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作 者:何文武[1] 黄国雄[1] 胡松[1] 冼磊[1] 陈铭伍[1]
机构地区:[1]广西医科大学第一附属医院心胸外科,广西南宁530021
出 处:《中华肿瘤防治杂志》2013年第10期757-760,共4页Chinese Journal of Cancer Prevention and Treatment
基 金:广西科技攻关与新产品试制基金(10124001A-47)
摘 要:目的:探讨配对同源结构域基因1(PITX1)和人端粒酶逆转录酶(hTERT)基因mRNA在非小细胞肺癌(NSCLC)组织中的表达水平与临床病理因素的关系及其相关性。方法:两步法RT-PCR技术检测91例NSCLC组织和21例支气管扩张或肺大疱等手术切除的良性肺组织中PITX1和hTERT基因mRNA的表达水平。结果:NSCLC组织PITX1基因阳性表达率为24.18%(22/91),明显低于良性肺组织的66.67%(14/21),差异有统计学意义,χ2=14.12,P=0.000。91例NSCLC组织中,hTERT基因过表达72例(79.12%),明显高于其在良性肺组织中的正常表达,χ2=46.52,P=0.000。NSCLC组织PITX1基因mRNA表达与淋巴结有无转移及分化程度(高、中分化与低分化)有关,P值分别为0.004和0.030。hTERT基因mRNA的过表达在不同病理类型中差异有统计学意义,P=0.003。PITX1与hTERT基因的mRNA表达存在相关性,P=0.000。结论:PITX1基因的表达可能对hTERT基因的过表达具有重要的抑制作用;PITX1和hTERT基因mRNA表达状况可能与NSCLC的发生与发展有关。OBJECTIVE:To explore the expression ievel of PITX1 and hTERT gene mRNA expression in non-small cell lung cancer(NSCLC). METHODS: The reverse transcription polymerase chain reaction (RT-PCR) was used to detect the PITX1 and hTERT mRNA in 91 cases of non-small cell lung cancer and 21 cases of lung benign diseases tissues sepa- rately. RESULTS: The expression rate of PITX1 gene in non-small cell lung cancer tissues was 24. 18 % (22/91), which was significantly lower than that in benign lung tissue 66.67% (14/21), and the difference was statistically significant (X^2= 14.12, P= 0. 000). hTERT gene overexpression in 72 (79.12 % ) of 91 patients with non-small cell lung cancer, sig- nificantly higher than its normal expression in benign lung tissue,and the difference was statistically significant (^(2^ 46.52, P=0. 000). The difference was statistically significant in the PITX1 gene mRNA expression in lymph node metas- tasis (P= 0. 004) and the degree of differentiation (high,moderately differentiated and poorly differentiated; P = 0. 030). hTERT gene mRNA overexpression in pathological type was statistically significant (P=0. 003). There was correlation between PITX1 gene mRNA and hTERT mRNA expression (P=0. 000). CONCLUSIONS: PITX1 gene expression may inhibit the over-expression of hTERT gene. mRNA expression of PITX1 and hTERT may be related to the occurrence and development of non-small cell lung cancer.
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