Mitochondrial Subversion in Cancer

被引:136
作者
Chatterjee, Aditi [1 ]
Dasgupta, Santanu [1 ]
Sidransky, David [1 ]
机构
[1] Johns Hopkins Univ, Dept Otolaryngol Head & Neck Surg, Head & Neck Canc Res Div, Baltimore, MD 21205 USA
关键词
BASE EXCISION-REPAIR; 8-OXOGUANINE DNA GLYCOSYLASE; D-LOOP MUTATIONS; SUPEROXIDE-DISMUTASE ACTIVITIES; NONCANCEROUS LIVER-TISSUE; GLUTATHIONE-S-TRANSFERASE; CATALASE GENE-EXPRESSION; CYTOCHROME-C-OXIDASE; BREAST-CANCER; COMPLEX-I;
D O I
10.1158/1940-6207.CAPR-10-0326
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mitochondria control essential cellular activities including generation of ATP via oxidative phosphorylation. Mitochondrial DNA (mtDNA) mutations in the regulatory D-loop region and somatic mtDNA mutations are common in primary human cancers. The biological impact of a given mutation may vary, depending on the nature of the mutation and the proportion of mutant mtDNAs carried by the cell. Identification of mtDNA mutations in precancerous lesions supports their early contribution to cell transformation and cancer progression. Introduction of mtDNA mutations in transformed cells has been associated with increased ROS production and tumor growth. Studies reveal that increased and altered mtDNA plays a role in the development of cancer but further work is required to establish the functional significance of specific mitochondrial mutations in cancer and disease progression. This review offers some insight into the extent of mtDNA mutations, their functional consequences in tumorigenesis, mitochondrial therapeutics, and future clinical application. Cancer Peer Res; 4(5); 638-54. (c) 2011 AACR.
引用
收藏
页码:638 / 654
页数:17
相关论文
共 185 条
[1]   Altered expression of 12S/MT-RNR1, MT-CO2/COX2, and MT-ATP6 mitochondrial genes in prostate cancer [J].
Abril, Jesus ;
Lopez de Heredia, Miguel ;
Gonzalez, Laura ;
Cleries, Ramon ;
Nadal, Marga ;
Condom, Enric ;
Aguilo, Fernando ;
Gomez-Zaera, Montserrat ;
Nunes, Virginia .
PROSTATE, 2008, 68 (10) :1086-1096
[2]   Association of mitochondrial DNA transversion mutations with familial medullary thyroid carcinoma/multiple endocrine neoplasia type 2 syndrome [J].
Abu-Amero, KK ;
Alzahrani, AS ;
Zou, M ;
Shi, Y .
ONCOGENE, 2006, 25 (05) :677-684
[3]   Different organization of base excision repair of uracil in DNA in nuclei and mitochondria and selective upregulation of mitochondrial uracil-DNA glycosylase after oxidative stress [J].
Akbari, M. ;
Otterlei, M. ;
Pena-Diaz, J. ;
Krokan, H. E. .
NEUROSCIENCE, 2007, 145 (04) :1201-1212
[4]   Mitochondrial base excision repair of uracil and AP sites takes place by single-nucleotide insertion and long-patch DNA synthesis [J].
Akbari, Mansour ;
Visnes, Torkild ;
Krokan, Hans E. ;
Otterlei, Marit .
DNA REPAIR, 2008, 7 (04) :605-616
[5]   Detection of somatic mutations in the mitochondrial DNA control region of colorectal and gastric tumors by heteroduplex and single-strand conformation analysis [J].
Alonso, A ;
Martin, P ;
Albarran, C ;
Aguilera, B ;
Garcia, O ;
Guzman, A ;
Oliva, H ;
Sancho, M .
ELECTROPHORESIS, 1997, 18 (05) :682-685
[6]   Mitochondrial DNA Mutation Stimulates Prostate Cancer Growth in Bone Stromal Environment [J].
Arnold, Rebecca S. ;
Sun, Carrie Q. ;
Richards, Jendai C. ;
Grigoriev, Galina ;
Coleman, Ilsa M. ;
Nelson, Peter S. ;
Hsieh, Chia-Ling ;
Lee, Jae K. ;
Xu, Zhiheng ;
Rogatko, Andre ;
Osunkoya, Adeboye O. ;
Zayzafoon, Majd ;
Chung, Leland ;
Petros, John A. .
PROSTATE, 2009, 69 (01) :1-11
[7]  
ATTARDI G, 1988, ANNU REV CELL BIOL, V4, P289, DOI 10.1146/annurev.cb.04.110188.001445
[8]   COMPLEMENTATION AND SEGREGATION BEHAVIOR OF DISEASE-CAUSING MITOCHONDRIAL-DNA MUTATIONS IN CELLULAR-MODEL SYSTEMS [J].
ATTARDI, G ;
YONEDA, M ;
CHOMYN, A .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1995, 1271 (01) :241-248
[9]   Altered antioxidant status and lipid peroxidation in Indian patients with urothelial bladder carcinoma [J].
Badjatia, Nitika ;
Satyam, Abhigyan ;
Singh, Prabhjot ;
Seth, Amlesh ;
Sharma, Alpana .
UROLOGIC ONCOLOGY-SEMINARS AND ORIGINAL INVESTIGATIONS, 2010, 28 (04) :360-367
[10]   Mitochondrial genetic background modifies breast cancer risk [J].
Bai, Ren-Kui ;
Leal, Suzanne M. ;
Covarrubias, Daniel ;
Liu, Aiyi ;
Wong, Lee-Jun C. .
CANCER RESEARCH, 2007, 67 (10) :4687-4694