
Zurück zum Zitat Maddox J, Shakya A, South S, Shelton D, Andersen JN, Chidester S, et al. Transcription factor oct1 is a somatic and cancer stem cell determinant. PLoS Genet. 2012;8:e1003048.PubMedCentralCrossRefPubMed Maddox J, Shakya A, South S, Shelton D, Andersen JN, Chidester S, et al. Transcription factor oct1 is a somatic and cancer stem cell determinant. PLoS Genet. 2012;8:e1003048.PubMedCentralCrossRefPubMed
Metadaten
Titel
OCT-1 overexpression is associated with poor prognosis in patients with well-differentiated gastric cancer
verfasst von
Sang-Ho Jeong
Young-Joon Lee
Bok-Im Cho
Woo-Song Ha
Sang-Kyung Choi
Eun-Jung Jung
Young-Tae Ju
Chi-Young Jeong
Gyung Hyuck Ko
Jiyun Yoo
Soon-Chan Hong
Publikationsdatum
01.06.2014
Verlag
Springer Netherlands
Erschienen in
Tumor Biology / Ausgabe 6/2014
Print ISSN: 1010-4283
Elektronische ISSN: 1423-0380
DOI
https://doi.org/10.1007/s13277-014-1724-4

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