Evidence map›Paper›PMID 33517899›Full record

ArticleWorld journal of surgical oncology2021

High GFPT1 expression predicts unfavorable outcomes in patients with resectable pancreatic ductal adenocarcinoma.

Yitao Gong, Yunzhen Qian, Guopei Luo, Yu Liu, Ruijie Wang, Shengming Deng, He Cheng, Kaizhou Jin, Quanxing Ni, Xianjun Yu and 2 more

Open access · goldAbstract read
In one paragraph

Article in World journal of surgical oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

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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

12 authors at 3 institutions in 1 country.

Yitao Gong *Department of Pancreatic Surgery, Fudan University Shanghai Cancer Center, No.270 DongAn Road, Shanghai, 200032, China.
Yunzhen Qian *Department of Pancreatic Surgery, Fudan University Shanghai Cancer Center, No.270 DongAn Road, Shanghai, 200032, China.
Guopei Luo *Department of Pancreatic Surgery, Fudan University Shanghai Cancer Center, No.270 DongAn Road, Shanghai, 200032, China.
Yu LiuDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, No.270 DongAn Road, Shanghai, 200032, China.
Ruijie WangDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, No.270 DongAn Road, Shanghai, 200032, China.
Shengming DengDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, No.270 DongAn Road, Shanghai, 200032, China.
He ChengDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, No.270 DongAn Road, Shanghai, 200032, China.
Kaizhou JinDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, No.270 DongAn Road, Shanghai, 200032, China.
Quanxing NiDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, No.270 DongAn Road, Shanghai, 200032, China.
Xianjun YuDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, No.270 DongAn Road, Shanghai, 200032, China.
Weiding WuDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, No.270 DongAn Road, Shanghai, 200032, China. weidingwu@126.com.
Chen LiuDepartment of Pancreatic Surgery, Fudan University Shanghai Cancer Center, No.270 DongAn Road, Shanghai, 200032, China. liuchen@fudanpci.org.
Shanghai Medical College of Fudan University · CNShanghai Cancer Institute · CNFudan University Shanghai Cancer Center · CN

Funding

Clinical and Scientific Innovation Project of Shanghai Hospital Development Center SHDC12018109Clinical Research Plan of Shanghai Hospital Development Center SHDC2020CR1006AFudan University Personalized Project for "Double Top" Original Research XM03190633National Natural Science Foundation of China 82072693, 81625016, 81871940, 81902417Scientific Innovation Project of Shanghai Education Committee 2019-01-07-00-07-E00057Shanghai Cancer Center Foundation for Distinguished Young Scholars YJJQ201803
6 · The paper itself

Abstract

backgroundGlutamine-fructose-6-phosphate transaminase 1 (GFPT1) is the first rate-limiting enzyme of the hexosamine biosynthesis pathway (HBP), which plays a pivotal role in the progression of pancreatic ductal adenocarcinoma (PDAC). Therefore, we investigated the prognostic significance of GFPT1 expression in patients with resectable PDAC.

methodsWe analyzed public datasets to compare GFPT1 expression in tumor tissues and normal/adjacent pancreatic tissues. We measured the relative GFPT1 expression of 134 resected PDAC specimens in our institution, using real-time polymerase chain reaction (PCR). Survival was compared between high and low GFPT1 expression groups using Kaplan-Meier curves and log-rank tests. Multivariate analyses were estimated using Cox regression and logistic regression models.

resultsGFPT1 is generally upregulated in PDAC tissues, according to the analysis of public datasets. The data from our institution shows that high GFPT1 expression was correlated with a high rate of lymph node (LN) metastasis (p = 0.038) and was an independent risk factor for LN metastasis (odds ratio (OR) = 3.14, 95% confidence interval (CI) = 1.42 to 6.90, P = 0.005). High GFPT1 expression was significantly associated with poor overall survival (OS; P = 0.019) in patients with resected PDAC. The multivariable-adjusted hazard ratio (HR) for mortality when comparing patients with high and low GFPT1 expression was 2.54 (95% CI = 1.35 to 4.79, P = 0.004).

conclusionsGFPT1 is generally upregulated in PDAC tissue and is associated with a high risk of LN metastasis and an unfavorable outcome in patients with resectable PDAC, suggesting its crucial role in PDAC progression.

Indexed as

AdenocarcinomaCarcinoma, Pancreatic DuctalPancreatic NeoplasmsBiomarkers, TumorGlutamine-Fructose-6-Phosphate Transaminase (Isomerizing)HumansPancreasPrognosisBiomarkers, TumorGFPT1 protein, humanGlutamine-Fructose-6-Phosphate Transaminase (Isomerizing)Glutamine-fructose-6-phosphate transaminase 1Hexosamine biosynthesis pathway (HBP)PrognosisSurvival

Identifiers

PMID33517899
PMCPMC7849098
OpenAlexW3126650285

What OpenQuestion holds

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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.