Evidence map›Paper›PMID 38270684›Full record

ArticleMolecular biology reports2024

Microarray data analysis of antileukemic action of Cinnamoylated benzaldehyde LQB-461 in Jurkat cell line.

Rachell R C Thimoteo, Pedro Nicolau Neto, Debora S S Costa, Fabrício da Mota Ramalho Costa, Douglas Cazaroti Brito, Paulo R R Costa, Tatiana de Almeida Simão, Ayres G Dias, Graça Justo

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Article in Molecular biology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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, 0 citations in OpenAlex.

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

9 authors at 4 institutions in 1 country.

Rachell R C ThimoteoDepartamento de Bioquímica, UERJ, Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0000-0002-6365-6491
Pedro Nicolau NetoPrograma de Carcinogênese Molecular, INCA, Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0000-0003-3322-2120
Debora S S CostaInstituto de Pesquisas Biomédicas - HNMD Marinha do Brazil, Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0000-0003-2405-3919
Fabrício da Mota Ramalho CostaLaboratório de Microbiologia Celular IOC/Fiocruz, Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0000-0002-6757-6587
Douglas Cazaroti BritoDepartamento de Química Orgânica, UERJ, Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0009-0009-5719-1155
Paulo R R CostaLaboratório de Química Bioorgânica, UFRJ, Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0000-0001-9541-1707
Tatiana de Almeida SimãoDepartamento de Bioquímica, UERJ, Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0000-0001-8509-2247
Ayres G DiasDepartamento de Química Orgânica, UERJ, Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0000-0002-5325-4421
Graça JustoDepartamento de Bioquímica, UERJ, Rio de Janeiro, RJ, Brazil. magrajusto@hotmail.com.ORCID http://orcid.org/0000-0001-5692-2571
Universidade do Estado do Rio de Janeiro · BRFundação Oswaldo Cruz · BRInstituto de Pesquisas da Marinha · BRUniversidade Federal do Rio de Janeiro · BR

Funding

Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ) no.E-26/211.931/2021Universidade do Estado do Rio de Janeiro Qualitec
6 · The paper itself

Abstract

backgroundLeukemias stand out for being the main type of childhood cancer in the world. Current treatments have strong side effects for patients, and there is still a high rate of development of resistance to multidrug therapy. Previously, our research group developed a structure-activity study with novel synthetic molecules analogous to LQB-278, described as an essential molecule with in vitro antileukemic action. Among these analogs, LQB-461 stood out, presenting more significant antileukemic action compared to its derivative LQB-278, with cytostatic and cytotoxicity effect by apoptosis, inducing caspase-3, and increased sub-G1 phase on cell cycle analysis. METHODS AND

resultsDeepening the study of the mechanism of action of LQB-461 in Jurkat cells in vitro, a microarray assay was carried out, which confirmed the importance of the apoptosis pathway in the LQB-461 activity. Through real-time PCR, we validated an increased expression of CDKN1A and BAX genes, essential mediators of the apoptosis intrinsic pathway. Through the extrinsic apoptosis pathway, we found an increased expression of the Fas receptor by flow cytometry, showing the presence of a more sensitive population and another more resistant to death. Considering the importance of autophagy in cellular resistance, it was demonstrated by western blotting that LQB-461 decreased LC-3 protein expression, an autophagic marker.

conclusionsThese results suggest that this synthetic molecule LQB-461 induces cell death by apoptosis in Jurkat cells through intrinsic and extrinsic pathways and inhibits autophagy, overcoming some mechanisms of cell resistance related to this process, which differentiates LQB-461 of other drugs used for the leukemia treatment.

Indexed as

BenzaldehydesIminesLeprostatic AgentsData AnalysisDrug Therapy, CombinationHumansJurkat CellsbenzaldehydeBenzaldehydesIminesLeprostatic AgentsLQB-278ApoptosisLeukemiaLQB-461MicroarrayResistance

Identifiers

PMID38270684
OpenAlexW4391218373

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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.