Evidence map›Paper›PMID 36642914›Full record

ArticleJournal of biomedical research2022

Role of mitophagy in the hallmarks of aging.

Jie Wen, Tingyu Pan, Hongyan Li, Haixia Fan, Jinhua Liu, Zhiyou Cai, Bin Zhao

Open access · diamondAbstract read
In one paragraph

Article in Journal of biomedical research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.3field-weighted citation impact, top 11% of its field
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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
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  6. Article
  7. GCN5L: a critical target in energy metabolism pathways.Frontiers in cell and developmental biology · 2025
    Review
  8. Review
  9. Article
  10. Review
  11. Kidney Aging and Chronic Kidney Disease.International journal of molecular sciences · 2024
    Review
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 at 3 institutions in 1 country.

Jie WenDepartment and Institute of Neurology, Guangdong Medical University, Zhanjiang, Guangdong 524001, China.
Tingyu PanChongqing Key Laboratory of Neurodegenerative Diseases, Chongqing 400013, China.
Hongyan LiChongqing Key Laboratory of Neurodegenerative Diseases, Chongqing 400013, China.
Haixia FanChongqing Medical University, Chongqing 400042, China.
Jinhua LiuDepartment and Institute of Neurology, Guangdong Medical University, Zhanjiang, Guangdong 524001, China.
Zhiyou CaiChongqing Key Laboratory of Neurodegenerative Diseases, Chongqing 400013, China.
Bin ZhaoDepartment and Institute of Neurology, Guangdong Medical University, Zhanjiang, Guangdong 524001, China.
First People's Hospital of Chongqing · CNGuangdong Medical College · CNChongqing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aging, subjected to scientific scrutiny, is extensively defined as a time-dependent decline in functions that involves the majority of organisms. The time-dependent accretion of cellular lesions is generally a universal trigger of aging, while mitochondrial dysfunction is a sign of aging. Dysfunctional mitochondria are identified and removed by mitophagy, a selective form of macroautophagy. Increased mitochondrial damage resulting from reduced biogenesis and clearance may promote the aging process. The primary purpose of this paper is to illustrate in detail the effects of mitophagy on aging and emphasize the associations between mitophagy and other signs of aging, including dietary restriction, telomere shortening, epigenetic alterations, and protein imbalance. The evidence regarding the effects of these elements on aging is still limited. And although the understanding of relationship between mitophagy and aging has been long-awaited, to analyze details of such a relationship remains the main challenge in aging studies.

Indexed as

agingdietary restrictionepigenetic alterationsmitophagyprotein imbalancetelomere shortening

Identifiers

PMID36642914
PMCPMC9898045
OpenAlexW4300712476

What OpenQuestion holds

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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 OpenQuestion graph.