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妊娠滋养细胞疾病中EMT相关蛋白CK19和N-cad表达的研究
引用本文:徐洁,薛艳,曾宪玲,安瑞芳. 妊娠滋养细胞疾病中EMT相关蛋白CK19和N-cad表达的研究[J]. 现代妇产科进展, 2014, 0(7): 517-519
作者姓名:徐洁  薛艳  曾宪玲  安瑞芳
作者单位:西安交通大学医学院第一附属医院,西安710061
基金项目:国家自然科学基金(No.81172489)
摘    要:目的:探讨上皮细胞向间质转化(EMT)相关蛋白细胞角蛋白19(CK19)和神经钙黏蛋白(N-cad)在妊娠滋养细胞疾病发生、发展中的作用。方法:采用免疫组化SP法检测了41例正常早孕绒毛(NP)、31例葡萄胎(HM)、32例妊娠滋养细胞肿瘤(GTN)[26例侵蚀性葡萄胎(IM)+6例绒癌(CCA)]中CK19和N-cad的定位及表达情况。结果:NP组中CK19和N-cad蛋白相对表达均显著高于HM、GTN组(P0.05),HM组显著高于GTN组(P0.05)。CK19与N-cad的表达无相关性(r=0.202,P=0.268)。结论:伴随着滋养细胞恶性程度的升高,CK19和N-cad表达逐渐降低,提示EMT可能与滋养细胞的恶性转化有关。

关 键 词:妊娠滋养细胞疾病  上皮细胞向间质转化  细胞角蛋白19  神经钙黏蛋白  免疫组织化学

The expression of epithelial to mesenchymal transition associated protein of CK19 and N-cad in gestational trophoblastic disease
Affiliation:Xu Jie, Xue Yan, Zeng Xianling, et al( The First Affiliated Hospital of Xi'an Jiaotong University Medical College,Xi'an 710061)
Abstract:Objective:To explore the role of epithelial to mesenchymal transition (EMT) associated protein of Cytokeratin 19 (CK19) and N-cadherin (N-cad) in oncogenesis, development of gestational trophoblastic disease ( GTD) . Methods:CK19 and N-cad were de-tected Immunohistochemically in paraffin-embedded tissue of 41 cases of normal placenta ( NP) ,31 cases of hydatidiform mole ( HM ) , 32 cases of gestational trophoblastic neoplasia ( GTN ) [ 26 cases of invasive hydatidiform mole ( IM ) and 6 cases of choriocarcinoma (CCA)]. Results:In NP,HM and GTN,the median mean density of CK19 was (7. 62±5. 54) ×10-2,(4. 76±3. 33)×10-2,(3. 20±3. 84)×10-2,respectively,the median mean density of N-cad was (10.6±8.39)×10-2,(4.15±4.19)×10-2,(2.28±3.05)×10-2,respectively. There were significant differences between NP and HM,GTN (P〈0. 05),and between HM and GTN ( P〈0 . 05 ) . There was no correlation between CK19 and N-cad ( r=0 . 202 , P=0 . 268 ) . Con-clusions:The expressions of CK19 and N-cad decrease with the increase of tropohblast malig-nancy which indicate that CK19 and N-cad may involve in the events of malignant transforma-tion of trophocytes,and EMT may play an important role in the malignant progression of GTD.
Keywords:Gestational trophoblastic disease  Epithelial to mesenchymal transition  N-cadherin  Immunohistochemistry
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