Evidence map›Paper›PMID 39895918›Full record

ArticleInternational journal of molecular and cellular medicine2024

Potential Otubain1 Inhibitor, an Approach for a Treatment against Breast Cancer.

Andrea Muñoz-Ayala, Victor G García-González, Angel Pulido-Capiz, Brenda Chimal-Vega, Ruth A García-Villarreal, José L Vique-Sánchez

Abstract read
In one paragraph

Article in International journal of molecular and cellular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

6 authors.

Andrea Muñoz-AyalaSchool of Medicine Campus Mexicali, Autonomous University of Baja California, Mexicali, 21000, BC, México.
Victor G García-GonzálezSchool of Medicine Campus Mexicali, Autonomous University of Baja California, Mexicali, 21000, BC, México.
Angel Pulido-CapizSchool of Medicine Campus Mexicali, Autonomous University of Baja California, Mexicali, 21000, BC, México.
Brenda Chimal-VegaSchool of Medicine Campus Mexicali, Autonomous University of Baja California, Mexicali, 21000, BC, México.
Ruth A García-VillarrealSchool of Medicine Campus Mexicali, Autonomous University of Baja California, Mexicali, 21000, BC, México.
José L Vique-SánchezSchool of Medicine Campus Mexicali, Autonomous University of Baja California, Mexicali, 21000, BC, México.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The develop of new anticancer drug continues worldwide and one of the new therapeutic targets to reach it is Otubain 1 (OTUB1), since OTUB1 has functions related to prognosis in a variety of tumors and is strongly related to tumor proliferation, migration, and apoptosis by their functions on deubiquitinating. This study uses OTUB1´s active site to develop a specific pharmacological treatment to regulate the OTUB1 functions. The aim of this research was to evaluate the effects of ten compounds (OT1 - OT10), that previously were selected by molecular docking to develop a new anticancer drug to decrease the OTUB1 functions in the cancer processes. We evaluated the cytotoxic effect of OT1 - OT10 compounds on MCF-7, BT474 and MDA-MB 231 cells by MTT assay, and we determined characteristics of apoptosis by western blot analysis. Then, the best compound (OT5) was analyzed by molecular docking, molecular dynamics and theoretical toxicity for describing the interactions of OT5 compound with the OTUB1´s active site. We proposed that the OT5 compound has a high probability to be selective against OTUB1, with an apoptosis (regulating caspase-8) and cytotoxic effect on some cancer lines; IC50 for MCF-7: 97 µM and MDA-MB 231:147 µM, as well as we described that this compound could have specific interactions in the catalytic domain of OTUB1, modifying this protein's activity, decreasing the OTUB1 functions, and probably safe for humans. These results show the high potential of this compound for promoting the development of this compound as a new drug against cancer.

Indexed as

Apoptosiscaspase-8drugMCF-7MDA-MB 231

Identifiers

PMID39895918
PMCPMC11786125

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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.