Evidence map›Paper›PMID 40595052›Full record

ArticleScientific reports2025

miR-210 locus deletion disrupts cellular homeostasis: an integrated genetic study.

Mihai Bogdan Preda, Evelyn Gabriela Nastase-Rusu, Carmen Alexandra Neculachi, Xiaoling Zhong, Christine Voellenkle, Nathalie M Mazure, Ovidiu Balacescu, Cristina Ivan, Xiao-Wei Zheng, Mihaela Gherghiceanu and 7 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

17 authors.

Mihai Bogdan PredaDepartment of Stem Cell Biology, Institute of Cellular Biology and Pathology "Nicolae Simionescu", 050568, Bucharest, Romania. bogdan.preda@icbp.ro.
Evelyn Gabriela Nastase-RusuDepartment of Stem Cell Biology, Institute of Cellular Biology and Pathology "Nicolae Simionescu", 050568, Bucharest, Romania.
Carmen Alexandra NeculachiDepartment of Stem Cell Biology, Institute of Cellular Biology and Pathology "Nicolae Simionescu", 050568, Bucharest, Romania.
Xiaoling ZhongDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Christine VoellenkleDepartment of Stem Cell Biology, Institute of Cellular Biology and Pathology "Nicolae Simionescu", 050568, Bucharest, Romania.
Nathalie M MazureINSERM U1065, C3M, Université Côte d'Azur, 151 Route de St Antoine de Ginestière, CEDEX 03, BP2 3194, 06204, Nice, France.
Ovidiu BalacescuDepartment of Genetics, Genomics and Experimental Pathology, The Oncology Institute "Prof. Dr. Ion Chiricuta", 400015, Cluj-Napoca, Romania.
Cristina IvanDepartment of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Xiao-Wei ZhengDepartment of Molecular Medicine and Surgery, Karolinska Institutet, 17177, Stockholm, Sweden.
Mihaela GherghiceanuVictor Babeș National Institute of Pathology, Bucharest, Romania.
Kevin LebrigandCNRS UMR7275 Inserm 1323, IPMC, FHU- OncoAge, IHU RespiERA, Sophia Antipolis, Université Côte d'Azur, 06560, Valbonne, France.
Maya SimionescuDepartment of Stem Cell Biology, Institute of Cellular Biology and Pathology "Nicolae Simionescu", 050568, Bucharest, Romania.
Fabio MartelliDepartment of Stem Cell Biology, Institute of Cellular Biology and Pathology "Nicolae Simionescu", 050568, Bucharest, Romania.
Bernard MariCNRS UMR7275 Inserm 1323, IPMC, FHU- OncoAge, IHU RespiERA, Sophia Antipolis, Université Côte d'Azur, 06560, Valbonne, France.
Sergiu-Bogdan CatrinaDepartment of Molecular Medicine and Surgery, Karolinska Institutet, 17177, Stockholm, Sweden.
Alexandrina BurlacuDepartment of Stem Cell Biology, Institute of Cellular Biology and Pathology "Nicolae Simionescu", 050568, Bucharest, Romania.
Mircea IvanDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, 46202, USA. mivan@iu.edu.

Funding

Role of Hypoxia-Induced miR-210 in Tumor MetabolismR01CA155332 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI IVAN, MIRCEA · 2011 to 2015
$1.7M
Ministero della Salute POS-T4 CAL.HUB.RIA T4-AN-09NCI NIH HHS R01 CA155332NIH R01 CA155332-01A1Romanian Ministry of Research, Innovation, and Digitization PN 23.16.01.01Romanian Ministry of Research, Innovation, and Digitization TE186/2021Romania's National Recovery and Resilience Plan 60062/23.05.2023
6 · The paper itself

Abstract

MiR-210 is widely recognized as the quintessential hypoxia-responsive miRNA and is thought to fine-tune various facets of cellular homeostasis. We hereby present an integrative appraisal of the phenotypic and molecular repercussions of disrupting the corresponding locus in human and mouse cells using multiple genetic strategies. In brief, MIR210 deletion led to decreased cellular fitness and suboptimal responses to several stress types. Transcriptomic comparisons via different profiling platforms, performed independently by members of this collaboration, revealed consistent deregulation of neighboring genes, in locus-disrupted cells. Interestingly, the anticipated enrichment of miR-210 targets failed to materialize in unbiased analyses. Our results point to the biological significance of unrecognized regulatory elements that overlap miRNA genes and should serve as a note of caution for studies based on the genetic disruption of such loci.

Indexed as

Gene DeletionHomeostasisMicroRNAsAnimalsGene Expression ProfilingGene Expression RegulationHumansMiceMicroRNAsMIRN210 microRNA, humanMIRN210 microRNA, mouseGene editing technologiesGenomic neighborhoodHypoxiamiR-210Targets

Identifiers

PMID40595052
PMCPMC12217331

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.