Knockdown of TIGAR by RNA interference induces apoptosis and autophagy in HepG2 hepatocellular carcinoma cells

Ling Ye, Xiaoping Zhao, Jian Lu, Guanxiang Qian, Jialin C. Zheng, Shengfang Ge

Research output: Contribution to journalArticlepeer-review

38 Scopus citations


Apoptosis and autophagy are crucial mechanisms regulating cell death, and the relationship between apoptosis and autophagy in the liver has yet to be thoroughly explored. TIGAR (TP53-induced glycolysis and apoptosis regulator), which is a p53-inducible gene, functions in the suppression of ROS (reactive oxygen species) and protects U2OS cells from undergoing cell death. In this study, silencing TIGAR by RNAi (RNA interference) in HepG2 cells down-regulated both TIGAR mRNA (~75%) and protein levels (~80%) and led to the inhibition of cell growth (P<. 0.01) by apoptosis (P<. 0.001) and autophagy. We demonstrated that TIGAR can increase ROS levels in HepG2 cells. The down-regulation of TIGAR led to the induction of LC-3 II (specific autophagic marker), the formation of the autophagosome, and increased Beclin-1 expression. 3-MA (3-Methyladenine), an inhibitor of autophagic sequestration blocker, inhibited TIGAR siRNA-enhanced autophagy, as indicated by the decrease in LC-3 II levels. Consequently, these data provide the first evidence that targeted silencing of TIGAR induces apoptotic and autophagic cell death in HepG2 cells, and our data raise hope for the future successful application of TIGAR siRNA in patients with hepatocellular carcinoma (HCC).

Original languageEnglish (US)
Pages (from-to)300-306
Number of pages7
JournalBiochemical and Biophysical Research Communications
Issue number2
StatePublished - Jul 26 2013


  • Apoptosis
  • Autophagy
  • Hepatocellular carcinoma
  • RNA interference

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Molecular Biology
  • Cell Biology


Dive into the research topics of 'Knockdown of TIGAR by RNA interference induces apoptosis and autophagy in HepG2 hepatocellular carcinoma cells'. Together they form a unique fingerprint.

Cite this