Evidence map›Paper›PMID 41555655›Full record

ArticleCancer science2026

Compound Library Screening Identified Cladribine as a Novel Radiosensitizer for Prostate Cancer.

Toshiki Oka, Koji Hatano, Shohei Katsuki, Tomohiro Kanaki, Shunsuke Inoguchi, Masaru Tani, Akihiro Yoshimura, Yuki Horibe, Yutong Liu, Nesrine Sassi and 17 more

Abstract read
In one paragraph

Article in Cancer science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

27 authors.

Toshiki OkaDepartment of Urology, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.ORCID https://orcid.org/0000-0002-2023-7211
Koji HatanoDepartment of Urology, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.ORCID https://orcid.org/0000-0002-8409-5152
Shohei KatsukiDepartment of Medical Physics and Engineering, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.
Tomohiro KanakiDepartment of Urology, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.
Shunsuke InoguchiDepartment of Urology, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.
Masaru TaniDepartment of Urology, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.ORCID https://orcid.org/0009-0001-3079-0520
Akihiro YoshimuraDepartment of Urology, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.
Yuki HoribeDepartment of Urology, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.
Yutong LiuDepartment of Urology, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.
Nesrine SassiDepartment of Urology, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.
Yohei OkudaDepartment of Urology, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.
Akinaru YamamotoDepartment of Urology, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.ORCID https://orcid.org/0000-0002-3565-5870
Toshihiro UemuraDepartment of Urology, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.
Gaku YamamichiDepartment of Urology, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.
Yu IshizuyaDepartment of Urology, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.
Takuji HayashiDepartment of Urology, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.
Yoshiyuki YamamotoDepartment of Urology, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.
Taigo KatoDepartment of Urology, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.ORCID https://orcid.org/0000-0002-8681-1407
Atsunari KawashimaDepartment of Urology, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.ORCID https://orcid.org/0000-0001-9369-4264
Keisuke TamariDepartment of Radiation Oncology, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.
Bangzhong LinCenter for Supporting Drug Discovery and Life Science Research, The University of Osaka Graduate School of Pharmaceutical Science, Suita, Osaka, Japan.
Akiyoshi TaniCenter for Supporting Drug Discovery and Life Science Research, The University of Osaka Graduate School of Pharmaceutical Science, Suita, Osaka, Japan.
Kazutake TsujikawaCenter for Supporting Drug Discovery and Life Science Research, The University of Osaka Graduate School of Pharmaceutical Science, Suita, Osaka, Japan.
Yutaka TakahashiDepartment of Medical Physics and Engineering, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.
Kazuhiko OgawaDepartment of Radiation Oncology, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.
Shawn E LupoldThe James Buchanan Brady Urological Institute and Department of Urology, The Johns Hopkins University Schoolof Medicine, Baltimore, Maryland, USA.
Norio NonomuraDepartment of Urology, The University of Osaka Graduate School of Medicine, Suita, Osaka, Japan.ORCID https://orcid.org/0000-0002-6522-6233

Funding

Japanese Urological AssociationJapan Society for the Promotion of Science KAKENHI (grant numbers: 24K12482)Research Support Project for Life Science and Drug Discovery (Basis for Supporting Innovative Drug Discovery and Life Science Research [BINDS]) from AMED JP24ama121054
6 · The paper itself

Abstract

Radiation therapy effectively treats prostate cancer, but tumor recurrence remains a clinical challenge, highlighting the need for strategies to enhance radiosensitivity. In this study, we developed a simple, high-throughput drug repurposing screening platform to find radiosensitizers from compounds approved by the U.S. Food and Drug Administration. A library of 1134 compounds was systematically screened at two concentrations (0.2 and 2 μM) using LNCaP cells stably expressing Metridia luciferase, allowing highly sensitive and quantitative assessment of cell viability through luciferase activity in culture supernatants. In the primary screening, 8 and 12 candidate radiosensitizers were identified at 0.2 μM and 2 μM, respectively. In the secondary screening, 19 compounds were evaluated at two radiation doses (4 Gy and 6 Gy) and six drug concentrations, identifying 5 radiation-sensitizing candidate compounds. Through this stepwise screening approach, cladribine was identified as the most potent radiosensitizer. Cladribine increased radiation-induced cytotoxicity in multiple prostate cancer cell lines (22Rv1, DU145, and PC3), with dose-modifying factors of 1.46, 1.55, and 1.43, respectively, based on the radiation dose needed to achieve 90% cell death. Mechanistically, cladribine prevented the repair of radiation-induced DNA double-strand breaks, shown by increased γH2AX levels. Importantly, its radiosensitizing effect was further confirmed in vivo using 22Rv1 and DU145 xenograft models. This study demonstrates that a luciferase-based high-throughput drug repurposing platform is useful for identifying clinically relevant radiosensitizers, revealing that cladribine is a promising candidate for further translational research in prostate cancer radiotherapy.

Indexed as

Prostatic NeoplasmsRadiation-Sensitizing AgentsAnimalsCell Line, TumorCell SurvivalDrug RepositioningHigh-Throughput Screening AssaysHumansMaleMiceXenograft Model Antitumor AssaysRadiation-Sensitizing Agentscladribinecompound library screeningprostate cancerradiationradiosensitizer

Identifiers

PMID41555655
PMCPMC13045248

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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 OpenQuestion graph.