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首页> 外文期刊>Acta Biochimica Polonica >Prognostic value of broad-spectrum keratin clones AE1/AE3 and CAM5.2 in small cell lung cancer patients undergoing pulmonary resection
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Prognostic value of broad-spectrum keratin clones AE1/AE3 and CAM5.2 in small cell lung cancer patients undergoing pulmonary resection

机译:广谱角蛋白克隆AE1 / AE3和CAM5.2在肺切除术中小细胞肺癌患者中的预后价值

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摘要

Introduction: Small cell lung carcinoma (SCLC) is an aggressive pulmonary neoplasm of neuroendocrine origin. Keratins form a large group of intermediate filaments, which are major structural proteins in epithelial cells and carcinomas. SCLC shows a wide spectrum of keratin expression, from very strong to completely negative. A prognostic role of keratin expression in SCLC is unknown. Material and Methods: Tumor tissue microarray samples from a unique series of 82 SCLC patients who underwent pulmonary resection were stained with keratin specific antibodies AE1/AE3 and CAM5.2. The percentage o1f positively stained cells and their staining pattern (diffusely membranous, partially membranous and dot-like) were evaluated. The median expression value was used for the distinction between keratin-negative and -positive patients. Overall survival in respective groups was compared using the log-rank test. Multivariate Cox proportional hazards regression analysis was performed adjusting for age, gender, tumor site, tumor stage, and tumor histology. Results: edian expression of AE1/AE3 and CAM5.2 was 80% and 90%, respectively. Five cases were completely negative for AE1/AE3 and three for Cam5.2. Median overall survival for patients with stronger and weaker AE1/AE3 staining was 24.7 and 13.8 months, respectively (p=0.019). There was no difference in survival in relation to the CAM5.2 expression (p=0.44). In multivariate analysis adjusted for CAM5.2, T and N stage, gender and age at diagnosis, stronger AE1/AE3 expression was an independent predictor of increased survival (HR 0.50; 95% CI, 0.27-0.94; p=0.031). Conclusion: High expression of AE1/AE3 is a favorable prognostic factor in surgically treated SCLC. The applicability of this finding to a typical patient population treated with non-surgical methods warrants further studies.
机译:介绍:小细胞肺癌(SCLC)是神经内分泌源的腐蚀性肺部肿瘤。角蛋白形成一大群中间细丝,是上皮细胞和癌中的主要结构蛋白。 SCLC显示出广谱的角蛋白表达,从非常强度完全消极。角蛋白表达在SCLC中的预后作用是未知的。材料和方法:肿瘤组织微阵列来自来自肺切除肺切除的独特系列82个SCLC患者的肿瘤组织微阵列样品用角蛋白特异性抗体AE1 / AE3和CAM5.2染色。评价O1F正染色细胞的百分比和它们的染色图案(漫反应,部分膜质和点状)。中值表达值用于角蛋白阴性和阳性患者之间的区别。使用对数级测试进行比较各组的整体生存。对年龄,性别,肿瘤部位,肿瘤阶段和肿瘤组织学进行了多元COX比例危害的回归分析。结果:AE1 / AE3和CAM5.2的EDian表达分别为80%和90%。对于AE1 / AE3和CAM5.2的三种情况完全为阴性。患有更强和较弱的AE1 / AE3染色的患者的中位数分别为24.7%和13.8个月(P = 0.019)。生存与CAM5.2表达没有差异(p = 0.44)。在调整CAM5.2,T和N期的多变量分析中,性别和年龄在诊断时,较强的AE1 / AE3表达是增长存活率的独立预测因子(HR 0.50; 95%CI,0.27-0.94; P = 0.031)。结论:AE1 / AE3的高表达是手术治疗SCLC的良好预后因素。这种发现对用非外科方法治疗的典型患者人群的适用性可证有进一步的研究。

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