Evidence map›Paper›PMID 30526300›Full record

ArticleCell cycle (Georgetown, Tex.)2018

MIR-300 in the imprinted DLK1-DIO3 domain suppresses the migration of bladder cancer by regulating the SP1/MMP9 pathway.

Huaqing Yan, Jiangfeng Li, Yufan Ying, Haiyun Xie, Hong Chen, Xin Xu, Xiangyi Zheng

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

  1. Function ofOncology letters · 2025
    Review
  2. Article
  3. Review
  4. Bladder cancer: non-coding RNAs and exosomal non-coding RNAs.Functional & integrative genomics · 2024
    Review
  5. Article
  6. Article
  7. UrinaryCancers · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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

7 authors at 1 institution in 1 country.

Huaqing Yana Department of Urology, First Affiliated Hospital , Zhejiang University , Hangzhou , Zhejiang Province , China.ORCID 0000-0001-9994-720X
Jiangfeng Lia Department of Urology, First Affiliated Hospital , Zhejiang University , Hangzhou , Zhejiang Province , China.
Yufan Yinga Department of Urology, First Affiliated Hospital , Zhejiang University , Hangzhou , Zhejiang Province , China.
Haiyun Xiea Department of Urology, First Affiliated Hospital , Zhejiang University , Hangzhou , Zhejiang Province , China.
Hong Chena Department of Urology, First Affiliated Hospital , Zhejiang University , Hangzhou , Zhejiang Province , China.
Xin Xua Department of Urology, First Affiliated Hospital , Zhejiang University , Hangzhou , Zhejiang Province , China.
Xiangyi Zhenga Department of Urology, First Affiliated Hospital , Zhejiang University , Hangzhou , Zhejiang Province , China.
First Affiliated Hospital Zhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Emerging research has suggested that miRNAs play a significant role in oncogenesis and tumor progression by regulating multiple molecular pathways. Here, we investigated miR-300, which inhibited bladder cancer (BCa) migration by regulating the SP1/MMP9 pathway. miR-300, belonging to the DLK1-DIO3 miRNA cluster, is frequently expressed at lower levels in BCa tissue than in adjacent normal tissue due to DNA methylation. Reinforced expression of miR-300 significantly suppressed the migration of BCa cells. We carried out a search of online databases to predict potential targets of miR-300. Further studies determined that miR-300 directly targeted SP1 and suppressed its expression by specifically binding to its 3'-untranslated region. Meanwhile, downregulated MMP9 may be the final effector of BCa cell mobility. Small interference RNAs silencing SP1 phenocopied the effects of miR-300 overexpression, while restoration of SP1 expression partially rescued the inhibition of metastasis induced by miR-300 overexpression in BCa cells. In conclusion, we unveiled a miR-300/SP1/MMP9 pathway in BCa. These findings demonstrate that miR-300 is a promising tumor suppressor in BCa.

Indexed as

3' Untranslated RegionsAntagomirsCalcium-Binding ProteinsCell Line, TumorCell MovementHumansIntercellular Signaling Peptides and ProteinsKaplan-Meier EstimateMatrix Metalloproteinase 9Membrane ProteinsMicroRNAsRNA InterferenceRNA, Small InterferingSp1 Transcription FactorUrinary Bladder Neoplasms3' Untranslated RegionsAntagomirsCalcium-Binding ProteinsDLK1 protein, humanIntercellular Signaling Peptides and ProteinsMatrix Metalloproteinase 9Membrane ProteinsMicroRNAsMIRN300 microRNA, humanMMP9 protein, humanRNA, Small InterferingSp1 Transcription Factormatrix metalloproteinasemigrationmiRNA

Identifiers

PMID30526300
PMCPMC6343712
OpenAlexW2904127812

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.