Evidence map›Paper›PMID 25645394›Full record

ArticleMolecular cancer2015

A molecular signature for the prediction of recurrence in colorectal cancer.

Lisha Wang, Xiaohan Shen, Zhimin Wang, Xiuying Xiao, Ping Wei, Qifeng Wang, Fei Ren, Yiqin Wang, Zebing Liu, Weiqi Sheng and 3 more

Abstract read
In one paragraph

Article in Molecular cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

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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

13 authors.

Lisha WangDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China. lishawang9@163.com.
Xiaohan ShenDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China. 21326217@qq.com.
Zhimin WangDepartment of Genetics, Shanghai-MOST Key Laboratory of Health and Disease Genomics, Chinese National Human Genome Center and Shanghai Industrial Technology Institute, Shanghai, 201203, China. wangzhm@chgc.sh.cn.
Xiuying XiaoDepartment of Oncology, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, 200127, China. xiaoxiuying2002@163.com.
Ping WeiDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China. ripplepz@gmail.com.
Qifeng WangDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China. wangqifeng19821982@126.com.
Fei RenDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China. renfei0319@163.com.
Yiqin WangDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China. yiqinwang11@fudan.edu.cn.
Zebing LiuDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China. zebing080@163.com.
Weiqi ShengDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China. shengweiqi2006@163.com.
Wei HuangDepartment of Genetics, Shanghai-MOST Key Laboratory of Health and Disease Genomics, Chinese National Human Genome Center and Shanghai Industrial Technology Institute, Shanghai, 201203, China. huangwei@chgc.sh.cn.
Xiaoyan ZhouDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China. 13524324387@163.com.
Xiang DuDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China. dx2008cn@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSeveral clinical and pathological factors have an impact on the prognosis of colorectal cancer (CRC), but they are not yet adequate for risk assessment. We aimed to identify a molecular signature that can reliably identify CRC patients at high risk for recurrence.

resultsTwo hundred eighty-one CRC samples (stage II/III) were included in this study. A two-step gene expression profiling study was conducted. First, gene expression measurements from 81 fresh frozen CRC samples were obtained using Affymetrix Human Genome U133 Plus 2.0 Arrays. Second, a focused gene expression assay, including prognostic genes and genes of interest from literature reviews, was performed using 200 fresh frozen samples and a Taqman low-density array (TLDA) analysis. An optimal 31-gene expression classifier for the prediction of recurrence among patients with stage II/III CRC was developed using logistic regression analysis. This gene expression signature classified 58.5% of patients as low-risk and 41.5% as high-risk (P < 0.001). The signature was the strongest independent prognostic factor in the multivariate analysis. The five-year relapse-free survival (RFS) rates for the low-risk patients and the high-risk patients were 88.5% and 41.3% (P < 0.001), respectively.

conclusionWe identified a 31-gene expression signature that is closely associated with the clinical outcome of stage II/III CRC patients.

Indexed as

AdultAgedColorectal NeoplasmsDisease-Free SurvivalFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedMultivariate AnalysisNeoplasm Recurrence, LocalNeoplasm StagingPrognosisProspective StudiesRiskTranscriptome

Identifiers

PMID25645394
PMCPMC4320628

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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.