Bcl-XL antisense oligodeoxynucleotide sensitizes human esophageal cancer cell line to 5-fluorouracil.
- Author:
Lei ZHANG
1
;
Hong-tao WEN
;
Liu-xing WANG
;
Lan ZHANG
;
Yun-han ZHANG
Author Information
- Publication Type:Journal Article
- MeSH: Antimetabolites, Antineoplastic; pharmacology; Apoptosis; drug effects; Cell Line, Tumor; Cell Proliferation; drug effects; Drug Resistance, Neoplasm; Esophageal Neoplasms; metabolism; pathology; Fluorouracil; pharmacology; Humans; Oligodeoxyribonucleotides, Antisense; pharmacology; RNA, Messenger; biosynthesis; genetics; Transfection; bcl-X Protein; biosynthesis; genetics
- From: Chinese Journal of Oncology 2006;28(3):173-177
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the effects of the Bcl-XL antisense oligodeoxynucleotides (ASODN) in suppressing the Bcl-XL expression and increasing the sensitivity of esophageal cancer cell line EC9706 to 5-fluorouracil (5-Fu).
METHODSThe proliferation inhibitory rate of EC9706 was assessed by MTT, the expression of Bcl-XL was detected by RT-PCR and Western blot, and the apoptotic changes were examined by acridine orange (AO) fluorescent staining and flow cytometry, respectively.
RESULTSIn the group of ASODN combined with 5-Fu, the proliferation inhibitory rate of esophageal cancer cells was 71.58%, the expression inhibitory rate of Bcl-XL mRNA was 81.25%, the expression of Bcl-XL protein was decreased significantly. The apoptosis rates detected by AO fluorescent staining and flow cytometry were 69.5% and (63.32 +/- 9.23)%, respectively. There were significant differences as compared with the cell control group, the vacuity control group, the N-ODN group, the ASODN group and the 5-Fu group, respectively (P < 0.05).
CONCLUSIONBcl-XL ASODN combined with 5-Fu can effectively inhibit the proliferation of esophageal cancer cells in vitro. Bcl-XL ASODN can significantly increase the sensitivity of esophageal cancer cells to 5-Fu through suppressing the expression of Bcl-XL.