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在肺癌中,c-erbB-2 的过表达和 p16 的缺失具有分子诊断相关性,但无预后价值。

Overexpression of c-erbB-2 and loss of p16 have molecular diagnostic relevance but no prognostic value in lung cancer.

机构信息

Department of Pathology, Cancer Hospital/Institute, Chinese Academy of Medical Sciences, 100021 Beijing, People's Republic of China.

出版信息

Med Oncol. 2011 Mar;28(1):336-41. doi: 10.1007/s12032-010-9452-0. Epub 2010 Mar 17.

Abstract

This study was designed to evaluate the expression of C-erbB-2 and p16 in lung cancers using tissue microarray technology and to determine their clinical and pathological significance. Immunohistochemical C-erbB-2 and p16 expressions and their associations with clinical and pathological features were analyzed in two tissue microarrays. The membranous and cytoplasmic expression rates of C-erbB-2 were 40.5 and 66.5% in non-small cell lung cancers (NSCLCs), and 0 and 9.5% in small cell lung cancers (SCLCs), respectively. The nuclear and cytoplasmic expression rates of p16 were 11.5 and 32.2% in NSCLs, and 45 and 80% in SCLCs, respectively. The cytoplasmic expression of both C-erbB-2 and p16 was more frequent than the membranous expression of C-erbB-2 and the nuclear expression of p16. The rates of overexpression of C-erbB-2 and loss of p16 expression were significantly higher in NSCLCs than in SCLCs (P < 0.05). Neither C-erbB-2 nor p16 expression was significantly associated with age, tumor grade or stage, presence of lymph node metastasis or survival duration. The abnormal expressions of p16 and C-erbB-2 may play a role in the progression of lung cancers. The variations in the expression patterns of C-erbB-2 and p16 between NSCLCs and SCLCs may aid the molecular classification of lung cancer. The abnormal expression of p16 may be involved in the development of NSCLCs, and the overexpression of C-erbB-2 in NSCLCs indicates that it can be a candidate target for gene therapy.

摘要

本研究旨在运用组织微阵列技术评估肺癌中 C-erbB-2 和 p16 的表达情况,并探讨其与临床病理特征的关系。在两个组织微阵列中,分析了 C-erbB-2 和 p16 的免疫组化表达及其与临床病理特征的关系。非小细胞肺癌(NSCLCs)中 C-erbB-2 的膜和细胞质表达率分别为 40.5%和 66.5%,小细胞肺癌(SCLCs)中分别为 0%和 9.5%。NSCLs 中 p16 的核和细胞质表达率分别为 11.5%和 32.2%,SCLCs 中分别为 45%和 80%。C-erbB-2 的细胞质表达和 p16 的核表达比 C-erbB-2 的膜表达和 p16 的核表达更为常见。C-erbB-2 过表达和 p16 表达缺失在 NSCLCs 中的发生率显著高于 SCLCs(P<0.05)。C-erbB-2 和 p16 的表达均与年龄、肿瘤分级或分期、淋巴结转移与否及生存时间无关。p16 和 C-erbB-2 的异常表达可能与肺癌的进展有关。NSCLCs 和 SCLCs 中 C-erbB-2 和 p16 的表达模式变化可能有助于肺癌的分子分类。p16 的异常表达可能与 NSCLCs 的发生有关,NSCLCs 中 C-erbB-2 的过表达表明其可能成为基因治疗的候选靶点。

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