Tumor-specific changes in mtDNA content in human cancer

被引:141
作者
Mambo, E
Chatterjee, A
Xing, MZ
Tallini, G
Haugen, BR
Yeung, SCJ
Sukumar, S
Sidransky, D
机构
[1] Johns Hopkins Univ, Sch Med, Dept Otolaryngol Head & Neck Surg, Head & Neck Canc Res Div, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Med, Div Endocrinol & Metab, Baltimore, MD 21205 USA
[3] Univ Bologna, Sch Med, Dept Pathol, Bologna, Italy
[4] Univ Colorado, Hlth Sci Ctr, Dept Med, Aurora, CO USA
[5] Univ Texas, MD Anderson Canc Ctr, Dept Endocrine Neoplasia & Hormonal Disorders, Houston, TX 77030 USA
[6] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Breast Canc Program, Baltimore, MD USA
关键词
mtDNA content; thyroid cancer; breast cancer;
D O I
10.1002/ijc.21110
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mitochondrial DNA (mtDNA) alterations are associated with various cancer types, suggesting that the mitochondrial genome may be a critical contributing factor in carcinogenesis: mtDNA alterations have been suggested as a potentially sensitive and specific biomarker for several cancer types. We examined mtDNA content in 25 pairs of normal and tumor breast tissue samples, 37 papillary thyroid carcinoma (PTC), 21 benign thyroid neoplasms and in 20 paired normal and PTC samples. Our results showed that mtDNA content was reduced in 80% of the breast tumors relative to their corresponding normal. mtDNA was increased in papillary thyroid carcinomas, however, when compared to the corresponding normal DNA taken from the same individual. Also, mtDNA content was increased in none-paired PTC samples compared to the normal controls. Our findings indicate that changes in mtDNA content during carcinogenesis may be regulated in a tumor specific manner. Additionally, changes in mtDNA levels did not correlate with tumor grade and metastasis, suggesting that these alterations may occur in the early stages of tumorigenesis. Our findings suggest that mtDNA content can be used as a molecular diagnostic tool to help identify genetic abnormalities in human tumors. (C) 2005 Wiley-Liss, Inc.
引用
收藏
页码:920 / 924
页数:5
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