RRC ID 37741
Author Karasawa H, Miura K, Fujibuchi W, Ishida K, Kaneko N, Kinouchi M, Okabe M, Ando T, Murata Y, Sasaki H, Takami K, Yamamura A, Shibata C, Sasaki I.
Title Down-regulation of cIAP2 enhances 5-FU sensitivity through the apoptotic pathway in human colon cancer cells.
Journal Cancer Sci
Abstract Currently 5-fluorouracil (5-FU) plays a central role in the chemotherapeutic regimens for colorectal cancers and thus it is important to understand the mechanisms that determine 5-FU sensitivity. The expression profiles of human colon cancer cell line DLD-1, its 5-FU-resistant subclone DLD-1/FU and a further 21 types of colon cancer cell lines were compared to identify the novel genes defining the sensitivity to 5-FU and to estimate which population of genes is responsible for 5-FU sensitivity. In the hierarchical clustering, DLD-1 and DLD-1/FU were most closely clustered despite over 100 times difference in their 50% inhibitory concentration of 5-FU. In DLD-1/FU, the population of genes differentially expressed compared to DLD-1 was limited to 3.3%, although it ranged from 4.8% to 24.0% in the other 21 cell lines, thus indicating that the difference of 5-FU sensitivity was defined by a limited number of genes. Next, the role of the cellular inhibitor of apoptosis 2 (cIAP2) gene, which was up-regulated in DLD-1/FU, was investigated for 5-FU resistance using RNA interference. The down-regulation of cIAP2 efficiently enhanced 5-FU sensitivity, the activation of caspase 3/7 and apoptosis under exposure to 5-FU. The immunohistochemistry of cIAP2 in cancer and corresponding normal tissues from colorectal cancer patients in stage III revealed that cIAP2 was more frequently expressed in cancer tissues than in normal tissues, and cIAP2-positive patients had a trend toward early recurrence after fluorouracil-based chemotherapy. Although the association between drug sensitivity and the IAP family in colorectal cancer has not yet been discussed, cIAP2 may therefore play an important role as a target therapy in colorectal cancer.
Volume 100(5)
Pages 903-13
Published 2009-5-1
DOI 10.1111/j.1349-7006.2009.01112.x
PII CAS1112
PMID 19302291
MeSH Apoptosis* Baculoviral IAP Repeat-Containing 3 Protein Caspase 3 / metabolism Caspase 7 / metabolism Cell Line, Tumor Colonic Neoplasms / metabolism* Colonic Neoplasms / pathology* Down-Regulation* Drug Resistance, Neoplasm / drug effects Enzyme Activation Fluorouracil / pharmacology* Gene Expression Regulation, Neoplastic Humans Inhibitor of Apoptosis Proteins / metabolism* Oligonucleotide Array Sequence Analysis Prognosis RNA, Small Interfering / genetics Signal Transduction / drug effects* Substrate Specificity Ubiquitin-Protein Ligases
IF 4.966
Times Cited 37
WOS Category ONCOLOGY
Resource
Human and Animal Cells COLO205(RCB2127) COLO-320(RCB1193) HCT116(RCB2979) LoVo(RCB1639)