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肺癌中的线粒体DNA 4977碱基对缺失突变

Mitochondrial DNA 4977 BP deletion mutations in lung carcinoma.

作者信息

Dai Ji Gang, Xiao Ying Bin, Min Jia Xin, Zhang Guo Qiang, Yao Ke, Zhou Ren Jie

机构信息

Department of Thoracic Cardiovascular Surgery of Xinqiao Hospital, The Third Military Medical University, Chongqing - 400037, China.

出版信息

Indian J Cancer. 2006 Jan-Mar;43(1):20-5. doi: 10.4103/0019-509x.25771.

DOI:10.4103/0019-509x.25771
PMID:16763358
Abstract

BACKGROUND

The most common and also the most often assayed mtDNA deletion mutation, degrees mtDNA 4,977 sub has been demonstrated in various types of human cancer. However, knowledge about degrees mtDNA 4,977 in lung carcinoma is poor.

AIM

To study the 4,977 bp deletions of mitochondrial DNA ( degrees mtDNA 4,977) in lung cancer, adjacent histologically normal and normal lung tissue and its potential roles in the development of cancer.

MATERIALS AND METHODS

Thirty-seven matched lung cancer/adjacent histologically normal and 20 histologically normal lung tissue samples in subjects without lung cancer were analyzed by PCR technique.

RESULTS

degrees mtDNA 4,977 deletions were detected in 54.1% (20/37) of lung cancers, 59.5% (22/37) of adjacent normal and 30.0% (6/20) of normal lung tissue samples. No significant difference was found in the frequency of degrees mtDNA 4,977 deletions between the tumor and adjacent normal lung tissues (P value = 0.815). Moreover, no significant difference was found in the frequency of degrees mtDNA 4,977 deletions between the tumor and histologically normal lung tissues in subjects without lung cancer (P value=0.101). However, the correlation between degrees mtDNA 4,977 deletion and age and smoking factors was present in our data.

STATISTICAL ANALYSIS

Fisher's exact test was used to assess the difference in different groups by the Scientific Package for Social Sciences (SPSS), version 10.0, Statistical analysis software.

CONCLUSIONS

Mitochondrial DNA 4,977 bp deletion, which is not specific to lung cancer, may reflect the environmental and aging process influences operative during tumor progression.

摘要

背景

最常见且最常检测的线粒体DNA(mtDNA)缺失突变——4977度线粒体DNA缺失已在各类人类癌症中得到证实。然而,关于肺癌中4977度线粒体DNA缺失的了解却很少。

目的

研究肺癌、组织学上相邻的正常肺组织及正常肺组织中线粒体DNA(4977度线粒体DNA)的4977bp缺失情况及其在癌症发生中的潜在作用。

材料与方法

采用聚合酶链反应(PCR)技术分析37例配对的肺癌/组织学上相邻的正常肺组织样本以及20例无肺癌受试者的组织学正常肺组织样本。

结果

在54.1%(20/37)的肺癌样本、59.5%(22/37)的相邻正常肺组织样本和30.0%(6/20)的正常肺组织样本中检测到4977度线粒体DNA缺失。肿瘤组织与相邻正常肺组织之间4977度线粒体DNA缺失的频率无显著差异(P值 = 0.815)。此外,在无肺癌受试者中,肿瘤组织与组织学正常肺组织之间4977度线粒体DNA缺失的频率也无显著差异(P值 = 0.101)。然而,我们的数据显示4977度线粒体DNA缺失与年龄和吸烟因素之间存在相关性。

统计分析

采用社会科学统计软件包(SPSS)10.0版统计分析软件中的Fisher精确检验来评估不同组间的差异。

结论

线粒体DNA 4977bp缺失并非肺癌所特有,可能反映了肿瘤进展过程中环境和衰老过程的影响。

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