Discovery of a small-molecule inhibitor of KSHV lytic replication from the MMV pandemic response box

被引:3
|
作者
Okpara, Michael O. [1 ]
Weaver, Frederick [2 ]
Whitehouse, Adrian [1 ,2 ,3 ,4 ]
Veale, Clinton G. L. [5 ]
Edkins, Adrienne L. [1 ,6 ]
机构
[1] Rhodes Univ, Dept Biochem & Microbiol, Biomed Biotechnol Res Unit BioBRU, Grahamstown, South Africa
[2] Univ Leeds, Fac Biol Sci, Sch Mol & Cellular Biol, Leeds LS2 9JT, England
[3] Univ Leeds, Astbury Ctr Struct Mol Biol, Leeds LS2 9JT, England
[4] Univ Leeds, LeedsOmics, Leeds LS2 9JT, England
[5] Univ Cape Town, Dept Chem, Cape Town, South Africa
[6] Rhodes Univ, Ctr Chem & Biomed Res CCBR, Grahamstown, South Africa
基金
英国医学研究理事会; 新加坡国家研究基金会;
关键词
Kaposi's sarcoma-associated herpesvirus; KSHV; ORF57; Lytic replication; MMV; Pandemic response box; Aminopyrimidone; SARCOMA-ASSOCIATED HERPESVIRUS; MULTICENTRIC CASTLEMAN-DISEASE; CARCINOMA IN-SITU; KAPOSIS-SARCOMA; ORAL BROPIRIMINE; ANTIVIRAL DRUGS; INTERFERON; PROTEIN; VIRUS; REACTIVATION;
D O I
10.1016/j.antiviral.2024.105990
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Kaposi's sarcoma-associated herpesvirus (KSHV) is the causative agent for primary effusion lymphoma (PEL), multicentric Castleman's disease (MCD) and Kaposi's sarcoma (KS). KSHV is one of the oncoviruses that contribute to 1.5 million new infection-related cancer cases annually. Currently, there are no targeted therapies for KSHV-associated diseases. Through the development of a medium-throughput phenotype-based ELISA screening platform based on KSHV ORF57 protein detection, we screened the Medicines for Malaria Venture (MMV) Pandemic Response Box for non-cytotoxic inhibitors of KSHV lytic replication. MMV1645152 was identified as a promising inhibitor of KSHV lytic replication, suppressing KSHV immediate-early and late lytic gene expression and blocking the production of infectious KSHV virion particles at non-cytotoxic concentrations in cell line models of KSHV infection with or without EBV coinfection. MMV1645152 is a promising hit compound for the development of future therapeutic agents against KSHV-associated malignancies.
引用
收藏
页数:15
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