靶向FoxO蛋白诱导KSHV的裂解性再激活用于治疗疱疹病毒原发性渗出性淋巴瘤。

IF 6.7 1区 医学 Q1 Immunology and Microbiology PLoS Pathogens Pub Date : 2023-08-18 eCollection Date: 2023-08-01 DOI:10.1371/journal.ppat.1011581
Jungang Lan, Yeqing Wang, Shusheng Yue, Duo Xu, Yinan Li, Xiangyu Peng, Jiao Hu, Enguo Ju, Shanping He, Tingting Li
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引用次数: 0

摘要

卡波西肉瘤相关疱疹病毒(KSHV)是一种由潜伏和裂解生命周期组成的致癌病毒。原发性渗出性淋巴瘤(PEL)是一种侵袭性B细胞谱系淋巴瘤,主要由KSHV潜伏感染。KSHV的潜伏感染是持续的,并对杀死肿瘤细胞构成障碍。与旨在消除潜在HIV库的“休克并杀死”策略一样,在潜在感染病毒的肿瘤中诱导病毒裂解再激活的方法代表了一种独特的抗肿瘤策略,因为它可能会增加癌症细胞毒性的特异性。受这一概念的启发,我们提出从潜伏期诱导KSHV裂解性再激活可能是KSHV相关癌症的潜在治疗策略。氧化应激是PEL的临床标志,是KSHV再激活最显著的诱导剂之一。矛盾的是,我们发现过氧化氢(H2O2)以剂量依赖的方式对KSHV阴性而非KSHV阳性的B淋巴瘤细胞触发强大的细胞毒性作用。从机制上讲,我们确定叉头盒蛋白O1(FoxO1)和FoxO3是不可撤销的抗氧化防御基因,它们都被KSHV潜伏感染上调,这对促进KSHV阳性B淋巴瘤细胞中ROS清除至关重要。FoxO1或FoxO3的药理学抑制或功能性敲除足以消除抗氧化能力,从而增加细胞内ROS水平,从而进一步逆转KSHV在PEL细胞中从潜伏到活性裂解复制,导致体外和体内的巨大细胞死亡。此外,通过抑制FoxO蛋白而升高的ROS水平进一步使PEL细胞对ROS诱导的细胞凋亡敏感。因此,我们的研究表明,通过抑制FoxO蛋白来裂解KSHV是一种很有前途的PEL治疗方法,可以进一步推广到其他病毒相关疾病。
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Targeting FoxO proteins induces lytic reactivation of KSHV for treating herpesviral primary effusion lymphoma.

Kaposi's sarcoma-associated herpesvirus (KSHV) is an oncogenic virus consisting of both latent and lytic life cycles. Primary effusion lymphoma (PEL) is an aggressive B-cell lineage lymphoma, dominantly latently infected by KSHV. The latent infection of KSHV is persistent and poses an obstacle to killing tumor cells. Like the "shock and kill" strategy designed to eliminate latent HIV reservoir, methods that induce viral lytic reactivation in tumor latently infected by viruses represent a unique antineoplastic strategy, as it could potentially increase the specificity of cytotoxicity in cancer. Inspired by this conception, we proposed that the induction of KSHV lytic reactivation from latency could be a potential therapeutic stratagem for KSHV-associated cancers. Oxidative stress, the clinical hallmark of PEL, is one of the most prominent inducers for KSHV reactivation. Paradoxically, we found that hydrogen peroxide (H2O2) triggers robust cytotoxic effects on KSHV-negative rather than KSHV-positive B lymphoma cells in a dose-dependent manner. Mechanistically, we identified forkhead box protein O1 (FoxO1) and FoxO3 as irrevocable antioxidant defense genes and both of them are upregulated by KSHV latent infection, which is essential for the promoted ROS scavenging in KSHV-positive B lymphoma cells. Pharmacological inhibition or functional knockdown of either FoxO1 or FoxO3 is sufficient to ablate the antioxidant ability and therefore increases the intracellular ROS level that further reverses KSHV from latency to active lytic replication in PEL cells, resulting in tremendous cell death both in vitro and in vivo. Additionally, the elevated level of ROS by inhibiting FoxO proteins further sensitizes PEL cells to ROS-induced apoptosis. Our study therefore demonstrated that the lytic reactivation of KSHV by inhibiting FoxO proteins is a promising therapeutic approach for PEL, which could be further extended to other virus-associated diseases.

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来源期刊
PLoS Pathogens
PLoS Pathogens 生物-病毒学
CiteScore
11.40
自引率
3.00%
发文量
598
审稿时长
2 months
期刊介绍: Bacteria, fungi, parasites, prions and viruses cause a plethora of diseases that have important medical, agricultural, and economic consequences. Moreover, the study of microbes continues to provide novel insights into such fundamental processes as the molecular basis of cellular and organismal function.
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