[Bcl-XL antisense oligodeoxynucleotide sensitizes human esophageal cancer cell line to 5-fluorouracil]

Zhonghua Zhong Liu Za Zhi. 2006 Mar;28(3):173-7.
[Article in Chinese]

Abstract

Objective: To 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).

Methods: The 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.

Results: In 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).

Conclusion: Bcl-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.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antimetabolites, Antineoplastic / pharmacology*
  • Apoptosis / drug effects
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Drug Resistance, Neoplasm
  • Esophageal Neoplasms / metabolism
  • Esophageal Neoplasms / pathology*
  • Fluorouracil / pharmacology*
  • Humans
  • Oligodeoxyribonucleotides, Antisense / pharmacology*
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Transfection
  • bcl-X Protein / biosynthesis
  • bcl-X Protein / genetics*

Substances

  • Antimetabolites, Antineoplastic
  • Oligodeoxyribonucleotides, Antisense
  • RNA, Messenger
  • bcl-X Protein
  • Fluorouracil