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线粒体 ND 基因中预测的致病性突变与 NSCLC 和结肠癌的远处转移相关。

Association of predicted pathogenic mutations in mitochondrial ND genes with distant metastasis in NSCLC and colon cancer.

机构信息

Laboratory of Cancer Genetics, Chiba Cancer Center Research Institute, 666-2 Nitona, Chuoh-ku, Chiba, 260-8717, Japan.

Department of Life Science, Shimane University Faculty of Medicine, 89-1 Enya, Izumo, Shimane, 693-8501, Japan.

出版信息

Sci Rep. 2017 Nov 14;7(1):15535. doi: 10.1038/s41598-017-15592-2.

Abstract

Cancer cells have more mutations in their mitochondrial DNA (mtDNA) than do normal cells, and pathogenic mutations in the genes encoding mitochondrial NADH dehydrogenase (ND) subunits have been found to enhance the invasive and metastatic ability of various tumour cells in animal experiments. However, it is unknown whether single-nucleotide variants (SNVs) of the ND genes that decrease complex I activity are involved in distant metastasis in human clinical samples. Here, we demonstrated the enhancement of the distant metastasis of Lewis lung carcinoma cells by the ND6 13885insC mutation, which is accompanied by the overexpression of metastasis-related genes, metabolic reprogramming, the enhancement of tumour angiogenesis and the acquisition of resistance to stress-induced cell death. We then sequenced ND genes in primary tumour lesions with or without distant metastases as well as metastatic tumour lesions from 115 patients with non-small cell lung cancer (NSCLC) and colon cancer, and we subsequently selected 14 SNVs with the potential to decrease complex I activity. Intriguingly, a significant correlation was observed (P < 0.05 by Chi-square test) between the incidence of the selected mutations and distant metastasis. Thus, these results strongly suggest that pathogenic ND gene mutations participate in enhancing distant metastasis in human cancers.

摘要

癌细胞的线粒体 DNA(mtDNA)比正常细胞有更多的突变,并且在编码线粒体 NADH 脱氢酶(ND)亚基的基因中发现的致病性突变可增强动物实验中各种肿瘤细胞的侵袭和转移能力。然而,在人类临床样本中,是否存在降低复合物 I 活性的 ND 基因单核苷酸变异(SNV)参与远处转移尚不清楚。在这里,我们通过 ND6 13885insC 突变证明了 Lewis 肺癌细胞远处转移的增强,该突变伴随着转移相关基因的过度表达、代谢重编程、肿瘤血管生成的增强以及对应激诱导细胞死亡的抗性的获得。然后,我们对来自 115 名非小细胞肺癌(NSCLC)和结肠癌患者的具有或不具有远处转移的原发性肿瘤病变以及转移性肿瘤病变进行了 ND 基因测序,并随后选择了 14 种具有降低复合物 I 活性潜力的 SNV。有趣的是,所选突变的发生率与远处转移之间存在显著相关性(卡方检验 P < 0.05)。因此,这些结果强烈表明致病性 ND 基因突变参与增强人类癌症的远处转移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3261/5686070/bc5dd0437b03/41598_2017_15592_Fig1_HTML.jpg

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