Evidence map›Paper›PMID 39408734›Full record

ArticleInternational journal of molecular sciences2024

Crosstalk between BER and NHEJ in XRCC4-Deficient Cells Depending on hTERT Overexpression.

Svetlana V Sergeeva, Polina S Loshchenova, Dmitry Yu Oshchepkov, Konstantin E Orishchenko

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

4 authors.

Svetlana V SergeevaInstitute of Cytology and Genetics, Russian Academy of Sciences, Lavrentieva 10, Novosibirsk 630090, Russia.ORCID 0000-0002-8585-7403
Polina S LoshchenovaInstitute of Cytology and Genetics, Russian Academy of Sciences, Lavrentieva 10, Novosibirsk 630090, Russia.
Dmitry Yu OshchepkovInstitute of Cytology and Genetics, Russian Academy of Sciences, Lavrentieva 10, Novosibirsk 630090, Russia.ORCID 0000-0002-6097-5155
Konstantin E OrishchenkoInstitute of Cytology and Genetics, Russian Academy of Sciences, Lavrentieva 10, Novosibirsk 630090, Russia.ORCID 0000-0001-9718-9038

Funding

IC&G state budget assignment FWNR-2022-0015Ministry of Education and Science of Russian Federation FSUS-2024-0018
6 · The paper itself

Abstract

Targeting DNA repair pathways is an important strategy in anticancer therapy. However, the unrevealed interactions between different DNA repair systems may interfere with the desired therapeutic effect. Among DNA repair systems, BER and NHEJ protect genome integrity through the entire cell cycle. BER is involved in the repair of DNA base lesions and DNA single-strand breaks (SSBs), while NHEJ is responsible for the repair of DNA double-strand breaks (DSBs). Previously, we showed that BER deficiency leads to downregulation of NHEJ gene expression. Here, we studied BER's response to NHEJ deficiency induced by knockdown of NHEJ scaffold protein XRCC4 and compared the knockdown effects in normal (TIG-1) and hTERT-modified cells (NBE1). We investigated the expression of the

Indexed as

DNA-Binding ProteinsDNA End-Joining RepairTelomeraseCell LineDNA Breaks, Double-StrandedDNA Ligase ATPDNA RepairGene Knockdown TechniquesHumansDNA-Binding ProteinsDNA Ligase ATPTelomeraseTERT protein, humanXRCC4 protein, humanbase excision repair (BER)cell cyclegenome stabilityhTERT overexpressionNHEJ deficiencynon-homologous end joining (NHEJ)p21 proteinscaffold protein XRCC4transcription factor p53transcription factor Sp1

Identifiers

PMID39408734
PMCPMC11476898

What OpenQuestion holds

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Registered trials

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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.