Evidence map›Paper›PMID 41484609›Full record

ArticleMolecular biology reports2026

Cell-free mitochondrial DNA as a potential predictor for hypoxic stress.

Qiaoping Qu, Can Xiao, Xuemei Liu, Aixue Huang, Hui Li, Gang Xu, Ningsheng Shao, Yuechao Zhao, Bo Gao

Erratum issuedAbstract read
In one paragraph

Article in Molecular biology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Qiaoping QuSchool of Basic Medical Sciences, Anhui Medical University, Anhui, 230032, China.
Can XiaoBeijing Institute of Basic Medical Sciences, 27 Taiping Road, Beijing, 100850, China.
Xuemei LiuBeijing Institute of Basic Medical Sciences, 27 Taiping Road, Beijing, 100850, China.
Aixue HuangBeijing Institute of Basic Medical Sciences, 27 Taiping Road, Beijing, 100850, China.
Hui LiBeijing Institute of Basic Medical Sciences, 27 Taiping Road, Beijing, 100850, China.
Gang XuSchool of Basic Medical Sciences, Anhui Medical University, Anhui, 230032, China.
Ningsheng ShaoBeijing Institute of Basic Medical Sciences, 27 Taiping Road, Beijing, 100850, China.
Yuechao ZhaoBeijing Institute of Basic Medical Sciences, 27 Taiping Road, Beijing, 100850, China. zhaoyuechao@bmi.ac.cn.
Bo GaoSchool of Basic Medical Sciences, Anhui Medical University, Anhui, 230032, China. gaobo1@bmi.ac.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHypoxia exerts a far-reaching influence on cellular metabolic activities, which in turn has profound implications on cell functions. Emerging evidence has demonstrated that cell-free mitochondrial DNA (cf-mtDNA) exhibits a prompt response to acute stress within a relatively short span. Nevertheless, to date, there is a lack of reports on how hypoxic stress affects cf-mtDNA.

methodsHypoxic stress cell models and mouse models were established. Western blot was used to examine the expression levels of HIF-1α and HIF-2α protein, and droplet digital PCR (ddPCR) was used to determine the copy numbers of cf-mtDNA in cell supernatants or in mice sera. Exosomes were isolated from the cell supernatants, with their characteristics analyzed by electron microscopy, nanoparticle tracking analysis (NTA), and Western blot. ELISA method was used to analyze the cortisol levels in mice sera. Receiver Operating Characteristic (ROC) curve was established to interpretate the ability of cf-mtDNA evaluating hypoxic stress.

resultsThe cf-mtDNA copy number alterations are associated with hypoxic stress. Cf-mtDNA levels were found to increase under hypoxic stress, which was primarily derived from exosomes. Cf-mtDNA and cortisol levels exhibited an ascending tendency in hypoxic mice sera, with the AUC values for cf-mtDNA being 0.8690 on Day 3 and 0.8976 on Day 7, indicating that cf-mtDNA could serve as a potential predictor for hypoxic stress.

conclusionsThe copy numbers of cf-mtDNA were increased under hypoxic stress. The extracellular release of cf-mtDNA was mainly derived from exosomes. Cf-mtDNA was proposed as a potential diagnostic predictor for acute mild hypoxic stress.

Indexed as

Cell-Free Nucleic AcidsDNA, MitochondrialHypoxiaStress, PhysiologicalAnimalsBasic Helix-Loop-Helix ProteinsCell HypoxiaDNA Copy Number VariationsEndothelial PAS Domain-Containing Protein 1ExosomesHumansHypoxia-Inducible Factor 1, alpha SubunitMaleMiceMice, Inbred C57BLMitochondriaBasic Helix-Loop-Helix ProteinsCell-Free Nucleic AcidsDNA, MitochondrialEndothelial PAS Domain-Containing Protein 1Hypoxia-Inducible Factor 1, alpha SubunitCf-mtDNADroplet digital PCRHypoxiaStress

Identifiers

PMID41484609
PMCPMC12764587

What OpenQuestion holds

Textmetadata
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.