Evidence map›Paper›PMID 33673002›Full record

ArticleInternational journal of molecular sciences2021

Microtubule Destabilizing Sulfonamides as an Alternative to Taxane-Based Chemotherapy.

Myriam González, María Ovejero-Sánchez, Alba Vicente-Blázquez, Raquel Álvarez, Ana B Herrero, Manuel Medarde, Rogelio González-Sarmiento, Rafael Peláez

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. 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
1.0field-weighted citation impact, top 22% of its field
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, 15 citations in OpenAlex.

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  10. Methoxy and bromo scans onJournal of enzyme inhibition and medicinal chemistry · 2021
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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

8 authors at 1 institution in 1 country.

Myriam GonzálezLaboratorio de Química Orgánica y Farmacéutica, Departamento de Ciencias Farmacéuticas, Facultad de Farmacia, Universidad de Salamanca, 37007 Salamanca, Spain.
María Ovejero-SánchezInstituto de Investigación Biomédica de Salamanca (IBSAL), Hospital Universitario de Salamanca, 37007 Salamanca, Spain.ORCID 0000-0003-1328-9491
Alba Vicente-BlázquezLaboratorio de Química Orgánica y Farmacéutica, Departamento de Ciencias Farmacéuticas, Facultad de Farmacia, Universidad de Salamanca, 37007 Salamanca, Spain.
Raquel ÁlvarezLaboratorio de Química Orgánica y Farmacéutica, Departamento de Ciencias Farmacéuticas, Facultad de Farmacia, Universidad de Salamanca, 37007 Salamanca, Spain.ORCID 0000-0002-6890-8416
Ana B HerreroInstituto de Investigación Biomédica de Salamanca (IBSAL), Hospital Universitario de Salamanca, 37007 Salamanca, Spain.ORCID 0000-0002-1414-6532
Manuel MedardeLaboratorio de Química Orgánica y Farmacéutica, Departamento de Ciencias Farmacéuticas, Facultad de Farmacia, Universidad de Salamanca, 37007 Salamanca, Spain.
Rogelio González-SarmientoInstituto de Investigación Biomédica de Salamanca (IBSAL), Hospital Universitario de Salamanca, 37007 Salamanca, Spain.ORCID 0000-0002-2726-6795
Rafael PeláezLaboratorio de Química Orgánica y Farmacéutica, Departamento de Ciencias Farmacéuticas, Facultad de Farmacia, Universidad de Salamanca, 37007 Salamanca, Spain.ORCID 0000-0003-1433-1612
Universidad de Salamanca · ES

Funding

Consejería de Educación de la Junta de Castilla y León, co-funded by the EU's European Regional Development Fund-FEDER SA030U16, SA262P18 and SA116P20health research program of the Instituto de Salud Carlos III (Spanish Ministry of Economy and Competitiveness) co-funded with FEDER founds. PI16/01920 and PI20/01569Spanish Ministry of Science, Innovation and Universities RTI2018-099474-BI00
6 · The paper itself

Abstract

Pan-Gyn cancers entail 1 in 5 cancer cases worldwide, breast cancer being the most commonly diagnosed and responsible for most cancer deaths in women. The high incidence and mortality of these malignancies, together with the handicaps of taxanes-first-line treatments-turn the development of alternative therapeutics into an urgency. Taxanes exhibit low water solubility that require formulations that involve side effects. These drugs are often associated with dose-limiting toxicities and with the appearance of multi-drug resistance (MDR). Here, we propose targeting tubulin with compounds directed to the colchicine site, as their smaller size offer pharmacokinetic advantages and make them less prone to MDR efflux. We have prepared 52 new Microtubule Destabilizing Sulfonamides (MDS) that mostly avoid MDR-mediated resistance and with improved aqueous solubility. The most potent compounds,

Indexed as

Antineoplastic AgentsApoptosisBreast NeoplasmsCell CycleCell Line, TumorCell ProliferationFemaleHeLa CellsHT29 CellsHumansMCF-7 CellsOvarian NeoplasmsPolymerizationSulfonamidesTaxoidsTubulinAntineoplastic AgentsSulfonamidesTaxoidsTubulinTubulin Modulatorsantitumorbreast cancercombretastatin A-4gynecologic cancersulfonamidetaxanetubulin

Identifiers

PMID33673002
PMCPMC7918738
OpenAlexW3132792674

What OpenQuestion holds

Textmetadata
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.