Evidence map›Paper›PMID 37092087›Full record

ArticleAfrican health sciences2022

MicroRNA-186 suppresses cell proliferation and metastasis in bladder cancer.

Jun Feng Liang, Pei Hua Li, Yong Zhu, Shuai Shuai Zheng, Jing Wei Liu, Shi Qiang Song

Open access · diamondAbstract read
In one paragraph

Article in African health sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Bladder cancer: non-coding RNAs and exosomal non-coding RNAs.Functional & integrative genomics · 2024
    Review
  2. Article
  3. Article
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

6 authors at 3 institutions in 1 country.

Jun Feng LiangDepartment of Urology, Qingdao Chengyang People's hospital, Qing dao, Shan dong Province, P.R.China.
Pei Hua LiDepartment of Urology, Qingdao Chengyang People's hospital, Qing dao, Shan dong Province, P.R.China.
Yong ZhuDepartment of Urology, Qingdao Chengyang People's hospital, Qing dao, Shan dong Province, P.R.China.
Shuai Shuai ZhengDepartment of Urology, Qingdao Chengyang People's hospital, Qing dao, Shan dong Province, P.R.China.
Jing Wei LiuDepartment of Urology, Qingdao Chengyang People's hospital, Qing dao, Shan dong Province, P.R.China.
Shi Qiang SongDepartment of Urology, Qingdao Chengyang People's hospital, Qing dao, Shan dong Province, P.R.China.
Wenzhou Medical University · CNDongyang People's Hospital · CNQingdao Eighth People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Bladder cancer (BCa) is a common malignancy in the urinary system. This study aims to explore the role of miR-186 in BCa tumorigenesis. Methods: The expression of miR-186 and ADAMTS12 in clinical BCa tissues and cell lines was detected. BCa cell lines T24, 5637 and EJ were used to transfect miR-186 mimics or inhibitors. Luciferase reporter gene detection confirmed the correlation between miR-186 and ADAMTS12. MTT method and flow cytometry were used to detect cell viability and apoptosis. Cell migration and invasion ability was detected by transwell assay. The protein level of ADAMTS12, β-catenin, GSK-3β and p-GSK-3β was determined using western blot analysis. Results: MiR-186 was negatively correlated with the expression of ADAMTS12 in BCa tissues. Further research confirmed that ADAMTS12 is the direct target of miR-186. In addition, overexpression of miR-186 down-regulated the expression of ADAMTS12, inhibiting cell viability and apoptosis, while knockout of miR-186 led to the opposite result. miR-186 also inhibits the phosphorylation of GSK-3 β and β-catenin without changing the total GSK-3β level. Our study shows that miR-186 has a negative regulatory effect on the expression of ADAMTS12 in clinical specimens and in vitro. miR-186 can inhibit the proliferation and invasion of BCa cells. Conclusions: miR-186 has the potential to be used as a biomarker in the early detection of BCa.

Indexed as

MicroRNAsUrinary Bladder NeoplasmsADAMTS Proteinsbeta CateninCell Line, TumorCell MovementCell ProliferationGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaHumansADAMTS12 protein, humanADAMTS Proteinsbeta CateninGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaMicroRNAsMIRN186 microRNA, humanADAMTS12bladder cancermetastasis biomarkermiR-186proliferation

Identifiers

PMID37092087
PMCPMC10117455
OpenAlexW4323059908

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.