Evidence map›Paper›PMID 32683666›Full record

ArticleJournal of molecular neuroscience : MN2021

miR-708 and miR-335-3p Inhibit the Apoptosis of Retinal Ganglion Cells Through Suppressing Autophagy.

Qiuli Zhang, Chang He, Ruizhuang Li, Yi Ke, Kaidi Sun, Jiaqi Wang

Abstract read
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In one paragraph

Article in Journal of molecular neuroscience : MN, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.2field-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

13 citing papers in PubMed, 22 citations in OpenAlex.

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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

6 authors at 3 institutions in 1 country.

Qiuli ZhangDepartment of Ophthalmology, Affiliated Hospital of Guangdong Medical University, No.57, South Renmin Avenue, Zhanjiang, 524001, Guangdong Province, China. Qiu_lizhang@126.com.ORCID http://orcid.org/0000-0001-5036-1152
Chang HeDepartment of Genetics, College of Basic Medical Sciences, Jilin University, Changchun, 130021, Jilin, China.
Ruizhuang LiDepartment of Ophthalmology, Affiliated Hospital of Guangdong Medical University, No.57, South Renmin Avenue, Zhanjiang, 524001, Guangdong Province, China.
Yi KeDepartment of Ophthalmology, Affiliated Hospital of Guangdong Medical University, No.57, South Renmin Avenue, Zhanjiang, 524001, Guangdong Province, China.
Kaidi SunDepartment of Ophthalmology, Affiliated Hospital of Inner Mongolia University for the Nationalities, Tongliao, 028007, Inner Mongolia, China.
Jiaqi WangDepartment of Ophthalmology, Affiliated Hospital of Inner Mongolia University for the Nationalities, Tongliao, 028007, Inner Mongolia, China.
Guangdong Medical College · CNInner Mongolia University for Nationalities · CNJilin University · CN

Funding

National Natural Science Foundation of China 81660734Natural Science Foundation of Inner Mongolia 2018MS08118
6 · The paper itself

Abstract

This study aimed to clarify the regulation role of miR-708 and miR-335-3p in retinal ganglion cell (RGC) autophagy and apoptosis in glaucoma. Chronic glaucoma mice were established by laser photocoagulation. RGCs were isolated and transfected with a series of plasmids and the cultured in 60 mmHg pressure. miR-335-3p, miR-708, and ATG3 mRNA expressions were detected by qRT-PCR. Protein levels of ATG3, autophagy-related protein LC3, and p62 were detected by Western blot. The apoptosis of RGCs was detected by flow cytometry. The regulation role of miR-335-3p/miR-708 in ATG3 was confirmed by the dual-luciferase reporter gene. The expressions of several miRNAs were measured in retinal tissues from chronic glaucoma mice and RGCs under pressure conditions, and results showed that both miR-335-3p and miR-708 were down-regulated. Besides, the inhibition of miR-708 and miR-335-3p induced the apoptosis of RGCs through promoting autophagy. Also, miR-708 and miR-335-3p could bind to ATG3 and targeted regulated ATG3. Furthermore, the interference with miR-708/miR-335-3p induced RGC apoptosis by up-regulating ATG3 to promote autophagy. In general, the down-regulation of miR-708 and miR-335-3p contributed to the apoptosis of RGCs through promoting autophagy in glaucoma.

Indexed as

AnimalsApoptosisAutophagyAutophagy-Related ProteinsCells, CulturedDown-RegulationGlaucomaIntraocular PressureMiceMice, Inbred C57BLMicroRNAsMicrotubule-Associated ProteinsPressureRetinal Ganglion CellsRNARNA InterferenceAtg3 protein, mouseAutophagy-Related ProteinsMap1lc3b protein, mouseMicroRNAsMicrotubule-Associated ProteinsMirn335 microRNA, mousemirn708 microRNA, mouseRNARNA, MessengerRNA, recombinantRNA, Small InterferingUbiquitin-Conjugating EnzymesApoptosisATG3AutophagyGlaucomamiR-335-3pmiR-708Retinal ganglion cells

Identifiers

PMID32683666
OpenAlexW3043680796

What OpenQuestion holds

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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.