Negoro Kenji, Yamano Yukio, Fushimi Kazuaki, Saito Kengo, Nakatani Ken, Shiiba Masashi, Yokoe Hidetaka, Bukawa Hiroki, Uzawa Katsuhiro, Wada Takeshi, Tanzawa Hideki, Fujita Shigeyuki
Department of Oral and Maxillofacial Surgery, School of Medicine, Wakayama Medical University, Japan.
Int J Oncol. 2007 Jun;30(6):1325-32. doi: 10.3892/ijo.30.6.1325.
To investigate the mechanism of the resistance to cisplatin (CDDP), we established the CDDP-resistant cell line, KB-R, from CDDP-sensitive oral carcinoma cell line, KB. The 3-(3, 4-dimethyl-thiazol-2-yl) 2, 5-diphenyltetrazolium bromide (MTT) assay indicated that KB-R is 5.5-fold more resistant to CDDP than KB. Microarray analysis indicated that the expression levels of 1,718 genes were elevated at least five-fold or more in KB-R, compared with KB. The expression status of ATP binding cassette (ABC) transporter genes, which belong to multi-drug resistance genes, was confirmed by semiquantitative reverse transcriptase-polymerase chain reaction and real-time PCR. MRP1 and MRP2 were up-regulated, whereas MDR1 was down-regulated. Pathway and ontology analysis using the Ingenuity Pathway Analysis tool indicated three highly significant genetic networks including 105 of the 1,718 overexpressed genes and one network including 35 'cell-to-cell signaling and interaction' related genes. Our results suggested that these cell lines, KB and KB-R, may be useful for searching the candidate genes responsible for CDDP-resistance and for further study to understand the mechanism of CDDP-resistance.
为研究顺铂(CDDP)耐药机制,我们从对CDDP敏感的口腔癌细胞系KB建立了CDDP耐药细胞系KB-R。3-(3,4-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)检测表明,KB-R对CDDP的耐药性是KB的5.5倍。基因芯片分析表明,与KB相比,KB-R中1718个基因的表达水平至少升高了5倍或更多。通过半定量逆转录聚合酶链反应和实时PCR确认了属于多药耐药基因的ATP结合盒(ABC)转运蛋白基因的表达状态。MRP1和MRP2上调,而MDR1下调。使用Ingenuity Pathway Analysis工具进行的通路和本体分析表明,有三个高度显著的基因网络,包括1718个过表达基因中的105个,以及一个包含35个“细胞间信号传导和相互作用”相关基因的网络。我们的结果表明,这些细胞系KB和KB-R可能有助于寻找导致CDDP耐药的候选基因,并有助于进一步研究以了解CDDP耐药的机制。