首页> 外文期刊>Acta histochemica et cytochemica. >Semi-Nested Real-Time Reverse Transcription Polymerase Chain Reaction Methods for the Successful Quantitation of Cytokeratin mRNA Expression Levels for the Subtyping of Non-Small-Cell Lung Carcinoma Using Paraffin-Embedded and Microdissected Lung Biopsy Specimens
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Semi-Nested Real-Time Reverse Transcription Polymerase Chain Reaction Methods for the Successful Quantitation of Cytokeratin mRNA Expression Levels for the Subtyping of Non-Small-Cell Lung Carcinoma Using Paraffin-Embedded and Microdissected Lung Biopsy Specimens

机译:半巢式实时逆转录聚合酶链反应方法用于成功定量使用石蜡包埋和显微解剖的肺活检标本的非小细胞肺癌亚型的细胞角蛋白mRNA表达水平

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In patients with inoperable advanced non-small cell lung carcinomas (NSCLCs), histological subtyping using small-mount biopsy specimens was often required to decide the indications for drug treatment. The aim of this study was to assess the utility of highly sensitive mRNA quantitation for the subtyping of advanced NSCLC using small formalin fixing and paraffin embedding (FFPE) biopsy samples. Cytokeratin (CK) 6, CK7, CK14, CK18, and thyroid transcription factor (TTF)-1 mRNA expression levels were measured using semi-nested real-time quantitative (snq) reverse-transcribed polymerase chain reaction (RT-PCR) in microdissected tumor cells collected from 52 lung biopsies. Our results using the present snqRT-PCR method showed an improvement in mRNA quantitation from small FFPE samples, and the mRNA expression level using snqRT-PCR was correlated with the immunohistochemical protein expression level. CK7, CK18, and TTF-1 mRNA were expressed at significantly higher levels (P
机译:对于无法手术的晚期非小细胞肺癌(NSCLC)患者,通常需要使用少量活检标本进行组织学分型,以确定药物治疗的适应症。这项研究的目的是评估使用小型福尔马林固定和石蜡包埋(FFPE)活检样品对晚期NSCLC进行亚型分型的高敏感性mRNA定量的实用性。使用半巢式实时定量(snq)逆转录聚合酶链反应(RT-PCR)在显微解剖中测量了细胞角蛋白(CK)6,CK7,CK14,CK18和甲状腺转录因子(TTF)-1 mRNA的表达水平从52个肺活检组织中收集到的肿瘤细胞。我们使用当前的snqRT-PCR方法的结果显示,从较小的FFPE样品中mRNA定量得到了改善,并且使用snqRT-PCR的mRNA表达水平与免疫组化蛋白表达水平相关。 CK7,CK18和TTF-1 mRNA的表达水平明显较高(P

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