KRAS突变阳性的结直肠癌患者体细胞突变分析  

Tumor-related somatic mutation in KRAS-mutated colorectal cancer

作　　者：董周寰[1] 石怀银[1] 吕亚莉[1] 钟梅[1] 朱凤伟[1] DONG Zhouhuan;SHI Huaiyin;LYU Yali;ZHONG Mei;ZHU Fengwei(Department of Pathology, Chinese PLA General Hospital, Beijing 100853, China)

机构地区：[1]解放军总医院病理科,北京100853

出　　处：《解放军医学院学报》2018年第12期1097-1101,共5页Academic Journal of Chinese PLA Medical School

摘　　要：目的分析KRAS突变阳性的结直肠癌患者的肿瘤相关基因突变特征,为其治疗和预后判断提供依据。方法入组2015年1月-2016年6月本院50例KRAS exon 2 G12/13突变阳性的结直肠癌肿瘤患者,用二代测序(NGS)技术检测其石蜡样本中59个常见肿瘤相关基因的热点突变。结果检测到除KRAS外的12个基因65种不同突变,其中突变样本超过10%的有TP53(62%)、APC(46%)、PIK3CA(22%)和SMAD4(14%)。这些基因的突变频率或者突变热点分布与肿瘤组织的生长存在相关性。结论 TP53、APC、PIK3CA、SMAD4与KRAS基因及其通路存在一定的相关性。Objective To analyze the characteristics of KRAS as well as other tumor-related gene mutation in colorectal cancer patients,and provide evidences for treatment and prognosis of these patients.Methods Totally 50 colorectal cancer patients with KRAS exon 2 G12/13 mutation admitted to our hospital from January 2015 to June 2016 were enrolled in this study.Next-generation sequencing(NGS)technology was used to detect the hot spot mutations of 59 tumor-related genes in FFPE samples.Results Totally 65 mutations in 12 genes were detected except KRAS.The abundance of mutations was over 10% in TP53(62%),APC(46%),PIK3CA(22%)and SMAD4(14%).The mutation frequency or hotspot distribution of these genes was associated with the growth of colorectal tumors.Conclusion TP53,APC,PIK3CA,SMAD4 may be related to KRAS gene and its pathway in colorectal cancer.

关 键 词：结直肠癌 KRAS基因 二代测序 体细胞突变 

分 类 号：R735.34[医药卫生—肿瘤]