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子宫颈癌不同活检组织中人乳头瘤病毒16型活性的特征分析

Characterization of human papillomavirus type 16 activity in separate biopsies from a carcinoma of the cervix uteri.

作者信息

Kube D, Janda J, Johannsmeyer K D, Bergmann S, Kiessling U

机构信息

Universitätskliniken Köln, Innere Medizin I, Germany.

出版信息

Virchows Arch. 1994;425(5):473-80. doi: 10.1007/BF00197550.

Abstract

Human papillomavirus (HPV) 16-specific nucleic acid sequences were analysed in separate biopsies taken from a patient with a poorly differentiated squamous cell carcinoma of the uterine cervix. Biopsies were obtained from histopathologically normal epithelium adjacent to the carcinomatous epithelium, the primary carcinoma and a metastatic lymph node. Signals characterizing viral DNA and oncogene transcription were obviously differentiation dependent as shown by in situ hybridization of viral nucleic acids and immunofluorescence of epithelial differentiation specific proteins. In histologically normal parts of the epithelium viral DNA was amplified at the transition from basal to maturing cells, whereas E6/E7 genes were actively transcribed mainly in maturing epithelial cells following the basal cell layer. Some of the cells in the primary carcinoma and in the metastatic lymph node expressed involucrin at increased levels. Signals for viral DNA and HPV 16-specific E6/E7 transcripts decreased in intensity during differentiation in an inverse relationship to the observed involucrin increase in those cells. The absence of Ki67 in cells expressing large amounts of involucrin as revealed by immunostaining, support the inverse correlation between differentiation of cancer cells, HPV 16 replication and E6/E7 transcription. The changes in cytokine expression may indicate an HPV 16 associated disruption of normal cytokine expression pattern in the carcinoma.

摘要

对一名患有子宫颈低分化鳞状细胞癌患者的不同活检样本进行了人乳头瘤病毒(HPV)16特异性核酸序列分析。活检样本取自癌上皮相邻的组织病理学正常上皮、原发性癌和一个转移性淋巴结。病毒核酸原位杂交和上皮分化特异性蛋白免疫荧光显示,表征病毒DNA和癌基因转录的信号明显依赖于分化。在组织学正常的上皮部分,病毒DNA在从基底细胞向成熟细胞转变时被扩增,而E6/E7基因主要在基底细胞层之后的成熟上皮细胞中活跃转录。原发性癌和转移性淋巴结中的一些细胞中,内披蛋白表达水平升高。在这些细胞中,病毒DNA和HPV 16特异性E6/E7转录本的信号强度在分化过程中降低,与观察到的内披蛋白增加呈负相关。免疫染色显示,大量表达内披蛋白的细胞中不存在Ki67,这支持了癌细胞分化、HPV 16复制和E6/E7转录之间的负相关。细胞因子表达的变化可能表明癌组织中存在与HPV 16相关的正常细胞因子表达模式破坏。

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