Literature DB >> 26622555

Expression of Oct-4 is significantly associated with the development and prognosis of colorectal cancer.

Huan Zhou1, Y U Hu2, Weipeng Wang3, Yong Mao2, Jingjie Zhu4, Bin Zhou5, Jing Sun6, Xueguang Zhang7.   

Abstract

Octamer-binding transcription factor 4 (Oct-4), is an essential transcription factor, which is required for pluripotency and self-renewal in embryonic stem cells and germ cells. It is also involved in maintaining cancer stem-like properties in certain types of tumor, and is an important biomarker for cancer stem cells. The present study investigated whether Oct-4 expression was associated with colorectal cancer (CRC). In order to achieve this, primary CRC tissues, matched non-tumor tissues and benign polyp tissues, representing different stages of carcinogenesis, were obtained, and Oct-4 expression was analyzed using reverse transcription-quantitative polymerase chain reaction, flow cytometry analysis and immunohistochemistry. Furthermore, the medical records of patients with CRC were reviewed, and clinicopathological analysis was performed in order to assess the association between Oct-4 expression and certain clinicopathological parameters. It was shown that the transcription and translation of Oct-4 increased in a stepwise manner, from non-tumor to benign polyp tissues, and from benign polyps to CRC tissues. Oct-4 expression in CRC was significantly correlated with histological grade (P=0.007), lymph node metastasis (P=0.027), distant metastasis (P=0.017) and TNM stage (P=0.041). Kaplan-Meier survival curve analysis demonstrated that Oct-4+ cases had a shorter median survival time (37.0 months) compared with Oct-4- cases (76.0 months; P=0.001). These results indicated that aberrant expression of Oct-4 may be involved in the development of CRC. Thus, Oct-4 may be a biomarker for the prediction, diagnosis or assessment of prognosis in CRC, in addition to a potential target for the treatment of this disease.

Entities:  

Keywords:  carcinogenesis; colorectal cancer; octamer-binding transcription factor 4; prognosis

Year:  2015        PMID: 26622555      PMCID: PMC4509036          DOI: 10.3892/ol.2015.3269

Source DB:  PubMed          Journal:  Oncol Lett        ISSN: 1792-1074            Impact factor:   2.967


  32 in total

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Journal:  J Pathol       Date:  2007-01       Impact factor: 7.996

2.  Ectopic expression of Oct-4 blocks progenitor-cell differentiation and causes dysplasia in epithelial tissues.

Authors:  Konrad Hochedlinger; Yasuhiro Yamada; Caroline Beard; Rudolf Jaenisch
Journal:  Cell       Date:  2005-05-06       Impact factor: 41.582

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Journal:  Cancer Lett       Date:  2012-03-16       Impact factor: 8.679

Review 4.  Stem cells in cancer: instigators and propagators?

Authors:  Malcolm R Alison; Shahriar Islam; Nicholas A Wright
Journal:  J Cell Sci       Date:  2010-07-15       Impact factor: 5.285

5.  High expression of octamer-binding transcription factor 4A, prominin-1 and aldehyde dehydrogenase strongly indicates involvement in the initiation of lung adenocarcinoma resulting in shorter disease-free intervals.

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Journal:  Eur J Cardiothorac Surg       Date:  2012-04-23       Impact factor: 4.191

6.  Oct-4 regulates alternative platelet-derived growth factor alpha receptor gene promoter in human embryonal carcinoma cells.

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Review 7.  Signalling, cell cycle and pluripotency in embryonic stem cells.

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10.  CD133 expression is not restricted to stem cells, and both CD133+ and CD133- metastatic colon cancer cells initiate tumors.

Authors:  Sergey V Shmelkov; Jason M Butler; Andrea T Hooper; Adilia Hormigo; Jared Kushner; Till Milde; Ryan St Clair; Muhamed Baljevic; Ian White; David K Jin; Amy Chadburn; Andrew J Murphy; David M Valenzuela; Nicholas W Gale; Gavin Thurston; George D Yancopoulos; Michael D'Angelica; Nancy Kemeny; David Lyden; Shahin Rafii
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1.  Apoptosis and cell cycle regulatory effects of adenosine by modulation of GLI-1 and ERK1/2 pathways in CD44+ and CD24- breast cancer stem cells.

Authors:  S M Jafari; H R Joshaghani; M Panjehpour; M Aghaei; N Zargar Balajam
Journal:  Cell Prolif       Date:  2017-03-29       Impact factor: 6.831

2.  Clinical significance of Fusobacterium nucleatum, epithelial-mesenchymal transition, and cancer stem cell markers in stage III/IV colorectal cancer patients.

Authors:  Xuebing Yan; Liguo Liu; Hao Li; Huanlong Qin; Zhenliang Sun
Journal:  Onco Targets Ther       Date:  2017-10-17       Impact factor: 4.147

Review 3.  Human Pluripotent Stem Cells-Based Therapies for Neurodegenerative Diseases: Current Status and Challenges.

Authors:  Elizabeth Ford; Jodie Pearlman; Travis Ruan; John Manion; Matthew Waller; Gregory G Neely; Leslie Caron
Journal:  Cells       Date:  2020-11-20       Impact factor: 6.600

4.  Identification of microRNA-451a as a Novel Circulating Biomarker for Colorectal Cancer Diagnosis.

Authors:  Zhen Zhang; Dai Zhang; Yaping Cui; Yongsheng Qiu; Changhong Miao; Xihua Lu
Journal:  Biomed Res Int       Date:  2020-08-27       Impact factor: 3.411

5.  Diagnostic significance and carcinogenic mechanism of pan-cancer gene POU5F1 in liver hepatocellular carcinoma.

Authors:  Dingdong He; Xiaokang Zhang; Jiancheng Tu
Journal:  Cancer Med       Date:  2020-09-26       Impact factor: 4.452

6.  A Pilot Study Investigating the Expression Levels of Pluripotency-Associated Genes in Rectal Swab Samples for Colorectal Polyp and Cancer Diagnosis and Prognosis.

Authors:  Ryan Wai-Yan Sin; Dominic Chi-Chung Foo; Deepak Narayanan Iyer; May Sau-Yee Fan; Xue Li; Oswens Siu-Hung Lo; Wai-Lun Law; Lui Ng
Journal:  Stem Cells Int       Date:  2021-07-22       Impact factor: 5.443

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