Original Articles
Copyright ©The Author(s) 2000. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Aug 15, 2000; 6(4): 532-539
Published online Aug 15, 2000. doi: 10.3748/wjg.v6.i4.532
Induction of apoptosis by arsenic trioxide and hydroxy camptothecin in gastriccancer cells in vitro
Shui-Ping Tu, Jie Zhong, Ji-Hong Tan, Xiao-Hua Jiang, Min-Min Qiao, Yu-Xin Wu, Shi-Hu Jiang
Shui-Ping Tu, Ji-Hong Tan, Xiao-Hua Jiang, Min-Min Qiao, Yu-Xin Wu, Shi-Hu Jiang, Jie-Zhong, Department of Gastroenterology, Ruijin Hospital, Shanghai Second Medical University, Shanghai 200025, China
Shui-Ping Tu, male, born on 1966-06-29 in Nanfeng, Jiangxi Province, grad uated from Suzhou Medical College with bachelor degree, now physician-in-charge, and PhD, majoring in gastrointestinal tumor research, having 8 papers published
Author contributions: All authors contributed equally to the work.
Supported by the Natural Science Foundation of Committee of Science andT echnology of Shanghai Municipality(No964119035)
Correspondence to: Shui-Ping Tu, Department of Gastroenterology, Ruijin Hospital, Shanghai Second Medical University, Shanghai 200025, China. Tushuiping@sohu.com
Telephone: +86-21-64370045 Ext, 661144
Received: February 12, 2000
Revised: February 27, 2000
Accepted: March 5, 2000
Published online: August 15, 2000
Abstract

AIM: To study the effects of arsenic trioxide and HCPT on different degrees of differentiated gastric cancer cells (SGC-7901, MKN-45, MKN-28) with respect to both cytotoxicity and induction of apoptosis in vitro.

METHODS: The cytotoxicity of As2O3 and HCPT on gastric cancer cells was determined by MTT assay. Morphologic changes of apoptosis of gastric cancer cells were observed by light microscopy and transmission electron microscopy. Apoptosis and cell cycle changes of gastric cancer cells induced by HCPT and As2O3 were investigated by TUNEL method and flow cytometry.

RESULTS: As2O3 and HCPT had remarkable cytotoxic effects on different degrees of differentiated gastric cancer cells. The IC50 of As2O3 on well differentiat ed gastric cancer cell MKN-28, moderately differentiated gastric cancer cell SG C-7901, and poorly differentiated gastric cancer cell MKN-28 were 8.91 μmol/L, 10.57 μmol/L, and 11.65 μmol/L, respectively. The IC50 of HCPT on MKN-28, SGC-7901, and MKN-45 were 9.35 mg/L, 10.21 mg/L, and 12.63 mg/L respectively after 48 h treatment. After 12 h of exposure to both drugs, gastric cancer cells exhibited morphologic features of apoptosis, including cell shrinkage, nuclear condensation, and formation of apoptotic bodies. A typical subdiploid peak before G0/G1 phase was observed by flow cytometry. The apoptotic rates of SGC-7901, MKN-45, and MKN-28 were 13.84%, 22.52%, and 9.68%, respectively after 48 h exposure to 10 μmol/L As2O3. The apoptotic rates of SGC-7901, MKN-45, and MKN-28 were 21.88%, 12.35%, and 30.26%, respectively after 48 h expo sure to 10 mg/L HCPT. The apoptotic indice were 7%-15% as assessed by TUNEL method. The effect of As2O3 on SGC-7901 showed remarkable cell cycle specificity, which induced cell death in G1 phase, and blocked G2/M phase. HCPT also showed a remarkable cell cycle specificity, by inducing cell death and apoptosis in G1 phase and arrest of proliferation at Sphase.

CONCLUSION: As2O3 and HCPT exhibit significant cytotoxicity on gastric cancer cells by induction of apoptosis. As2O3 and HCPT might have a promising prospect in the treatment of gastric cancer, which needs to be further studied.

Keywords: gastric cancer, apoptosis, arsenic trioxide, hydroxycamptothecin