Association of a variant in MIR 196A2 with susceptibility to hepatocellular carcinoma in male Chinese patients with chronic hepatitis B virus infection

被引:130
作者
Qi, Peng [1 ]
Dou, Tong-hai [2 ]
Geng, Li [3 ]
Zhou, Fei-guo [4 ]
Gu, Xing [1 ]
Wang, Hao [5 ]
Gao, Chun-fang [1 ]
机构
[1] Second Mil Med Univ, Eastern Hepatobiliary Hosp, Dept Lab Med, Shanghai 200438, Peoples R China
[2] Fudan Univ, Sch Life Sci, Dept Microbiol, Shanghai 200433, Peoples R China
[3] Second Mil Med Univ, Eastern Hepatobiliary Hosp, Dept Special Treatment, Shanghai 200438, Peoples R China
[4] Second Mil Med Univ, Eastern Hepatobiliary Hosp, Dept Hepat Surg, Shanghai 200438, Peoples R China
[5] Second Mil Med Univ, Changzheng Hosp, Dept Lab Med, Shanghai 200438, Peoples R China
基金
中国国家自然科学基金;
关键词
Chronic hepatitis; Hepatitis B virus; Hepatocellular carcinoma; MIR196A2; Single nucleotide polymorphism; NON-TUMOROUS TISSUES; MICRORNA EXPRESSION; GENETIC POLYMORPHISMS; SUPPRESSOR GENE; DOWN-REGULATION; LUNG-CANCER; RISK; TARGET; POPULATION; APOPTOSIS;
D O I
10.1016/j.humimm.2010.02.017
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
MicroRNAs (miRNAs) are small noncoding RNAs with regulatory functions as tumor suppressors and oncogenes. Recent studies have implicated that the rs11614913 SNP in MIR196A2 was associated with susceptibility of lung cancer, congenital heart disease, breast cancer and shortened survival time of nonsmall cell lung cancer. To assess whether this polymorphism is associated with susceptibility to and clinicopathologic characteristics of hepatitis B virus (HBV)-related hepatocellular carcinoma (HCC), a total of 560 patients with chronic HBV infection and 391 healthy volunteers were enrolled, and MIR196A2 polymorphism was genotyped by polymerase chain reaction-ligation detection reaction (PCR-LDR). In our study group, there was no significant association between MIR196A2 polymorphism and the risk of HBV-related HCC in all subjects, however, the risk of HCC was significantly higher with MIR196A2 rs11614913 CC genotype or C allele compared with those with the genotype or T allele in male patients. Furthermore, in a subsequent analysis of the association between this polymorphism and clinicopathologic characteristics, there was still no significant difference in both the distribution of genotype or allelic frequency. However, we observed that the T allele was significantly more frequent in male HCC patients with lymphatic metastasis. Our results suggested that MIR196A2 polymorphism was associated with susceptibility to HBV-related HCC in a male Chinese population. (C) 2010 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:621 / 626
页数:6
相关论文
共 50 条
[31]   Variants Identified by Hepatocellular Carcinoma and Chronic Hepatitis B Virus Infection Susceptibility GWAS Associated with Survival in HBV-Related Hepatocellular Carcinoma [J].
Li, Cong ;
Bi, Xinyu ;
Huang, Ying ;
Zhao, Jianjun ;
Li, Zhiyu ;
Zhou, Jianguo ;
Zhang, Meng ;
Huang, Zhen ;
Zhao, Hong ;
Cai, Jianqiang .
PLOS ONE, 2014, 9 (07)
[32]   Hepatitis B Virus Core Promoter Mutations in Patients With Chronic Hepatitis B and Hepatocellular Carcinoma in Bucharest, Romania [J].
Constantinescu, Ileana ;
Dinu, Andrei-Antoniu ;
Boscaiu, Voicu ;
Niculescu, Marius .
HEPATITIS MONTHLY, 2014, 14 (10)
[33]   Statin and the risk of hepatocellular carcinoma in patients with hepatitis B virus or hepatitis C virus infection: a meta-analysis [J].
Li, Xiaofei ;
Sheng, Lina ;
Liu, Liwen ;
Hu, Yongtao ;
Chen, Yongxin ;
Lou, Lianqing .
BMC GASTROENTEROLOGY, 2020, 20 (01)
[34]   High viral load is a risk factor for hepatocellular carcinoma in patients with chronic hepatitis B virus infection [J].
Ohata, K ;
Hamasaki, K ;
Toriyama, K ;
Ishikawa, H ;
Nakao, K ;
Eguchi, K .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2004, 19 (06) :670-675
[35]   Association of Interleukin-17 gene polymorphisms with susceptibility to chronic hepatitis B virus infection and clearance in Iranian population [J].
Tayefinasrabadi, Hamideh ;
Mohebbi, Seyed Reza ;
Hosseini, Seyed Masoud ;
Azimzadeh, Pedram ;
Pourhoseingholi, Mohamad Amin ;
Ghaemi, Amir ;
Sharifian, Afsaneh ;
Aghdaei, Hamid Asadzadeh ;
Zali, Mohammad Reza .
MICROBIAL PATHOGENESIS, 2020, 144
[36]   Treatment of chronic hepatitis B virus infection and hepatocellular carcinoma prevention [J].
Soudan, Damien ;
Sultanik, Philippe ;
Pol, Stanislas .
PRESSE MEDICALE, 2015, 44 (12) :1251-1255
[37]   Surveillance for hepatocellular carcinoma in chronic hepatitis B virus infection: for whom [J].
Jihyun An ;
Lee, Han Chu .
HEPATIC ONCOLOGY, 2015, 2 (03) :225-229
[38]   Association of transforming growth factor-β1 gene polymorphisms with a hepatocellular carcinoma risk in patients with chronic hepatitis B virus infection [J].
Yoon Jun Kim ;
Hyo-Suk Lee ;
Jong Pil Im ;
Byung-Hoon Min ;
Hyun Dae Kim ;
Ji Bong Jeong ;
Jung-Hwan Yoon ;
Chung Yong Kim ;
Myung Soo Kim ;
Jun Yeon Kim ;
Ji Hyun Jung ;
Lyoung Hyo Kim ;
Byung Lae Park ;
Hyoung Doo Shin .
Experimental & Molecular Medicine, 2003, 35 :196-202
[39]   Effect of previous infection with hepatitis B virus on the incidence of hepatocellular carcinoma after sustained virologic response in patients with chronic hepatitis C virus infection [J].
Toyoda, Hidenori ;
Koshiyama, Yuichi ;
Yasuda, Satoshi ;
Kumada, Takashi ;
Chayama, Kazuaki ;
Akita, Tomoyuki ;
Tanaka, Junko .
JOURNAL OF VIRAL HEPATITIS, 2024, 31 (03) :137-142
[40]   Diagnostic value of PIVKA-II in detecting hepatocellular carcinoma in Chinese patients with hepatitis B virus infection [J].
Tang, Xiao-Qiong ;
Li, Hong ;
Yan, Li-Bo ;
Zhou, Ling-Yun ;
Chen, En-Qiang ;
Liu, Miao ;
Zhang, Dong-Mei ;
Tang, Hong .
FUTURE VIROLOGY, 2017, 12 (05) :259-267