Silencing Fas-associated phosphatase 1 expression enhances efficiency of chemotherapy for colon carcinoma with oxaliplatin

World J Gastroenterol. 2010 Jan 7;16(1):112-8. doi: 10.3748/wjg.v16.i1.112.

Abstract

Aim: To investigate whether silencing Fas-associated phosphatase 1 (FAP-1) expression enhances the efficiency of chemotherapy for colon carcinoma with oxaliplatin.

Methods: Expression of FAP-1 in mRNA and protein was detected by reverse transcription polymerase chain reaction (RT-PCR) and flow cytometry. Small interfering RNA (siRNA) was designed according to the FAP-1 mRNA sequence. Cell proliferation was evaluated by methyl thiazolyl tetrazolium (MTT) assay. Anenxin V- and propidine iodine (PI) were assayed by flow cytometry for the detection of apoptosis.

Results: The expression of FAP-1 was increased in SW480 cells after chemotherapy with oxaliplatin. Transfection of FAP-1 siRNA into SW480 cells silenced the expression of FAP-1 and consequently abolished the inhibitory function of Fas/FasL-mediated apoptosis pathway, thus increasing the efficacy of chemotherapy for colon carcinoma with oxaliplatin.

Conclusion: RNA interference combined with conventional chemotherapy is more effective against colon cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / enzymology
  • Adenocarcinoma / genetics
  • Adenocarcinoma / pathology
  • Adenocarcinoma / therapy*
  • Antineoplastic Agents / pharmacology*
  • Apoptosis / drug effects
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Chemotherapy, Adjuvant
  • Colonic Neoplasms / enzymology
  • Colonic Neoplasms / genetics
  • Colonic Neoplasms / pathology
  • Colonic Neoplasms / therapy*
  • Flow Cytometry
  • Genetic Therapy / methods*
  • Humans
  • Organoplatinum Compounds / pharmacology*
  • Oxaliplatin
  • Protein Tyrosine Phosphatase, Non-Receptor Type 13 / genetics*
  • Protein Tyrosine Phosphatase, Non-Receptor Type 13 / metabolism
  • RNA Interference*
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Time Factors
  • Transfection

Substances

  • Antineoplastic Agents
  • Organoplatinum Compounds
  • RNA, Messenger
  • Oxaliplatin
  • PTPN13 protein, human
  • Protein Tyrosine Phosphatase, Non-Receptor Type 13