Evidence map›Paper›PMID 40871468›Full record

ReviewMolecules (Basel, Switzerland)2025

Recent Advances in Microtubule Targeting Agents for Cancer Therapy.

Henrique C Assunção, Patrícia M A Silva, Hassan Bousbaa, Honorina Cidade

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 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

4 authors.

Henrique C AssunçãoLaboratory of Organic and Pharmaceutical Chemistry, Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, Rua de Jorge de Viterbo Ferreira, 288, 4050-313 Porto, Portugal.ORCID 0009-0008-7647-7477
Patrícia M A SilvaAssociate Laboratory i4HB-Institute for Health and Bioeconomy, University Institute of Health Sciences-CESPU, 4585-116 Gandra, Portugal.ORCID 0000-0002-0694-7321
Hassan BousbaaUNIPRO-Oral Pathology and Rehabilitation Research Unit, IUCS-CESPU, University Institute of Health Sciences, 4585-116 Gandra, Portugal.ORCID 0000-0002-4006-5779
Honorina CidadeLaboratory of Organic and Pharmaceutical Chemistry, Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, Rua de Jorge de Viterbo Ferreira, 288, 4050-313 Porto, Portugal.ORCID 0000-0003-0715-1779

Funding

Cooperativa de Ensino Superior Politécnico e Universitário FlavScreen_GI2-CESPU-2023Fundação para a Ciência e Tecnologia LA/P/0101/2020 (https://doi.org/10.54499/LA/P/0101/2020)Fundação para a Ciência e Tecnologia UIDB/04423/2020 (https://doi.org/10.54499/UIDB/04423/2020)Fundação para a Ciência e Tecnologia UIDP/04423/2020 (https://doi.org/10.54499/UIDP/04423/2020)
6 · The paper itself

Abstract

Cancer mortality and the development of cancer resistance present significant challenges that must be addressed to ensure global health. Among anticancer agents, microtubule-targeting agents (MTAs) represent a well-recognized therapeutic approach that disrupts microtubule dynamics, thereby inhibiting cell division, and has been widely used to treat several types of cancers. However, even though MTAs are widely regarded as effective, their potential is limited primarily due to cancer resistance and toxicity. Consequently, in the last years, the exploration of new MTAs with the aim of identifying agents with improved cytotoxicity, selectivity, and adequate pharmacokinetic profile, as well as the ability to evade drug resistance mechanisms, has remained a major concern in the development of anticancer treatment. This review highlights the discovery of new MTAs since 2020, with the goal of understanding the advancements made in this field and its future directions. Special attention is given to structure-activity relationship (SAR) studies that could be important for the discovery of more effective MTAs in the future.

Indexed as

Antineoplastic AgentsMicrotubulesNeoplasmsTubulin ModulatorsAnimalsDrug Resistance, NeoplasmHumansMolecular Targeted TherapyStructure-Activity RelationshipAntineoplastic AgentsTubulin Modulatorscancermicrotubule-targeting agentsnatural productsstructure-activity relationship studies

Identifiers

PMID40871468
PMCPMC12388312

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.