Effects of tachyplesin on the regulation of cell cycle in human hepatocarcinoma SMMC-7721 cells
To investigate the effects of tachyplesin on the cell cycle regulation in human hepatcarcinoma cells. Effects of tachyplesin on the cell cycle in human hepatocarcinoma SMMC-7721 cells were assayed with flow cytometry. The protein levels of p53, p16, cyclin D1 and CDK4 were assayed by immunocytochemi...
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Published in | World journal of gastroenterology : WJG Vol. 9; no. 3; pp. 454 - 458 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
United States
The Key Laboratory of China Education Ministry for Cell Biology and Tumor Cell Engineering, School of Life Sciences, Xiamen University, Xiamen 361005, Fujian Province, China%Laboratory of Cell Biology, School of Life Sciences, Xiamen University, Xiamen 361005, Fujian Province, China
01.03.2003
Baishideng Publishing Group Inc |
Subjects | |
Online Access | Get full text |
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Summary: | To investigate the effects of tachyplesin on the cell cycle regulation in human hepatcarcinoma cells.
Effects of tachyplesin on the cell cycle in human hepatocarcinoma SMMC-7721 cells were assayed with flow cytometry. The protein levels of p53, p16, cyclin D1 and CDK4 were assayed by immunocytochemistry. The mRNA levels of p21(WAF1/CIP1) and c-myc genes were examined with in situ hybridization assay.
After tachyplesin treatment, the cell cycle arrested at G0/G1 phase, the protein levels of mutant p53, cyclin D1 and CDK4 and the mRNA level of c-myc gene were decreased, whereas the levels of p16 protein and p21(WAF1/CIP1) mRNA increased.
Tachyplesin might arrest the cell at G0/G1 phase by upregulating the levels of p16 protein and p21(WAF1/CIP1) mRNA and downregulating the levels of mutant p53, cyclin D1 and CDK4 proteins and c-myc mRNA, and induce the differentiation of human hepatocacinoma cells. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Telephone: +86-592-2183619 Fax: +86-592-2186392 Author contributions: All authors contributed equally to the work. Correspondence to: Dr. Qi-Fu Li, The Key Laboratory of China Education Ministry for Cell Biology and Tumor Cell Engineering, School of Life Sciences, Xiamen University, Xiamen 361005, Fujian Province, China. chifulee@163.net |
ISSN: | 1007-9327 2219-2840 |
DOI: | 10.3748/wjg.v9.i3.454 |