Section of Virology, Imperial College London, Norfolk Place, London W2 1PG, United Kingdom; National Centre for Human Retrovirology, Imperial College Healthcare NHS Trust, London, United Kingdom; Department of Haematology, Imperial College Healthcare NHS Trust, United Kingdom.
Section of Virology, Imperial College London, Norfolk Place, London W2 1PG, United Kingdom.
Curr Opin Virol. 2017 Oct;26:125-131. doi: 10.1016/j.coviro.2017.07.013. Epub 2017 Aug 18.
Human T-lymphotropic virus type-1 (HTLV-1) is the causative agent of adult T-cell leukaemia/lymphoma (ATL), an aggressive CD4+ T-cell malignancy. The mechanisms of leukaemogenesis in ATL are incompletely understood. Insertional mutagenesis has not previously been thought to contribute to the pathogenesis of ATL. However, the recent discovery that HTLV-1 binds the key chromatin architectural protein CTCF raises the hypothesis that HTLV-1 deregulates host gene expression by causing abnormal chromatin looping, bringing the strong HTLV-1 promoter-enhancer near to host genes that lie up to 2Mb from the integrated provirus. Here we review current opinion on the mechanisms of oncogenesis in ATL, with particular emphasis on the local and distant impact of HTLV-1 on the structure and expression of the host genome.
人类 T 淋巴细胞白血病病毒 1 型(HTLV-1)是成人 T 细胞白血病/淋巴瘤(ATL)的病原体,这是一种侵袭性的 CD4+T 细胞恶性肿瘤。ATL 中的白血病发生机制尚未完全了解。插入突变在过去并未被认为会导致 ATL 的发病机制。然而,最近发现 HTLV-1 结合关键染色质结构蛋白 CTCF,提出了这样的假设:HTLV-1 通过导致异常染色质环化来调节宿主基因表达,从而将强 HTLV-1 启动子增强子带到距离整合前病毒长达 2Mb 的宿主基因附近。在这里,我们回顾了 ATL 中致癌机制的现有观点,特别强调了 HTLV-1 对宿主基因组结构和表达的局部和远距离影响。