A common pathway for genetic events leading to pheochromocytoma
- PMID: 16098460
- DOI: 10.1016/j.ccr.2005.07.012
A common pathway for genetic events leading to pheochromocytoma
Abstract
Mutations in VHL, RET, NF1, SDHB, SDHC, and SDHD can give rise to pheochromocytoma/paraganglioma. These different genetic lesions may all act by decreasing the activity of a 2-oxoglutarate-dependent oxygenase, SM-20/EglN3/PHD3, resulting in reduced apoptosis of neural crest cells during development.
Comment on
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Neuronal apoptosis linked to EglN3 prolyl hydroxylase and familial pheochromocytoma genes: developmental culling and cancer.Cancer Cell. 2005 Aug;8(2):155-67. doi: 10.1016/j.ccr.2005.06.015. Cancer Cell. 2005. PMID: 16098468
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