Evidence mapPaperPMID 41828574Full record

ReviewInternational journal of molecular sciences2026

Ubiquitin System-Driven Proteostasis in DNA Damage Response.

Renata Kusuma, Audrey Regina Valerie, Sisi Qin, Kitty Ichiwa, Kenneth Joshua, Gayoung Seo, Wootae Kim

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2026. 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

7 authors.

Renata KusumaDepartment of Integrated Biomedical Science, Soonchunhyang Institute of Medi-bio-Science (SIMS), Soonchunhyang University, Cheonan 31151, Republic of Korea.
Audrey Regina ValerieDepartment of Integrated Biomedical Science, Soonchunhyang Institute of Medi-bio-Science (SIMS), Soonchunhyang University, Cheonan 31151, Republic of Korea.
Sisi QinDepartment of Pathology, University of Chicago, Chicago, IL 60637, USA.
Kitty IchiwaDepartment of Integrated Biomedical Science, Soonchunhyang Institute of Medi-bio-Science (SIMS), Soonchunhyang University, Cheonan 31151, Republic of Korea.ORCID 0009-0006-6849-8521
Kenneth JoshuaDepartment of Integrated Biomedical Science, Soonchunhyang Institute of Medi-bio-Science (SIMS), Soonchunhyang University, Cheonan 31151, Republic of Korea.
Gayoung SeoDepartment of Integrated Biomedical Science, Soonchunhyang Institute of Medi-bio-Science (SIMS), Soonchunhyang University, Cheonan 31151, Republic of Korea.
Wootae KimDepartment of Integrated Biomedical Science, Soonchunhyang Institute of Medi-bio-Science (SIMS), Soonchunhyang University, Cheonan 31151, Republic of Korea.ORCID 0000-0003-4364-3260

Funding

National Research Foundation of Korea (NRF) 2022R1A2C1091563National Research Foundation of Korea (NRF) RS-2025-02293074National Research Foundation of Korea (NRF) - Global-Learning & Academic research institution for Master's PhD students and Post-docs (G-LAMP) Program (Ministry of Education) RS-2025-25441283Soonchunhyang University Research Fund N/A
6 · The paper itself

Abstract

Proteostasis is essential for maintaining the proper function of the proteome and diverse cellular processes. The ubiquitin system plays a central role in proteostasis by regulating protein stability, trafficking, and termination. Under cellular stress, rapid proteome remodeling is required to maintain proteostasis and support adaptive cellular stress-response pathways, including the DNA damage response (DDR). Proper DDR function relies on precise control of protein abundance and signaling dynamics, primarily achieved through ubiquitin-mediated proteostatic regulation involving both proteolytic degradation and non-proteolytic scaffolding function. Dysregulation of the ubiquitin system alters the dynamic control of the DDR cascade, leading to genomic instability and disease progression. Therefore, targeting key components of the ubiquitin system may restore proper DDR signaling regulation and offer novel therapeutic opportunities for disease treatment. In this review, we summarize the role of the ubiquitin system in proteostasis-mediated DDR regulation and explore the potential of targeting ubiquitin system components as therapeutic strategies in cancer treatment.

Indexed as

DNA DamageDNA RepairProteostasisUbiquitinAnimalsGenomic InstabilityHumansNeoplasmsProteotoxic StressSignal TransductionUbiquitincancer therapyDNA damage responsegenomic instabilityproteostasisubiquitin-system

Identifiers

PMID41828574
PMCPMC12985048

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.