SDH mutations in cancer

The SDHA, SDHB, SDHC, SDHD genes encode the four subunits of succinate dehydrogenase (SDH; mitochondrial complex II), a mitochondrial enzyme involved in two essential energy-producing metabolic processes of the cell, the Krebs cycle and the electron transport chain. Germline loss-of-function mutatio...

Full beskrivning

Bibliografiska uppgifter
Huvudupphovsmän: Bardella, C, Pollard, P, Tomlinson, I
Materialtyp: Journal article
Språk:English
Publicerad: 2011
_version_ 1826281490107858944
author Bardella, C
Pollard, P
Tomlinson, I
author_facet Bardella, C
Pollard, P
Tomlinson, I
author_sort Bardella, C
collection OXFORD
description The SDHA, SDHB, SDHC, SDHD genes encode the four subunits of succinate dehydrogenase (SDH; mitochondrial complex II), a mitochondrial enzyme involved in two essential energy-producing metabolic processes of the cell, the Krebs cycle and the electron transport chain. Germline loss-of-function mutations in any of the SDH genes or assembly factor (SDHAF2) cause hereditary paraganglioma/phaeochromocytoma syndrome (HPGL/PCC) through a mechanism which is largely unknown. Owing to the central function of SDH in cellular energy metabolism it is important to understand its role in tumor suppression. Here is reported an overview of genetics, clinical and molecular progress recently performed in understanding the basis of HPGL/PCC tumorigenesis. © 2011 Elsevier B.V. All rights reserved.
first_indexed 2024-03-07T00:29:35Z
format Journal article
id oxford-uuid:7f4b982f-3a1c-44e4-b9b7-2416603fa4e8
institution University of Oxford
language English
last_indexed 2024-03-07T00:29:35Z
publishDate 2011
record_format dspace
spelling oxford-uuid:7f4b982f-3a1c-44e4-b9b7-2416603fa4e82022-03-26T21:16:06ZSDH mutations in cancerJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:7f4b982f-3a1c-44e4-b9b7-2416603fa4e8EnglishSymplectic Elements at Oxford2011Bardella, CPollard, PTomlinson, IThe SDHA, SDHB, SDHC, SDHD genes encode the four subunits of succinate dehydrogenase (SDH; mitochondrial complex II), a mitochondrial enzyme involved in two essential energy-producing metabolic processes of the cell, the Krebs cycle and the electron transport chain. Germline loss-of-function mutations in any of the SDH genes or assembly factor (SDHAF2) cause hereditary paraganglioma/phaeochromocytoma syndrome (HPGL/PCC) through a mechanism which is largely unknown. Owing to the central function of SDH in cellular energy metabolism it is important to understand its role in tumor suppression. Here is reported an overview of genetics, clinical and molecular progress recently performed in understanding the basis of HPGL/PCC tumorigenesis. © 2011 Elsevier B.V. All rights reserved.
spellingShingle Bardella, C
Pollard, P
Tomlinson, I
SDH mutations in cancer
title SDH mutations in cancer
title_full SDH mutations in cancer
title_fullStr SDH mutations in cancer
title_full_unstemmed SDH mutations in cancer
title_short SDH mutations in cancer
title_sort sdh mutations in cancer
work_keys_str_mv AT bardellac sdhmutationsincancer
AT pollardp sdhmutationsincancer
AT tomlinsoni sdhmutationsincancer