Evidence map›Paper›PMID 39891599›Full record

ArticleJournal of medical virology2025

Identification of RP-54745, an IL-1 Inhibitor Displaying Anticancer Activities for KSHV-Related Primary Effusion Lymphoma.

Lu Dai, Amrita Choudhary, Jiaojiao Fan, Lu Huang, Zhen Lin, Zhiqiang Qin

Abstract read
In one paragraph

Article in Journal of medical virology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Lu DaiDepartment of Pathology, Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Amrita ChoudharyLittle Rock Central High School, Little Rock, Arkansas, USA.
Jiaojiao FanDepartment of Pathology, Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Lu HuangDepartment of Microbiology and Immunology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Zhen LinDepartment of Pathology & Laboratory Medicine, Tulane University Health Sciences Center, Tulane Cancer Center, New Orleans, Louisiana, USA.
Zhiqiang QinDepartment of Pathology, Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.ORCID 0000-0002-9905-1275

Funding

Translational Genomics Core (TGC)P20GM121288 · NIGMS · LSU HEALTH SCIENCES CENTER · PI Arunava Roy · 2017 to 2026
$22.4M
Ontogeny and metabolism of lung alveolar macrophages in tuberculosisR01AI184960 · NIAID · UNIV OF ARKANSAS FOR MED SCIS · PI Lu Huang · 2024 to 2026
$2.2M
Vitamin D in viral associated lung cancersR01CA261258 · NCI · TULANE UNIVERSITY OF LOUISIANA · PI LIN, ZHEN · 2021 to 2025
$1.9M
Macrophage metabolism in diabetes and tuberculosis comorbidityR21AI175738 · NIAID · UNIV OF ARKANSAS FOR MED SCIS · PI HUANG, LU · 2023 to 2024
$438k
Development of O’PROTACs-based degraders targeting an oncogenic viral proteinR21AI186566 · NIAID · UNIV OF ARKANSAS FOR MED SCIS · PI Lu Dai · 2025 to 2026
$415k
Targeting ILlRAP in virus-associated malignanciesR03DE031978 · NIDCR · UNIV OF ARKANSAS FOR MED SCIS · PI DAI, LU · 2022 to 2023
$304k
NCI NIH HHS R01 CA261258NIAID NIH HHS R01 AI184960NIAID NIH HHS R21 AI175738NIAID NIH HHS R21 AI186566NIDCR NIH HHS R03 DE031978NIGMS NIH HHS P20 GM121288The study was supported by the National Institutes of Health (R03DE031978, R21AI186566, R21AI175738, and R01AI184960), National Cancer Institute (R01CA261258), National Institute of General Medical Sciences COBRE (P20GM121288), U.S.-Japan Cooperative Medical Sciences Program Collaborative Award from the National Institute of Allergy and Infectious Diseases and CRDF Global (DAA3-19-65602-1).
6 · The paper itself

Abstract

Kaposi's sarcoma-associated herpesvirus (KSHV) is the etiologic agent of several human cancers, including primary effusion lymphoma (PEL), usually seen in immunocompromised patients while lack of effective therapeutic options. Interleukin-1 (IL-1) family is a major mediator for inflammatory responses and has functional role in both innate and adaptive immunity. We previously showed high activation of multiple IL-1 signaling molecules during KSHV latent and lytic stages, as well as in clinical samples from patients with KSHV-related malignancies. In the current study, we identified RP-54745, a potential antirheumatic compound as IL-1 inhibitor, effectively repressed KSHV + PEL cell growth through inducing tumor cell apoptosis. By using an established PEL xenograft model, we found that RP-54745 treatment suppressed tumor expansion in mice. Also, RP-54745 treatment significantly reduced hyperinflammation in tumor microenvironment including myeloid cells and neutrophils infiltration, as well as blocking IL-1 signaling molecules expression in vivo. In addition, our transcriptome analysis revealed novel cellular genes and mechanisms for anticancer activities of RP-54745. Taken together, our data indicate targeting IL-1 production and signaling may represent promising therapeutic strategies against these virus-associated diseases.

Indexed as

Antineoplastic AgentsHerpesvirus 8, HumanInterleukin-1Lymphoma, Primary EffusionAnimalsApoptosisCell Line, TumorCell ProliferationDisease Models, AnimalGene Expression ProfilingHumansMiceTumor MicroenvironmentXenograft Model Antitumor AssaysAntineoplastic AgentsInterleukin-1IL‐1KSHVlymphomaPEL

Identifiers

PMID39891599
PMCPMC12326551

What Socratic holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.