›› 2009, Vol. 40 ›› Issue (1): 63-66.doi:

• 肿瘤基础研究专题报道 • 上一篇    下一篇

Raf-1基因可能与口腔上皮癌细胞多药耐药性发生机制有关

董岩1 ;杨佩满2* ;牛卫东1   

  1. 1.大连医科大学口腔医学院,辽宁 大连 116044 ;2.大连医科大学组织胚胎学教研室, 辽宁 大连 116044
  • 收稿日期:2008-01-07 修回日期:2008-04-30 出版日期:2009-01-06
  • 通讯作者: 杨佩满

Raf-1 is possibly related with the multidrug resistance in oral squamous cell carcinoma

  1. 1.Stomatology School, Dalian Medical University, Liaoning Dalian 116044,China;2.Department of Histology and Embryology, Dalian Medical University,Liaoning Dalian 116044,China
  • Received:2008-01-07 Revised:2008-04-30 Online:2009-01-06
  • Contact: YANG Pei-man

关键词: 口腔上皮癌耐药株(KBV)/敏感株(KB, Raf-1, 多药耐药性, 反转录-聚合酶链式反应, 免疫印迹法,

Abstract: Objective Multidrug resistance is a major barrier for most patients with oral squamous cell carcinoma. In this study, we investigated the difference of the expression of Raf-1 mRNA and protein between multidrug resistant (KBV) and sensitive (KB) human oral squamous carcinoma cells to explore the effect of Raf-1 on the multidrug resistance in the human oral squamous carcinoma. Methods The changes of the mRNA and protein levels of Raf-1 in both KBV cells and KB cells were determined by RT-PCR,Western blotting assay and immunofluorescent method. By MTT and flow cytometry (FCM), ICSUB>50/SUB> and apoptosis rates in both KBV and KB cells were detected. Results The findings indicated that expressions of Raf-1 mRNA and protein levels in KB cells were lower than those in KBV cells statistically (P<0.01). Immunofluorescent image showed that Raf-1 protein expression in KBV cells were much stronger than that in KB cells. The ICSUB>50/SUB> in KB cells was (21.33±2.25)μg/L and that in KBV cells was (352.68±12.36)μg/L.The resistance index (RI) was 16.5The apoptosis rate in KB cells was (98.8±1.2)% and that in KBV cells was (23.5±2.1)%.These results showed that differences in the chemosensitivity to VCR between KBV cells and KB cells were significant statistically (P<0.01). Conclusion

Key words: KBV/KB, Raf-1, Multidrug resistance, RT-PCR, Western blotting, Human

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