Evidence map›Paper›PMID 26917489›Full record

ArticleBMC cancer2016

Aberrant KDM5B expression promotes aggressive breast cancer through MALAT1 overexpression and downregulation of hsa-miR-448.

Oluwaseun Adebayo Bamodu, Wen-Chien Huang, Wei-Hwa Lee, Alexander Wu, Liang Shun Wang, Michael Hsiao, Chi-Tai Yeh, Tsu-Yi Chao

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 1 pooled it
6.5field-weighted citation impact, top 3% 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

73 citing papers in PubMed, 1 synthesis or guideline pooled it, 119 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
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  9. Role of microRNA in colorectal carcinoma (CRC): a narrative review.Annals of medicine and surgery (2012) · 2024
    Review
  10. Review
  11. Review
  12. Article
  13. Interplay between LncRNAs and microRNAs in Breast Cancer.International journal of molecular sciences · 2023
    Review
  14. Article
  15. Article
  16. Article
  17. Cancers · 2022
    Article
  18. Review
  19. Article
  20. Article

13 more citing papers are in PubMed but not listed here.

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

8 authors at 4 institutions in 1 country.

Oluwaseun Adebayo BamoduGraduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei City, Taiwan. dr_bamodu@yahoo.com.
Wen-Chien HuangDepartment of Thoracic Surgery, Mackay Memorial Hospital, Taipei, 10449, Taiwan. wjhuang0@yahoo.com.tw.
Wei-Hwa LeeDepartment of Pathology, Taipei Medical University-Shuang Ho Hospital, Taipei, Taiwan. whlpath97616@s.tmu.edu.tw.
Alexander WuGraduate Institute of Translational Medicine, Taipei Medical University, Taipei City, Taiwan. chaw1211@tmu.edu.tw.
Liang Shun WangGraduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei City, Taiwan. wangls72269@yahoo.com.tw.
Michael HsiaoGenomics Research Center, Academia Sinica, Taipei, Taiwan. mhsiao@gate.sinica.edu.tw.
Chi-Tai YehGraduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei City, Taiwan. ctyeh@s.tmu.edu.tw.
Tsu-Yi ChaoGraduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei City, Taiwan. j0607@ms6.hinet.net.
Taipei Medical University · TWTaipei Medical University-Shuang Ho Hospital · TWGenomics Research Center, Academia Sinica · TWMackay Memorial Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTriple negative breast cancers (TNBC) possess cell dedifferentiation characteristics, carry out activities connate to those of cancer stem cells (CSCs) and are associated with increased metastasis, as well as, poor clinical prognosis. The regulatory mechanism of this highly malignant phenotype is still poorly characterized. Accruing evidence support the role of non-coding RNAs (ncRNAs) as potent regulators of CSC and metastatic gene expression, with their dysregulation implicated in tumorigenesis and disease progression.

methodsIn this study, we investigated TNBC metastasis, metastasis-associated genes and potential inhibitory mechanisms using bioinformatics, tissue microarray analyses, immunoblotting, polymerase chain reaction, loss and gain of gene function assays and comparative analyses of data obtained.

resultsCompared with other breast cancer types, the highly metastatic MDA-MB-231 cells concurrently exhibited increased expression levels of Lysine-specific demethylase 5B protein (KDM5B) and long non-coding RNA (lncRNA), MALAT1, suggesting their functional association. KDM5B-silencing in the TNBC cells correlated with the upregulation of hsa-miR-448 and led to suppression of MALAT1 expression with decreased migration, invasion and clonogenic capacity in vitro, as well as, poor survival in vivo. This projects MALAT1 as a mediator of KDM5B oncogenic potential and highlights the critical role of this microRNA, lncRNA and histone demethylase in cancer cell motility and metastatic colonization. Increased expression of KDM5B correlating with disease progression and poor clinical outcome in breast cancer was reversed by hsa-miR-448.

conclusionsOur findings demonstrate the critical role of KDM5B and its negative regulator hsa-miR-448 in TNBC metastasis and progression. Hsa-miR-448 disrupting KDM5B-MALAT1 signalling axis and associated activities in TNBC cells, projects it as a putative therapeutic factor for selective eradication of TNBC cells. Graphical abstract KDM5B, MALAT1 and hsa-miR-448 are active looped components of the epigenetic poculo mortis in aggressive breast cancer.

Indexed as

Gene Expression Regulation, NeoplasticBase SequenceBreast NeoplasmsCell Line, TumorCell MovementCell ProliferationCell Transformation, NeoplasticCluster AnalysisDisease ProgressionFemaleGene Expression ProfilingGene Knockdown TechniquesGene SilencingHumansImmunohistochemistryJumonji Domain-Containing Histone DemethylasesJumonji Domain-Containing Histone DemethylasesKDM5B protein, humanMALAT1 long non-coding RNA, humanMicroRNAsMIRN448 microRNA, humanNuclear ProteinsRepressor ProteinsRNA, Long Noncoding

Identifiers

PMID26917489
PMCPMC4768424
OpenAlexW2278682036

What OpenQuestion holds

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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.