Evidence map›Paper›PMID 42326010›Full record

ArticleFrontiers in cell and developmental biology2026

FGFR inhibitor resistance in cervical cancer: a role for integrin α2 and mTOR signalling.

Nauf Bou Antoun, Richard P Grose, Anthony J Walker, Helmout Modjtahedi, Athina Myrto Chioni

Abstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 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

5 authors.

Nauf Bou AntounSchool of Life Sciences Pharmacy and Chemistry, Faculty of Health, Science, Social Care and Education, Kingston University London, Kingston-upon-Thames, United Kingdom.
Richard P GroseCentre for Tumour Biology, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Anthony J WalkerSchool of Life Sciences Pharmacy and Chemistry, Faculty of Health, Science, Social Care and Education, Kingston University London, Kingston-upon-Thames, United Kingdom.
Helmout ModjtahediSchool of Life Sciences Pharmacy and Chemistry, Faculty of Health, Science, Social Care and Education, Kingston University London, Kingston-upon-Thames, United Kingdom.
Athina Myrto ChioniSchool of Life Sciences Pharmacy and Chemistry, Faculty of Health, Science, Social Care and Education, Kingston University London, Kingston-upon-Thames, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cervical cancer is the fourth most common cancer among women worldwide and is often diagnosed at advanced stages, highlighting the need for effective systemic therapies, including those targeting key cancer-related pathways. Fibroblast growth factor (FGF) signalling plays a critical role in cell biology, activating FGF receptors (FGFRs) to regulate proliferation, migration and apoptosis. Aberrant activation of the pathway contributes to tumour progression in many cancers, including cervical cancer. FGFR inhibitors (FGFRi) have shown clinical promise but are limited by emergence of therapeutic resistance. Here, we describe mechanisms underpinning FGFRi resistance in three human cervical cancer cell lines (CaSki, HeLa, and SiHa). Transcriptomic analysis identified several genes differentially expressed between parental and resistant lines, including downregulation of Pleckstrin Homology Like Domain Family A Member 1 (

Indexed as

cervical cancerdrug resistanceFAKFGF(R)integrin α2mTORPHLDA1

Identifiers

PMID42326010
PMCPMC13276803

What OpenQuestion holds

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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.