Literature DB >> 24608572

Identification of transmembrane protein 98 as a novel chemoresistance-conferring gene in hepatocellular carcinoma.

Kevin Tak-Pan Ng1, Chung Mau Lo, Dong Yong Guo, Xiang Qi, Chang Xian Li, Wei Geng, Xiao Bing Liu, Chang Chun Ling, Yuen Yuen Ma, Wai Ho Yeung, Yan Shao, Ronnie Tung-Ping Poon, Sheung Tat Fan, Kwan Man.   

Abstract

Chemoresistance is one of the major obstacles in systemic chemotherapy and targeted therapy for patients with advanced hepatocellular carcinoma. To identify novel chemoresistance-associated targets in hepatocellular carcinoma, chemoresistant hepatocellular carcinoma cell lines were established. By comparing the global gene expression profiles between chemoresistant and chemosensitive cell lines, eight novel chemoresistance-associated genes were identified to be significantly associated with the commonly augmented chemoresistance of hepatocellular carcinoma cells. One upregulated candidate named transmembrane protein 98 (TMEM98) was found to be overexpressed in 80 of 118 (67.80%) of patients with hepatocellular carcinoma. TMEM98 mRNA in tumor tissues was significantly higher than nontumor tissues of patients with hepatocellular carcinoma (P < 0.0001). Upregulation of TMEM98 was significantly correlated with advanced tumor stage (P = 0.048), high incidence of early tumor recurrence (P = 0.005), poor overall survival (P = 0.029), and poor disease-free survival (P = 0.011) of patients with hepatocellular carcinoma after hepatectomy. Importantly, upregulation of TMEM98 mRNA in patients with hepatocellular carcinoma who received transarterial chemoembolization (TACE) treatment was significantly higher than in patients without TACE treatment (P = 0.046). Moreover, patients with poor response to TACE treatment had higher degree of TMEM98 upregulation than the responsive patients. In vitro and in vivo studies showed that suppression of TMEM98 in chemoresistant hepatocellular carcinoma cells restored their chemosensitivity, while forced overexpression of TMEM98 enhanced their chemoresistance. The mechanism of TMEM98 in conferring chemoresistance of hepatocellular carcinoma might be possibly through activation of the AKT pathway and deactivation of p53. In conclusion, we identified a panel of novel common chemoresistance-associated genes and demonstrated that TMEM98 is a chemoresistance-conferring gene in hepatocellular carcinoma.

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Year:  2014        PMID: 24608572     DOI: 10.1158/1535-7163.MCT-13-0806

Source DB:  PubMed          Journal:  Mol Cancer Ther        ISSN: 1535-7163            Impact factor:   6.261


  18 in total

1.  Alcohol Consumption Modulates Host Defense in Rhesus Macaques by Altering Gene Expression in Circulating Leukocytes.

Authors:  Tasha Barr; Thomas Girke; Suhas Sureshchandra; Christina Nguyen; Kathleen Grant; Ilhem Messaoudi
Journal:  J Immunol       Date:  2015-11-30       Impact factor: 5.422

2.  The Secreted Form of Transmembrane Protein 98 Promotes the Differentiation of T Helper 1 Cells.

Authors:  Weiwei Fu; Yingying Cheng; Yanfei Zhang; Xiaoning Mo; Ting Li; Yuanfeng Liu; Pingzhang Wang; Wen Pan; Yingyu Chen; Yintong Xue; Dalong Ma; Yu Zhang; Wenling Han
Journal:  J Interferon Cytokine Res       Date:  2015-05-06       Impact factor: 2.607

3.  Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse.

Authors:  Sally H Cross; Lisa Mckie; Margaret Keighren; Katrine West; Caroline Thaung; Tracey Davey; Dinesh C Soares; Luis Sanchez-Pulido; Ian J Jackson
Journal:  Invest Ophthalmol Vis Sci       Date:  2019-07-01       Impact factor: 4.799

4.  Interactive Repression of MYRF Self-Cleavage and Activity in Oligodendrocyte Differentiation by TMEM98 Protein.

Authors:  Hao Huang; Peng Teng; Junqing Du; Jun Meng; Xuemei Hu; Tao Tang; Zunyi Zhang; Yingchuan B Qi; Mengsheng Qiu
Journal:  J Neurosci       Date:  2018-09-24       Impact factor: 6.167

5.  Clinical relevance and therapeutic potential of angiopoietin-like protein 4 in hepatocellular carcinoma.

Authors:  Kevin Tak-Pan Ng; Aimin Xu; Qiao Cheng; Dong Yong Guo; Zophia Xue-Hui Lim; Chris Kin-Wai Sun; Jeffrey Hon-Sing Fung; Ronnie Tung-Ping Poon; Sheung Tat Fan; Chung Mau Lo; Kwan Man
Journal:  Mol Cancer       Date:  2014-08-22       Impact factor: 27.401

6.  Early-phase circulating miRNAs predict tumor recurrence and survival of hepatocellular carcinoma patients after liver transplantation.

Authors:  Kevin Tak-Pan Ng; Chung Mau Lo; Nathalie Wong; Chang Xian Li; Xiang Qi; Xiao Bing Liu; Wei Geng; Oscar Wai-Ho Yeung; Yuen Yuen Ma; See Ching Chan; Kwan Man
Journal:  Oncotarget       Date:  2016-04-12

7.  Glutathione S-transferase A2 promotes hepatocellular carcinoma recurrence after liver transplantation through modulating reactive oxygen species metabolism.

Authors:  Kevin Tak-Pan Ng; Oscar Wai-Ho Yeung; Yin Fan Lam; Jiang Liu; Hui Liu; Li Pang; Xin Xiang Yang; Jiye Zhu; Weiyi Zhang; Matthew Y H Lau; Wen Qi Qiu; Hoi Chung Shiu; Man Kit Lai; Chung Mau Lo; Kwan Man
Journal:  Cell Death Discov       Date:  2021-07-21

8.  The Clinical Significance and Potential Therapeutic Role of GPx3 in Tumor Recurrence after Liver Transplantation.

Authors:  Xiang Qi; Kevin Tak-Pan Ng; Yan Shao; Chang Xian Li; Wei Geng; Chang Chun Ling; Yuen Yuen Ma; Xiao Bing Liu; Hui Liu; Jiang Liu; Wai Ho Yeung; Chung Mau Lo; Kwan Man
Journal:  Theranostics       Date:  2016-08-08       Impact factor: 11.556

9.  A hemoglobin-based oxygen carrier sensitized Cisplatin based chemotherapy in hepatocellular carcinoma.

Authors:  Xiang Qi; Bing L Wong; Sze Hang Lau; Kevin Tak-Pan Ng; Sui Yi Kwok; Chris Kin-Wai Sun; Fei Chuen Tzang; Yan Shao; Chang Xian Li; Wei Geng; Chang Chun Ling; Yuen Yuen Ma; Xiao Bing Liu; Hui Liu; Jiang Liu; Wai Ho Yeung; Chung Mau Lo; Kwan Man
Journal:  Oncotarget       Date:  2017-07-28

10.  Inhibition of IL-8-mediated endothelial adhesion, VSMCs proliferation and migration by siRNA-TMEM98 suggests TMEM98's emerging role in atherosclerosis.

Authors:  Guangxin Lv; Hongmei Zhu; Cai Li; Jingyu Wang; Dandan Zhao; Shuyao Li; Le Ma; Guohua Sun; Fang Li; Ying Zhao; Ying Gao
Journal:  Oncotarget       Date:  2017-09-30
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