Evidence map›Paper›PMID 21203532›Full record

ArticlePloS one2010

Identification of C16orf74 as a marker of progression in primary non-muscle invasive bladder cancer.

Won Tae Kim, Seok Joong Yun, Cheol Park, Isaac Yi Kim, Sung-Kwon Moon, Tae Gyun Kwon, Yung Hyun Choi, Wun-Jae Kim

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 28% 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

7 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  5. Article
  6. Upregulated MiR-1269 in hepatocellular carcinoma and its clinical significance.International journal of clinical and experimental medicine · 2015
    Article
  7. Aberrant methylation of CDH13 is a potential biomarker for predicting the recurrence and progression of non muscle invasive bladder cancer.Medical science monitor : international medical journal of experimental and clinical research · 2014
    Article
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 3 institutions in 2 countries.

Won Tae KimDepartment of Urology, College of Medicine, Chungbuk National University, Cheongju, Republic of Korea.
Seok Joong Yun
Cheol Park
Isaac Yi Kim
Sung-Kwon Moon
Tae Gyun Kwon
Yung Hyun Choi
Wun-Jae Kim
Chungbuk National University · KRKorea National University of Transportation · KRDong-Eui University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeMethylation-induced silencing of PRSS3 has been shown to be significantly associated with invasive bladder cancer, and expression of the C16orf74 gene locus has been shown to correlate positively with PRSS3. The aim of the current study was to evaluate the relationship between C16orf74 expression level and progression in non-muscle invasive bladder cancer (NMIBC). MATERIALS AND

methodsC16orf74 mRNA levels were examined by real-time reverse transcriptase polymerase chain reaction (RT-PCR) analysis of 193 tumor specimens from patients with primary NMIBC. Expression data were analyzed in terms of clinical and experimental parameters. Kaplan-Meier curves and multivariate Cox regression models, respectively, were used to determine progression-free survival and to identify independent predictive parameters of progression.

resultsAnalysis using Kaplan-Meier curves revealed prolonged progression-free survival of high-C16orf74-expressors as compared to low-expressors (p<0.001). Multivariate Cox regression analysis revealed that low C16orf74 mRNA expression levels are a significant risk factor for disease progression in patients with primary NMIBC (HR: 10.042, CI:2.699-37.360, p = 0.001).

conclusionsDecreased expression of C16orf74 correlates significantly with progression in primary NMIBC. C16orf74 expression level represents a potentially useful marker for predicting progression in primary NMIBC patients.

Indexed as

Gene Expression Regulation, NeoplasticAdultAgedBiomarkers, TumorCarcinoma in SituDisease ProgressionDNA, ComplementaryFemaleHumansMaleMiddle AgedNeoplasm InvasivenessProportional Hazards ModelsReverse Transcriptase Polymerase Chain ReactionRisk FactorsROC CurveBiomarkers, TumorDNA, Complementary

Identifiers

PMID21203532
PMCPMC3006390
OpenAlexW2010855588

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.