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...
Huvudupphovsmän: | , , |
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Materialtyp: | Journal article |
Språk: | English |
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2011
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_version_ | 1826281490107858944 |
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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 |