Evidence map›Paper›PMID 30117016›Full record

ArticleInternational urology and nephrology2018

miR-129-5p inhibits gemcitabine resistance and promotes cell apoptosis of bladder cancer cells by targeting Wnt5a.

Jingyi Cao, Qichao Wang, Gang Wu, Shasha Li, Qian Wang

Abstract read
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In one paragraph

Article in International urology and nephrology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 41 citations in OpenAlex.

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  12. Suppressive effect of platycodin D on bladder cancer through microRNA-129-5p-mediated PABPC1/PI3K/AKT axis inactivation.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2021
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  18. miR-129-5p Inhibits Bone Formation Through TCF4.Frontiers in cell and developmental biology · 2020
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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 at 2 institutions in 1 country.

Jingyi CaoDepartment of Urology, Xuzhou Cancer Hospital, Xuzhou, 221005, Jiangsu, People's Republic of China.
Qichao WangDepartment of Urology, Xuzhou Cancer Hospital, Xuzhou, 221005, Jiangsu, People's Republic of China.
Gang WuDepartment of Urology, Xuzhou Cancer Hospital, Xuzhou, 221005, Jiangsu, People's Republic of China. wugang567@163.com.
Shasha LiDepartment of Urology, Xuzhou Cancer Hospital, Xuzhou, 221005, Jiangsu, People's Republic of China.
Qian WangDepartment of Urology, Xuzhou Cancer Hospital, Xuzhou, 221005, Jiangsu, People's Republic of China. wangqian0013@sina.com.
Xuzhou Cancer Hospital · CNJiangsu University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesGemcitabine resistance is a major obstacle for effective treatment of bladder cancer. This study was aimed to investigate the potential role of miR-129-5p in the development of gemcitabine resistance in bladder cancer cells and its underlying mechanism.

methodsThe IC50 for gemcitabine in 20 bladder cancer cells was first profiled from Genomics of Drug Sensitivity in Cancer. miR-129-5p level and gene mRNA expression were detected using quantitative real-time PCR (qRT-PCR). Cell viability, apoptosis, and gene protein level were assessed by MTT, flow cytometry, and Western blot, respectively. Regulatory relationship between Wnt5a and miR-129-5p was determined using luciferase reporter assay.

resultsWe found that down-regulated miR-129-5p level contributed to gemcitabine resistance in bladder cancer cells and tissues. We also observed restoration of miR-129-5p could significantly increase cell sensitivity to gemcitabine and promote cell apoptosis. Mechanism analysis revealed that Wnt5a is a direct target gene of miR-129-5p and knock-down of Wnt5a reversed gemcitabine resistance.

conclusionsTaken together, our findings indicate that miR-129-5p and Wnt5a may be novel therapeutic targets for overcoming gemcitabine resistance in bladder cancer treatment.

Indexed as

AgedAged, 80 and overAntimetabolites, AntineoplasticApoptosisCell Line, TumorCell SurvivalDeoxycytidineDown-RegulationDrug Resistance, NeoplasmFemaleGemcitabineHumansInhibitory Concentration 50MaleMicroRNAsMiddle AgedAntimetabolites, AntineoplasticDeoxycytidineGemcitabineMicroRNAsMirn129 microRNA, humanWnt-5a ProteinWNT5A protein, humanApoptosisBladder cancerGemcitabine resistancemiR-129-5pWnt5a

Identifiers

PMID30117016
OpenAlexW2887558650

What OpenQuestion holds

Textmetadata
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.