Scott Tristan A, Soemardy Citradewi, Ray Roslyn M, Morris Kevin V
Center for Gene Therapy, City of Hope - Beckman Research Institute and Hematological Malignancy and Stem Cell Transplantation Institute at the City of Hope. 1500 E. Duarte Rd., Duarte, CA 91010, USA.
Menzies Health Institute Queensland, School of Pharmacy and Medical Science, Griffith University, Gold Coast Campus 4222, Australia.
NAR Cancer. 2023 Jan 11;5(1):zcac046. doi: 10.1093/narcan/zcac046. eCollection 2023 Mar.
Human T-lymphotropic virus type I (HTLV-I) infects CD4+ T-cells resulting in a latent, life-long infection in patients. Crosstalk between oncogenic viral factors results in the transformation of the host cell into an aggressive cancer, adult T-cell leukemia/lymphoma (ATL). ATL has a poor prognosis with no currently available effective treatments, urging the development of novel therapeutic strategies. Recent evidence exploring those mechanisms contributing to ATL highlights the viral anti-sense gene HTLV-I bZIP factor (HBZ) as a tumor driver and a potential therapeutic target. In this work, a series of zinc-finger protein (ZFP) repressors were designed to target within the HTLV-I promoter that drives HBZ expression at highly conserved sites covering a wide range of HTLV-I genotypes. ZFPs were identified that potently suppressed HBZ expression and resulted in a significant reduction in the proliferation and viability of a patient-derived ATL cell line with the induction of cell cycle arrest and apoptosis. These data encourage the development of this novel ZFP strategy as a targeted modality to inhibit the molecular driver of ATL, a possible next-generation therapeutic for aggressive HTLV-I associated malignancies.
人类嗜T淋巴细胞病毒I型(HTLV-I)感染CD4+ T细胞,导致患者发生潜伏性终身感染。致癌病毒因子之间的相互作用导致宿主细胞转化为侵袭性癌症,即成人T细胞白血病/淋巴瘤(ATL)。ATL预后较差,目前没有有效的治疗方法,因此迫切需要开发新的治疗策略。最近探索导致ATL的机制的证据表明,病毒反义基因HTLV-I bZIP因子(HBZ)是肿瘤驱动因子和潜在的治疗靶点。在这项研究中,设计了一系列锌指蛋白(ZFP)阻遏物,靶向HTLV-I启动子内驱动HBZ表达的高度保守位点,这些位点涵盖了广泛的HTLV-I基因型。已鉴定出能有效抑制HBZ表达的ZFP,导致患者来源的ATL细胞系的增殖和活力显著降低,并诱导细胞周期停滞和凋亡。这些数据鼓励将这种新型ZFP策略开发为一种靶向方法,以抑制ATL的分子驱动因子,这可能是侵袭性HTLV-I相关恶性肿瘤的下一代治疗方法。