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Tissue Microarray Analysis of Fas and FasL Expressions in Human Non-small Cell Lung Carcinomas; with Reference to the p53 and bcl-2 Overexpressions

机译:非小细胞肺癌中Fas和FasL表达的组织芯片分析参考p53和bcl-2过表达

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摘要

Lack of surface Fas expression is a main route for apoptotic resistance which is considered an important mechanism of tumorigenesis and tumor progression. Fas and FasL expressions in 110 non-small cell lung carcinomas (NSCLCs) were investigated to evaluate their roles in pulmonary carcinogenesis and to examine the clinicopathologic significance of Fas expression with its relationship with p53 and bcl-2 overexpressions. Immunohistochemical analysis using tissue microarray demonstrated that a large proportion of NSCLC patients (60%) showed lack of membranous Fas expression. The Fas-negative cases revealed the significantly lower survival rate than Fas-positive ones. Also, the loss of Fas receptor expression was found more frequently in advanced stage and higher nodal status. FasL protein was increased in most NSCLCs (89%) compared to normal lungs. p53 and bcl-2 overexpressions showed no association with Fas expression. Conclusively, reduced membranous Fas expression as a mechanism of apoptotic resistance is considered to play an important part of the pulmonary carcinogenesis, which may predict poor survival and have a bad prognostic influence. Increased FasL expression is thought to be a basis for the immune evasion in NSCLCs. The rare bcl-2 overexpression suggests that this anti-apoptotic protein is unlikely to play a role in the apoptotic resistance of NSCLCs.
机译:表面Fas表达的缺乏是凋亡抗性的主要途径,其被认为是肿瘤发生和肿瘤进展的重要机制。研究了110例非小细胞肺癌(NSCLC)中Fas和FasL的表达,以评估其在肺癌发生中的作用,并研究Fas的表达及其与p53和bcl-2过表达的关系,在临床病理上具有重要意义。使用组织芯片进行的免疫组织化学分析表明,大部分NSCLC患者(60%)显示缺乏膜Fas表达。 Fas阴性病例的生存率明显低于Fas阳性病例。另外,在晚期和更高的淋巴结状态中更频繁地发现Fas受体表达的丧失。与正常肺部相比,大多数NSCLC中的FasL蛋白增加(89%)。 p53和bcl-2的过表达与Fas表达无关。结论是,降低的膜Fas表达作为凋亡抗性的机制被认为在肺致癌作用中起着重要的作用,这可能预示着不良的生存率和不良的预后影响。 FasL表达的增加被认为是NSCLCs逃避免疫的基础。罕见的bcl-2过表达表明,这种抗凋亡蛋白不太可能在NSCLC的凋亡抗性中发挥作用。

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