Attenuation of argininosuccinate lyase inhibits cancer growth via cyclin A2 and nitric oxide

Hau Lun Huang, Hui Ping Hsu, Shu Chus Shieh, Yung Sheng Chang, Wei Ching Chen, Chien Yu Cho, Chiao Fang Teng, Ih Jen Su, Wen Chun Hung, Ming Derg Lai

研究成果: Article同行評審

17 引文 斯高帕斯(Scopus)

摘要

Arginine biosynthesis and nitric oxide (NO) production are important for cancer homeostasis. Degradation of arginine may be used to inhibit liver tumors with low argininosuccinate synthetase (ASS) expression. In this report, we investigated an alternative therapeutic approach by targeting argininosuccinate lyase (ASL). ASL is transcriptionally induced by endoplasmic reticulum stress and is overexpressed in some human liver tumors. Knockdown of ASL expression by short hairpin RNA (shRNA) in three liver cancer cell lines, ML-1, HuH-7, and HepG2, decreased colony formation in vitro and tumor growth in vivo. Furthermore, lentiviral infection of ASL shRNA inhibited tumor growth in a therapeutic animal tumor model. Analysis of ASL shRNA on the cellcycle progression revealed a G2-M delay. Among cell-cycle regulatory molecules, cyclin A2 expression was reduced. Reintroduction of exogenous cyclin A2 restored the cell growth in ASL-knockdown cells. Autophagy was observed in the cells treated with ASL shRNA, as shown by an increase in LC3-II levels and autophagosome formation. The total cellular arginine level was not altered significantly. Inhibition of autophagy further attenuated cell growth, suggesting that autophagy induced by ASL shRNA plays a feedback prosurvival function. Knockdown of ASL reduced NO content, and addition of NO donor partially recovered the growth inhibition by ASL shRNA. In summary, downregulation of ASL attenuated tumor growth and the inhibition was mainly mediated by a decrease of cyclin A2 and NO. Mol Cancer Ther; 12(11); 2505-16.

原文English
頁(從 - 到)2505-2516
頁數12
期刊Molecular Cancer Therapeutics
12
發行號11
出版狀態Published - 2013 十一月

All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research

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