Regulation of the Tumor Microenvironment by KSHV

KSHV 对肿瘤微环境的调节

• 批准号: 8588216
• 负责人: Christopher H Parsons
• 金额: $ 17.39万
• 依托单位: LSU HEALTH SCIENCES CENTER
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-02-01 至 2014-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8588216
• 关键词: Regulation; Tumor; Microenvironment; KSHV

DESCRIPTION (provided by applicant): Kaposi's sarcoma (KS) remains the most common tumor arising in patients with HIV/AIDS, and involvement of the oral cavity represents one of the most common clinical manifestations of this tumor. Kaposi's sarcoma-associated herpesvirus (KSHV) replication and ongoing infection of target cells plays an important role in KS pathogenesis. An amino acid membrane transport protein subunit, xCT, maintains intracellular glutathione stores to enhance the survival of cells producing reactive nitrogen species (RNS), and xCT was recently identified as a fusion-entry receptor for KSHV (Kaleeba and Berger, Science, 2006). A number of intracellular and extracellular triggers regulate xCT expression, including binding of the xCT promoter by transcription regulators and the activation of positive transcription regulators by RNS. We have determined recently that xCT is expressed by multiple cell types within KS lesions and circulating mononuclear cells from HIV-infected patients, with cells from KSHV/HIV co-infected patients exhibiting the highest xCT expression. However, it is unknown whether KSHV itself regulates xCT expression to promote KSHV infection and persistence in the local environment. KSHV infects macrophages within KS lesions, and macrophages are a principal source of RNS. Using a novel macrophage cell culture system, our preliminary data suggest that KSHV microRNA suppress BACH-1, a negative transcription regulator of xCT expression, and that KSHV induces RNS secretion by macrophages. Based on these preliminary data, we hypothesize that KSHV promotes its own persistence in the local environment by upregulating xCT expression through both paracrine and autocrine mechanisms, and that targeting xCT regulatory pathways reduces KSHV infection and persistence in the microenvironment. To address this hypothesis, we propose two independent aims: 1) to determine mechanisms and functional outcomes for xCT regulation by KSHV; and 2) to determine clinical relationships between KSHV infection, xCT expression and RNS production in HIV-infected patients at greatest risk for KS. Through these efforts, we hope to provide the framework for developing novel therapeutic strategies for KS through the targeting of xCT and the reduction of KSHV infection and persistence within the tumor microenvironment. PUBLIC HEALTH RELEVANCE: Tumors etiologically linked to the Kaposi's sarcoma-associated herpesvirus (KSHV/HHV8), including Kaposi's sarcoma (KS), are among the most common tumors encountered in the setting of HIV infection and other forms of immune suppression. KS remains an important cause of morbidity and mortality for these patients in the modern era, and the efficacy and toxicity of available therapies for KS are limiting. Therefore, understanding mechanisms for how KSHV regulates expression of its own receptors and the longevity of KSHV-infected cells could provide a scientific basis for developing novel preventive and therapeutic targets for KS.

描述（由申请人提供）：卡波西肉瘤（KS）仍然是HIV/AIDS患者中最常见的肿瘤，口腔受累是该肿瘤最常见的临床表现之一。卡波西肉瘤相关疱疹病毒（KSHV）的复制和持续感染的靶细胞在KS发病机制中起着重要作用。氨基酸膜转运蛋白亚基xCT维持细胞内谷胱甘肽储存以增强产生活性氮物质（RNS）的细胞的存活，并且xCT最近被鉴定为KSHV的融合进入受体（Kaleeba和Berger，Science，2006）。许多细胞内和细胞外触发因子调节xCT表达，包括转录调节因子与xCT启动子的结合以及RNS对正转录调节因子的激活。我们最近已经确定，xCT由KS病变内的多种细胞类型和来自HIV感染患者的循环单核细胞表达，来自KSHV/HIV共感染患者的细胞表现出最高的xCT表达。然而，尚不清楚KSHV本身是否调节xCT表达以促进KSHV感染并在局部环境中持续存在。KSHV感染KS病变内的巨噬细胞，巨噬细胞是RNS的主要来源。使用一种新的巨噬细胞培养系统，我们的初步数据表明，KSHV microRNA抑制BACH-1，一种xCT表达的负转录调节因子，KSHV诱导巨噬细胞分泌RNS。基于这些初步数据，我们假设KSHV通过旁分泌和自分泌机制上调xCT表达来促进其自身在局部环境中的持久性，并且靶向xCT调节途径减少了KSHV感染和在微环境中的持久性。为了解决这一假设，我们提出了两个独立的目标：1）确定KSHV调节xCT的机制和功能结局; 2）确定KS风险最高的HIV感染患者中KSHV感染、xCT表达和RNS产生之间的临床关系。通过这些努力，我们希望通过靶向xCT和减少KSHV感染和在肿瘤微环境中的持久性，为开发KS的新治疗策略提供框架。 公共卫生关系：与卡波西肉瘤相关疱疹病毒（KSHV/HHV 8）病因相关的肿瘤，包括卡波西肉瘤（KS），是HIV感染和其他形式免疫抑制中最常见的肿瘤之一。KS仍然是现代这些患者发病率和死亡率的重要原因，并且KS的可用疗法的疗效和毒性是有限的。因此，了解KSHV如何调节其自身受体的表达和KSHV感染细胞的寿命的机制可以为开发KS的新的预防和治疗靶点提供科学依据。