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首页> 外文期刊>In vivo. >Expression of multi-drug resistance genes (mdr1, mrp1, bcrp) in primary oral squamous cell carcinoma.
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Expression of multi-drug resistance genes (mdr1, mrp1, bcrp) in primary oral squamous cell carcinoma.

机译:原发性口腔鳞状细胞癌中多药耐药基因(mdr1,mrp1,bcrp)的表达。

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The expression of resistance genes can cause the ineffectiveness of chemotherapeutics for the treatment of cancer. Therefore, known resistance genes were investigated in oral squamous cell carcinoma (OSCC) and the results were compared with clinico-pathological findings. MATERIALS AND METHODS: Fresh frozen samples of 45 primary OSCC were investigated for the expression of mdr1 (p-glycoprotein-mediated multi-drug resistance), mrp1 (multi-drug resistance-related protein) and bcrp (breast cancer-related protein), using a reverse transcriptase PCR. The gene products were revealed immunohistochemically on representative slices of the same tumor sample. The results were compared with TNM stage grouping [SG, (UICC, 1987)], HPV infection and p53 mutations (exons 5-8). RESULTS: The expression of the resistance genes was independent of age, sex, localisation of the tumor, HPV infection and p53 mutations. SG did not correlate to mdr1 and mrp1. On the other hand, bcrp expression increased 2.7-fold between SG III and IV OSCC. Loss of differentiation was associated with an increased expression of mdr1 (p=0.06), mrp1 (p<0.01) and bcrp (p<0.01). The bcrp expression correlated with shorter survival periods. Expression of mrp1 and mdr1 did not correlate positively in a linear pattern. Expression of mdr1 and bcrp moderately positively correlated (p<0.01). DISCUSSION: Multi-drug resistance genes can be up-regulated in OSCC. The expression of at least one of these genes is up-regulated in SG-IV OSCC. Determining these genes could probably support current studies on therapeutic effects in OSCC, e.g. new cytostatic drugs.
机译:抗性基因的表达可导致化学疗法对于治疗癌症无效。因此,在口腔鳞状细胞癌(OSCC)中研究了已知的耐药基因,并将结果与​​临床病理结果进行了比较。材料与方法:研究了45例原发性食管鳞癌的新鲜冷冻样品中mdr1(p-糖蛋白介导的多药耐药性),mrp1(多药耐药相关蛋白)和bcrp(乳腺癌相关蛋白)的表达,使用逆转录酶PCR。基因产物在同一肿瘤样品的代表性切片上免疫组织化学显示。将结果与TNM分期分组[SG,(UICC,1987)],HPV感染和p53突变(外显子5-8)进行比较。结果:耐药基因的表达与年龄,性别,肿瘤部位,HPV感染和p53突变无关。 SG与mdr1和mrp1不相关。另一方面,SG III和IV OSCC之间的bcrp表达增加了2.7倍。分化的丧失与mdr1(p = 0.06),mrp1(p <0.01)和bcrp(p <0.01)的表达增加有关。 bcrp表达与较短的生存期相关。 mrp1和mdr1的表达没有线性关系正相关。 mdr1和bcrp的表达呈正相关(p <0.01)。讨论:OSCC中的多药耐药基因可以被上调。这些基因中至少一种的表达在SG-IV OSCC中被上调。确定这些基因可能支持当前有关OSCC治疗效果的研究,例如新的抑制细胞生长的药物。

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