Evidence map›Paper›PMID 26818536›Full record

ArticleJournal of cellular and molecular medicine2016

Role of long non-coding RNA MIAT in proliferation, apoptosis and migration of lens epithelial cells: a clinical and in vitro study.

Yi Shen, Ling-Feng Dong, Rong-Mei Zhou, Jin Yao, Yu-Chen Song, Hong Yang, Qin Jiang, Biao Yan

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
7.2field-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

64 citing papers in PubMed, 114 citations in OpenAlex.

  1. Article
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  5. Article
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  19. Long Noncoding RNACirculation · 2021
    Article
  20. Retina stem cells, hopes and obstacles.World journal of stem cells · 2021
    Review

4 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

8 authors at 2 institutions in 1 country.

Yi ShenEye Hospital, Nanjing Medical University, Nanjing, China.
Ling-Feng DongEye Hospital, Nanjing Medical University, Nanjing, China.
Rong-Mei ZhouEye Hospital, Nanjing Medical University, Nanjing, China.
Jin YaoEye Hospital, Nanjing Medical University, Nanjing, China.
Yu-Chen SongThe Fourth School of Clinical Medicine, Nanjing Medical University, Nanjing, China.
Hong YangThe Fourth School of Clinical Medicine, Nanjing Medical University, Nanjing, China.
Qin JiangEye Hospital, Nanjing Medical University, Nanjing, China.
Biao YanThe Fourth School of Clinical Medicine, Nanjing Medical University, Nanjing, China.
Second Affiliated Hospital of Nanjing Medical University · CNNanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Age-related cataract is among the most common chronic disorders of ageing and is the world's leading blinding disorder. Long non-coding RNAs play important roles in several biological processes and complicated diseases. However, the role of lncRNAs in the setting of cataract is still unknown. Here, we extracted total RNAs from the transparent and age-matched cataractous human lenses, and determined lncRNA expression profiles using microarray analysis. We found that 38 lncRNAs were differentially expressed between transparent and cataractous lenses. 17 of 20 differentially expressed lncRNAs were further verified by quantitative RT-PCRs. One top abundant lncRNA, MIAT, was specifically up-regulated both in the plasma fraction of whole blood and aqueous humor of cataract patients. MIAT knockdown could affect the proliferation, apoptosis and migration of Human lens epithelial cells (HLECs) upon oxidative stress. Posterior capsule opacification (PCO) is a common complication of cataract surgery, which is associated with abnormal production of inflammatory factors. MIAT knockdown could repress tumour necrosis factor-α-induced abnormal proliferation and migration of HLECs, suggesting a potential role of MIAT in PCO-related pathological process. Moreover, we found that MIAT acted as a ceRNA, and formed a feedback loop with Akt and miR-150-5p to regulate HLEC function. Collectively, this study provides a novel insight into the pathogenesis of age-related cataract.

Indexed as

AgedApoptosisBiomarkersCataractCell LineCell MovementCell ProliferationEpithelial CellsFemaleGene ExpressionHumansLens, CrystallineMaleMicroRNAsMiddle AgedProto-Oncogene Proteins c-aktBiomarkersMiat long non-coding RNAMicroRNAsMIR150, humanProto-Oncogene Proteins c-aktRNA, Long Noncodingcataractcell migrationcell viabilitycirculating RNAlong non-coding RNA

Identifiers

PMID26818536
PMCPMC4759467
OpenAlexW2279993917

What OpenQuestion holds

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LicenceCC BY
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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.