Pheochromocytoma and paraganglioma pathogenesis: learning from genetic heterogeneity
@article{Dahia2014PheochromocytomaAP, title={Pheochromocytoma and paraganglioma pathogenesis: learning from genetic heterogeneity}, author={P. Dahia}, journal={Nature Reviews Cancer}, year={2014}, volume={14}, pages={108-119} }
The neuroendocrine tumours pheochromocytomas and paragangliomas carry the highest degree of heritability in human neoplasms, enabling genetic alterations to be traced to clinical phenotypes through their transmission in families. Mutations in more than a dozen distinct susceptibility genes have implicated multiple pathways in these tumours, offering insights into kinase downstream signalling interactions and hypoxia regulation, and uncovering links between metabolism, epigenetic remodelling and… CONTINUE READING
Paper Mentions
Observational Patient Registry Clinical Trial
Pheochromocytomas and paragangliomas are neural crest-derived tumors of the nervous system
that are often inherited and genetically heterogeneous. Genetic screening is recommended for… Expand
Conditions | Associated Conditions, Bone Cancer, Inherited Cancer Syndrome, (+5 more) |
---|---|
Intervention | Genetic |
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