通过核因子-κB和磷脂酰肌醇3激酶信号通路激活的碳酸酐酶IX在人t细胞白血病病毒1型引起的成人t细胞白血病/淋巴瘤多步骤癌变中的重要作用

Sakitani M
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引用次数: 0

摘要

人t细胞白血病病毒1型(HTLV-1)是成人t细胞白血病/淋巴瘤(ATL)的病原体。ATL的癌变过程非常复杂,htlv -1衍生蛋白Tax和HBZ可能在ATL的癌变过程中没有发挥主要作用,这是一个谜。因此,人们提出了几种多步骤肿瘤发生的模型。本文首先简要介绍了ATL的多步骤肿瘤发生模型。然后,总结了宿主细胞中可能独立于Tax和HBZ的其他致癌事件。特别讨论了核因子κB (NFκB)/缺氧诱导因子(HIF)/碳酸酐酶IX (CA9)轴和磷脂酰肌醇3-激酶(PI3K)/HIF/CA9轴在其肿瘤发生的最后阶段的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Essential Role of Carbon Anhydrase IX, Activated Via the Nuclear Factor-κB and Phosphatidylinositol 3-Kinase Signaling Pathways, In Multistep Oncogenesis of Adult T-Cell Leukemia/Lymphoma Caused by Human T-Cell Leukemia Virus Type 1
Human T-cell leukemia virus type 1 (HTLV-1) is a causative agent of adult T-cell leukemia/lymphoma (ATL). Oncogenic processes of ATL are highly complicated, and there is an enigma that the HTLV-1-derived proteins Tax and HBZ may not play major roles in completion of its oncogenesis. Thus several models of multistep oncogenesis have been proposed. In this review, first, the multistep oncogenesis models of ATL were concisely presented. Then, additional oncogenic events in host cells, probably independent of Tax and HBZ, were summarized. In particular, importance of the nuclear factor kappa B (NFκB)/hypoxia inducible factor (HIF)/carbon anhydrase IX (CA9) axis and the phosphatidylinositol 3-kinase (PI3K)/HIF/CA9 axis at the final stage of its oncogenesis was discussed.
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