Oct4, a Novel Marker for Human Gastric Cancer

被引:86
作者
Chen, Zhong [1 ,2 ,3 ]
Xu, Wen-Rong [1 ,2 ]
Qian, Hui [1 ,2 ]
Zhu, Wei [1 ,2 ]
Bu, Xue-Feng [4 ]
Wang, Sheng [4 ]
Yan, Yong-Min [1 ,2 ]
Mao, Fei [1 ,2 ]
Gu, Hong-Bing [4 ]
Cao, Hui-Ling [1 ,2 ]
Xu, Xue-Jing [1 ,2 ]
机构
[1] Jiangsu Univ, Sch Med Sci, Zhenjiang 212013, Jiangsu, Peoples R China
[2] Jiangsu Univ, Lab Med, Key Inst Clin Lab Sci, Zhenjiang 212013, Jiangsu, Peoples R China
[3] Peoples Hosp Danyang, Dept Clin Lab Med, Danyang, Jiangsu, Peoples R China
[4] First Peoples Hosp Zhenjiang, Dept Surg, Zhenjiang, Peoples R China
关键词
Oct4; stem cells; gastric cancer; STEM-LIKE CELLS; TRANSCRIPTION FACTOR; PROSPECTIVE IDENTIFICATION; MAMMALIAN EMBRYO; SIDE POPULATION; BREAST-CANCER; SELF-RENEWAL; LUNG-CANCER; BONE-MARROW; EXPRESSION;
D O I
10.1002/jso.21270
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background and Objective: Octamer-4 (Oct4), a transcription factor involved in regulating human embryonic stern cells (ESCs), may play a role in tumorigenesis. Since little is known about the efficacy of Oct4 its a potential biomarker for gastric cancer (GC), we investigated its expression in GC tissues and its relationship to various clinicopathological parameters. Methods: Primary tumor tissues and matching, adjacent non-cancerous tissues were obtained from 62 GC patients, and Oct4 expression was examined by reverse transcription-PCR (RT-PCR) and real-time PCR. Twenty biopsy specimens of atrophic gastritis and gastric ulcer individually were collected as control. To detect Oct4 expression in the paired GC and non-cancerous tissues at the protein level, Western blotting and immunohistochemistry (IHC) were employed. Correlation analyses were conducted to assess the relationship between Oct4 expression and clinicopathological parameters. Results: Oct4 expression levels were higher in GC tissues compared to matching, adjacent non-cancerous tissues, atrophic gastritis and gastric ulcer tissues. Additionally. Oct4 expression in GC tumors correlated with their differentiation status. but not with patient age or gender, tumor size, TNM stage. depth of invasion, Or the presence of lymph node metastasis. Conclusions: Oct4 may be a potential biomarker for the initiation, progression. and differentiation of human GC. J. Surg. Oncol. 2009;99:414-419. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:414 / 419
页数:6
相关论文
共 54 条
[1]
Prospective identification of tumorigenic breast cancer cells [J].
Al-Hajj, M ;
Wicha, MS ;
Benito-Hernandez, A ;
Morrison, SJ ;
Clarke, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3983-3988
[2]
Self-renewal and solid tumor stem cells [J].
Al-Hajj, M ;
Clarke, MF .
ONCOGENE, 2004, 23 (43) :7274-7282
[3]
OCT-4, an embryonic stem cell marker, is highly expressed in bladder cancer [J].
Atlasi, Yaser ;
Mowla, Seyed J. ;
Ziaee, Seyed A. M. ;
Bahrami, Ahmad-Reza .
INTERNATIONAL JOURNAL OF CANCER, 2007, 120 (07) :1598-1602
[4]
An embryonic stem cell-like gene expression signature in poorly differentiated aggressive human tumors [J].
Ben-Porath, Ittai ;
Thomson, Matthew W. ;
Carey, Vincent J. ;
Ge, Ruping ;
Bell, George W. ;
Regev, Aviv ;
Weinberg, Robert A. .
NATURE GENETICS, 2008, 40 (05) :499-507
[5]
Opinion - The origin of the cancer stem cell: current controversies and new insights [J].
Bjerkvig, R ;
Tysnes, BB ;
Aboody, KS ;
Najbauer, J ;
Terzis, AJA .
NATURE REVIEWS CANCER, 2005, 5 (11) :899-904
[7]
Chang CC, 2001, RADIAT RES, V155, P201, DOI 10.1667/0033-7587(2001)155[0201:AHBECT]2.0.CO
[8]
2
[9]
Oct-4 Expression Maintained Cancer Stem-Like Properties in Lung Cancer-Derived CD133-Positive Cells [J].
Chen, Yu-Chih ;
Hsu, Han-Shui ;
Chen, Yi-Wei ;
Tsai, Tung-Hu ;
How, Chorng-Kuang ;
Wang, Chien-Ying ;
Hung, Shih-Chieh ;
Chang, Yuh-Lih ;
Tsai, Ming-Long ;
Lee, Yi-Yen ;
Ku, Hung-Hai ;
Chiou, Shih-Hwa .
PLOS ONE, 2008, 3 (07)
[10]
Aberrant expression and distribution of the OCT-4 transcription factor in seminomas [J].
Cheng, Chien-Jui ;
Wu, Yu-Chih ;
Shu, Jye-An ;
Ling, Thai-Yen ;
Kuo, Hung-Chih ;
Wu, Jui-Yu ;
Chang, E. E. ;
Chang, Shyh-Chern ;
Huang, Yen-Hua .
JOURNAL OF BIOMEDICAL SCIENCE, 2007, 14 (06) :797-807