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A common pathway for genetic events leading to pheochromocytoma
- Source :
- Cancer Cell. 8:91-93
- Publication Year :
- 2005
- Publisher :
- Elsevier BV, 2005.
-
Abstract
- SummaryMutations 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.
- Subjects :
- Cancer Research
Oxygenase
endocrine system diseases
SDHB
Adrenal Gland Neoplasms
Procollagen-Proline Dioxygenase
Down-Regulation
Apoptosis
Pheochromocytoma
Biology
Bioinformatics
Dioxygenases
Hypoxia-Inducible Factor-Proline Dioxygenases
03 medical and health sciences
0302 clinical medicine
Paraganglioma
medicine
Humans
Genetic Predisposition to Disease
neoplasms
030304 developmental biology
0303 health sciences
Neural crest
Cell Biology
medicine.disease
Gene Expression Regulation, Neoplastic
Oncology
030220 oncology & carcinogenesis
Mutation
Cancer research
SDHD
Subjects
Details
- ISSN :
- 15356108
- Volume :
- 8
- Database :
- OpenAIRE
- Journal :
- Cancer Cell
- Accession number :
- edsair.doi.dedup.....d0c4ebabc9761f3d1448922aad822c4e
- Full Text :
- https://doi.org/10.1016/j.ccr.2005.07.012