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在良性人乳头瘤病毒(HPV)诱导的病变中,干扰素抗性与拷贝数无关。

Interferon resistance is independent from copy numbers in benign HPV-induced lesions.

作者信息

Arany I, Nagamani K, Tyring S K

机构信息

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

出版信息

Anticancer Res. 1995 May-Jun;15(3):1003-6.

PMID:7645918
Abstract

Interferons (IFNs) are successfully used in treatment of different human papillomavirus (HPV)-related diseases, such as condyloma acuminatum. Unresponsiveness can be seen in a number of patients which is related to a differential expression of early (E7) and late (L1) viral genes, according to our preliminary studies rather than to impaired IFN-signalling. The molecular basis for this differential expression might imply differential viral replication (copy numbers) in responder vs. nonresponder patients. PCR analysis revealed that the two groups did not differ significantly in HPV copy numbers before treatment. In contrast E7 and L1 levels significantly differed in responders versus nonresponders, regardless of copy numbers. Also, the IFN-mediated antiproliferative effect was mostly influenced by other factors rather than just the copy number. Our data imply that the unresponsiveness of certain patients to IFN treatment may relate to differential viral gene transcription rather than different copy numbers of infecting HIVs.

摘要

干扰素(IFNs)已成功用于治疗多种与人类乳头瘤病毒(HPV)相关的疾病,如尖锐湿疣。根据我们的初步研究,许多患者出现无反应性,这与病毒早期(E7)和晚期(L1)基因的差异表达有关,而非与干扰素信号传导受损有关。这种差异表达的分子基础可能意味着在有反应者与无反应者患者中病毒复制(拷贝数)存在差异。PCR分析显示,两组在治疗前HPV拷贝数上无显著差异。相比之下,无论拷贝数如何,有反应者与无反应者的E7和L1水平存在显著差异。此外,干扰素介导的抗增殖作用主要受其他因素影响,而非仅仅受拷贝数影响。我们的数据表明,某些患者对干扰素治疗无反应可能与病毒基因转录差异有关,而非与感染的HPV拷贝数不同有关。

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引用本文的文献

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Binase treatment increases interferon sensitivity and apoptosis in SiHa cervical carcinoma cells by downregulating E6 and E7 human papilloma virus oncoproteins.Binase治疗通过下调人乳头瘤病毒E6和E7癌蛋白来提高SiHa宫颈癌细胞对干扰素的敏感性并诱导其凋亡。
Oncotarget. 2017 Aug 10;8(42):72666-72675. doi: 10.18632/oncotarget.20199. eCollection 2017 Sep 22.