Evidence map›Paper›PMID 39695918›Full record

ReviewCellular & molecular biology letters2024

Inter- and intracellular mitochondrial communication: signaling hubs in aging and age-related diseases.

Meng Zhang, Jin Wei, Chang He, Liutao Sui, Chucheng Jiao, Xiaoyan Zhu, Xudong Pan

Abstract readReview
In one paragraph

Review in Cellular & molecular biology letters, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
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  5. Article
  6. Review
  7. A novelBiology methods & protocols · 2025
    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

7 authors.

Meng Zhang *Department of Neurology, The Affiliated Hospital of Qingdao University, Qingdao, 266000, China.
Jin Wei *Department of Neurology, The Affiliated Hospital of Qingdao University, Qingdao, 266000, China.
Chang He *Department of Critical Care Medicine, The Affiliated Hospital of Qingdao University, Qingdao, 266000, China.
Liutao SuiDepartment of Critical Care Medicine, The Affiliated Hospital of Qingdao University, Qingdao, 266000, China.
Chucheng JiaoDepartment of Critical Care Medicine, The Affiliated Hospital of Qingdao University, Qingdao, 266000, China.
Xiaoyan ZhuDepartment of Critical Care Medicine, The Affiliated Hospital of Qingdao University, Qingdao, 266000, China. zxysdjm@qdu.edu.cn.ORCID http://orcid.org/0000-0002-1078-4123
Xudong PanDepartment of Neurology, The Affiliated Hospital of Qingdao University, Qingdao, 266000, China. drpan022@qdu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondria are versatile and complex organelles that can continuously communicate and interact with the cellular milieu. Deregulated communication between mitochondria and host cells/organelles has significant consequences and is an underlying factor of many pathophysiological conditions, including the process of aging. During aging, mitochondria lose function, and mitocellular communication pathways break down; mitochondrial dysfunction interacts with mitochondrial dyscommunication, forming a vicious circle. Therefore, strategies to protect mitochondrial function and promote effective communication of mitochondria can increase healthy lifespan and longevity, which might be a new treatment paradigm for age-related disorders. In this review, we comprehensively discuss the signal transduction mechanisms of inter- and intracellular mitochondrial communication, as well as the interactions between mitochondrial communication and the hallmarks of aging. This review emphasizes the indispensable position of inter- and intracellular mitochondrial communication in the aging process of organisms, which is crucial as the cellular signaling hubs. In addition, we also specifically focus on the status of mitochondria-targeted interventions to provide potential therapeutic targets for age-related diseases.

Indexed as

AgingMitochondriaSignal TransductionAnimalsHumansAge-related diseasesAgingMitochondrial communicationMitochondrial dysfunctionSignaling hubs

Identifiers

PMID39695918
PMCPMC11653655

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Registered trials

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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.