首页> 中文期刊> 《世界核心医学期刊文摘:胃肠病学分册》 >患有早发型胃癌的Peutz-Jeghers综合征患者的一种LKB1基因新型种系突变

患有早发型胃癌的Peutz-Jeghers综合征患者的一种LKB1基因新型种系突变

         

摘要

cqvip:The gene responsible for Peutz-Jeghers syndrome (PJS), LKB1 (also called STK11) was mapped to chromosome 19p13.3 and was found to encode a putative serine/threonine protein kinase,LKB1. As only a limited number (~100) of germline mutations of the gene have been reported, and because the protein function is still unclear, information about LKB1 mutations and their expression should be accumulated to understand the phenotypegenotype correlation of this disease. Here we report a patient with sporadic PJS with early-onset gastric cancer. We found a novel germline frameshift mutation (757-758insT) in the LKB1 gene and a marked reduction in LKB1 protein expression in the carcinoma cells, suggesting that the loss of LKB1 function may have led to the carcinogenesis of the gastric cancer.

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