Published December 4, 2014 | Version v1
Journal article

Galangin suppresses HepG2 cell proliferation by activating the TGF-β receptor/Smad pathway

  • 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.2014.09.010

Additional 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.