肿瘤与非肿瘤性胆囊病变中Cyclin D1、E-cadherin、EGFR、HER- 2、Ki67、p53肿瘤标志物表达及其临床病理相关性的研究

A. Agarwal, R. Bansal, Mamta Gupta
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摘要

背景:在世界范围内,胆囊癌(GBC)是胆道最常见的恶性肿瘤。它是最具侵袭性的胆道癌,自诊断以来中位生存期较短。癌的侵袭性生物学行为和缺乏早期发现的敏感筛查试验可能是导致GBC预后不良的原因。材料和方法:纳入印度Subharti医学院病理科诊断为肿瘤和非肿瘤胆囊病变的患者。收集胆囊活检结果和临床病理资料,研究不同免疫标记物的诊断和治疗价值。结果:51 ~ 60岁年龄组24例(24.0%)。38例(38.0%)病变部位为眼底,55例(55.0%)合并结石。其中P53强过表达36例(36.0%),ki67强过表达40例(40.0%),EGFR强过表达25例(25.0%),Her2/Neu阴性61例(61.0%)。Cyclin D1:中度过表达27例(27.0%),E-cadherin中度过表达22例(23.2%)。结论:新的预后生物标志物有望为胆囊癌的诊断和治疗带来必要的突破。我们的结论是,我们研究的生物标志物可能有助于识别可能从辅助和靶向治疗中获益的病例。关键词:Cyclin D1, E-cadherin, EGFR, HER- 2, Ki67, p53,肿瘤标志物,肿瘤性,非肿瘤性,胆囊病变
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A Study of Cyclin D1, E-cadherin, EGFR, HER- 2, Ki67, and p53 Tumor Marker Expressions in Neoplastic and Non -neoplastic Gall Bladder Lesions and their Clinico-pathological Correlation
Background: Worldwide gall bladder cancer (GBC) is known to be the commonest malignant tumour of the biliary tract. It is the most aggressive carcinoma of the biliary tract with short median survival from the time of diagnosis. The aggressive biologic behaviour of the carcinoma and non-availability of sensitive screening tests for early detection may be responsible for the poor prognosis associated with GBC. Material and Methods: Patients diagnosed with neoplastic and non-neoplastic gallbladder lesions in the Department of Pathology, Subharti Medical College in India were included in the study. Gall bladder biopsies findings and the clinic-pathological data were compiled and different immune-markers  diagnostic and therapeutic usefulness were studied . Results: 24 (24.0%) of the cases were in the age group of 51-60 Years.  In 38 (38.0%) of the cases the site of lesion was Fundus. 55 (55.0%) of cases had associated stones. 36 (36.0%) of them had P53: strong over expression, 40 (40.0%) of the them had ki67: strong over expression, 25 (25.0%) had EGFR: strong over expression whereas negative expression for  Her2/Neu was found in 61 (61.0%) of the cases. Cyclin D1: moderate over expression was found in 27 (27.0%) of them and moderate over expression of E-cadherin were found in  22 (23.2%) cases. Conclusions: Novel prognostic biomarkers could bring about the needed breakthrough in gall bladder cancer diagnosis and treatment. We conclude that the biomarkers studied by us  may help in the identification of cases who may benefit tremendously from adjuvant and targeted therapies. Key words: Cyclin D1, E-cadherin, EGFR, HER- 2, Ki67,  p53, tumour marker, neoplastic , non –neoplastic, Gall bladder lesions.
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