Evidence map›Paper›PMID 24573672›Full record

ArticleThe Journal of biological chemistry2014

MicroRNA-137 is a novel hypoxia-responsive microRNA that inhibits mitophagy via regulation of two mitophagy receptors FUNDC1 and NIX.

Wen Li, Xingli Zhang, Haixia Zhuang, He-Ge Chen, Yinqin Chen, Weili Tian, Wenxian Wu, Ying Li, Sijie Wang, Liangqing Zhang and 6 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed, 4 pooled it
8.6field-weighted citation impact, top 2% 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

83 citing papers in PubMed, 4 syntheses or guidelines pooled it, 136 citations in OpenAlex.

  1. Pooled it
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  13. Review
  14. The Role of miR-137 in Neurodegenerative Disorders.International journal of molecular sciences · 2024
    Review
  15. Review
  16. Article
  17. The role of ferroptosis-related non-coding RNA in liver fibrosis.Frontiers in cell and developmental biology · 2024
    Review
  18. Review
  19. Therapeutic potential for KCC2-targeted neurological diseases.The Japanese dental science review · 2023
    Review
  20. Article

23 more citing papers are in PubMed but not listed here.

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

16 authors at 2 institutions in 1 country.

Wen LiInstitute of Neurology, Guangdong Key Laboratory of Age-related Cardiac-cerebral Vascular Disease, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524001, Guangdong.
Xingli ZhangInstitute of Neurology, Guangdong Key Laboratory of Age-related Cardiac-cerebral Vascular Disease, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524001, Guangdong.
Haixia ZhuangDepartment of Anesthesiology, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524001, Guangdong.
He-Ge ChenDepartment of Urology, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524001, Guangdong.
Yinqin ChenDepartment of Interventional Radiology, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524001, Guangdong.
Weili TianInstitute of Neurology, Guangdong Key Laboratory of Age-related Cardiac-cerebral Vascular Disease, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524001, Guangdong.
Wenxian WuInstitute of Neurology, Guangdong Key Laboratory of Age-related Cardiac-cerebral Vascular Disease, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524001, Guangdong.
Ying LiCell Biology Core Facility, Center for Biomedical Analysis, Tsinghua University, Beijing 100084.
Sijie WangDepartment of Clinic Research Center, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524001, Guangdong.
Liangqing ZhangDepartment of Anesthesiology, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524001, Guangdong.
Yusen ChenInstitute of Neurology, Guangdong Key Laboratory of Age-related Cardiac-cerebral Vascular Disease, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524001, Guangdong.
Longxuan LiInstitute of Neurology, Guangdong Key Laboratory of Age-related Cardiac-cerebral Vascular Disease, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524001, Guangdong; Department of Neurology, Gongli Hospital, Pudong New Area, Shanghai 200135.
Bin ZhaoInstitute of Neurology, Guangdong Key Laboratory of Age-related Cardiac-cerebral Vascular Disease, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524001, Guangdong.
Senfang SuiState Key Laboratory of Biomembrane and Membrane Biotechnology, School of Life Sciences, Tsinghua University, Beijing 100084, China.
Zhe HuDepartment of Anesthesiology, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524001, Guangdong. Electronic address: biohuzhe@hotmail.com.
Du FengInstitute of Neurology, Guangdong Key Laboratory of Age-related Cardiac-cerebral Vascular Disease, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524001, Guangdong. Electronic address: feng_du@foxmail.com.
Guangdong Medical College · CNTsinghua University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitophagy receptors mediate the selective recognition and targeting of damaged mitochondria by autophagosomes. The mechanism for the regulation of these receptors remains unknown. Here, we demonstrated that a novel hypoxia-responsive microRNA, microRNA-137 (miR-137), markedly inhibits mitochondrial degradation by autophagy without affecting global autophagy. miR-137 targets the expression of two mitophagy receptors NIX and FUNDC1. Impaired mitophagy in response to hypoxia caused by miR-137 is reversed by re-expression of FUNDC1 and NIX expression vectors lacking the miR-137 recognition sites at their 3' UTR. Conversely, miR-137 also suppresses the mitophagy induced by fundc1 (CDS+3'UTR) but not fundc1 (CDS) overexpression. Finally, we found that miR-137 inhibits mitophagy by reducing the expression of the mitophagy receptor thereby leads to inadequate interaction between mitophagy receptor and LC3. Our results demonstrated the regulatory role of miRNA to mitophagy receptors and revealed a novel link between miR-137 and mitophagy.

Indexed as

Autophagy3' Untranslated RegionsAnimalsCell HypoxiaFibroblastsGene Expression RegulationGenetic VectorsHEK293 CellsHeLa CellsHumansMembrane ProteinsMiceMice, Inbred C57BLMicroRNAsMitochondriaMitochondrial Proteins3' Untranslated RegionsFUNDC1 protein, mouseMembrane ProteinsMicroRNAsMIRN137 microRNA, mouseMitochondrial ProteinsNix protein, mouseAutophagyFUNDC1HypoxiaMicroRNAMitochondriaMitophagyNIXParkin

Identifiers

PMID24573672
PMCPMC4036186
OpenAlexW1969728632

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.