病毒蛋白质与人类蛋白质相似,可能干扰人类途径。

Systems and Synthetic Biology Pub Date : 2014-12-01 Epub Date: 2014-05-24 DOI:10.1007/s11693-014-9141-y
Zhao Jin, Masaaki Kotera, Susumu Goto
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引用次数: 3

摘要

现在,癌症在世界上任何地方都不罕见,全球癌症负担每年都在大幅增加。先前关于感染和癌症的研究报告称,全球约17.8%的癌症,即190多万例癌症病例,与病毒感染有关。迄今为止,已知的致癌病毒至少有6种,包括乙型肝炎病毒、丙型肝炎病毒、eb病毒(EBV或HHV-4)、人乳头瘤病毒、人T淋巴细胞1型病毒、卡波西肉瘤相关疱疹病毒(KSHV或HHV-8),但其致病机制尚不完全清楚。在本研究中,假设发现与病毒癌蛋白显著相似的人类蛋白会导致目前尚不清楚的癌症相关途径的分类,我们根据它们的相似性分析了不同类型的病毒引起的癌症,以阐明未知的癌症机制。因此,我们获得了几个潜在的肿瘤通路,这些通路可能在癌变过程中具有重要和必要的意义,这将有助于进一步研究癌变机制和开发新的药物靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Virus proteins similar to human proteins as possible disturbance on human pathways.

Virus proteins similar to human proteins as possible disturbance on human pathways.

Virus proteins similar to human proteins as possible disturbance on human pathways.

Virus proteins similar to human proteins as possible disturbance on human pathways.

Cancer is not rare anywhere in the world now, and the global burden of cancer continues to increase largely every year. Previous research on infections and cancers reported that, about 17.8 % of the cancers worldwide, which are over 1.9 million cases of cancer, are related to viral infections. At least six oncoviruses, cancer-causing viruses, have been known so far, which include hepatitis B virus, hepatitis C virus, Epstein-Barr virus (EBV or HHV-4), human papillomavirus, human T lymphotropic virus type 1, Kaposi's sarcoma-associated herpesvirus (KSHV or HHV-8), but the pathogenic mechanism is far from being completely understood. In this study, assuming that finding human proteins significantly similar to viral oncoproteins leads to a categorization of the cancer-related pathways that are currently not clearly known, we analyzed different types of virus-caused cancers based on their similarity in order to clarify the unknown cancer mechanisms. As a result, we obtained several potential tumor pathways that may be significant and essential in oncogenic cancer process, which will be helpful for further study on cancer mechanisms and the development of new drug targets.

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