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线粒体 DNA 4977 碱基对缺失及其在结直肠癌中拷贝数改变的意义。

The mitochondrial DNA 4,977-bp deletion and its implication in copy number alteration in colorectal cancer.

机构信息

Zhejiang Provincial Key Laboratory of Medical Genetics, School of Laboratory Medicine of Wenzhou Medical College, Zhejiang 325035, PRChina.

出版信息

BMC Med Genet. 2011 Jan 13;12:8. doi: 10.1186/1471-2350-12-8.

Abstract

BACKGROUND

qualitative and quantitative changes in human mitochondrial DNA (mtDNA) have been implicated in various cancer types. A 4,977 bp deletion in the major arch of the mitochondrial genome is one of the most common mutations associated with a variety of human diseases and aging.

METHODS

we conducted a comprehensive study on clinical features and mtDNA of 104 colorectal cancer patients in the Wenzhou area of China. In particular, using a quantitative real time PCR method, we analyzed the 4,977 bp deletion and mtDNA content in tumor tissues and paired non-tumor areas from these patients.

RESULTS

we found that the 4,977 bp deletion was more likely to be present in patients of younger age (≤65 years, p = 0.027). In patients with the 4,977 bp deletion, the deletion level decreased as the cancer stage advanced (p = 0.031). Moreover, mtDNA copy number in tumor tissues of patients with this deletion increased, both compared with that in adjacent non-tumor tissues and with in tumors of patients without the deletion. Such mtDNA content increase correlated with the levels of the 4,977 bp deletion and with cancer stage (p < 0.001).

CONCLUSIONS

our study indicates that the mtDNA 4,977 bp deletion may play a role in the early stage of colorectal cancer, and it is also implicated in alteration of mtDNA content in cancer cells.

摘要

背景

人类线粒体 DNA(mtDNA)的定性和定量变化与各种癌症类型有关。线粒体基因组主要环上的 4977bp 缺失是与多种人类疾病和衰老相关的最常见突变之一。

方法

我们对中国温州地区的 104 例结直肠癌患者的临床特征和 mtDNA 进行了综合研究。特别是,我们使用定量实时 PCR 方法分析了这些患者肿瘤组织及其配对非肿瘤区域中的 4977bp 缺失和 mtDNA 含量。

结果

我们发现,4977bp 缺失更可能发生在年龄较小的患者(≤65 岁,p=0.027)中。在有 4977bp 缺失的患者中,随着癌症分期的进展,缺失水平降低(p=0.031)。此外,缺失患者肿瘤组织中的 mtDNA 拷贝数增加,与相邻非肿瘤组织中的 mtDNA 拷贝数相比,以及与无缺失患者的肿瘤中的 mtDNA 拷贝数相比,均增加。这种 mtDNA 含量的增加与 4977bp 缺失的水平和癌症分期相关(p<0.001)。

结论

我们的研究表明,mtDNA 4977bp 缺失可能在结直肠癌的早期阶段发挥作用,并且还与癌细胞中 mtDNA 含量的改变有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b029/3025938/5a1cff48313a/1471-2350-12-8-1.jpg

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