Treatment with sodium butyrate and rapamycin inhibit growth of human cervical cancer cells.
- Author:
Yong Jun JEON
1
;
Chi Heum CHO
;
So Jin SHIN
;
Sang Hoon KWON
;
Soon Do CHA
Author Information
1. Department of Obstetrics and Gynecology, School of Medicine, Keimyung University, Daegu, Korea. sdcha@dsmc.or.kr
- Publication Type:In Vitro ; Original Article
- Keywords:
HeLa cell;
Rapamycin;
Sodium butyrate;
Apotosis
- MeSH:
Blotting, Western;
Butyric Acid*;
Cell Cycle;
Cell Line;
Cell Survival;
Cyclin A;
Cyclin B1;
Cyclin D1;
Flow Cytometry;
HeLa Cells;
Histone Deacetylases;
Humans*;
Mental Competency;
Sirolimus*;
Sodium*;
Uterine Cervical Neoplasms*
- From:Korean Journal of Gynecologic Oncology
2007;18(3):165-171
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
OBJECTIVE: To evaluate whether mTOR inhibition by rapamycin can enhance the inhibitory effect of sodium butyrate, a histone deacetylase (HDAC) inhibitor on human cervical cancer cell line HeLa. METHODS: Cervical cancer cells (HeLa) were treated with sodium butyrate alone or in combination with rapamycin. Cell viability was analyzed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTS) assay and flow cytometry was performed to ascertain the effects of sodium butyrate and combinations of sodium butyrate with rapamycin. Expression of cell cycle related proteins were evaluated by Western blot analysis. RESULTS: As proven previously rapamycin, the mTOR inhibitor was effective in reducing the cell growth of cervical cancer cell line HeLa. Rapamycin and sodium butyrate induced growth inhibition in a dose dependent manner, with 100 nM/L rapamycin and 10 mM/L sodium butyrate blocked 78% cell growth. FACS analysis data substantiated the competence of rapamycin in inducing G1 arrest of mammalian cells, and this ability was greatly enhanced by the combination of sodium butyrate and rapamycin. The percentage of sub G1 fraction of cells was remarkably increased by the combination of sodium butyrate and rapamycin. Sodium butyrate in combination with rapamycin showed the increased expression of CDK inhibitors p21, p27, and dephosphorylation of Rb whereas the expression levels of cyclin A, cyclin D1 and cyclin B1 were reduced. CONCLUSION: The findings implicate that rapamycin could enhance the anti-cancer effect of sodium butyrate. Further in depth studies and in vitro studies would throw more light on the growth inhibitory mechanism and its potential use as therapeutic drugs of butyric acid and rapamycin.
