Evidence map›Paper›PMID 39816554›Full record

ArticleTranslational cancer research2024

KIF18A and CDK1 as combined therapeutic targets in cervical and endometrial carcinomas: based on bioinformatics analysis and

Mengjie Wang, David Lukanovic, Fabio Barra, Aoli Lei

Abstract read
In one paragraph

Article in Translational cancer research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

4 authors.

Mengjie WangDepartment of Pharmacy, Shaanxi Cancer Hospital, Xi'an, China.
David LukanovicDivision of Gynecology and Obstetrics, Department of Gynecology, Ljubljana University Medical Center, Ljubljana, Slovenia.
Fabio BarraDepartment of Health Sciences (DISSAL), University of Genoa, Genoa, Italy.
Aoli LeiDepartment of Gynecology, the First Hospital of Weinan City, Weinan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Chromosomal instability (CIN) has been identified as a factor that increases the susceptibility of tumor cells to kinesin family member 18A (KIF18A) inhibitors. Limited research exists on genes that are associated with sensitization to KIF18A inhibitors (KIF18Ais). Our study aimed to identify a gene linked to heightened sensitivity to KIF18Ais in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC) and uterine corpus endometrial carcinoma (UCEC). Methods: The Cancer Genome Atlas (TCGA) and X2K Appyter databases were used to analyze potential kinases associated with Results: Our findings indicated that the combination of Conclusions: This study provides evidence that targeting both KIF18A and CDK1 exerts synergistic anti-tumor effects in CESC and UCEC via inhibiting cell proliferation and migration and inducing apoptosis, suggesting a promising therapeutic strategy for these cancers.

Indexed as

Cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC)cyclin-dependent kinase 1 (CDK1)kinesin family member 18A (KIF18A)synergistic effectuterine corpus endometrial carcinoma (UCEC)

Identifiers

PMID39816554
PMCPMC11730454

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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.