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作 者:罗华荣[1,2] 甘梅富 徐铖 徐伟铭 梁勇 LUO Huarong;GAN Meifu;XU Cheng;XU Weiming;LIANG Yong(The First Clinical Medical College,Wenzhou Medical University,Whenzhou,325035;Department of Pathology,Enze Hospital,Taizhou Enze Medical Center(Group),Taizhou,318050;Medical College of Taizhou University,Taizhou,318000)
机构地区:[1]温州医科大学第一临床医学院,浙江温州325035 [2]台州恩泽医疗中心(集团)恩泽医院病理科,浙江台州318050 [3]台州学院医学院,浙江台州318000
出 处:《温州医科大学学报》2018年第10期718-722,共5页Journal of Wenzhou Medical University
基 金:浙江省自然科学基金资助项目(LY14H160036);台州市科技计划项目(1701KY56)
摘 要:目的:探讨甲状腺乳头状癌(PTC)中PD-L1蛋白表达与BRAF V600E基因突变的相关性。方法:应用免疫组织化学Envision两步法检测74例PTC及癌旁正常甲状腺组织的PD-L1蛋白表达,Q-PCR法检测PTC组织中BRAF V600E基因突变情况,分析PD-L1蛋白表达与PTC各临床病理特征及BRAF V600E基因突变的相关性。结果:PD-L1阳性表达于48.6%(36/74)的PTC组织中,高于癌旁对照组(P<0.01)。PD-L1蛋白在PTC中的表达与年龄、肿瘤大小、淋巴细胞性甲状腺炎(CLT)背景、肿瘤浸润淋巴细胞(TILs)以及临床分期有关(P<0.05)。BRAF V600E基因突变的阳性率为79.7%(59/74)。BRAF V600E基因突变与PTC的组织学分型有关(P<0.01)。PD-L1蛋白表达与BRAF V600E基因突变之间无明显相关性(Kappa=-0.091,P>0.05)。多因素logistic回归分析显示CLT背景是影响PD-L1蛋白表达的独立因素(OR=18.675,95%CI:3.074~113.453,P<0.01)。结论:PD-L1蛋白在PTC组织中有过量表达,其阳性表达与PTC的临床病理特征有关,而与BRAF V600E基因突变无关。Objective: To investigate the correlation between PD-L1 protein expression and BRAF V600E gene mutation in papillary thyroid carcinoma (PTC). Methods: 74 cases of PTC and normal thyroid tissue speci-mens were used to detect PD-L1 protein expression by immunohistochemical EnVision two step method. Gene mutation of BRAF V600E was detected by Q-PCR. And the correlation between PD-L1 protein expression and the clinicopathological parameters of PTC including BRAF V600E gene mutation was evaluated. Results: The positive rate of PD-L1 protein expression was 48.6% (36/74) in PTC tissues, signifcantly higher than that in con-trol group (P〈0.01). The expression of PD-L1 protein was correlated with age, tumor size, chronic lymphocytic thyroiditis (CLT) background, tumor-infltrating lymphocytes (TILs) and clinical stage (P〈0.05). The positive rate of BRAF V600E gene mutation was 79.7% (59/74) in PTC tissues. The gene mutation of BRAF V600E was correlated with histological classifcation of PTC (P〈0.01). Consistency analysis showed that there was no rela-tionship between PD-L1 protein expression and BRAF V600E gene mutation (Kappa=-0.091, P〉0.05). Among these parameters, background CLT was independent factor affecting PD-L1 protein expression (OR=18.675, 95%CI: 3.074-113.453, P〈0.01). Conclusion: PD-L1 protein is over-expressed in PTC tissues. The expression of PD-L1 protein is correlated with clinicopathologic features of PTC, but there is no relationship between PD-L1 protein expression and BRAF V600E gene mutation in PTC.
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