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干扰素反应取决于含人乳头瘤病毒病变中的病毒转录。

Interferon response depends on viral transcription in human papillomavirus-containing lesions.

作者信息

Arany I, Goel A, Tyring S K

机构信息

Department of Microbiology, University of Texas Medical Branch, Galveston 77555-1019, USA.

出版信息

Anticancer Res. 1995 Nov-Dec;15(6B):2865-9.

PMID:8669880
Abstract

Human papillomaviruses (HPVs) express various proteins which have been proven to interact with some cellular functions playing a role in cell cycle progression and differentiation. Therefore, these viral gene products might be candidates for interfering with IFN-mediated antiproliferative actions. Condyloma biopsies from patients subsequently demonstrated to be responsive or non-responsive to IFN treatment were investigated. mRNA levels of HPV genes and IFN-responsive genes were determined by RT-PCR and correlated with IFN responsiveness. Patients clinically nonresponsive to IFN demonstrated a characteristic HPV transcriptional activity differing from responder patients. Nonresponders expressed mostly early E7 mRNAs; responders demonstrated higher expression of the late L1 gene. This differential transcription of infecting HPV also correlated with the extent of IFN mediated antiproliferative effect. A hypothesis for further study is that HPV E7 may inhibit IFN responsiveness, while HPV L1 may promote IFN responsiveness.

摘要

人乳头瘤病毒(HPV)表达多种蛋白质,这些蛋白质已被证明可与一些在细胞周期进程和分化中起作用的细胞功能相互作用。因此,这些病毒基因产物可能是干扰干扰素介导的抗增殖作用的候选物质。对随后证明对干扰素治疗有反应或无反应的患者的尖锐湿疣活检样本进行了研究。通过逆转录聚合酶链反应(RT-PCR)测定HPV基因和干扰素反应基因的mRNA水平,并将其与干扰素反应性相关联。临床上对干扰素无反应的患者表现出与有反应患者不同的特征性HPV转录活性。无反应者主要表达早期E7 mRNA;有反应者则表现出晚期L1基因的更高表达。感染HPV的这种差异转录也与干扰素介导的抗增殖作用程度相关。进一步研究的一个假设是,HPV E7可能抑制干扰素反应性,而HPV L1可能促进干扰素反应性。

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