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甲状腺乳头状癌与非肿瘤性甲状腺组织中Met表达模式的差异。

Difference in patterns of Met expression in papillary thyroid carcinomas and nonneoplastic thyroid tissue.

作者信息

Haugen D R, Lillehaug J R, Varhaug J E

机构信息

Department of Molecular Biology, University of Bergen, Thormøhlens gt 55, N-5020 Bergen, Norway.

出版信息

World J Surg. 2001 May;25(5):623-31. doi: 10.1007/s002680020167.

Abstract

Met protein is a tyrosine kinase receptor for hepatocyte growth factor (HGF). c-Met has morphogenic, mitogenic, and motogenic properties and is overexpressed in many solid tumors. We studied c-met mRNA and protein expression in papillary thyroid carcinomas and nonneoplastic thyroid tissue. The c-met mRNA was detected in all biopsies by reverse transcriptase-polymerase chain reaction and by hybridization of complex cDNA probes to a c-met-specific DNA fragment in a dot blot array. Immunohistochemistry on fresh frozen biopsies showed Met protein localized along the basal cell membrane of normal thyrocytes in 32 of 35 nonneoplastic thyroid tissue specimens, sometimes associated with weak cytoplasmic reactivity but without apical cell membrane staining. In papillary carcinomas an increased Met protein expression was seen, comprising a cytoplasmic (33 of 49) and apical cell membrane (24 of 49) immunoreactivity, whereas only 1 of 49 biopsies showed basal cell membrane staining. A 145-kDa Met-specific band was detected by Western immunoblotting on protein extracts from papillary carcinomas. The tight junction protein zona occludens-1 (ZO-1), studied by immunohistochemistry, was weakly expressed along the apical cell membrane in 10 nonneoplastic biopsies. In contrast, increased and cytoplasmic/apical membranous ZO-1 immunostaining was seen in 11 of 15 papillary carcinomas. Nuclear ZO-1 staining was present in a few papillary carcinomas with partial dedifferentiation. The concomitant overexpression and subcellular redistribution of Met and ZO-1 proteins indicate a change in cell polarity in papillary carcinomas compared to nonneoplastic thyroid tissue. These observations may reflect an important feature of the tumorigenesis of papillary thyroid carcinomas. No significant association was found between semiquantitative immunohistochemical assessment of Met protein and clinical parameters in papillary carcinoma patients.

摘要

Met蛋白是肝细胞生长因子(HGF)的酪氨酸激酶受体。c-Met具有形态发生、促有丝分裂和促运动特性,在许多实体瘤中过表达。我们研究了甲状腺乳头状癌和非肿瘤性甲状腺组织中c-met mRNA和蛋白的表达。通过逆转录聚合酶链反应以及在斑点印迹阵列中用复合cDNA探针与c-met特异性DNA片段杂交,在所有活检样本中均检测到了c-met mRNA。对新鲜冷冻活检样本进行的免疫组织化学检测显示,在35个非肿瘤性甲状腺组织标本中的32个中,Met蛋白定位于正常甲状腺细胞的基底细胞膜,有时伴有弱细胞质反应,但无顶端细胞膜染色。在甲状腺乳头状癌中,可见Met蛋白表达增加,包括细胞质免疫反应性(49个样本中的33个)和顶端细胞膜免疫反应性(49个样本中的24个),而49个活检样本中只有1个显示基底细胞膜染色。通过对甲状腺乳头状癌蛋白提取物进行Western免疫印迹检测到一条145 kDa的Met特异性条带。通过免疫组织化学研究的紧密连接蛋白闭合蛋白-1(ZO-1),在10个非肿瘤性活检样本中沿顶端细胞膜弱表达。相比之下,在15个甲状腺乳头状癌样本中的11个中,可见ZO-1免疫染色增加且呈细胞质/顶端膜性。在一些部分去分化的甲状腺乳头状癌中存在核ZO-1染色。与非肿瘤性甲状腺组织相比,Met和ZO-1蛋白的同时过表达和亚细胞重新分布表明甲状腺乳头状癌中细胞极性发生了变化。这些观察结果可能反映了甲状腺乳头状癌发生的一个重要特征。在甲状腺乳头状癌患者中,Met蛋白的半定量免疫组织化学评估与临床参数之间未发现显著关联。

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