Evidence map›Paper›PMID 34318435›Full record

ArticleMolecular biology reports2021

Identification of miRNA signatures and their therapeutic potentials in prostate cancer.

Abdullah Karadag, Ata Ozen, Mete Ozkurt, Cavit Can, Ibrahim Bozgeyik, Selda Kabadere, Ruhi Uyar

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular biology reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Role of miRNA-145, 148, and 185 and Stem Cells in Prostate Cancer.International journal of molecular sciences · 2022
    Review
  8. Review
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 2 institutions in 1 country.

Abdullah KaradagDepartment of Physiology, Faculty of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey. abdullahtbb63@gmail.com.ORCID http://orcid.org/0000-0003-3620-9589
Ata OzenDepartment of Urology, Faculty of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey.ORCID http://orcid.org/0000-0002-0890-486X
Mete OzkurtDepartment of Physiology, Faculty of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey.ORCID http://orcid.org/0000-0003-4000-2345
Cavit CanDepartment of Urology, Faculty of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey.ORCID http://orcid.org/0000-0003-2267-2759
Ibrahim BozgeyikDepartment of Medical Biology, Faculty of Medicine, Adiyaman University, Adiyaman, Turkey.ORCID http://orcid.org/0000-0003-1483-2580
Selda KabadereDepartment of Physiology, Faculty of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey.ORCID http://orcid.org/0000-0002-9589-0063
Ruhi UyarDepartment of Physiology, Faculty of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey.ORCID http://orcid.org/0000-0002-7608-7531
Eskişehir Osmangazi University · TRAdıyaman University · TR

Funding

Eskişehir Osmangazi Üniversitesi (TR) 2016-1228
6 · The paper itself

Abstract

backgroundHerein, we identified miRNA signatures that were able to differentiate malignant prostate cancer from benign prostate hyperplasia and revealed the therapeutic potential of these miRNAs against prostate cancer development. METHODS AND

resultsMicroRNA expressions were determined by qPCR. MTT was used for cell viability analysis and immunohistochemistry was performed for Bax/Bcl-2 staining. ELISA was used to measure MMP2/9 levels. Wound healing assay was used for the evaluation of cell migration. Notably, expression levels of miR-125b-5p, miR-145-5p and miR-221-3p were significantly reduced in prostate cancer patients as compared to BPH patients. Moreover, ectopic expression of miR-125b-5p, miR-145-5p and miR-221-3p resulted in significant inhibition of cell proliferation and altered cell morphology. Also, expression level of Bax protein was increased while Bcl-2 level was reduced in cells treated with miR-125b-5p, miR-145-5p and miR-221-3p mimics. Enhanced expression of miR-125b-5p, miR-145-5p and miR-221-3p was also significantly altered the expression of caspase 3 and 8 levels. In addition, MMP9 levels were significantly reduced in cells ectopically expressing miR-221-3p. All miRNA mimics significantly interfered with the migration of prostate cancer cells.

conclusionsConsequently, our findings point to an important role of these three miRNAs in prostate cancer and indicate that miR-125b-5p, miR-145-5p and miR-221-3p are potential therapeutic targets against prostate cancer.

Indexed as

Gene Expression ProfilingGene Expression Regulation, NeoplasticTranscriptomeAgedBiomarkers, TumorCell Line, TumorCirculating MicroRNAComputational BiologyDisease ManagementDisease SusceptibilityEnzyme-Linked Immunosorbent AssayHumansMaleMicroRNAsMiddle AgedNeoplasm MetastasisBiomarkers, TumorCirculating MicroRNAMicroRNAsBPHmiR-125b-5pmiR-145-5pmiR-221-3pmiRNAProstate cancer

Identifiers

PMID34318435
OpenAlexW3183396903

What OpenQuestion holds

Textmetadata
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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.