Evidence map›Paper›PMID 30674952›Full record

ArticleScientific reports2019

MicroRNA 141 is associated to outcome and aggressive tumor characteristics in prostate cancer.

Elin Richardsen, Sigve Andersen, Christian Melbø-Jørgensen, Mehrdad Rakaee, Nora Ness, Samer Al-Saad, Yngve Nordby, Mona I Pedersen, Tom Dønnem, Roy M Bremnes and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 57 citations in OpenAlex.

  1. Pooled it
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  7. Article
  8. Article
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  11. The Role of MiRNA in Cancer: Pathogenesis, Diagnosis, and Treatment.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  12. Review
  13. Article
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  15. Article
  16. Article
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  19. Article
  20. Small RNAs, Big Diseases.International journal of molecular sciences · 2020
    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

11 authors at 3 institutions in 1 country.

Elin RichardsenTranslational Cancer Research Group, Institute of Medical Biology, UiT The Arctic University of Norway, 9037, Tromsø, Norway. elin-ri@live.no.
Sigve AndersenTranslational Cancer Research Group, Institute of Clinical Medicine, UiT The Arctic University of Norway, 9037, Tromsø, Norway.
Christian Melbø-JørgensenNORMENT, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Mehrdad RakaeeTranslational Cancer Research Group, Institute of Medical Biology, UiT The Arctic University of Norway, 9037, Tromsø, Norway.
Nora NessTranslational Cancer Research Group, Institute of Medical Biology, UiT The Arctic University of Norway, 9037, Tromsø, Norway.
Samer Al-SaadTranslational Cancer Research Group, Institute of Medical Biology, UiT The Arctic University of Norway, 9037, Tromsø, Norway.
Yngve NordbyTranslational Cancer Research Group, Institute of Clinical Medicine, UiT The Arctic University of Norway, 9037, Tromsø, Norway.ORCID 0000-0003-2237-4401
Mona I PedersenTranslational Cancer Research Group, Institute of Clinical Medicine, UiT The Arctic University of Norway, 9037, Tromsø, Norway.
Tom DønnemTranslational Cancer Research Group, Institute of Clinical Medicine, UiT The Arctic University of Norway, 9037, Tromsø, Norway.
Roy M BremnesTranslational Cancer Research Group, Institute of Clinical Medicine, UiT The Arctic University of Norway, 9037, Tromsø, Norway.
Lill-Tove BusundTranslational Cancer Research Group, Institute of Medical Biology, UiT The Arctic University of Norway, 9037, Tromsø, Norway.
University Hospital of North Norway · NOUiT The Arctic University of Norway · NOUniversity of Oslo · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A large number of miRNAs influence key cellular processes involved in prostate tumorigenesis. Previous studies have demonstrated high expression of miRNAs in human prostate cancer (PC) tissues and cell lines. In previous microarray data, we found miR-141 to be upregulated and miR-145 to be downregulated in PC. In this large PC cohort (n = 535), we explored the prognostic role of miR-141 and miR-145 in PC. Tumor epithelial (TE) and tumor stromal (TS) areas were evaluated separately and combined (TE + TS). In situ hybridization was used to evaluate the expression of the miRNAs. We found that miR-141 (TE) correlated significantly to Gleason score ≥8 (p = 0.040) and large tumor size (≥20 mm, p = 0.025) and miR-141 (TE + TS) to Gleason grade (p = 0.001). MiR-145 correlated to pT-stage (p = 0.038), tumor size (p = 0.025), Gleason grade (p = 0.051) and PSA (p = 0.032). In univariate analysis miR-141 (TE + TS) was significantly associated with biochemical failure-free survival (BFFS, p = 0.007) and clinical failure-free survival (CFFS, p = 0.021). For miR-145, there were no differences between patients with high versus low expression. In multivariate analysis overexpression of miR-141 in tumor epithelium and tumor stroma was significantly associated with BFFS (HR = 1.07 CI95% 1.00-1.14, p = 0.007). To conclude, high expression of miR-141 appears associated with increased risk of biochemical PC recurrence.

Indexed as

Gene Expression Regulation, NeoplasticUp-RegulationAgedDisease-Free SurvivalFollow-Up StudiesHumansMaleMicroRNAsMiddle AgedProstatic NeoplasmsRNA, NeoplasmSurvival RateMicroRNAsMIRN141 microRNA, humanRNA, Neoplasm

Identifiers

PMID30674952
PMCPMC6344505
OpenAlexW2913334316

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.