Evidence map›Paper›PMID 28641312›Full record

ArticleBritish journal of cancer2017

Impact of novel miR-145-3p regulatory networks on survival in patients with castration-resistant prostate cancer.

Yusuke Goto, Akira Kurozumi, Takayuki Arai, Nijiro Nohata, Satoko Kojima, Atsushi Okato, Mayuko Kato, Kazuto Yamazaki, Yasuo Ishida, Yukio Naya and 2 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 2 pooled it
11.7field-weighted citation impact, top 1% 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

77 citing papers in PubMed, 2 syntheses or guidelines pooled it, 110 citations in OpenAlex.

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  13. Role and mechanism ofFrontiers in pharmacology · 2024
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17 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

12 authors at 3 institutions in 2 countries.

Yusuke GotoDepartment of Functional Genomics, Chiba University Graduate School of Medicine, Chiba, Japan.
Akira KurozumiDepartment of Functional Genomics, Chiba University Graduate School of Medicine, Chiba, Japan.
Takayuki AraiDepartment of Functional Genomics, Chiba University Graduate School of Medicine, Chiba, Japan.
Nijiro NohataMoores Cancer Center, University of California, San Diego, La Jolla, CA 92093, USA.
Satoko KojimaDepartment of Urology, Teikyo University Chiba Medical Center, Ichihara, Japan.
Atsushi OkatoDepartment of Functional Genomics, Chiba University Graduate School of Medicine, Chiba, Japan.
Mayuko KatoDepartment of Functional Genomics, Chiba University Graduate School of Medicine, Chiba, Japan.
Kazuto YamazakiDepartment of Pathology, Teikyo University Chiba Medical Center, Ichihara, Japan.
Yasuo IshidaDepartment of Pathology, Teikyo University Chiba Medical Center, Ichihara, Japan.
Yukio NayaDepartment of Urology, Teikyo University Chiba Medical Center, Ichihara, Japan.
Tomohiko IchikawaDepartment of Urology, Chiba University Graduate School of Medicine, Chiba, Japan.
Naohiko SekiDepartment of Functional Genomics, Chiba University Graduate School of Medicine, Chiba, Japan.
Chiba University · JPTeikyo University Chiba Medical Center · JPUniversity of California, San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite recent advancements, metastatic castration-resistant prostate cancer (CRPC) is not considered curative. Novel approaches for identification of therapeutic targets of CRPC are needed.

methodsNext-generation sequencing revealed 945-1248 miRNAs from each lethal mCRPC sample. We constructed miRNA expression signatures of CRPC by comparing the expression of miRNAs between CRPC and normal prostate tissue or hormone-sensitive prostate cancer (HSPC). Genome-wide gene expression studies and in silico analyses were carried out to predict miRNA regulation and investigate the functional significance and clinical utility of the novel oncogenic pathways regulated by these miRNAs in prostate cancer (PCa).

resultsBased on the novel miRNA expression signature of CRPC, miR-145-5p and miR-145-3p were downregulated in CRPC. By focusing on miR-145-3p, which is a passenger strand and has not been well studied in previous reports, we showed that miR-145-3p targeted 4 key molecules, i.e., MELK, NCAPG, BUB1, and CDK1, in CPRC. These 4 genes significantly predicted survival in patients with PCa.

conclusionsSmall RNA sequencing for lethal CRPC and in silico analyses provided novel therapeutic targets for CRPC.

Indexed as

Gene Expression Regulation, NeoplasticArgonaute ProteinsCDC2 Protein KinaseCell Cycle ProteinsCell Line, TumorComputer SimulationCyclin-Dependent KinasesDisease-Free SurvivalDown-RegulationGene ExpressionGenome-Wide Association StudyHumansLymphatic MetastasisMaleMicroRNAsMiddle AgedAGO2 protein, humanArgonaute ProteinsBUB1 protein, humanCDC2 Protein KinaseCDK1 protein, humanCell Cycle ProteinsCyclin-Dependent KinasesMELK protein, humanMicroRNAsMIRN145 microRNA, humanNCAPG protein, humanProtein Serine-Threonine KinasesRNA-Induced Silencing Complex

Identifiers

PMID28641312
PMCPMC5537499
OpenAlexW2627977620

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.