ArticleBMC genomics2026
MitoCommun: a database for decoding mitochondrial communication networks.
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.
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.
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.
Who cites it
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
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
Identifiers
What Socratic holds
Registered trials
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.