Evidence map›Paper›PMID 30042171›Full record

ArticleBioscience reports2018

Knockdown of long non-coding RNA linc00511 suppresses proliferation and promotes apoptosis of bladder cancer cells via suppressing Wnt/β-catenin signaling pathway.

Jun Li, Yan Li, Fandong Meng, Liye Fu, Chuize Kong

Abstract read
In one paragraph

Article in Bioscience reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 3 pooled it
–field-weighted citation impact
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

23 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
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  13. Role of Long Non-coding RNAs on Bladder Cancer.Frontiers in cell and developmental biology · 2021
    Review
  14. Article
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  16. Article
  17. LINC00511 promotes gastric cancer cell growth by acting as a ceRNA.World journal of gastrointestinal oncology · 2020
    Article
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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

5 authors.

Jun LiDepartment of Urology, The First Hospital of China Medical University, Shenyang 110001, China.
Yan LiDepartment of Biotherapy, Cancer Research Institute, the First Affiliated Hospital of China Medical University, Shenyang 110001, China.
Fandong MengDepartment of Biotherapy, Cancer Research Institute, the First Affiliated Hospital of China Medical University, Shenyang 110001, China.
Liye FuDepartment of Biotherapy, Cancer Research Institute, the First Affiliated Hospital of China Medical University, Shenyang 110001, China.
Chuize KongDepartment of Urology, The First Hospital of China Medical University, Shenyang 110001, China kongchuize_emu@sina.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

More and more studies have shown that long non-coding RNAs (lncRNAs) play critical roles in various biological processes of bladder cancer, including proliferation, apoptosis, migration and cell cycle arrest. LncRNA long intergenic noncoding RNA 00511 (linc00511) is one of the lncRNAs highly expressed in bladder cancer tissues and cells. However, little is known about the roles and mechanisms of linc00511 in bladder cancer. Here, we demonstrated that linc00511 was highly expressed in bladder cancer tissues and cells. Linc00511 knockdown could cause the cell proliferation suppression and cell cycle arrest, which were mediated by p18, p21, CDK4, cyclin D1 and phosphorylation Rb. Suppressed linc00511 could induce the apoptosis in T24 and BIU87 cells via activating the caspase pathway. Down-regulation of linc00511 could also suppress the migration and invasion of T24 and BIU87 cells. In addition, we found that the expression of linc00511 was negatively correlated with that of miR-15a-3p in the clinical bladder cancer samples. Further mechanistic studies showed that linc00511 knockdown induced proliferation inhibition, and apoptosis increase might be regulated through suppressing the activities of Wnt/β-catenin signaling pathway. Thus, we revealed that knockdown of linc00511 suppressed the proliferation and promoted apoptosis of bladder cancer cells through suppressing the activities of Wnt/β-catenin signaling pathway. Moreover, we suggested that linc00511 could be a potential therapeutic target and novel biomarker in bladder cancer.

Indexed as

ApoptosisCell ProliferationGene Expression Regulation, NeoplasticGene Knockdown TechniquesWnt Signaling PathwayAnimalsCell Cycle CheckpointsCell MovementDown-RegulationGenetic TherapyHumansMaleMice, Inbred BALB CRNA, Long NoncodingUrinary Bladder NeoplasmsRNA, Long Noncodingapoptosisbladder cancerLINC00511proliferationWnt/beta-catenin

Identifiers

PMID30042171
PMCPMC6131201

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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.