Skip to Main content Skip to Navigation
Journal articles

Growth factor-antagonized rexinoid apoptosis involves permissive PPARgamma/RXR heterodimers to activate the intrinsic death pathway by NO.

Abstract : Growth factor (GF) deprivation and/or blocking of cognate signaling can induce apoptosis and is the basis of several cancer treatment paradigms. We observed that RXR agonists (rexinoids) induce apoptosis of tumor cells when GF support is abrogated. This "rexinoid apoptosis" involves activation of both iNOS and eNOS by RXR-PPARgamma and results in production of apoptogenic NO. IGF/EGF-induced IGF receptor 1-mediated MAP kinase blocks rexinoid apoptosis by RXR phosphorylation. Combining rexinoids with the MAPK inhibitor U0126 induced apoptosis in human cancer cells in vitro and ex vivo and blocked xenograft growth in vivo. Our results suggest a regulatory mechanism in which GF signaling antagonizes RXR-PPARgamma-mediated default apoptosis to sustain cell life.
Document type :
Journal articles
Complete list of metadatas

https://www.hal.inserm.fr/inserm-00420821
Contributor : Maité Peney <>
Submitted on : Tuesday, September 29, 2009 - 4:53:04 PM
Last modification on : Tuesday, May 26, 2020 - 11:50:03 AM

Identifiers

Collections

Citation

Pattabhiraman Shankaranarayanan, Aurélie Rossin, Harshal Khanwalkar, Susana Alvarez, Rosana Alvarez, et al.. Growth factor-antagonized rexinoid apoptosis involves permissive PPARgamma/RXR heterodimers to activate the intrinsic death pathway by NO.. Cancer Cell, Elsevier, 2009, 16 (3), pp.220-31. ⟨10.1016/j.ccr.2009.07.029⟩. ⟨inserm-00420821⟩

Share

Metrics