Literature DB >> 16778197

Bmi-1 is a novel molecular marker of nasopharyngeal carcinoma progression and immortalizes primary human nasopharyngeal epithelial cells.

Li-Bing Song1, Mu-Sheng Zeng, Wen-Ting Liao, Ling Zhang, Hao-Yuan Mo, Wan-Li Liu, Jian-Yong Shao, Qiu-Liang Wu, Man-Zhi Li, Yun-Fei Xia, Li-Wu Fu, Wen-Lin Huang, Goberdhan P Dimri, Vimla Band, Yi-Xin Zeng.   

Abstract

The Bmi-1 oncoprotein regulates proliferation and oncogenesis in human cells. Its overexpression leads to senescence bypass in human fibroblasts and immortalization of human mammary epithelial cells. In this study, we report that compared with normal nasopharyngeal epithelial cells (NPEC), Bmi-1 is overexpressed in nasopharyngeal carcinoma cell lines. Importantly, Bmi-1 was also found to be overexpressed in 29 of 75 nasopharyngeal carcinoma tumors (38.7%) by immunohistochemical analysis. In contrast to nasopharyngeal carcinoma, there was no detectable expression of Bmi-1 in noncancerous nasopharyngeal epithelium. Moreover, high Bmi-1 expression positively correlated with poor prognosis of nasopharyngeal carcinoma patients. We also report that the overexpression of Bmi-1 leads to bypass of senescence and immortalization of NPECs, which normally express p16(INK4a) and exhibit finite replicative life span. Overexpression of Bmi-1 in NPECs led to the induction of human telomerase reverse transcriptase activity and reduction of p16(INK4a) expression. Mutational analysis of Bmi-1 showed that both RING finger and helix-turn-helix domains of it are required for immortalization of NPECs. Our findings suggest that Bmi-1 plays an important role in the development and progression of nasopharyngeal carcinoma, and that Bmi-1 is a valuable marker for assessing the prognosis of nasopharyngeal carcinoma patients. Furthermore, this study provides the first cellular proto-oncogene immortalized nasopharyngeal epithelial cell line, which may serve as a cell model system for studying the mechanisms involved in the tumorigenesis of nasopharyngeal carcinoma.

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Year:  2006        PMID: 16778197     DOI: 10.1158/0008-5472.CAN-06-0094

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  161 in total

1.  Bmi-1, c-myc, and Snail expression in primary breast cancers and their metastases--elevated Bmi-1 expression in late breast cancer relapses.

Authors:  Kristiina Joensuu; Jaana Hagström; Marjut Leidenius; Caj Haglund; Leif C Andersson; Hannu Sariola; Päivi Heikkilä
Journal:  Virchows Arch       Date:  2011-06-03       Impact factor: 4.064

2.  IGF-1R and Bmi-1 expressions in lung adenocarcinoma and their clinicopathologic and prognostic significance.

Authors:  Xueyan Zhang; Jiayuan Sun; Huimin Wang; Yuqing Lou; Yanwei Zhang; Huifang Sha; Jiuxian Feng; Baohui Han
Journal:  Tumour Biol       Date:  2013-08-29

3.  The prognostic significance of BMI1 expression in invasive breast cancer is dependent on its molecular subtypes.

Authors:  Maryam Althobiti; Abir A Muftah; Mohammed A Aleskandarany; Chitra Joseph; Michael S Toss; Andrew Green; Emad Rakha
Journal:  Breast Cancer Res Treat       Date:  2020-06-10       Impact factor: 4.872

4.  Inverse association between Bmi-1 and RKIP affecting clinical outcome of gastric cancer and revealing the potential molecular mechanisms underlying tumor metastasis and chemotherapy resistance.

Authors:  Yinting Chen; Guoda Lian; Guangsheng Ou; Kege Yang; Jianning Chen; Haigang Li; Shaojie Chen; Jiajia Li; Linjuan Zeng; Kaihong Huang
Journal:  Gastric Cancer       Date:  2015-03-13       Impact factor: 7.370

5.  Bmi-1-shRNA inhibits the proliferation of lung adenocarcinoma cells by blocking the G1/S phase through decreasing cyclin D1 and increasing p21/p27 levels.

Authors:  Xiangyu Zheng; Yifang Wang; Ben Liu; Chunqing Liu; Dandan Liu; Jie Zhu; Chunhui Yang; Jiangzhou Yan; Xiaobo Liao; Xiuxiang Meng; Hong Yang
Journal:  Nucleic Acid Ther       Date:  2014-02-19       Impact factor: 5.486

6.  The Bmi-1 polycomb protein antagonizes the (-)-epigallocatechin-3-gallate-dependent suppression of skin cancer cell survival.

Authors:  Sivaprakasam Balasubramanian; Gautam Adhikary; Richard L Eckert
Journal:  Carcinogenesis       Date:  2009-12-16       Impact factor: 4.944

7.  PTEN inhibits BMI1 function independently of its phosphatase activity.

Authors:  Catherine Fan; Lizhi He; Anil Kapoor; Adrian P Rybak; Jason De Melo; Jean-Claude Cutz; Damu Tang
Journal:  Mol Cancer       Date:  2009-11-10       Impact factor: 27.401

8.  Distinct population of highly malignant cells in a head and neck squamous cell carcinoma cell line established by xenograft model.

Authors:  Chi-Yuan Chen; Shih-Hwa Chiou; Chih-Yang Huang; Chia-Ing Jan; Shu-Chun Lin; Ming-Long Tsai; Jeng-Fan Lo
Journal:  J Biomed Sci       Date:  2009-11-16       Impact factor: 8.410

9.  Upregulation of CENP-H in tongue cancer correlates with poor prognosis and progression.

Authors:  Wen-Ting Liao; Chun-Ping Yu; Dong-Hui Wu; Ling Zhang; Li-Hua Xu; Gui-Xiang Weng; Mu-Sheng Zeng; Li-Bing Song; Jin-Song Li
Journal:  J Exp Clin Cancer Res       Date:  2009-06-05

10.  BMI1 cooperates with H-RAS to induce an aggressive breast cancer phenotype with brain metastases.

Authors:  M J Hoenerhoff; I Chu; D Barkan; Z-y Liu; S Datta; G P Dimri; J E Green
Journal:  Oncogene       Date:  2009-06-22       Impact factor: 9.867

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