دورية أكاديمية

Succinate Mediates Tumorigenic Effects via Succinate Receptor 1: Potential for New Targeted Treatment Strategies in Succinate Dehydrogenase Deficient Paragangliomas.

التفاصيل البيبلوغرافية
العنوان: Succinate Mediates Tumorigenic Effects via Succinate Receptor 1: Potential for New Targeted Treatment Strategies in Succinate Dehydrogenase Deficient Paragangliomas.
المؤلفون: Matlac, Dieter M., Hadrava Vanova, Katerina, Bechmann, Nicole, Richter, Susan, Folberth, Julica, Ghayee, Hans K., Ge, Guang-Bo, Abunimer, Luma, Wesley, Robert, Aherrahrou, Redouane, Dona, Margo, Martínez-Montes, Ángel M., Calsina, Bruna, Merino, Maria J., Schwaninger, Markus, Deen, Peter M. T., Zhuang, Zhengping, Neuzil, Jiri, Pacak, Karel, Lehnert, Hendrik
المصدر: Frontiers in Endocrinology; 3/12/2021, Vol. 11, pN.PAG-N.PAG, 11p
مصطلحات موضوعية: PARAGANGLIOMA, SUCCINATE dehydrogenase, PROGNOSIS, PROGENITOR cells, TARGETED drug delivery, THERAPEUTICS
مستخلص: Paragangliomas and pheochromocytomas (PPGLs) are chromaffin tumors associated with severe catecholamine-induced morbidities. Surgical removal is often curative. However, complete resection may not be an option for patients with succinate dehydrogenase subunit A-D (SDHx) mutations. SDHx mutations are associated with a high risk for multiple recurrent, and metastatic PPGLs. Treatment options in these cases are limited and prognosis is dismal once metastases are present. Identification of new therapeutic targets and candidate drugs is thus urgently needed. Previously, we showed elevated expression of succinate receptor 1 (SUCNR1) in SDHB PPGLs and SDHD head and neck paragangliomas. Its ligand succinate has been reported to accumulate due to SDHx mutations. We thus hypothesize that autocrine stimulation of SUCNR1 plays a role in the pathogenesis of SDHx mutation-derived PPGLs. We confirmed elevated SUCNR1 expression in SDHx PPGLs and after SDHB knockout in progenitor cells derived from a human pheochromocytoma (hPheo1). Succinate significantly increased viability of SUCNR1 -transfected PC12 and ERK pathway signaling compared to control cells. Candidate SUCNR1 inhibitors successfully reversed proliferative effects of succinate. Our data reveal an unrecognized oncometabolic function of succinate in SDHx PPGLs, providing a growth advantage via SUCNR1. [ABSTRACT FROM AUTHOR]
Copyright of Frontiers in Endocrinology is the property of Frontiers Media S.A. and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
قاعدة البيانات: Complementary Index
الوصف
تدمد:16642392
DOI:10.3389/fendo.2021.589451