Literature DB >> 31367972

Pheochromocytoma/Paraganglioma: Is This a Genetic Disorder?

Lauren Fishbein1.   

Abstract

Pheochromocytomas and paragangliomas (PCC/PGL) are neuroendocrine tumors of the adrenal medulla and extra-adrenal ganglia which often over-secrete catecholamines leading to cardiovascular morbidity and even mortality. These unique tumors have the highest heritability of all solid tumor types with up to 35-40% of patients with PCC/PGL having a germline predisposition. PURPOSE OF REVIEW: To review the germline susceptibility genes and clinical syndromes associated with PCC/PGL. RECENT
FINDINGS: There are over 12 PCC/PGL susceptibility genes identified in a wide range of pathways. Each gene is associated with a clinical syndrome with varying penetrance for both primary and metastatic PCC/PGL and often includes increased risk for additional tumors besides PCC/PGL. Patients with sporadic or hereditary PCC/PGL should be monitored for life given the risk of multiple primary tumors, recurrence, and metastatic disease. All patients with PCC/PGL should be referred for consideration for clinical genetic testing given the high heritability of disease.

Entities:  

Keywords:  Genetics; Hereditary; Metastatic pheochromocytoma; Paraganglioma; Pheochromocytoma

Mesh:

Year:  2019        PMID: 31367972     DOI: 10.1007/s11886-019-1184-y

Source DB:  PubMed          Journal:  Curr Cardiol Rep        ISSN: 1523-3782            Impact factor:   2.931


  78 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.  Biochemical diagnosis of pheochromocytoma: which test is best?

Authors:  Jacques W M Lenders; Karel Pacak; McClellan M Walther; W Marston Linehan; Massimo Mannelli; Peter Friberg; Harry R Keiser; David S Goldstein; Graeme Eisenhofer
Journal:  JAMA       Date:  2002-03-20       Impact factor: 56.272

3.  Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndrome.

Authors:  B Parfait; D Chretien; A Rötig; C Marsac; A Munnich; P Rustin
Journal:  Hum Genet       Date:  2000-02       Impact factor: 4.132

4.  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

5.  Succinate links TCA cycle dysfunction to oncogenesis by inhibiting HIF-alpha prolyl hydroxylase.

Authors:  Mary A Selak; Sean M Armour; Elaine D MacKenzie; Houda Boulahbel; David G Watson; Kyle D Mansfield; Yi Pan; M Celeste Simon; Craig B Thompson; Eyal Gottlieb
Journal:  Cancer Cell       Date:  2005-01       Impact factor: 31.743

6.  Structure of an HIF-1alpha -pVHL complex: hydroxyproline recognition in signaling.

Authors:  Jung-Hyun Min; Haifeng Yang; Mircea Ivan; Frank Gertler; William G Kaelin; Nikola P Pavletich
Journal:  Science       Date:  2002-05-09       Impact factor: 47.728

7.  Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer.

Authors:  Ian P M Tomlinson; N Afrina Alam; Andrew J Rowan; Ella Barclay; Emma E M Jaeger; David Kelsell; Irene Leigh; Patricia Gorman; Hanan Lamlum; Shamima Rahman; Rebecca R Roylance; Simon Olpin; Stephen Bevan; Karen Barker; Nicholas Hearle; Richard S Houlston; Maija Kiuru; Rainer Lehtonen; Auli Karhu; Susa Vilkki; Päivi Laiho; Carita Eklund; Outi Vierimaa; Kristiina Aittomäki; Marja Hietala; Pertti Sistonen; Anders Paetau; Reijo Salovaara; Riitta Herva; Virpi Launonen; Lauri A Aaltonen
Journal:  Nat Genet       Date:  2002-02-25       Impact factor: 38.330

Review 8.  von Recklinghausen's disease and pheochromocytomas.

Authors:  M M Walther; J Herring; E Enquist; H R Keiser; W M Linehan
Journal:  J Urol       Date:  1999-11       Impact factor: 7.450

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

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

10.  Pheochromocytoma in Italy: a multicentric retrospective study.

Authors:  M Mannelli; L Ianni; A Cilotti; A Conti
Journal:  Eur J Endocrinol       Date:  1999-12       Impact factor: 6.664

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  3 in total

Review 1.  What Have We Learned from Molecular Biology of Paragangliomas and Pheochromocytomas?

Authors:  Thomas G Papathomas; Diederik P D Suurd; Alfred K Lam; Ronald R de Krijger; Karel Pacak; Arthur S Tischler; Menno R Vriens
Journal:  Endocr Pathol       Date:  2021-01-12       Impact factor: 3.943

2.  Novel DNMT3A Germline Variant in a Patient with Multiple Paragangliomas and Papillary Thyroid Carcinoma.

Authors:  Sara Mellid; Javier Coloma; Bruna Calsina; María Monteagudo; Juan M Roldán-Romero; María Santos; Luis J Leandro-García; Javier Lanillos; Ángel M Martínez-Montes; Cristina Rodríguez-Antona; Cristina Montero-Conde; Joaquín Martínez-López; Rosa Ayala; Xavier Matias-Guiu; Mercedes Robledo; Alberto Cascón
Journal:  Cancers (Basel)       Date:  2020-11-09       Impact factor: 6.639

3.  Long-term in vitro 2D-culture of SDHB and SDHD-related human paragangliomas and pheochromocytomas.

Authors:  Jean-Pierre Bayley; Heggert G Rebel; Kimberly Scheurwater; Dominique Duesman; Juan Zhang; Francesca Schiavi; Esther Korpershoek; Jeroen C Jansen; Abbey Schepers; Peter Devilee
Journal:  PLoS One       Date:  2022-09-30       Impact factor: 3.752

  3 in total

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