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首页> 外文期刊>Virology >Subcellular localization of the human papillomavirus 16 E7 oncoprotein in CaSki cells and its detection in cervical adenocarcinoma and adenocarcinoma in situ.
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Subcellular localization of the human papillomavirus 16 E7 oncoprotein in CaSki cells and its detection in cervical adenocarcinoma and adenocarcinoma in situ.

机译:人乳头瘤病毒16 E7癌蛋白在CaSki细胞中的亚细胞定位及其在宫颈腺癌和腺癌中的原位检测。

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摘要

E7 is the major oncoprotein of high-risk human papillomaviruses (HPV) which causes cervical cancer. To date E7 oncoproteins have not been investigated in cervical adenocarcinoma. In this study we generated a rabbit monoclonal anti-HPV-16 E7 antibody, RabMab42-3, which recognizes a conformational epitope in the E7 carboxy-terminal zinc-finger resulting in a strong increase in the sensitivity for the detection of cell-associated HPV-16 E7 protein relative to conventional polyclonal anti-HPV-16 E7 antibodies. Using RabMab42-3, we show that the subcellular localization of endogenous HPV-16 E7 oncoprotein varies during the cell cycle in cervical cancer cells. Moreover, we demonstrate for the first time that the HPV-16 E7 oncoprotein is abundantly expressed in cervical adenocarcinoma in situ and adenocarcinoma, suggesting an important role of HPV-16 E7 for the development of these tumors. Our findings suggest that the HPV-16 E7 oncoprotein could be a useful marker for the detection of cervical adenocarcinoma and their precursors.
机译:E7是导致宫颈癌的高危人类乳头瘤病毒(HPV)的主要癌蛋白。迄今为止,尚未在宫颈腺癌中研究E7癌蛋白。在这项研究中,我们生成了兔抗HPV-16 E7单克隆抗体RabMab42-3,该抗体识别E7羧基末端锌指中的构象表位,导致检测与细胞相关的HPV的敏感性大大提高。相对于常规多克隆抗HPV-16 E7抗体的-16 E7蛋白。使用RabMab42-3,我们显示内源性HPV-16 E7癌蛋白的亚细胞定位在子宫颈癌细胞的细胞周期中变化。此外,我们首次证明HPV-16 E7癌蛋白在宫颈腺癌和腺癌中大量表达,提示HPV-16 E7在这些肿瘤的发展中具有重要作用。我们的发现表明,HPV-16 E7癌蛋白可能是检测宫颈腺癌及其前体的有用标志物。

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