Evidence map›Paper›PMID 30095171›Full record

ArticleThe Prostate2018

Overexpression of MCM10 promotes cell proliferation and predicts poor prognosis in prostate cancer.

Feilun Cui, Jianpeng Hu, Songyi Ning, Jian Tan, Huaming Tang

Open access · hybridAbstract read
In one paragraph

Article in The Prostate, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

33 citing papers in PubMed, 45 citations in OpenAlex.

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  7. Pan-cancer analysis of telomere maintenance mechanisms.The Journal of biological chemistry · 2024
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  9. Activation of Glycolysis by MCM10 Increases Stemness and Paclitaxel Resistance in Gastric Cancer Cells.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2023
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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

5 authors at 1 institution in 1 country.

Feilun CuiDepartment of Urology, The Affiliated People's Hospital of Jiangsu University, Zhenjiang, Jiangsu, P.R. China.
Jianpeng HuDepartment of Urology, The Affiliated People's Hospital of Jiangsu University, Zhenjiang, Jiangsu, P.R. China.ORCID 0000-0002-6511-6448
Songyi NingMedical College of Jiangsu University, Zhenjiang, Jiangsu, P.R. China.
Jian TanDepartment of Urology, The Affiliated People's Hospital of Jiangsu University, Zhenjiang, Jiangsu, P.R. China.
Huaming TangDepartment of Urology, The Affiliated People's Hospital of Jiangsu University, Zhenjiang, Jiangsu, P.R. China.
Jiangsu University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProstate cancer (PCa) is one of the most malignant tumors of the male urogenital system. There is an urgent need to identify novel biomarkers for PCa.

methodsIn this study, we evaluated the expression levels of MCM10 in prostate cancer by analyzing public datasets (including The Cancer Genome Atlas and GSE21032). Furthermore, loss of function assays was performed to evaluate the effects of MCM10 on cell proliferation, apoptosis, and colony formation. Furthermore, we performed microarray and bioinformatics analyses to explore the potential mechanisms of MCM10.

resultsIn the present study, we for the first time revealed MCM10 was significantly upregulated in PCa. Moreover, we found increased MCM10 expression was significantly associated with advanced clinical stage and high Gleason score PCa. Kaplan-Meier analysis demonstrated higher MCM10 expression was associated with a poorer patient prognosis in PCa. Furthermore, loss of function assays showed that MCM10 knockdown inhibited cell proliferation and colony formation, but promoted cell apoptosis. Additionally, we performed microarray and bioinformatics analysis and found MCM10 regulated PCa progression by regulating a series of biological processes including cancer, cell death, and apoptosis.

conclusionsThese results suggest that MCM10 may be a potential diagnostic and therapeutic target for PCa.

Indexed as

Gene Expression Regulation, NeoplasticApoptosisCell ProliferationDatabases, FactualDisease-Free SurvivalDisease ProgressionHumansMaleMinichromosome Maintenance ProteinsNeoplasm GradingPrognosisProstatic NeoplasmsSurvival RateMCM10 protein, humanMinichromosome Maintenance ProteinsMCM10prognosisproliferationprostate cancersurvival

Identifiers

PMID30095171
PMCPMC6282949
OpenAlexW2886934235

What OpenQuestion holds

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LicenceCC BY-NC
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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.