Evidence map›Paper›PMID 41545919›Full record

ArticleBMC genomics2026

MitoCommun: a database for decoding mitochondrial communication networks.

Xueyan Wu, Danlei Chen, Jitong Feng, Xueying Bu, Shengbo Wu, Jianjun Qiao

Abstract read
In one paragraph

Article in BMC genomics, 2026. 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

6 authors.

Xueyan WuSchool of Synthetic Biology and Biomanufacturing, State Key Laboratory of Synthetic Biology, Key Laboratory of Systems Bioengineering (Ministry of Education), Tianjin University, Tianjin, 300350, China.
Danlei ChenZhejiang Institute of Tianjin University (Shaoxing), Shaoxing, 312300, China.
Jitong FengZhejiang Institute of Tianjin University (Shaoxing), Shaoxing, 312300, China.
Xueying BuSchool of Synthetic Biology and Biomanufacturing, State Key Laboratory of Synthetic Biology, Key Laboratory of Systems Bioengineering (Ministry of Education), Tianjin University, Tianjin, 300350, China.
Shengbo WuSchool of Synthetic Biology and Biomanufacturing, State Key Laboratory of Synthetic Biology, Key Laboratory of Systems Bioengineering (Ministry of Education), Tianjin University, Tianjin, 300350, China. wushengbo@tju.edu.cn.
Jianjun QiaoSchool of Synthetic Biology and Biomanufacturing, State Key Laboratory of Synthetic Biology, Key Laboratory of Systems Bioengineering (Ministry of Education), Tianjin University, Tianjin, 300350, China. jianjunq@tju.edu.cn.

Funding

National Key Research and Development Program of China 2024YFA0920200"Pioneer" and "Leading Goose" R&D Program of Zhejiang 2025C01102
6 · The paper itself

Abstract

Mitochondria are highly dynamic signaling organelles that engage in continuous bidirectional communication with the cytoplasm and participate in biological processes such as cell death, inflammation, and epigenetic modification. Mitochondria receive, process and export various types of signals, ranging from metabolites to non-coding RNAs. Despite their central importance, progress in understanding mitochondrial signaling has been hampered by the fragmented characterization of their communication networks. In this study, we present MitoCommun, a manually curated database comprising 580 mitochondria-derived signaling events from five model species: Homo sapiens, Mus musculus, Rattus norvegicus, Saccharomyces cerevisiae, and Caenorhabditis elegans. Specifically, MitoCommun features 233 well-annotated mitochondrial signaling molecules, defined by either mitochondrial origin or specific organelle localization. These molecular entities have been systematically paired with their receptors and functionally mapped into explicit pathways and interaction networks. Furthermore, we have reconstructed signaling networks across phylogenetically divergent species, functionally distinct biological processes, and inter-organelle communication systems, yielding comprehensive topological maps of mitochondrial signaling cascades. By integrating these resources, MitoCommun establishes a foundational framework for decoding mitochondrial communication and serves as a versatile, user-friendly platform for exploring organelle signaling networks, which is freely accessible at http://mitocommun.qscn.online/ .

Indexed as

Databases, GeneticMitochondriaSignal TransductionAnimalsBiocurationCaenorhabditis elegansHumansMiceRatsSaccharomyces cerevisiaeIntercellular crosstalkMitochondriaMitochondrial-nuclear interactionOrganelle communicationSignaling networksSignaling transduction

Identifiers

PMID41545919
PMCPMC12896290

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.