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Fungal secondary metabolites rasfonin induces autophagy, apoptosis and necroptosis in renal cancer cell line.

Abstract
Rasfonin (A304) is a fungal natural product isolated from the fermentation substrate of Talaromyces sp. 3656-A1, which was named according to its activity against the small G-protein Ras. In a former study, we demonstrated that it induced autophagy and apoptosis; however, whether rasfonin activated necroptosis remained unknown. Moreover, the interplay among different cell death processes induced by rasfonin was unexplored. In the present study, we revealed that, in addition of promoting autophagy and caspase-dependent apoptosis, rasfonin also activated necroptosis. Nectrostatin-1 (Nec-1), an inhibitor of necroptosis, affected rasfonin-induced autophagy in a time-dependent manner concurring with an increased caspase-dependent apoptosis. The aforementioned results were confirmed by knockdown of receptor-interacting protein 1 (RIP1), a crucial necrostatin-1-targeted adaptor kinase mediating cell death and survival. Taken together, the data presented indicate that rasfonin activates various cell death pathways, and RIP1 plays a critical role in rasfonin-induced autophagy and apoptosis.
AuthorsHui Sun, Weijun Wang, Yongsheng Che, Xuejun Jiang
JournalMycology (Mycology) Vol. 7 Issue 2 Pg. 81-87 ( 2016) ISSN: 2150-1203 [Print] England
PMID30123619 (Publication Type: Journal Article)

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