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(−)-Gossypol enhances the anticancer activity of epirubicin via downregulating survivin in hepatocellular carcinoma.
- Source :
-
Chemico-Biological Interactions . Sep2022, Vol. 364, pN.PAG-N.PAG. 1p. - Publication Year :
- 2022
-
Abstract
- Epirubicin (EPI)-based transarterial chemoembolization is an effective therapy for advanced hepatocellular carcinoma (HCC). However, EPI-induced survivin expression limits its tumor-killing potential in HCC. Interestingly, (−)-gossypol ((−)-Gsp), a male contraceptive, suppresses various malignancies. More importantly, (−)-Gsp also holds promise for enhancing the antitumor effects of chemotherapy in numerous cancer types. In the present study, we demonstrated for the first time that (−)-Gsp-sensitized EPI inhibited cell growth and induced apoptosis of HCC cells in vitro. Furthermore, (−)-Gsp sensitized EPI by attenuating the EPI-elevated survivin protein levels. Mechanistic studies showed that EPI stimulated survivin protein synthesis by promoting translation initiation, which was alleviated by (−)-Gsp mainly through suppressing the AKT-4EBP1/p70S6K-survivin and ERK-4EBP1-survivin pathways. HCC xenograft experiments in nude mice also showed that (−)-Gsp treatment acted synergistically with EPI to repress xenograft tumor growth. Overall, our proof-of-concept results may pave the way for novel strategies for the treatment of HCC based on the combination of EPI and (−)-Gsp. • (−)-Gossypol ((−)-Gsp) enhances epirubicin (EPI)-caused apoptosis of hepatocellular carcinoma cells in vitro and in vivo. • (−)-Gsp sensitizes EPI by attenuating EPI-induced survivin expression. • (−)-Gsp attenuates EPI-induced survivin by suppressing cap-dependent translation of survivin. • (−)-Gsp alleviates EPI-elicited 4EBP1 phosphorylation via AKT and ERK inactivation. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00092797
- Volume :
- 364
- Database :
- Academic Search Index
- Journal :
- Chemico-Biological Interactions
- Publication Type :
- Academic Journal
- Accession number :
- 158423323
- Full Text :
- https://doi.org/10.1016/j.cbi.2022.110060