Mutation analysis of HIF-prolylhydroxylases (PHD/EGLN) in individuals with features of phaeochromocytoma and renal cell carcinoma susceptibility.

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Mutation analysis of HIF-prolylhydroxylases (PHD/EGLN) in individuals with features of phaeochromocytoma and renal cell carcinoma susceptibility. / Astuti, Dewi; Ricketts, Christopher; Chowdury, R; McDonough, MA; Gentle, Dean; Kirby, Gail; Schlisio, S; Kenchappa, R; Carter, B; Kaelin, WG; Ratcliffe, PJ; Schofield, CJ; Latif, Farida; Maher, Eamonn.

In: Endocrine-related cancer, 19.10.2010.

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Astuti, Dewi ; Ricketts, Christopher ; Chowdury, R ; McDonough, MA ; Gentle, Dean ; Kirby, Gail ; Schlisio, S ; Kenchappa, R ; Carter, B ; Kaelin, WG ; Ratcliffe, PJ ; Schofield, CJ ; Latif, Farida ; Maher, Eamonn. / Mutation analysis of HIF-prolylhydroxylases (PHD/EGLN) in individuals with features of phaeochromocytoma and renal cell carcinoma susceptibility. In: Endocrine-related cancer. 2010.

Bibtex

@article{314b9420feb7442494919598da2b5fa5,
title = "Mutation analysis of HIF-prolylhydroxylases (PHD/EGLN) in individuals with features of phaeochromocytoma and renal cell carcinoma susceptibility.",
abstract = "Germline mutations in the von Hippel–Lindau disease (VHL) and succinate dehydrogenase subunit B (SDHB) genes can cause inherited phaeochromocytoma and/or renal cell carcinoma(RCC). Dysregulation of the hypoxia-inducible factor (HIF) transcription factors has been linked to VHL and SDHB-related RCC; both HIF dysregulation and disordered function of a prolyl hydroxylase domain isoform 3 (PHD3/EGLN3)-related pathway of neuronal apoptosis have been linked to the development of phaeochromocytoma. The 2-oxoglutarate-dependent prolyl hydroxylase enzymes PHD1 (EGLN2), PHD2 (EGLN1) and PHD3 (EGLN3) have a key role in regulating the stability of HIF-a subunits (and hence expression of the HIF-a transcription factors). A germline PHD2 mutation has been reported in association with congenital erythrocytosis and recurrent extra-adrenal phaeochromocytoma. We undertook mutation analysis of PHD1, PHD2 and PHD3 in two cohorts of patients with features of inherited phaeochromocytoma (nZ82) and inherited RCC (nZ64) and no evidence of germline mutations in known susceptibility genes. No confirmed pathogenic mutations were detected suggesting that mutations in these genes are not a frequent cause of inherited phaeochromocytoma or RCC.",
author = "Dewi Astuti and Christopher Ricketts and R Chowdury and MA McDonough and Dean Gentle and Gail Kirby and S Schlisio and R Kenchappa and B Carter and WG Kaelin and PJ Ratcliffe and CJ Schofield and Farida Latif and Eamonn Maher",
year = "2010",
month = oct,
day = "19",
doi = "10.1677/ERC-10-0113",
language = "English",
journal = "Endocrine-related cancer",
issn = "1351-0088",
publisher = "BioScientifica",

}

RIS

TY - JOUR

T1 - Mutation analysis of HIF-prolylhydroxylases (PHD/EGLN) in individuals with features of phaeochromocytoma and renal cell carcinoma susceptibility.

AU - Astuti, Dewi

AU - Ricketts, Christopher

AU - Chowdury, R

AU - McDonough, MA

AU - Gentle, Dean

AU - Kirby, Gail

AU - Schlisio, S

AU - Kenchappa, R

AU - Carter, B

AU - Kaelin, WG

AU - Ratcliffe, PJ

AU - Schofield, CJ

AU - Latif, Farida

AU - Maher, Eamonn

PY - 2010/10/19

Y1 - 2010/10/19

N2 - Germline mutations in the von Hippel–Lindau disease (VHL) and succinate dehydrogenase subunit B (SDHB) genes can cause inherited phaeochromocytoma and/or renal cell carcinoma(RCC). Dysregulation of the hypoxia-inducible factor (HIF) transcription factors has been linked to VHL and SDHB-related RCC; both HIF dysregulation and disordered function of a prolyl hydroxylase domain isoform 3 (PHD3/EGLN3)-related pathway of neuronal apoptosis have been linked to the development of phaeochromocytoma. The 2-oxoglutarate-dependent prolyl hydroxylase enzymes PHD1 (EGLN2), PHD2 (EGLN1) and PHD3 (EGLN3) have a key role in regulating the stability of HIF-a subunits (and hence expression of the HIF-a transcription factors). A germline PHD2 mutation has been reported in association with congenital erythrocytosis and recurrent extra-adrenal phaeochromocytoma. We undertook mutation analysis of PHD1, PHD2 and PHD3 in two cohorts of patients with features of inherited phaeochromocytoma (nZ82) and inherited RCC (nZ64) and no evidence of germline mutations in known susceptibility genes. No confirmed pathogenic mutations were detected suggesting that mutations in these genes are not a frequent cause of inherited phaeochromocytoma or RCC.

AB - Germline mutations in the von Hippel–Lindau disease (VHL) and succinate dehydrogenase subunit B (SDHB) genes can cause inherited phaeochromocytoma and/or renal cell carcinoma(RCC). Dysregulation of the hypoxia-inducible factor (HIF) transcription factors has been linked to VHL and SDHB-related RCC; both HIF dysregulation and disordered function of a prolyl hydroxylase domain isoform 3 (PHD3/EGLN3)-related pathway of neuronal apoptosis have been linked to the development of phaeochromocytoma. The 2-oxoglutarate-dependent prolyl hydroxylase enzymes PHD1 (EGLN2), PHD2 (EGLN1) and PHD3 (EGLN3) have a key role in regulating the stability of HIF-a subunits (and hence expression of the HIF-a transcription factors). A germline PHD2 mutation has been reported in association with congenital erythrocytosis and recurrent extra-adrenal phaeochromocytoma. We undertook mutation analysis of PHD1, PHD2 and PHD3 in two cohorts of patients with features of inherited phaeochromocytoma (nZ82) and inherited RCC (nZ64) and no evidence of germline mutations in known susceptibility genes. No confirmed pathogenic mutations were detected suggesting that mutations in these genes are not a frequent cause of inherited phaeochromocytoma or RCC.

U2 - 10.1677/ERC-10-0113

DO - 10.1677/ERC-10-0113

M3 - Article

C2 - 20959442

JO - Endocrine-related cancer

JF - Endocrine-related cancer

SN - 1351-0088

ER -