Evidence map›Paper›PMID 41526033›Full record

ArticleBMJ open ophthalmology2026

Impact of anticancer drugs on human Tenon's fibroblast proliferation: implications for glaucoma surgery.

Viviana Villa, Barbara Marengo, Carlo Alberto Cutolo, Mario Passalacqua, Stefania Vernazza, Giulia Montalto, Maria A Pronzato, Michele Iester, Roberta Ricciarelli

Abstract read
In one paragraph

Article in BMJ open ophthalmology, 2026. 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

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

9 authors.

Viviana VillaDepartment of Experimental Medicine, University of Genoa, Genoa, Italy.
Barbara MarengoDepartment of Experimental Medicine, University of Genoa, Genoa, Italy.
Carlo Alberto CutoloUniversità degli Studi di Genova Dipartimento di Neuroscienze Riabilitazione Oftalmologia Genetica e Scienze Materno-Infantili, Genoa, Italy.
Mario PassalacquaDepartment of Experimental Medicine, University of Genoa, Genoa, Italy.
Stefania VernazzaDepartment of Experimental Medicine, University of Genoa, Genoa, Italy.
Giulia MontaltoDepartment of Experimental Medicine, University of Genoa, Genoa, Italy.
Maria A PronzatoDepartment of Experimental Medicine, University of Genoa, Genoa, Italy.
Michele IesterUniversità degli Studi di Genova Dipartimento di Neuroscienze Riabilitazione Oftalmologia Genetica e Scienze Materno-Infantili, Genoa, Italy.
Roberta RicciarelliDepartment of Experimental Medicine, University of Genoa, Genoa, Italy ricciarelli@medicina.unige.it.ORCID http://orcid.org/0000-0002-2053-2501

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveElevated intraocular pressure (IOP) is a major risk factor for glaucoma and the primary target of current therapies. When IOP-lowering drugs are insufficient, surgical intervention may be required; however, conjunctival and subconjunctival scarring often limits long-term success. Although intraoperative and postoperative antimetabolite treatments help preserve surgical outcomes, they are associated with ocular side effects. This study investigated the effects of selected anticancer drugs on the proliferation of human Tenon's fibroblasts (HTFs), key mediators of postoperative scarring. METHODS AND ANALYSIS: Primary HTFs were isolated from explants obtained during glaucoma surgery and characterised by immunofluorescence. The cytotoxic effects of candidate drugs were assessed using the MTT and LDH assays, while HTF migration and proliferation were evaluated by wound-healing assays. Additional cytotoxicity testing was performed on primary human trabecular meshwork cells (HTMCs) to assess ocular safety.

resultsUnder the experimental conditions used, HTF proliferation, rather than migration, was the main driver of wound closure. Among the drugs tested, pemigatinib and sorafenib significantly slowed wound closure. Pemigatinib showed no cytotoxicity in either HTFs or HTMCs, whereas sorafenib induced a moderate (28%) cytotoxic effect in HTMCs.

conclusionsPemigatinib and sorafenib, two Food and Drug Administration-approved anticancer agents, effectively reduced HTF proliferation, with pemigatinib showing a more favourable safety profile. These findings identify selective fibroblast growth factor receptor (FGFR) inhibition as a promising strategy for modulating postoperative fibrosis and support further preclinical studies to evaluate the safety and efficacy of FGFR inhibitors as potential adjuncts in glaucoma surgery.

Indexed as

Antineoplastic AgentsCell ProliferationFibroblastsFiltering SurgeryGlaucomaTenon CapsuleCell MovementCells, CulturedHumansIntraocular PressureTrabecular MeshworkWound HealingAntineoplastic AgentsAqueous humourDrugsGlaucomaIntraocular pressureSclera and Episclera

Identifiers

PMID41526033
PMCPMC12815085

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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.