Galangin suppresses HepG2 cell proliferation by activating the TGF-β receptor/Smad pathway
Creators
- 1. Affiliated Hospital of Guangdong Medical College, Zhanjiang, Guangdong 524001 (China)
- 2. Department of Biochemistry and Molecular Biology, Guangdong Medical College, Dongguan, Guangdong 523808 (China)
- 3. Department of Chemistry, Guangdong Medical College, Zhanjiang, Guangdong 524023 (China)
Description
Galangin can suppress hepatocellular carcinoma (HCC) cell proliferation. In this study, we demonstrated that galangin induced autophagy by activating the transforming growth factor (TGF)-β receptor/Smad pathway and increased TGF-β receptor I (RI), TGF-βRII, Smad1, Smad2, Smad3 and Smad4 levels but decreased Smad6 and Smad7 levels. Autophagy induced by galangin appears to depend on the TGF-β receptor/Smad signalling pathway because the down-regulation of Smad4 by siRNA or inhibition of TGF-β receptor activation by LY2109761 blocked galangin-induced autophagy. The down-regulation of Beclin1, autophagy-related gene (ATG) 16L, ATG12 and ATG3 restored HepG2 cell proliferation and prevented galangin-induced apoptosis. Our findings indicate a novel mechanism for galangin-induced autophagy via activation of the TGF-β receptor/Smad pathway. The induction of autophagy thus reflects the anti-proliferation effect of galangin on HCC cells
Availability note (English)
Available from http://dx.doi.org/10.1016/j.tox.2014.09.010Additional details
Identifiers
- DOI
- 10.1016/j.tox.2014.09.010;
- PII
- S0300-483X(14)00186-3;
Publishing Information
- Journal Title
- Toxicology
- Journal Volume
- 326
- Journal Page Range
- p. 9-17
- ISSN
- 0300-483X
- CODEN
- TXCYAC
INIS
- Country of Publication
- Ireland
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47008055
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- APOPTOSIS; CELL PROLIFERATION; GENES; GROWTH FACTORS; HEPATOMAS; RECEPTORS
- Descriptors DEC
- CARCINOMAS; DISEASES; MEMBRANE PROTEINS; MITOGENS; NEOPLASMS; ORGANIC COMPOUNDS; PROTEINS
Optional Information
- Copyright
- Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.