Evidence map›Paper›PMID 32228440›Full record

ArticleBMC molecular and cell biology2020

LncRNA MALAT1 exhibits positive effects on nucleus pulposus cell biology in vivo and in vitro by sponging miR-503.

Hongyu Zheng, Tingting Wang, Xiangmin Li, Wei He, Zhiqiang Gong, Zhenkai Lou, Bing Wang, Xingguo Li

Open access · goldAbstract read
In one paragraph

Article in BMC molecular and cell biology, 2020. 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
1.9field-weighted citation impact, top 14% 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, 17 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

8 authors at 4 institutions in 1 country.

Hongyu ZhengDepartment of Emergency Medical, First Affiliated Hospital of Kunming Medical University, Kunming, China.
Tingting WangDepartment of Geriatrics, Yan' An Hospital of Kunming City, Kunming, China.
Xiangmin LiDepartment of Panicaceae, First Affiliated Hospital of Kunming Medical University, Kunming, China.
Wei HeDepartment of Orthopedics, Qianjiang Central Hospital, Qianjiang, China.
Zhiqiang GongDepartment of Orthopedics, First Affiliated Hospital of Kunming Medical University, No. 295 Xichang Road, Kunming, Yunnan, China.
Zhenkai LouDepartment of Orthopedics, First Affiliated Hospital of Kunming Medical University, No. 295 Xichang Road, Kunming, Yunnan, China.
Bing WangDepartment of Orthopedics, First Affiliated Hospital of Kunming Medical University, No. 295 Xichang Road, Kunming, Yunnan, China.
Xingguo LiDepartment of Orthopedics, First Affiliated Hospital of Kunming Medical University, No. 295 Xichang Road, Kunming, Yunnan, China. XingguoLi@tom.com.
First Affiliated Hospital of Kunming Medical University · CNKunming Medical University · CNQianjiang Central Hospital · CNYan'an Hospital Affiliated To Kunming Medical University · CN

Funding

Applied Basic Research Fundation of Yunnan Province(Kunming Medical University Joint Project) 2015FB030Joint Project on Applied Basic Research Foundation of Yunnan Science and Technology Department-Kunming Medical University 2015FB030; 2018FE001-146 and 2018FE001-213Kunming Health and Family Planning Commission Medical and Health Science and Technology Program - Reserve Talents (Thousand Project) 2019-03-07-003Kunming Medical University young and middle-aged academic and technical talents fund 60117190455National Natural Science Foundation of China 81760029National Natural Science Foundation of China 81760030Scientific and Technological Innovation Team of Spinal Degenerative Diseases Research in Kunming Medical University CXTD201805Yunnan Health Science and Technology Project 2017NS022
6 · The paper itself

Abstract

backgroundIntervertebral disc degeneration (IDD) is characterized by the loss of nucleus pulposus cells (NPCs) and phenotypic abnormalities. Accumulating evidence suggests that long noncoding RNAs (lncRNAs) are involved in the pathogenesis of IDD. In this study, we aimed to investigate the functional effects of lncRNA MALAT1 on NPCs in IDD and the possible mechanism governing these effects.

resultsWe validated the decreased expression of MALAT1 in the IDD tissues, which was associated with decreased Collagen II and Aggrecan expression. In vitro, overexpressed MALAT1 could attenuate the effect of IL-1β on NPC proliferation, apoptosis, and Aggrecan degradation. In vivo, MALAT1 overexpression attenuated the severity of disc degeneration in IDD model rats. Our molecular study further demonstrated that MALAT1 could sponge miR-503, modulate the expression of miR-503, and activate downstream MAPK signaling pathways. The effects of MALAT1 on NPCs were partially reversed/aggregated by miR-503 mimics/inhibitor treatment.

conclusionOur data suggested that the MALAT1-miR-503-MAPK pathway plays a critical role in NPCs, which may be a potential strategy for alleviating IDD.

Indexed as

Nucleus PulposusAdultAggrecansAnimalsApoptosisCollagen Type IIDisease Models, AnimalFemaleHumansInterleukin-1betaIntervertebral Disc DegenerationMaleMAP Kinase Signaling SystemMicroRNAsMiddle AgedPeptide FragmentsAggrecansCollagen Type IIIL1B protein, humanInterleukin-1betainterleukin-1beta (163-171)MALAT1 long non-coding RNA, humanMALAT1 long noncoding RNA, ratMicroRNAsMIRN503 microRNA, humanMIRN503 microRNA, ratPeptide FragmentsRNA, Long NoncodingApoptosisIntervertebral disc degenerationLong noncoding RNA MALAT1MAPK pathwaymicroRNA-503Nucleus pulposus cells

Identifiers

PMID32228440
PMCPMC7106590
OpenAlexW3013635252

What OpenQuestion holds

Textmetadata
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.