Evidence map›Paper›PMID 26090723›Full record

ArticleOncotarget2015

DNMT1-dependent suppression of microRNA424 regulates tumor progression in human bladder cancer.

Chun-Te Wu, Wei-Yu Lin, Ying-Hsu Chang, Paul-Yang Lin, Wen-Cheng Chen, Miao-Fen Chen

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
2.6field-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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Role of miR-424 in the carcinogenesis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Review
  4. Article
  5. Sequence Requirements for miR-424-5p Regulating and Function in Cancers.International journal of molecular sciences · 2022
    Review
  6. Article
  7. Article
  8. MicroRNAs and target molecules in bladder cancer.Medical oncology (Northwood, London, England) · 2020
    Review
  9. Article
  10. Article
  11. Article
  12. Role of miRNA-424 in Cancers.OncoTargets and therapy · 2020
    Review
  13. Review
  14. MicroRNAs: Key Players in Bladder Cancer.Molecular diagnosis & therapy · 2019
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Unmasking molecular profiles of bladder cancer.Investigative and clinical urology · 2018
    Review
  20. 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 2 institutions in 1 country.

Chun-Te WuDepartment of Urology, Chang Gung Memorial Hospital at Keelung, Keelung, Taiwan.
Wei-Yu LinChang Gung University, College of Medicine, Taoyuan City, Taiwan.
Ying-Hsu ChangChang Gung University, College of Medicine, Taoyuan City, Taiwan.
Paul-Yang LinChang Gung University, College of Medicine, Taoyuan City, Taiwan.
Wen-Cheng ChenChang Gung University, College of Medicine, Taoyuan City, Taiwan.
Miao-Fen ChenChang Gung University, College of Medicine, Taoyuan City, Taiwan.
Chang Gung University · TWChiayi Chang Gung Memorial Hospital · TW

Funding

NTP INFORMATION SYSTEMS SUPPORT27305C0011 · NIEHS · Z-TECH CORPORATION · 2007 to 2009
$4.3M
PROVIDE RABBITS, RATS, MICE, HAMSTERS, GERBILS, GUINEA PIGS27307C0011 · NIEHS · PI BOLEN, WAYNE · 2007 to 2007
$500k
NIEHS NIH HHS 27305C0011NIEHS NIH HHS 27307C0011NIEHS NIH HHS 27398C0011
6 · The paper itself

Abstract

The aim of this study was to examine the role of miRNAs regulation by DNMT1 and its underlying mechanisms in bladder cancer. The choice of target miRNAs was based on the analysis of a TaqMan MicroRNA Panel assay. The role of target miRNA in tumor behavior and the related signaling pathways were assessed using the human bladder cancer cell lines. We also evaluated the predictive power of the target miRNA and its link to DNMT1 from 124 clinical bladder cancer specimens. Our results revealed that the miR-424 level is significantly increased when blocking DNMT1 in bladder cancer cells. From the clinical specimen analysis, the staining of miR-424 was inversely correlated with DNMT1 immunoreactivity. The lack of miR-424 expression was significantly linked to aggressive tumor growth, advanced clinical stage and poor prognosis in bladder cancer. Increased miR-424 suppressed the tumor growth rate and invasion ability determined in vitro and in vivo. Furthermore, the EGFR pathway plays a role in the transmission of the miR-424 signal that regulates cell growth and the epithelial-to-mesenchymal transition. These results highlight a potential role for miR-424 as a molecular predictor and therapeutic target in bladder cancer.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsCell Line, TumorCell ProliferationDisease ProgressionDNA (Cytosine-5-)-Methyltransferase 1DNA (Cytosine-5-)-MethyltransferasesEpithelial-Mesenchymal TransitionErbB ReceptorsFemaleGene Expression ProfilingHumansMiceMice, NudeMicroRNAsNeoplasm InvasivenessDNA (Cytosine-5-)-Methyltransferase 1DNA (Cytosine-5-)-MethyltransferasesDNMT1 protein, humanDnmt1 protein, mouseEGFR protein, humanErbB ReceptorsMicroRNAsMIRN424 microrna, humanMIRN424 microRNA, mousebladder cancerDNMT1EGFRmiR424

Identifiers

PMID26090723
PMCPMC4695174
OpenAlexW1959021249

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.