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线粒体基因突变而非大规模缺失是具有线粒体微卫星不稳定性的结直肠癌的一个特征。

Mitochondrial gene mutation, but not large-scale deletion, is a feature of colorectal carcinomas with mitochondrial microsatellite instability.

作者信息

Habano W, Sugai T, Yoshida T, Nakamura S

机构信息

Division of Pathology, Central Clinical Laboratory, School of Medicine, Iwate Medical University, Morioka City, Japan.

出版信息

Int J Cancer. 1999 Nov 26;83(5):625-9. doi: 10.1002/(sici)1097-0215(19991126)83:5<625::aid-ijc10>3.0.co;2-n.

Abstract

We have shown that microsatellite instability (MSI) occurs in mitochondrial DNA (mtDNA) of colorectal carcinomas. To determine whether such mitochondrial microsatellite instability (mtMSI) is associated with certain forms of mitochondrial gene alterations, we extended the screening in the same series of 45 carcinomas. Analysis by whole mtDNA amplification (16.5 kb) and digestion revealed no detectable large-scale change in these carcinomas. In contrast, single-strand conformation polymorphism (SSCP) analysis demonstrated NADH dehydrogense (ND) gene alterations in 7 carcinomas (16%), including 3 mononucleotide repeat alterations, 2 missense mutations and 1 small (15 bp) deletion. Six of these 7 carcinomas also exhibited mtMSI of the (C)n sequence in the displacement-loop (D-loop) region. Thus, frameshift or missense mutations rather than large-scale changes in the mtDNA were more common features in colorectal carcinomas with mtMSI. By analogy to mutational features of nuclear MSI, mtMSI most likely results from certain repair deficiencies in the mtDNA and probably plays a role in the tumor development of certain colorectal carcinomas.

摘要

我们已经证明,微卫星不稳定性(MSI)存在于结直肠癌的线粒体DNA(mtDNA)中。为了确定这种线粒体微卫星不稳定性(mtMSI)是否与某些形式的线粒体基因改变相关,我们在同一组45例癌症中扩大了筛查范围。通过对整个mtDNA(16.5 kb)进行扩增和酶切分析,未发现这些癌症中存在可检测到的大规模变化。相比之下,单链构象多态性(SSCP)分析显示,7例癌症(16%)中存在NADH脱氢酶(ND)基因改变,包括3个单核苷酸重复改变、2个错义突变和1个小(15 bp)缺失。这7例癌症中有6例在置换环(D-loop)区域也表现出(C)n序列的mtMSI。因此,移码或错义突变而非mtDNA的大规模变化是具有mtMSI的结直肠癌中更常见的特征。与核MSI的突变特征类似,mtMSI很可能是由mtDNA中的某些修复缺陷导致的,并且可能在某些结直肠癌的肿瘤发生中起作用。

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