期刊
BREAST CANCER RESEARCH AND TREATMENT
卷 108, 期 3, 页码 427-434出版社
SPRINGER
DOI: 10.1007/s10549-007-9613-9
关键词
benign breast disease; breast cancer; mtDNA 4977-bp deletion; quantitative real-time PCR assay
类别
资金
- NCI NIH HHS [R01 CA 064277, R01 CA064277] Funding Source: Medline
The mitochondrial DNA (mtDNA) 4977-bp deletion (Delta mtDNA(4977) mutation) is one of the most frequently observed mtDNA mutations in human tissues and may play a role in carcinogenesis. Only a few studies have evaluated Delta mtDNA(4977) mutation in breast cancer tissue, and the findings have been inconsistent, which may be due to methodological differences. In this study, we developed a quantitative real-time PCR assay to assess the level of the Delta mtDNA(4977) mutation in tumor tissue samples from 55 primary breast cancer patients and 21 patients with benign breast disease (BBD). The Delta mtDNA(4977) mutation was detected in all of the samples with levels varying from 0.000149% to 7.0%. The Delta mtDNA(4977) mutation levels were lower in tumor tissues than in adjacent normal tissues in both breast cancer and BBD subjects. The differences, however, were not statistically significant. No significant difference between breast cancer and BBD patients was found in the Delta mtDNA(4977) mutation levels of tumor tissues and adjacent normal tissues. The Delta mtDNA(4977) mutation levels were not significantly associated with clinicopathological characteristics (age, histology, tumor stage, and ER/PR status) in breast cancer or BBD patients. These results do not support the notion that the mitochondrial DNA 4977-bp deletion plays a major role in breast carcinogenesis.
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