Evidence map›Paper›PMID 40989716›Full record

ReviewBiochemistry and biophysics reports2025

The structure and function of FBXW5 in human diseases.

Yuyang Han, Tao Yu, Zhaowu Ma

Abstract readReview
In one paragraph

Review in Biochemistry and biophysics reports, 2025. 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

3 authors.

Yuyang HanSchool of Basic Medicine, Yangtze University, Health Science Center, Jingzhou, China.
Tao YuSchool of Basic Medicine, Yangtze University, Health Science Center, Jingzhou, China.
Zhaowu MaSchool of Basic Medicine, Yangtze University, Health Science Center, Jingzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

FBXW5, a member of the F-box protein family, plays a pivotal role in various cellular processes through its involvement in ubiquitin-mediated proteolysis as a component of the SCF complex. Recent studies have highlighted the potential of targeting FBXW5 for therapeutic interventions, making it a promising candidate for drug development. Thus, it is of great importance to provide a comprehensive overview of the structure and function of FBXW5, with a particular focus on its binding motifs for gene regulation and activities to recruitment and recognition. Herein, this review summarizes the biological significance of FBXW5 in different diseases, including cancers, neurological disorders, and other pathological conditions. This review also discusses the current challenges and future perspectives in research on FBXW5 in human diseases. Although direct inhibitors are lacking, therapeutic vulnerability is achieved via SCF inhibition or targeting hyperactivated downstream signaling nodes, emphasizing the need for further studies to fully elucidate its biological functions and therapeutic potential.

Indexed as

CancerF-box proteinFBXW5Neurological diseasesRecruitment and cognitionTherapeutic targetingUbiquitin-mediated proteolysis

Identifiers

PMID40989716
PMCPMC12452546

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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.