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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.

Original publication

DOI

10.1038/nrc1737

Type

Journal article

Journal

Nat Rev Cancer

Publication Date

11/2005

Volume

5

Pages

857 - 866

Keywords

Animals, Genes, Tumor Suppressor, Genetic Predisposition to Disease, Humans, Mitochondria, Mutation, Neoplasms, Tumor Suppressor Proteins