Evidence map›Paper›PMID 33282949›Full record

ArticleBioMed research international2020

Downregulation of Long Noncoding RNA LUCAT1 Suppresses the Migration and Invasion of Bladder Cancer by Targeting miR-181c-5p.

Yifan Chen, Wentao Zhang, Liliang Shen, Aimaitiaji Kadier, Jianhua Huang, Ruiliang Wang, Pengfei Wu, Xudong Yao

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in BioMed research international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Yifan ChenDepartment of Urology, Shanghai Tenth People's Hospital, Tongji University, Shanghai 200072, China.ORCID https://orcid.org/0000-0002-8433-3210
Wentao ZhangDepartment of Urology, Shanghai Tenth People's Hospital, Tongji University, Shanghai 200072, China.ORCID https://orcid.org/0000-0002-5733-4875
Liliang ShenDepartment of Urology, The Affiliated People's Hospital of Ningbo University, 251 East Baizhang Road, Ningbo City, Zhejiang Province, China.ORCID https://orcid.org/0000-0001-8765-5883
Aimaitiaji KadierDepartment of Urology, Shanghai Tenth People's Hospital, Tongji University, Shanghai 200072, China.ORCID https://orcid.org/0000-0001-7217-5721
Jianhua HuangDepartment of Urology, Shanghai Tenth People's Hospital, Tongji University, Shanghai 200072, China.ORCID https://orcid.org/0000-0002-6923-007X
Ruiliang WangDepartment of Urology, Shanghai Tenth People's Hospital, Tongji University, Shanghai 200072, China.ORCID https://orcid.org/0000-0001-5508-2785
Pengfei WuDepartment of Urology, Shanghai Tenth People's Hospital, Tongji University, Shanghai 200072, China.ORCID https://orcid.org/0000-0002-0592-3432
Xudong YaoDepartment of Urology, Shanghai Tenth People's Hospital, Tongji University, Shanghai 200072, China.ORCID https://orcid.org/0000-0001-7234-3940
Tongji University · CNNingbo University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe long noncoding RNA LUCAT1 (lung cancer-associated transcript 1) has been reported to be highly expressed in bladder cancer samples, but its role and molecular mechanisms need to be elucidated.

methodsBioinformatics methods show that miR-181c-5p is a target of LUCAT1. Here, we aimed to reveal whether LUCAT1 participates in the development of bladder cancer via targeting miR-181c-5p. The expression levels of LUCAT1 and miR-181c-5p were detected by RT-PCR technology in bladder cells and tissues. The effects of the LUCAT1/miR-181c-5p axis on cell proliferation, migration, invasion, and apoptosis were tested by CCK-8, wound healing, Transwell chambers, and flow cytometry assays. The expressions of apoptosis/migration-related proteins were detected by western blotting assays.

resultsThe results demonstrated that LUCAT1 was overexpressed in bladder cancer tissue and cells, while miR-181c-5p showed a low expression pattern as compared to normal bladder cells and tissues. Cell proliferation, migration, and invasion capacities were significantly impaired, and cell apoptosis was enhanced when LUCAT1 was silenced in UM-UC-3 and T24 cell lines, but this effect was abolished by miR-181c-5p downregulation. In addition, miR-181c-5p downregulation impaired LUCAT1 downregulation which mediated the decreased expressions of Bcl2 and N-cadherin and the increased expressions of Bax and E-cadherin. Moreover, we found that KRAS was a direct target of miR-181c-5p and was under the positive regulation of LUCAT1.

conclusionCollectively, this study reveals that knockdown of LUCAT1 inhibits the migration and invasion of bladder cancer cells in a miR-181c-5p-dependent manner, which may be related to KRAS downregulation.

Indexed as

Gene Expression Regulation, NeoplasticApoptosisBase SequenceCell Line, TumorCell MovementDown-RegulationGene Knockdown TechniquesHumansMicroRNAsNeoplasm InvasivenessNeoplasm ProteinsPrognosisRNA, Long NoncodingUrinary Bladder Neoplasmslong non-coding RNA LUCAT1, humanMicroRNAsMIrn181 microRNA, humanNeoplasm ProteinsRNA, Long Noncoding

Identifiers

PMID33282949
PMCPMC7685804
OpenAlexW3098440918

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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.