FTY720 induces apoptosis of human hepatoma cell lines through cell lines through P13-K-mediated Akt dephosphorylation

Kin Wah Lee, Kwan Man, Joanna W. Ho, Chris K. Sun, Kevin T. Ng, Xiang Hong Wang, Yong Chuan Wong, Irene O. Ng, Ray Xu, Sheung Tat Fan

Research output: Journal article publicationJournal articleAcademic researchpeer-review

77 Citations (Scopus)

Abstract

Our aim was to study the anticancer effect of the novel immunomodulator FTY720 in vitro and in vivo by investigation of cell cycle entry, cell cycle regulation, cell survival and apoptosis pathways. Three hepatoma cell lines with different p53 statuses (HepG2, Huh-7 and Hep3B) and one non-tumorigenic immortalized liver cell line (MIHA) were used for an in vitro study. The in vivo effects of FTY720 were evaluated in a nude mouse tumor model. Cell cycle distribution and cell cycle regulator proteins p27Kip1and cyclin D1, together with the PI3-K/Akt pathway, mitogen-activated protein kinases and cleaved caspase-3 and caspase-9, were evaluated. FTY720 selectively induced cell apoptosis in hepatoma cell lines with overexpression of cleaved caspase-3 and caspase-9, but the same phenomena were not found in MIHA cells. FTY720 induced Akt dephosphorylation at Ser473 mediated by phosphoinositide 3-kinase (PI3-K) inhibition. Dephosphorylation led to down-regulation of p42/p44 and dephosphorylation of Forkhead transcription factor and GSK-3β and, subsequently, up-regulation of p27Kip1and down-regulation of cyclin D1. In our in vivo model FTY720 induced apoptosis of tumor cells by down-regulation of the Akt pathway. FTY720 suppressed tumor growth without notable side-effects in normal liver. In conclusion, FTY720 is a novel anticancer agent that induces apoptosis of hepatoma cell lines both in vitro and in vivo through PI3-K-mediated Akt dephosphorylation in a p53-independent manner.
Original languageEnglish
Pages (from-to)2397-2405
Number of pages9
JournalCarcinogenesis
Volume25
Issue number12
DOIs
Publication statusPublished - 1 Dec 2004
Externally publishedYes

ASJC Scopus subject areas

  • Cancer Research

Cite this