Evidence map›Paper›PMID 38438751›Full record

ReviewCell biochemistry and biophysics2024

Drp1: Focus on Diseases Triggered by the Mitochondrial Pathway.

Fulin Sun, Min Fang, Huhu Zhang, Qinghang Song, Shuang Li, Ya Li, Shuyao Jiang, Lina Yang

Abstract readReview
PubMed Publisher
In one paragraph

Review in Cell biochemistry and biophysics, 2024. 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
3.5field-weighted citation impact, top 7% 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, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. DRP1, fission and apoptosis.Cell death discovery · 2025
    Review
  9. Review
  10. Review
  11. 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

8 authors at 2 institutions in 1 country.

Fulin Sun *Department of Genetics and Cell Biology, Basic Medical College, Qingdao University, Qingdao, China.
Min Fang *Department of Gynaecology, Qingdao Women and Children's Hospital, Qingdao, 266021, Shandong, China.
Huhu ZhangDepartment of Genetics and Cell Biology, Basic Medical College, Qingdao University, Qingdao, China.
Qinghang SongDepartment of Genetics and Cell Biology, Basic Medical College, Qingdao University, Qingdao, China.
Shuang LiDepartment of Genetics and Cell Biology, Basic Medical College, Qingdao University, Qingdao, China.
Ya LiDepartment of Genetics and Cell Biology, Basic Medical College, Qingdao University, Qingdao, China.
Shuyao JiangDepartment of Genetics and Cell Biology, Basic Medical College, Qingdao University, Qingdao, China.
Lina YangDepartment of Genetics and Cell Biology, Basic Medical College, Qingdao University, Qingdao, China. yanglina@qdu.edu.cn.
Qingdao University · CNQingdao Women and Children's Hospital · CN

Funding

China Postdoctoral Science Foundation No.2020M682131National Natural Science Foundation of China No.81803895Shandong Province Natural Science Foundation ZR2021YQ57
6 · The paper itself

Abstract

Drp1 (Dynamin-Related Protein 1) is a cytoplasmic GTPase protein encoded by the DNM1L gene that influences mitochondrial dynamics by mediating mitochondrial fission processes. Drp1 has been demonstrated to play an important role in a variety of life activities such as cell survival, proliferation, migration, and death. Drp1 has been shown to play different physiological roles under different physiological conditions, such as normal and inflammation. Recently studies have revealed that Drp1 plays a critical role in the occurrence, development, and aggravation of a series of diseases, thereby it serves as a potential therapeutic target for them. In this paper, we review the structure and biological properties of Drp1, summarize the biological processes that occur in the inflammatory response to Drp1, discuss its role in various cancers triggered by the mitochondrial pathway and investigate effective methods for targeting Drp1 in cancer treatment. We also synthesized the phenomena of Drp1 involving in the triggering of other diseases. The results discussed herein contribute to our deeper understanding of mitochondrial kinetic pathway-induced diseases and their therapeutic applications. It is critical for advancing the understanding of the mechanisms of Drp1-induced mitochondrial diseases and preventive therapies.

Indexed as

DynaminsMitochondriaNeoplasmsAnimalsHumansInflammationMitochondrial DynamicsMitochondrial ProteinsDNM1L protein, humanDynaminsMitochondrial ProteinsAlzheimer’s diseaseCancerDynamin-Related Protein 1Inflammation responseMitochondrial dynamicsParkinson’s disease

Identifiers

PMID38438751
OpenAlexW4392382916

What OpenQuestion holds

Textmetadata
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.