Targeted sequencing of cancer-associated genes in hepatocellular carcinoma using next generation sequencing

被引:13
作者
Lu, Jianguo [1 ]
Yin, Jikai [1 ]
Dong, Rui [1 ]
Yang, Tao [1 ]
Yuan, Lijuan [1 ]
Zang, Li [1 ]
Xu, Cheng [2 ]
Peng, Bo [2 ]
Zhao, Jiangman [2 ]
Du, Xilin [1 ]
机构
[1] Fourth Mil Med Univ, Tangdu Hosp, Dept Gen Surg, Xian 710038, Shaanxi, Peoples R China
[2] Shanghai Zhangjiang Translat Med Res Ctr, Dept Med, Shanghai 201203, Peoples R China
关键词
hepatocellular carcinoma; mutations; next generation sequencing; HEPATITIS-B-VIRUS; TRANSGENIC MICE; JANUS KINASES; LIVER-CANCER; HBX GENE; MUTATIONS; P53; HEPATOCARCINOGENESIS; PROTEIN; DOMAIN;
D O I
10.3892/mmr.2015.3952
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Liver cancer is one of the most common causes of cancer-associated mortality. Hepatocellular carcinoma (HCC) is the major histological subtype among types of primary liver cancer. China is an area of high incidence of HCC, and >50% of the cases of HCC worldwide are in China. At present, the mechanism underlying the development of HCC remains to be fully elucidated, and previous studies have predominantly focused on HCC in southern and eastern China, with molecular data of the HCC cases in Western China remains limited. In the present study, a panel of 372 cancer-associated genes were screened using a next generation sequencing platform, which included a total of 12 cases from western China. The results confirmed mutations in previously identified HCC drivers, including p53 and Kras. Additionally, mutations in several cancer genes, which had not been previously associated with HCC, were identified, including RUNX1 and JAK3. The present study provided a mutation spectrum of HCC tissue in cases from western China, assisting in the investigation of the mechanism of liver carcinogenesis.
引用
收藏
页码:4678 / 4682
页数:5
相关论文
共 25 条
[1]   The RUNX genes: Gain or loss of function in cancer [J].
Blyth, K ;
Cameron, ER ;
Neil, JC .
NATURE REVIEWS CANCER, 2005, 5 (05) :376-387
[2]   The enigmatic X gene of hepatitis B virus [J].
Bouchard, MJ ;
Schneider, RJ .
JOURNAL OF VIROLOGY, 2004, 78 (23) :12725-12734
[3]   Transcriptome classification of HCC is related to gene alterations and to new therapeutic targets [J].
Boyault, Sandrine ;
Rickman, David S. ;
de Reynies, Aurelien ;
Balabaud, Charles ;
Rebouissou, Sandra ;
Jeannot, Emmanuelle ;
Herault, Aurelie ;
Saric, Jean ;
Belghiti, Jacques ;
Franco, Dominique ;
Bioulac-Sage, Paulette ;
Laurent-Puig, Pierre ;
Zucman-Rossi, Jessica .
HEPATOLOGY, 2007, 45 (01) :42-52
[4]   International Trends in Liver Cancer Incidence Rates [J].
Center, Melissa M. ;
Jemal, Ahmedin .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2011, 20 (11) :2362-2368
[5]   CRYSTAL-STRUCTURE OF A P53 TUMOR-SUPPRESSOR DNA COMPLEX - UNDERSTANDING TUMORIGENIC MUTATIONS [J].
CHO, YJ ;
GORINA, S ;
JEFFREY, PD ;
PAVLETICH, NP .
SCIENCE, 1994, 265 (5170) :346-355
[6]   FERM domain mutations induce gain of function in JAK3 in adult T-cell leukemia/lymphoma [J].
Elliott, Natalina E. ;
Cleveland, Susan M. ;
Grann, Victor ;
Janik, John ;
Waldmann, Thomas A. ;
Dave, Utpal P. .
BLOOD, 2011, 118 (14) :3911-3921
[7]  
GANDEVIA B, 1964, Med J Aust, V2, P320
[8]   The aflatoxin-induced TP53 mutation at codon 249 (R249S): Biomarker of exposure, early detection and target for therapy [J].
Gouas, Doriane ;
Shi, Hong ;
Hainaut, Pierre .
CANCER LETTERS, 2009, 286 (01) :29-37
[9]   MUTATIONAL HOTSPOT IN THE P53 GENE IN HUMAN HEPATOCELLULAR CARCINOMAS [J].
HSU, IC ;
METCALF, RA ;
SUN, T ;
WELSH, JA ;
WANG, NJ ;
HARRIS, CC .
NATURE, 1991, 350 (6317) :427-428
[10]   Exome sequencing of hepatitis B virus-associated hepatocellular carcinoma [J].
Huang, Jian ;
Deng, Qing ;
Wang, Qun ;
Li, Kun-Yu ;
Dai, Ji-Hong ;
Li, Niu ;
Zhu, Zhi-Dong ;
Zhou, Bo ;
Liu, Xiao-Yan ;
Liu, Rui-Fang ;
Fei, Qian-Lan ;
Chen, Hui ;
Cai, Bing ;
Zhou, Boping ;
Xiao, Hua-Sheng ;
Qin, Lun-Xiu ;
Han, Ze-Guang .
NATURE GENETICS, 2012, 44 (10) :1117-+