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

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.

Authors

Institutions

Publication Details

Journal
Antiviral Research
Published
2024-08-16
DOI
https://doi.org/10.1016/j.antiviral.2024.105990
Citations
10
Primary Topic
Viral-associated cancers and disorders
Type
article
Field-Weighted Citation Impact
2.83

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

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

Michael Okpara, Adrienne L. Edkins, Adrian Whitehouse, Clinton G. L. Veale et al.
10 citations
Antiviral Research
Viral-associated cancers and disorders
2.83
article

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

Michael Okpara, Adrienne L. Edkins, Adrian Whitehouse, Clinton G. L. Veale, Frederick Weaver
article en
10 citations

Abstract

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.

Antiviral ResearchVol. 230
University of Leeds (GB), University of Cape Town (ZA), Rhodes University (ZA)
Government of the United Kingdom, Global Challenges Research Fund, Academy of Medical Sciences, National Research Foundation, Rhodes University, Department of Science and Technology, Republic of South Africa, Medicines for Malaria Venture, African Academy of Sciences, Foreign, Commonwealth and Development Office, Medical Research Council, European and Developing Countries Clinical Trials Partnership
Good health and well-being
Openalex Percentile: Top 8%
Viral-associated cancers and disorders
2.83
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.