Fang Yu, Huang Jie, Zhang Jing, Wang Jun, Qiao Fei, Chen Hua-Mei, Hong Zhi-Peng
Department of Anesthesiology and.
Mitochondrial DNA. 2015 Feb;26(1):56-60. doi: 10.3109/19401736.2013.823168. Epub 2013 Sep 6.
To detect the somatic mutations and character its spectrum in Chinese lung cancer patients. In this study, we sequenced the whole mitochondrial DNA (mtDNA) genomes for 10 lung cancer patients including the primary cancerous, matched paracancerous normal and distant normal tissues. By analyzing the 30 whole mtDNA genomes, eight somatic mutations were identified from five patients investigated, which were confirmed with the cloning and sequencing of the somatic mutations. Five of the somatic mutations were detected among control region and the rests were found at the coding region. Heterogeneity was the main character of the somatic mutations in Chinese lung cancer patients. Further potential disease-related screening showed that, except the C deletion at position 309 showed AD-weakly associated, most of them were not disease-related. Although the role of aforementioned somatic mutations was unknown, however, considering the relative higher frequency of somatic mutations among the whole mtDNA genomes, it hints that detecting the somatic mutation(s) from the whole mtDNA genomes can serve as a useful tool for the Chinese lung cancer diagnostic to some extent.
为检测中国肺癌患者的体细胞突变并描绘其突变谱。在本研究中,我们对10例肺癌患者的整个线粒体DNA(mtDNA)基因组进行了测序,包括原发癌组织、配对的癌旁正常组织和远处正常组织。通过分析这30个完整的mtDNA基因组,在5例受调查患者中鉴定出8个体细胞突变,并通过体细胞突变的克隆和测序得到证实。其中5个体细胞突变在控制区被检测到,其余的在编码区被发现。异质性是中国肺癌患者体细胞突变的主要特征。进一步的潜在疾病相关筛查表明,除了309位的C缺失显示与常染色体显性遗传呈弱关联外,大多数突变与疾病无关。尽管上述体细胞突变的作用尚不清楚,然而,考虑到整个mtDNA基因组中体细胞突变的相对较高频率,这提示从整个mtDNA基因组中检测体细胞突变在一定程度上可作为中国肺癌诊断的有用工具。