Evidence map›Paper›PMID 38675620›Full record

ArticleMolecules (Basel, Switzerland)2024

Design and Evaluation of NSAID Derivatives as AKR1C3 Inhibitors for Breast Cancer Treatment through Computer-Aided Drug Design and In Vitro Analysis.

Victoria Fonseca-Benítez, Paola Acosta-Guzmán, Juan Esteban Sánchez, Zaira Alarcón, Ronald Andrés Jiménez, James Guevara-Pulido

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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

6 authors at 1 institution in 1 country.

Victoria Fonseca-BenítezInvestigación en Química Aplicada INQA, Química Farmacéutica, Universidad El Bosque, Bogotá 11001, Colombia.ORCID 0000-0002-4471-4115
Paola Acosta-GuzmánInvestigación en Química Aplicada INQA, Química Farmacéutica, Universidad El Bosque, Bogotá 11001, Colombia.ORCID 0000-0003-4979-9928
Juan Esteban SánchezInvestigación en Química Aplicada INQA, Química Farmacéutica, Universidad El Bosque, Bogotá 11001, Colombia.ORCID 0000-0002-2402-917X
Zaira AlarcónInvestigación en Química Aplicada INQA, Química Farmacéutica, Universidad El Bosque, Bogotá 11001, Colombia.
Ronald Andrés JiménezInvestigación en Química Aplicada INQA, Química Farmacéutica, Universidad El Bosque, Bogotá 11001, Colombia.ORCID 0000-0002-1364-154X
James Guevara-PulidoInvestigación en Química Aplicada INQA, Química Farmacéutica, Universidad El Bosque, Bogotá 11001, Colombia.ORCID 0000-0001-9134-3719
Universidad El Bosque · CO

Funding

Diseño Racional de Farmacos UEB PCI 2022-11039
6 · The paper itself

Abstract

Breast cancer is a major global health issue, causing high incidence and mortality rates as well as psychological stress for patients. Chemotherapy resistance is a common challenge, and the Aldo-keto reductase family one-member C3 enzyme is associated with resistance to anthracyclines like doxorubicin. Recent studies have identified celecoxib as a potential treatment for breast cancer. Virtual screening was conducted using a quantitative structure-activity relationship model to develop similar drugs; this involved backpropagation of artificial neural networks and structure-based virtual screening. The screening revealed that the C-6 molecule had a higher affinity for the enzyme (-11.4 kcal/mol), a lower half-maximal inhibitory concentration value (1.7 µM), and a safer toxicological profile than celecoxib. The compound C-6 was synthesized with an 82% yield, and its biological activity was evaluated. The results showed that C-6 had a more substantial cytotoxic effect on MCF-7 cells (62%) compared to DOX (63%) and celecoxib (79.5%). Additionally, C-6 had a less harmful impact on healthy L929 cells than DOX and celecoxib. These findings suggest that C-6 has promising potential as a breast cancer treatment.

Indexed as

Aldo-Keto Reductase Family 1 Member C3Anti-Inflammatory Agents, Non-SteroidalBreast NeoplasmsDrug DesignAntineoplastic AgentsCelecoxibCell ProliferationComputer-Aided DesignEnzyme InhibitorsFemaleHumansMCF-7 CellsMolecular Docking SimulationQuantitative Structure-Activity RelationshipAKR1C3 protein, humanAldo-Keto Reductase Family 1 Member C3Anti-Inflammatory Agents, Non-SteroidalAntineoplastic AgentsCelecoxibEnzyme Inhibitorsartificial neural networks (ANNs)breast cancerCADDorganic synthesis

Identifiers

PMID38675620
PMCPMC11052204
OpenAlexW4394847266

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.