Evidence map›Paper›PMID 38367174›Full record

ArticleBiological trace element research2024

Boric Acid Affects the Expression of DNA Double-Strand Break Repair Factors in A549 Cells and A549 Cancer Stem Cells: An In Vitro Study.

Tuğba Semerci Sevimli, Aynaz Ghorbani, Bahar Demir Cevizlidere, Burcugül Altuğ, Murat Sevimli

Open access · hybridAbstract read
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Article in Biological trace element research, 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
0.2field-weighted citation impact, top 47% 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

0 citing papers in PubMed, 1 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

5 authors at 1 institution in 1 country.

Tuğba Semerci SevimliCellular Therapy and Stem Cell Production, Application, and Research Center (ESTEM), Eskişehir Osmangazi University, Eskişehir, 26040, Turkey. tssevimli@ogu.edu.tr.ORCID http://orcid.org/0000-0003-4856-2304
Aynaz GhorbaniCellular Therapy and Stem Cell Production, Application, and Research Center (ESTEM), Eskişehir Osmangazi University, Eskişehir, 26040, Turkey.ORCID http://orcid.org/0000-0001-5516-027X
Bahar Demir CevizlidereCellular Therapy and Stem Cell Production, Application, and Research Center (ESTEM), Eskişehir Osmangazi University, Eskişehir, 26040, Turkey.ORCID http://orcid.org/0000-0002-2444-8833
Burcugül AltuğCellular Therapy and Stem Cell Production, Application, and Research Center (ESTEM), Eskişehir Osmangazi University, Eskişehir, 26040, Turkey.
Murat SevimliDepartment of Histology and Embryology, Faculty of Medicine, Eskisehir Osmangazi University, 26040, Eskişehir, Turkey.ORCID http://orcid.org/0000-0001-8463-6943
Eskişehir Osmangazi University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA double-strand break (DSB) repair genes interact with tumor stemness- and resistance-associated processes in cancer stem cells (CSCs). Therefore, targeting DNA DSB genes in cancer treatment is important for the CSC phenotype. Although the anti-cancer effect of boric acid (BA) has been studied, its effect on DNA DSB is unclear. Moreover, no studies investigate BA's effects on DNA DSB of lung cancer stem cells (LC-SCs). To fill the gap, we aimed to assess the effects of BA on A549 cancer stem cells. CSCs were isolated from human non-small cell lung cancer cells (A549) and characterized by flow cytometry. Different concentrations of BA (at doses ranging from 1 to 100 mM) were applied to cancer stem cells. Cytotoxic activities were determined using the cell viability assay (MTT assay) at 24 and 48 h. Expression levels of DNA DSB genes that BRCA1, BRCA2, RAD51, KU70/80, ATM, and XRCC4 were evaluated by RT-qPCR. Additionally, immunofluorescence staining analysis was exploited for caspase-3 and E-cadherin. ATM expression increased significantly (p < 0.001). No significant change was observed in the expression of other genes. Moreover, BA up-regulated caspase-3 and E-cadherin expression. Consequently, we can say that BA affects DNA DSB and the apoptotic abilities of LC-SCs.

Indexed as

Boric AcidsDNA Breaks, Double-StrandedDNA RepairNeoplastic Stem CellsA549 CellsAntineoplastic AgentsApoptosisAtaxia Telangiectasia Mutated ProteinsBRCA1 ProteinBRCA2 ProteinCell SurvivalDNA-Binding ProteinsDose-Response Relationship, DrugHumansLung NeoplasmsRad51 RecombinaseAntineoplastic AgentsAtaxia Telangiectasia Mutated Proteinsboric acidBoric AcidsBRCA1 ProteinBRCA2 ProteinDNA-Binding ProteinsRad51 RecombinaseXRCC4 protein, humanBoric acidCytotoxicityDNA DSBLung cancer stem cell

Identifiers

PMID38367174
PMCPMC11442501
OpenAlexW4391914547

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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.