首页|甲状腺乳头状癌组织中miR-338-3p、PLCD3表达及其与病理参数、上皮—间质转化、预后的关系

甲状腺乳头状癌组织中miR-338-3p、PLCD3表达及其与病理参数、上皮—间质转化、预后的关系

Expression of miR-338-3p and PLCD3 in papillary thyroid carcinoma tissues and association with pathological pa-rameters,epithelial-mesenchymal transition and prognosis

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目的 探讨甲状腺乳头状癌(PTC)组织中微小核糖核酸-338-3p(miR-338-3p)、磷脂酶C8-3(PLCD3)表达及与病理参数、上皮—间质转化(EMT)、预后的关系.方法 选取2016年1月-2020年12月商洛市中心医院乳甲外科收治接受手术切除的PTC患者152例,取其癌组织及对应癌旁组织,采用实时荧光定量聚合酶链式反应检测miR-338-3p、PLCD3 mRNA表达,免疫组织化学法检测EMT相关蛋白[N-钙黏蛋白(N-Cad)、E-钙黏蛋白(E-Cad)、波形蛋白(VIM)];分析miR-338-3p、PLCD3 mRNA表达与PTC病理参数的关系;通过Targetscan数据库预测miR-338-3p与PLCD3的结合位点,采用Pearson法和二列相关性分析miR-338-3p与PLCD3 mRNA及二者与EMT相关蛋白在PTC组织中表达的相关性;根据PTC组织miR-338-3p、PLCD3 mRNA表达均值分为高/低miR-338-3p、PLCD3 mRNA表达组,通过Kaplan-Meier法绘制高/低miR-338-3p、PLCD3 mRNA表达PTC患者无病生存率(DFS)生存曲线;通过Cox回归分析PTC患者DFS的影响因素.结果 与癌旁组织比较,PTC组织miR-338-3p和E-Cad蛋白阳性表达率降低,PLCD3 mRNA 和 N-Cad、VIM 蛋白阳性表达率升高(t/x2/P=32.875/<0.001、15.575/<0.001、37.351/<0.001、21.984/<0.001、16.604/<0.001);miR-338-3p 与 PLCD3 mRNA 在 PTC 组织中表达呈负相关(r/P=-0.712/<0.001).PTC组织中miR-338-3p与N-Cad、VIM蛋白阳性表达呈负相关,与E-Cad蛋白阳性表达呈正相关(r/P=-0.642/<0.001、-0.617/<0.001、0.622/<0.001);PTC 组织中 PLCD3 mRNA 与 N-Cad、VIM 蛋白阳性表达呈正相关,与 E-Cad 蛋白阳性表达呈负相关(r/P=0.657/<0.001、0.624/<0.001、-0.632/<0.001).不同 TNM 分期、淋巴结转移的PTC组织miR-338-3p、PLCD3 mRNA表达差异有统计学意义(F/t/P=30.778/<0.001、3.430/0.001).miR-338-3p高表达组3年DFS高于低表达组,PLCD3 mRNA高表达组3年DFS低于低表达组(x2/P=15.615/<0.001、16.088/<0.001).TNM 分期Ⅲ期、淋巴结转移、PLCD3 mRNA≥ 1.83 为 PTC 患者 DFS 的独立危险因素[HR(95%CI)=3.127(1.361~7.604)、2.546(1.115~5.817)、2.854(1.178~6.919)],miR-338-3p≥0.57 为独立保护因素[HR(95%CI)=0.306(0.116~0.804)].结论 PTC 组织中 miR-338-3p 低表达和 PLCD3 mRNA 高表达,与TNM分期、淋巴结转移、EMT和预后有关,可能成为PTC诊治新靶点.
Objective To investigate the expression of micro ribonucleic acid-338-3p(miR-338-3p)and phospho-lipase C delta-3(PLCD3)in papillary thyroid carcinoma(PTC)tissues and their relationship with pathological parameters,epi-thelial-mesenchymal transition(EMT)and prognosis.Methods 152 cases of PTC patients admitted to the Breast and Thy-roid Surgery Department of Shangluo Central Hospital who underwent surgical resection from January 2016 to December 2020 were selected,and real-time fluorescence quantitative polymerase chain reaction was used to detect the expression of miR-338-3p and PLCD3 mRNA in cancer tissues and corresponding para-cancerous tissues,and immunohistochemistry was used to detect the expression of EMT-associated proteins[N-calmodulin(N-Cad),E-calmodulin(E-Cad),and vimentin(VIM)].The relationship between miR-338-3p,PLCD3 mRNA expression and pathological parameters of PTC were analyzed.The binding sites of miR-338-3p and PLCD3 were predicted by Targetscan database,and the correlation between mriR-338-3p and PLCD3 mRNA and the expression of both with EMT-related proteins in PTC tissues was analyzed by Pearson's method and dichotomous correlation.PTC tissues were divided into high/low miR-338-3p,PLCD3 mRNA expression groups accord-ing to the mean values of miR-338-3p,PLCD3 mRNA expression,and the survival curves of disease-free survival(DFS)of PTC patients with high/low miR-338-3p,PLCD3 mRNA expression were plotted by Kaplan-Meier method.Factors of DFS in PTC patients were analyzed by Cox regression.Results Compared with para-cancerous tissues,miR-338-3p expression and E-Cad protein positive expression rate were decreased in PTC tissues,and PLCD3 mRNA expression and N-Cad and VIM protein positive expression rate were increased(t/x2/P=32.875/<0.001,15.575/<0.001,37351/<0.001,21.984/<0.001,16.604/<0.001).miR-338-3p was negatively correlated with PLCD3 mRNA expression in PTC tissues(r/P=-0.712/<0.001).miR-338-3p was negatively correlated with the positive expression rate of N-Cad and VIM proteins,and positively correlated with that of E-Cad proteins in PTC tissues(r/P=-0.642/<0.001,-0.617/<0.001,0.622/<0.001);PLCD3 mRNA was negatively correlated with N-Cad in PTC tissues,VIM protein positive expression rate was positively correlated with E-Cad protein pos-itive expression rate(r/P=0.657/<0.001,0.624/<0.001,-0.632/<0.001).Comparison of miR-338-3p and PLCD3 mRNA ex-pression in PTC tissues with different TNM stages and lymph node metastasis showed differences(F/t/P=30.778/<0.001,3.430/0.001).3-year DFS was higher in the miR-338-3p high-express ion group than that in the miR-338-3p low-expression group,and 3-year DFS was lower in the PLCD3 mRNA high-expression group than that in the PLCD3 mRNA low-expression group(x2/P=15.615/<0.001,16.088/<0.001).TNM stage Ⅲ,lymph node metastasis,and PLCD3 mRNA ≥ 1.83 were inde-pendent risk factors for DFS in PTC patients,and miR-338-3p ≥0.57 was an independent protective factor[HR(95%CI)=3.127(1361-7.604),2-46(1.115-5.817),2.854(1.178-6.919),0.306(0.116-0.804)].Conclusion Low expression of miR-338-3p and high expression of PLCD3 mRNA in PTC tissues are associated with TNM staging,lymph node metastasis,EMT and prognosis,and may become a new target for PTC diagnosis and treatment.

Papillary thyroid carcinomaMicro ribonucleic acid-338-3pPhospholipase C delta 3Pathological pa-rametersEpithelial-mesenchymal transitionPrognosis

柯贤锋、李强、向辉、崔仪、雷珍珍

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726000 陕西省商洛市中心医院乳甲外科

甲状腺乳头状癌 微小核糖核酸-338-3p 磷脂酶Cδ-3 病理参数 上皮—间质转化 预后

陕西省卫生健康委卫生健康科研项目

2018C006

2024

疑难病杂志
中国医师协会

疑难病杂志

CSTPCD
影响因子:1.171
ISSN:1671-6450
年,卷(期):2024.23(6)