Induction of endoplasmic reticulum stress and apoptosis by a marine prostanoid in human hepatocellular carcinoma
Journal
Journal of Hepatology
Journal Volume
43
Journal Issue
4
Pages
679-686
Date Issued
2005
Author(s)
Abstract
Background/Aims: Hepatocellular carcinoma is a very common malignancy and is highly chemoresistant to currently available chemotherapeutic agents. We isolated a marine prostanoid, bromovulone III, from soft coral Clavularia viridis and found that it displayed effective anti-tumor activity in human hepatocellular carcinoma. The anti-tumor mechanism has been delineated in this study. Methods: Anti-tumor efficacy and apoptotic cell death were examined by sulforhodamine B and Hoechst 33342 assays. Rhodamine 123 was used to measure the change of mitochondrial membrane potential. Immunoprecipitation and Western blotting detect the involvement of several apoptosis-related proteins. Electron microscopic examination detects the morphological change of mitochondria and endoplasmic reticulum (ER). Results: Bromovulone III primarily induced mitochondria-related activation of caspase-9 and -3 in several tumor types, such as prostate cancer PC-3 and acute promyelocytic leukemia HL-60 cells. However, it primarily induced the activation of m-calpain, caspase-12, and transcription factor CHOP/GADD153 in hepatocellular carcinoma Hep3B cells, suggesting the involvement of ER stress. Furthermore, a secondary mitochondrial swelling and depolarization of mitochondrial membrane potential were subsequently triggered after ER stress, suggesting the crosstalk between ER and mitochondria. Conclusions: It is suggested that bromovulone III induces apoptosis in Hep3B cells through a mechanism that induces ER stress and leads to activation of CHOP/GADD153 and caspase-12. ? 2005 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
SDGs
Other Subjects
bromovulone iii; calpain; caspase 12; caspase 3; caspase 9; growth arrest and DNA damage inducible protein 153; hoe 33342; prostanoid; rhodamine 123; sulforhodamine B; unclassified drug; antineoplastic activity; apoptosis; article; cancer cell culture; clavularia viridis; controlled study; coral; depolarization; drug efficacy; electron microscopy; endoplasmic reticulum; enzyme activation; human; human cell; immunoprecipitation; liver cell carcinoma; liver mitochondrion; membrane potential; mitochondrial membrane; mitochondrion swelling; priority journal; promyelocytic leukemia; prostate cancer; signal transduction; Western blotting; Apoptosis; Carcinoma, Hepatocellular; Cell Line, Tumor; Endoplasmic Reticulum; Humans; Liver Neoplasms; Oxidative Stress; Prostaglandins
Type
journal article