Literature DB >> 19596260

Loss of heterozygosity of succinate dehydrogenase B mutation by direct sequencing in synchronous paragangliomas.

Pinki Prasad1, Jeffrey A Kant, Marcia Wills, Mandy O'Leary, Harold Lovvorn, Elizabeth Yang.   

Abstract

Extraadrenal pheochromocytomas and paragangliomas are rare entities within the pediatric population. We report the presentation of three synchronous extra-adrenal abdominal paragangliomas in an adolescent boy who carries a germline mutation in the succinate dehydrogenase B (SDHB) gene. Loss of heterozygosity of this allele was demonstrated by direct sequencing of DNA from two of his tumors, confirming loss of tumor suppressor function in the pathogenesis of these paragangliomas.

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Year:  2009        PMID: 19596260      PMCID: PMC2927361          DOI: 10.1016/j.cancergencyto.2009.04.009

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN: 0165-4608


  11 in total

1.  Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.

Authors:  B E Baysal; R E Ferrell; J E Willett-Brozick; E C Lawrence; D Myssiorek; A Bosch; A van der Mey; P E Taschner; W S Rubinstein; E N Myers; C W Richard; C J Cornelisse; P Devilee; B Devlin
Journal:  Science       Date:  2000-02-04       Impact factor: 47.728

2.  Pediatric paraganglioma: an early manifestation of an adult disease secondary to germline mutations.

Authors:  Jaume Mora; Alberto Cascón; Mercedes Robledo; Albert Catala
Journal:  Pediatr Blood Cancer       Date:  2006-11       Impact factor: 3.167

3.  Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma.

Authors:  D Astuti; F Latif; A Dallol; P L Dahia; F Douglas; E George; F Sköldberg; E S Husebye; C Eng; E R Maher
Journal:  Am J Hum Genet       Date:  2001-06-12       Impact factor: 11.025

4.  Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

Authors:  S Niemann; U Müller
Journal:  Nat Genet       Date:  2000-11       Impact factor: 38.330

5.  Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas.

Authors:  Diana E Benn; Michael S Croxson; Kathy Tucker; Christopher P Bambach; Anne Louise Richardson; Leigh Delbridge; Peter T Pullan; Jeremy Hammond; Deborah J Marsh; Bruce G Robinson
Journal:  Oncogene       Date:  2003-03-06       Impact factor: 9.867

6.  Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations.

Authors:  Hartmut P H Neumann; Christian Pawlu; Mariola Peczkowska; Birke Bausch; Sarah R McWhinney; Mihaela Muresan; Mary Buchta; Gerlind Franke; Joachim Klisch; Thorsten A Bley; Stefan Hoegerle; Carsten C Boedeker; Giuseppe Opocher; Jörg Schipper; Andrzej Januszewicz; Charis Eng
Journal:  JAMA       Date:  2004-08-25       Impact factor: 56.272

7.  Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility.

Authors:  Dewi Astuti; Niki Hart-Holden; Farida Latif; Fiona Lalloo; Graeme C Black; Caron Lim; Anthony Moran; Ashley B Grossman; Shirley V Hodgson; Anthony Freemont; Richard Ramsden; Charis Eng; D Gareth R Evans; Eamonn R Maher
Journal:  Clin Endocrinol (Oxf)       Date:  2003-12       Impact factor: 3.478

8.  Functional consequences of a SDHB gene mutation in an apparently sporadic pheochromocytoma.

Authors:  Anne-Paule Gimenez-Roqueplo; Judith Favier; Pierre Rustin; Claudine Rieubland; Véronique Kerlan; Pierre-François Plouin; Agnès Rötig; Xavier Jeunemaitre
Journal:  J Clin Endocrinol Metab       Date:  2002-10       Impact factor: 5.958

Review 9.  Clinical and molecular progress in hereditary paraganglioma.

Authors:  B E Baysal
Journal:  J Med Genet       Date:  2008-11       Impact factor: 6.318

10.  The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency.

Authors:  Jean-Pierre Bayley; Peter Devilee; Peter E M Taschner
Journal:  BMC Med Genet       Date:  2005-11-16       Impact factor: 2.103

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  3 in total

1.  Succinate dehydrogenase B-deficient cancer cells are highly sensitive to bromodomain and extra-terminal inhibitors.

Authors:  Satoshi Kitazawa; Shunsuke Ebara; Ayumi Ando; Yuji Baba; Yoshinori Satomi; Tomoyoshi Soga; Takahito Hara
Journal:  Oncotarget       Date:  2017-04-25

Review 2.  Clinical Practice Guidance: Surveillance for phaeochromocytoma and paraganglioma in paediatric succinate dehydrogenase gene mutation carriers.

Authors:  Mei Yin Wong; Katrina A Andrews; Benjamin G Challis; Soo-Mi Park; Carlo L Acerini; Eamonn R Maher; Ruth T Casey
Journal:  Clin Endocrinol (Oxf)       Date:  2019-01-29       Impact factor: 3.478

Review 3.  Model systems in SDHx-related pheochromocytoma/paraganglioma.

Authors:  Krisztina Takács-Vellai; Zsolt Farkas; Fanni Ősz; Gordon W Stewart
Journal:  Cancer Metastasis Rev       Date:  2021-12-27       Impact factor: 9.264

  3 in total

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