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Extracellular Vesicles From SDHB Deficient hPheo1 Cells Activate STAT3 in Wild-Type Cells

Pheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors that originate from the adrenal medulla and extra-adrenal paraganglia, respectively. Inactivating mutations in succinate dehydrogenase (SDHx) genes leads to succinate accumulation, increased HIF1-α levels, and uncontrollable...

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Détails bibliographiques
Publié dans:J Endocr Soc
Auteurs principaux: Ghayee, Hans K, Patel, Sujal, Tuna, Kubra M, Liu, Lauren, Xu, Yiling, Alli, Abdel A
Format: Artigo
Langue:Inglês
Publié: Oxford University Press 2021
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC8265752/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvab048.138
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