Evidence map›Paper›PMID 39434056›Full record

ArticleMolecular medicine (Cambridge, Mass.)2024

Upregulation of PRRX2 by silencing Marveld3 as a protective mechanism against radiation-induced ferroptosis in skin cells.

Jinming Cao, Mengyao Wu, Wei Mo, Min Zhao, Liming Gu, Xi Wang, Bin Zhang, Jianping Cao

Abstract read
In one paragraph

Article in Molecular medicine (Cambridge, Mass.), 2024. 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

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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. P53 Competitively Binds P300 to Suppress HIF-1α/TFRC-Mediated Ferroptosis and Promote Doxorubicin Resistance in Breast Cancer.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    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

8 authors.

Jinming Cao *Department of Nuclear Medicine, The First Affiliated Hospital of Soochow University, Suzhou, China.
Mengyao Wu *Department of Oncology, The First Affiliated Hospital of Soochow University, Suzhou, China.
Wei MoSchool of Radiation Medicine and Protection, Suzhou Medical College of Soochow University, Suzhou, China.
Min ZhaoDepartment of Nuclear Medicine, The First Affiliated Hospital of Soochow University, Suzhou, China.
Liming GuSchool of Radiation Medicine and Protection, Suzhou Medical College of Soochow University, Suzhou, China.
Xi WangSchool of Radiation Medicine and Protection, Suzhou Medical College of Soochow University, Suzhou, China.
Bin ZhangDepartment of Nuclear Medicine, The First Affiliated Hospital of Soochow University, Suzhou, China. zbnuclmd@126.com.
Jianping CaoSchool of Radiation Medicine and Protection, Suzhou Medical College of Soochow University, Suzhou, China. jpcao@suda.edu.cn.

Funding

National Natural Science Foundation of China 82103772Natural Science Foundation of the Jiangsu Higher Education Institutions of China 23KJB320014Project of State Key Laboratory of Radiation Medicine and Protection, Soochow University GZK1202205Suzhou Science and Technology Plan Project SKJY2021069
6 · The paper itself

Abstract

backgroundRadiation-induced skin injury (RISI) represents a significant complication in patients receiving radiotherapy and individuals exposed to nuclear accidents, characterized by a protracted wound-healing process relative to injuries from other etiologies. Current preventive and management approaches remain inadequate. Consequently, investigating efficacious intervention strategies that target the disease's progression characteristics holds significant practical importance.

methodsSmall interfering RNA (siRNA) and overexpression plasmid were used to modulate the expression of Marvel domain containing 3 (Marveld3) and paired related homeobox 2 (PRRX2). Protein and mRNA levels were estimated by Western Blot and real-time PCR, respectively. Intracellular levels of Malondialdehyde (MDA), a terminal product of lipid peroxidation, were measured following the manufacturer's protocol for MDA assay kit. Similarly, intracellular levels of ferrous iron (Fe

resultsIn this study, our findings indicated that Marveld3 suppression could effectively inhibit lipid peroxidation levels in irradiated skin cells, concomitantly reducing intracellular Fe

conclusionsThis study elucidates the role of Marveld3 in radiation-induced ferroptosis in skin cells. Inhibition of Marveld3 led to the upregulation of PRRX2, which subsequently resulted in a reduction of Fe

Indexed as

FerroptosisHomeodomain ProteinsMembrane ProteinsSkinAnimalsCell LineGene SilencingHumansIronLipid PeroxidationMaleRatsReactive Oxygen SpeciesTranscription FactorsUp-RegulationHomeodomain ProteinsIronMembrane ProteinsPrrx2 protein, ratReactive Oxygen SpeciesTranscription FactorsFerroptosisMarveld3PRRX2Radiation-induced skin injury

Identifiers

PMID39434056
PMCPMC11494952

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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.