Evidence map›Paper›PMID 31981466›Full record

Observational studyCancer medicine2020

LINC-PINT alleviates lung cancer progression via sponging miR-543 and inducing PTEN.

Shu Wang, Wenyang Jiang, Xinghua Zhang, Zilong Lu, Qing Geng, Wei Wang, Nan Li, Xinyong Cai

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Cancer medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
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  18. Molecular Signatures of Idiopathic Pulmonary Fibrosis.American journal of respiratory cell and molecular biology · 2021
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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 3 institutions in 1 country.

Shu WangDepartment of Gerontology, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Wenyang JiangDepartment of Thoracic Surgery, Renmin Hospital of Wuhan University, Wuhan, China.
Xinghua ZhangDepartment of Thoracic Surgery, Renmin Hospital of Wuhan University, Wuhan, China.
Zilong LuDepartment of Thoracic Surgery, Renmin Hospital of Wuhan University, Wuhan, China.
Qing GengDepartment of Thoracic Surgery, Renmin Hospital of Wuhan University, Wuhan, China.
Wei WangDepartment of Thoracic Surgery, Renmin Hospital of Wuhan University, Wuhan, China.ORCID 0000-0002-3953-489X
Nan LiDepartment of Cardiology, Shangrao People's Hospital, Shangrao, China.
Xinyong CaiDepartment of Cardiology, Jiangxi Provincial People's Hospital Affiliated to Nanchang University, Nanchang, China.
Wuhan University · CNNanchang University · CNShangrao Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long intergenic nonprotein coding RNA p53-induced transcript (LINC-PINT) has been reported to participate in various cancers. Here, we investigated the effects of LINC-PINT on lung cancer progression. Firstly, in our study, we implied that LINC-PINT was obviously decreased in NSCLC. Thereafter, in A549 and H1299 cells, LINC-PINT was upregulated via transfecting LV-LINC-PINT. As exhibited, LINC-PINT repressed cell proliferation and cell colony formation of A549 and H1299 cells. Subsequently, flow cytometry evidenced that A549 and H1299 cell apoptosis was obviously triggered and the cell cycle was arrested in G1 phase. Then, migration and transwell invasion experiments were carried out to detect the cell migration and invasion capacity. We found A549 and H1299 cell migration and invasion capacity were restrained by the upregulation of LINC-PINT. Meanwhile, we predicted that miR-543 could function as the target of LINC-PINT and the association was verified. Moreover, we exhibited that miR-543 was remarkably increased in lung cancer, which could be regulated by LINC-PINT negatively. Furthermore, PTEN could act as the downstream target of miR-543 and upregulation of miR-543 repressed PTEN, which was reversed by LV-PINT in A549 and H1299 cells. Finally, xenografts were utilized to confirm the function of LINC-PINT on lung cancer. All these findings concluded that LINC-PINT exerted crucial biological roles in NSCLC through sponging miR-543 and inducing PTEN.

Indexed as

A549 CellsAnimalsApoptosisBiomarkers, TumorCell MovementDisease ProgressionFemaleGene Expression Regulation, NeoplasticHumansLungLung NeoplasmsMaleMiceMicroRNAsMiddle AgedNeoplasm InvasivenessBiomarkers, TumorMicroRNAsMIRN543 microRNA, humanPTEN PhosphohydrolasePTEN protein, humanRNA, Long NoncodinglncRNAlung cancermiR-543PINTPTEN

Identifiers

PMID31981466
PMCPMC7064031
OpenAlexW3002731675

What OpenQuestion holds

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LicenceCC BY
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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.