Evidence map›Paper›PMID 24949429›Full record

ArticleBioMed research international2014

Coexpression of SFRP1 and WIF1 as a prognostic predictor of favorable outcomes in patients with colorectal carcinoma.

Shiyong Huang, XiaoMing Zhong, Jun Gao, Rongfeng Song, Hongyu Wu, Shuming Zi, Shijie Yang, Peng Du, Long Cui, Chun Yang and 1 more

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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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

11 authors at 5 institutions in 1 country.

Shiyong HuangDepartment of Anorectal Surgery and Colorectal Cancer Center, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, No. 1665 Kongjiang Road, Shanghai 200092, China.
XiaoMing ZhongDepartment of Tumor Radiotherapy and Chemotherapy, Jiangxi Tumor Hospital, Nanchang, China.
Jun GaoDepartment of Gastroenterology, Changhai Hospital, Second Military Medical University, Shanghai, China.
Rongfeng SongDepartment of Tumor Radiotherapy and Chemotherapy, Jiangxi Tumor Hospital, Nanchang, China.
Hongyu WuDepartment of Gastroenterology, Changhai Hospital, Second Military Medical University, Shanghai, China.
Shuming ZiDepartment of Anorectal Surgery and Colorectal Cancer Center, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, No. 1665 Kongjiang Road, Shanghai 200092, China.
Shijie YangDepartment of Anorectal Surgery and Colorectal Cancer Center, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, No. 1665 Kongjiang Road, Shanghai 200092, China.
Peng DuDepartment of Anorectal Surgery and Colorectal Cancer Center, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, No. 1665 Kongjiang Road, Shanghai 200092, China.
Long CuiDepartment of Anorectal Surgery and Colorectal Cancer Center, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, No. 1665 Kongjiang Road, Shanghai 200092, China.
Chun YangDepartment of Gastrointestinal Surgery, Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, Chengdu, Sichuan, China.
Zikang LiDepartment of Oncology, Ya'an People's Hospital, No. 358 Chenghou Road, Ya'an, Sichuan 610072, China.
XinHua Hospital · CNChanghai Hospital · CNJiangxi Provincial Cancer Hospital · CNShanghai Jiao Tong University · CNSichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal tumorigenesis is ascribed to the activity of Wnt signaling pathway in a ligand-independent manner mainly through APC and CTNNB1 gene mutations and in a ligand-dependent manner through low expression of Wnt inhibitors such as WNT inhibitory factor 1 (WIF1) and secreted frizzled related protein 1 (SFRP1). In this study we found that WIF1 protein expression was increased and SFRP1 was decreased significantly in CRC tissue versus normal tissue, and high expression of WIF1 was associated with big tumor diameters and deep invasion, and loss of SFRP1 expression was associated with the left lesion site, deep invasion, and high TNM stage. Among the four expression patterns (WIF+/SFRP1+, WIF+/SFRP1-, WIF-/SFRP1+, and WIF-/SFRP1-) only coexpression of WIF1 and SFRP1 (WIF+/SFRP1+) was associated with favorable overall survival, together with low TNM stage, as an independent prognostic factor as shown in a multivariate survival model. The results indicated that WIF1 seemed to play an oncogenic role, while SFRP1 seemed to play an oncosuppressive role although both of them are secreted Wnt antagonists. Coexpression of SFRP1 and WIF1, rather than SFRP1 or WIF1 alone, could be used, together with low TNM stage, as a prognostic predictor of favorable outcomes in CRC.

Indexed as

PrognosisAdaptor Proteins, Signal TransducingAgedCarcinogenesisColorectal NeoplasmsDNA MethylationFemaleGene Expression Regulation, NeoplasticHumansIntercellular Signaling Peptides and ProteinsMaleMembrane ProteinsMiddle AgedRepressor ProteinsSecreted Frizzled-Related ProteinsSignal TransductionAdaptor Proteins, Signal TransducingIntercellular Signaling Peptides and ProteinsMembrane ProteinsRepressor ProteinsSecreted Frizzled-Related ProteinsSFRP1 protein, humanWIF1 protein, human

Identifiers

PMID24949429
PMCPMC4053147
OpenAlexW2162243281

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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.