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Derrone induces autophagic cell death through induction of ROS and ERK in A549 cells
Author(s) -
Myung-Ji Kang,
Sooyeon Kim,
EunBin Kwon,
Yang Hee Jo,
Mi Kyeong Lee,
Hyun-Sun Lee,
DongOh Moon,
Mun-Ock Kim
Publication year - 2019
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0218659
Subject(s) - autophagy , programmed cell death , mapk/erk pathway , microbiology and biotechnology , a549 cell , apoptosis , viability assay , intracellular , cell growth , phosphorylation , chemistry , kinase , cancer cell , cancer research , biology , cancer , biochemistry , genetics
We studied the effect of derrone (DR), one of the major compounds of unripe fruits of Cudrania tricuspidata , on cancer cell death. DR inhibited cell growth of various cancer cells, and that was partially associated with apoptosis in A549 cells. DR showed the autophagic features, such as the conversion of LC3-I to LC3-II, the formation of autophagosome and the downregulation of SQSTM1/p62 (p62). The treatment of autophagy inhibitor reversed DR-mediated cell death, suggesting that DR induces autophagic cell death. The increase of cytoplasmic Ca 2+ and ROS by DR treatment significantly influences the formation of autophagosomes; however, only ROS scavengers significantly rescued the reduced cell viability. Additional results revealed that treatment of DR induces sustained phosphorylation of ERK and the inhibition of ERK phosphorylation using U0126 (ERK inhibitor) markedly attenuated DR-induced cell death. Overall, these results suggest that DR induces autophagic cell death through intracellular ROS and sustained ERK phosphorylation in A549 cells.

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