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通过定量PCR对CaSki细胞中HPV-16 E6/E7转录进行表征。

Characterization of HPV-16 E6/E7 transcription in CaSki cells by quantitative PCR.

作者信息

Hsu E M, McNicol P J

机构信息

Department of Medical Microbiology, University of Manitoba, Canada.

出版信息

Mol Cell Probes. 1992 Dec;6(6):459-66. doi: 10.1016/0890-8508(92)90042-v.

DOI:10.1016/0890-8508(92)90042-v
PMID:1480186
Abstract

Human papillomavirus (HPV) is associated with specific benign and malignant lesions of the epithelial and mucosal surfaces. Of the sexually transmitted types, HPV type 16 (HPV-16) is the most commonly associated with carcinoma of the uterine cervix. Expression of the E6/E7 open reading frame of the viral genome is considered critical in the development of neoplasia. Using the CaSki cervical carcinoma cell line as a model system, we have adapted the polymerase chain reaction to quantify the transcripts expressed from this region. It was found that 97.1% of the total spliced transcript is E6I, which putatively encodes the E7 oncoprotein, while E6II comprises 2.9% of spliced product. The ratio of E6I to E6II expression may be an important parameter in evaluating the disease risk associated with HPV-16 infection.

摘要

人乳头瘤病毒(HPV)与上皮和粘膜表面的特定良性及恶性病变相关。在性传播类型中,HPV 16型(HPV - 16)与子宫颈癌最为相关。病毒基因组E6/E7开放阅读框的表达被认为在肿瘤形成过程中至关重要。以CaSki宫颈癌细胞系作为模型系统,我们采用聚合酶链反应来定量该区域表达的转录本。结果发现,总剪接转录本的97.1%是E6I,其可能编码E7癌蛋白,而E6II占剪接产物的2.9%。E6I与E6II的表达比例可能是评估与HPV - 16感染相关疾病风险的一个重要参数。

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