Evidence map›Paper›PMID 25403684›Full record

ArticleDiagnostic pathology2014

Partner of Sld five 3: a potential prognostic biomarker for colorectal cancer.

Xiaoli Sun, Wu Sui, Miaoling Huang, Yeli Wang, Yuanjie Xuan, Zaiqiu Wang

Open access · goldAbstract read
In one paragraph

Article in Diagnostic pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact, top 86% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. A novel prognostic biomarker:Translational cancer research · 2023
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  2. Identification ofTranslational cancer research · 2023
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  3. Review
  4. Bioinformatics Analysis Identifies a Novel Role ofCancer management and research · 2020
    Article
  5. Review
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

6 authors at 1 institution in 1 country.

Xiaoli SunDepartment of Laboratory, Yuhuangding Hospital, No. 20 Yuhuangding East Road, Yantai, 264000, Shandong, China. dr_xl_sun@126.com.
Wu SuiGeneral Surgery, Yuhuangding Hospital, No. 20 Yuhuangding East Road, Yantai, 264000, Shandong, China. wu_sui@yeah.net.
Miaoling HuangAnorectal Surgery, Yuhuangding Hospital, No. 20 Yuhuangding East Road, Yantai, 264000, Shandong, China. huang_ml@yeah.net.
Yeli WangAnorectal Surgery, Yuhuangding Hospital, No. 20 Yuhuangding East Road, Yantai, 264000, Shandong, China. doctor_wangyl@163.com.
Yuanjie XuanAnorectal Surgery, Yuhuangding Hospital, No. 20 Yuhuangding East Road, Yantai, 264000, Shandong, China. xuan_yuanjie@126.com.
Zaiqiu WangAnorectal Surgery, Yuhuangding Hospital, No. 20 Yuhuangding East Road, Yantai, 264000, Shandong, China. zaiqiu_wang@yeah.net.
Yuhuangding Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPartner of Sld five 3 (PSF3) is a member of the evolutionarily conserved heterotetrameric complex "Go-Ichi-Ni-San" (GINS), which consists of SLD5, PSF1, PSF2, and PSF3. Previous studies have suggested that some GINS complex members are upregulated in cancer, but the status of PSF3 expression in colorectal cancer has not been investigated.

methodsWe investigated the status of PSF3 expression in 137 consecutive resected colorectal caners by quantitative reverse-transcription polymerase chain reaction. Univariable and multivariable Cox regression analyses were performed to assess independent prognostic factors for overall survival in colorectal cancer.

resultsIn 137 restected colorectal cancer samples, median messenger RNA (mRNA) expression levels of PSF3 were significantly higher in tumor tissues (1.35 × 10(-3), range 2.88 × 10(-4) to 3.16 × 10(-2)) than in adjacent normal tissues (2.94 × 10(-4), range 5.48 × 10(-5) to 1.27 × 10(-3)) (P < 0.05). Moreover, high expression of PSF3 in tumor tissues was associated with shorter disease-free survival and overall survival. When analyzed with a Cox regression model, the PSF3 expression was an independent prognostic factor for overall survival. In addition, in patients with early stage (stage I and II) colorectal cancer, the overall survival rate of the high PSF3 expression group was significantly lower than that of the low PSF3 expression group (P < 0.001).

conclusionsThe PSF3 expression plays an important role in the progression of colorectal cancer and acts as a factor significantly affecting the prognosis of patients. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/13000_2014_217.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorChi-Square DistributionChromosomal Proteins, Non-HistoneColorectal NeoplasmsDisease-Free SurvivalFemaleGene Expression Regulation, NeoplasticHumansKaplan-Meier EstimateMaleMiddle AgedMultivariate AnalysisNeoplasm StagingBiomarkers, TumorChromosomal Proteins, Non-HistoneGINS3 protein, humanRNA, Messenger

Identifiers

PMID25403684
PMCPMC4244056
OpenAlexW2120994349

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LicenceCC BY
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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.