| Literature DB >> 25824057 |
Xiaoli Tang1, Libin Deng2, Qi Chen3, Yao Wang4, Rong Xu3, Chao Shi4, Jia Shao4, Guohui Hu4, Meng Gao4, Hai Rao5, Shiwen Luo4, Quqin Lu6.
Abstract
Multiple lines of evidence implicate that aberrant activation of Hedgehog (Hh) signaling is involved in a variety of human cancers. However, the molecular mechanisms underlying how cancer cells respond to Hh inhibition remain to be elucidated. In this study, we found that blockade of Hh signaling suppresses cell proliferation in human cancer cells. Microarray analysis revealed that differentially expressed genes (DEGs) in human cancer cells are enriched in autophagy pathway in response to the inhibition of Hh signaling. Interestingly, inhibition of Hh signaling induced autophagy, whereas activation of Hh signaling by ligand treatments prevented the induction of autophagy. In addition, inhibition of autophagy by 3-methyladenine (3-MA) partially suppressed cytotoxicity induced by inhibition of Hh signaling. Finally, in autophagy deficient cells, cytotoxic effect triggered by inhibition of Hh signaling was partially reversed, indicating the modulation of autophagy by Hh signaling is autophagy-specific. These results suggest that inhibition of Hh signaling impedes cancer cell proliferation in part through induction of autophagy.Entities:
Keywords: Autophagy; Cell proliferation; Hedgehog signaling; SQSTM1/p62; Transcription factor Gli
Mesh:
Substances:
Year: 2015 PMID: 25824057 DOI: 10.1016/j.ejcb.2015.03.003
Source DB: PubMed Journal: Eur J Cell Biol ISSN: 0171-9335 Impact factor: 4.492