Mitochondrial tumour suppressors: A genetic and biochemical update

被引:490
作者
Gottlieb, E
Tomlinson, IPM
机构
[1] Beatson Inst Canc Res, Canc Res UK, Apoptosis & Tumour Physiol Lab, Glasgow G61 1BD, Lanark, Scotland
[2] Canc Res UK, Mol & Populat Genet Lab, London WC2A 3PX, England
关键词
D O I
10.1038/nrc1737
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Since the discovery 5 years ago that the D-subunit of succinate dehydrogenase ( SDHD) can behave as a classic tumour suppressor, other nuclear-encoded mitochondrial proteins (SDHB, SDHC and fumarate hydratase) have been implicated in tumour susceptibility. Mutations in these proteins are principally involved in familial predisposition to benign tumours, but the spectrum of inherited lesions is increasingly recognized to include malignant tumours, such as malignant phaeochromocytomas and renal cell carcinomas. Here we review recent advances in the field of mitochondrial tumour suppressors, the biochemical pathway that links mitochondrial dysfunction with tumorigenesis, and potential therapeutic approaches to these malignancies.
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收藏
页码:857 / 866
页数:10
相关论文
共 98 条
[81]   Oxygen sensing by HIF hydroxylases [J].
Schofield, CJ ;
Ratcliffe, PJ .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2004, 5 (05) :343-354
[82]   Succinate links TCA cycle dysfunction to oncogenesis by inhibiting HIF-α prolyl hydroxylase [J].
Selak, MA ;
Armour, SM ;
MacKenzie, ED ;
Boulahbel, H ;
Watson, DG ;
Mansfield, KD ;
Pan, Y ;
Simon, MC ;
Thompson, CB ;
Gottlieb, E .
CANCER CELL, 2005, 7 (01) :77-85
[83]   HIF-1 and tumor progression: pathophysiology and therapeutics [J].
Semenza, GL .
TRENDS IN MOLECULAR MEDICINE, 2002, 8 (04) :S62-S67
[84]   Targeting HIF-1 for cancer therapy [J].
Semenza, GL .
NATURE REVIEWS CANCER, 2003, 3 (10) :721-732
[85]   Positive contribution of pathogenic mutations in the mitochondrial genome to the promotion of cancer by prevention from apoptosis [J].
Shidara, Y ;
Yamagata, K ;
Kanamori, T ;
Nakano, K ;
Kwong, JQ ;
Manfredi, G ;
Oda, H ;
Ohta, S .
CANCER RESEARCH, 2005, 65 (05) :1655-1663
[86]  
Sowter HM, 2001, CANCER RES, V61, P6669
[87]   Reactive oxygen species in tumor progression [J].
Storz, P .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2005, 10 :1881-1896
[88]   Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene [J].
Taschner, PEM ;
Jansen, JC ;
Baysal, BE ;
Bosch, A ;
Rosenberg, EH ;
Bröcker-Vriends, AHJT ;
van der Mey, AGL ;
van Ommen, GJB ;
Cornelisse, CJ ;
Devilee, P .
GENES CHROMOSOMES & CANCER, 2001, 31 (03) :274-281
[89]   Direct evidence for expression of Type II flavoprotein subunit in human complex II (succinate-ubiquinone reductase) [J].
Tomitsuka, E ;
Goto, Y ;
Taniwaki, M ;
Kita, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 311 (03) :774-779
[90]   Direct evidence for two distinct forms of the flavoprotein subunit of human mitochondrial complex II (succinate-ubiquinone reductase) [J].
Tomitsuka, E ;
Hirawake, H ;
Goto, Y ;
Taniwaki, M ;
Harada, S ;
Kita, K .
JOURNAL OF BIOCHEMISTRY, 2003, 134 (02) :191-195