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Genome-wide scan for familial nasopharyngeal carcinoma reveals evidence of linkage to chromosome 4
Authors:Feng Bing-Jian  Huang Wei  Shugart Yin Yao  Lee Ming K  Zhang Feng  Xia Jian-Chuan  Wang Hui-Yun  Huang Teng-Bo  Jian Shao-Wen  Huang Ping  Feng Qi-Sheng  Huang Li-Xi  Yu Xing-Juan  Li Duang  Chen Li-Zheng  Jia Wei-Hua  Fang Yan  Huang Hui-Ming  Zhu Jing-Liu  Liu Xiao-Ming  Zhao Yan  Liu Wang-Qing  Deng Mang-Quan  Hu Wei-Han  Wu Shao-Xiong  Mo Hao-Yuan  Hong Ming-Fang  King Mary Claire  Chen Zhu  Zeng Yi-Xin
Institution:Cancer Institute, Cancer Center, Sun Yat-sen University, GuangZhou, China.
Abstract:Nasopharyngeal carcinoma (NPC) occurs with high frequency in Asian populations, especially among people of Cantonese ancestry. In areas with high incidence, NPC clusters in families, which suggests that both geography and genetics may influence disease risk. Although the HLA-Bw46 locus is associated with increased risk of NPC, no predisposing genes have been identified so far. Here we report the results of a genome-wide search carried out in families at high risk of NPC from Guangdong Province, China. Parametric analyses provide evidence of linkage to the D4S405 marker on chromosome 4 with a logarithm of odds for linkage (lod) score of 3.06 and a heterogeneity-adjusted lod (hlod) score of 3.21. Fine mapping with additional markers flanking D4S405 resulted in a lod score of 3.54 and hlod score of 3.67 for the region 4p15.1-q12. Multipoint nonparametric linkage analysis gives lod scores of 3.54 at D4S405 (P = 5.4 x 10(-5)) and 4.2 at D4S3002 (P = 1.1 x 10(-5)), which is positioned 4.5 cM away from D4S405. When Epstein Barr virus antibody titer was included as a covariate, the lod scores reached 4.70 (P = 2.0 x 10(-5)) and 5.36 (P = 4.36 x 10(-6)) for D4S405 and D4S3002, respectively. Our findings provide evidence of a major susceptibility locus for NPC on chromosome 4 in a subset of families.
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