Yasunaga Jun-Ichirou
Department of Hematology, Rheumatology and Infectious Diseases, Kumamoto University Faculty of life Sciences.
Rinsho Ketsueki. 2025;66(8):773-780. doi: 10.11406/rinketsu.66.773.
Adult T-cell leukemia-lymphoma (ATL) is a malignancy of peripheral CD4+ T cells induced by human T-cell leukemia virus type 1 (HTLV-1). HTLV-1 encodes two oncogenic viral factors, Tax and HTLV-1 bZIP factor (HBZ) in the sense and antisense strands of the provirus respectively. Both Tax and HBZ dysregulate the expression and activities of a large number of host genes and cellular signaling pathways via their multimodal functions. Tax is a potent transactivator of viral replication and various cancer-related genes in HTLV-1-infected cells; however, Tax expression is generally suppressed in ATL cells owing to its high immunogenicity. Previously, we reported that Tax is transiently expressed in a small subpopulation of ATL cells, leading to drastic changes in the host transcriptional profile. In contrast, HBZ is conserved and expressed in all ATL patients. The HBZ gene is thought to be essential in the pathogenesis of HTLV-1. It is unique in that its transcript not only encodes HBZ protein but also acts in a similar way to long non-coding RNAs. Among the functions of HBZ, activation of the TGF-β/Smad pathway is critical for proliferation of ATL cells. These multimodal actions of Tax and HBZ genes are thought to be critical for ATL leukemogenesis.
成人T细胞白血病-淋巴瘤(ATL)是由1型人类T细胞白血病病毒(HTLV-1)诱导的外周CD4+ T细胞恶性肿瘤。HTLV-1在前病毒的正义链和反义链中分别编码两种致癌病毒因子,即Tax和HTLV-1 bZIP因子(HBZ)。Tax和HBZ都通过其多模式功能失调大量宿主基因的表达和活性以及细胞信号通路。Tax是HTLV-1感染细胞中病毒复制和各种癌症相关基因的有效反式激活因子;然而,由于其高免疫原性,Tax表达在ATL细胞中通常受到抑制。此前,我们报道Tax在一小部分ATL细胞中短暂表达,导致宿主转录谱发生剧烈变化。相比之下,HBZ在所有ATL患者中都是保守且表达的。HBZ基因被认为在HTLV-1的发病机制中至关重要。它的独特之处在于其转录本不仅编码HBZ蛋白,还以类似于长链非编码RNA的方式发挥作用。在HBZ的功能中,TGF-β/Smad信号通路的激活对ATL细胞的增殖至关重要。Tax和HBZ基因的这些多模式作用被认为对ATL白血病发生至关重要。