Evidence map›Paper›PMID 39063187›Full record

ArticleInternational journal of molecular sciences2024

Overcoming Vemurafenib Resistance in Metastatic Melanoma: Targeting Integrins to Improve Treatment Efficacy.

Asiye Busra Boz Er, Helen M Sheldrake, Mark Sutherland

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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.

Asiye Busra Boz ErInstitute of Cancer Therapeutics, School of Pharmacy and Medical Sciences, University of Bradford, Bradford BD7 1DP, UK.
Helen M SheldrakeInstitute of Cancer Therapeutics, School of Pharmacy and Medical Sciences, University of Bradford, Bradford BD7 1DP, UK.ORCID 0000-0003-4111-2132
Mark SutherlandSchool of Chemistry and Biosciences, University of Bradford, Bradford BD7 1DP, UK.ORCID 0000-0003-3171-2281

Funding

The ministry of National Education Turkey
6 · The paper itself

Abstract

Metastatic melanoma, a deadly form of skin cancer, often develops resistance to the BRAF inhibitor drug vemurafenib, highlighting the need for understanding the underlying mechanisms of resistance and exploring potential therapeutic strategies targeting integrins and TGF-β signalling. In this study, the role of integrins and TGF-β signalling in vemurafenib resistance in melanoma was investigated, and the potential of combining vemurafenib with cilengitide as a therapeutic strategy was investigated. In this study, it was found that the transcription of

Indexed as

Drug Resistance, NeoplasmMelanomaSnake VenomsVemurafenibAntineoplastic AgentsCell Line, TumorCell ProliferationCyclin-Dependent Kinase Inhibitor p21Gene Expression Regulation, NeoplasticHumansIndolesIntegrin alpha5Integrin beta3IntegrinsSignal TransductionSkin NeoplasmsAntineoplastic AgentsCilengitideCyclin-Dependent Kinase Inhibitor p21IndolesIntegrin alpha5Integrin beta3IntegrinsITGB3 protein, humanSnake VenomsSulfonamidesTransforming Growth Factor betaVemurafenibBRAFdrug resistanceintegrinmelanoma

Identifiers

PMID39063187
PMCPMC11277089

What OpenQuestion holds

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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 OpenQuestion graph.