Evidence map›Paper›PMID 40582249›Full record

ReviewDNA repair2025

FBH1 and the replication stress response: Implications for genome stability and cancer development.

Joshua L Turner, Jennifer M Mason

Abstract readReview
In one paragraph

Review in DNA repair, 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. Article
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

2 authors.

Joshua L TurnerDepartment of Genetics and Biochemistry, Clemson University, United States.
Jennifer M MasonDepartment of Genetics and Biochemistry, Clemson University, United States. Electronic address: jmason4@clemson.edu.

Funding

Role of homologous recombination in the replication stress responseR35GM142512 · NIGMS · CLEMSON UNIVERSITY · PI MASON, JENNIFER · 2021 to 2025
$2.1M
NIGMS NIH HHS R35 GM142512
6 · The paper itself

Abstract

The replication stress response plays important roles in maintaining genome stability.In this review article, we focus on the role of FBH1 in the replication stress response and promoting death in cells with excessive DNA damage. FBH1-deficiency results in resistance to replication stress. We discuss how loss and gain of FBH1 in a wide variety of cancers can contribute to tumor-associated phenotypes, impact cancer therapies and be exploited for potential targeted therapies.

Indexed as

DNA-Binding ProteinsDNA ReplicationGenomic InstabilityNeoplasmsAnimalsDNA DamageDNA RepairHumansDNA-Binding ProteinscancerFBH1replication stress

Identifiers

PMID40582249
PMCPMC13200063

What OpenQuestion 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 OpenQuestion graph.