Evidence map›Paper›PMID 31305441›Full record

ArticleMedicine2019

The clinical significance of PYCR1 expression in renal cell carcinoma.

Fu Weijin, Xie Zhibin, Zheng Shengfeng, Yang Xiaoli, Ding Qijian, Liu Jiayi, Liang Qiumei, Chen Yilong, Mi Hua, Liu Deyun and 1 more

Open access · goldAbstract read
In one paragraph

Article in Medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
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  6. Novel Fragment Inhibitors of PYCR1 from Docking-Guided X-ray Crystallography.Journal of chemical information and modeling · 2024
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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 2 institutions in 1 country.

Fu WeijinDepartment of Urology, The First Affiliated Hospital of GuangXi Medical University, NanNing.
Xie ZhibinDepartment of Urology, The First Affiliated Hospital of GuangXi Medical University, NanNing.
Zheng ShengfengDepartment of Urology, The First Affiliated Hospital of GuangXi Medical University, NanNing.
Yang XiaoliScientific Research Center, GuiLin Medical University, GuiLin.
Ding QijianDepartment of Urology, The First Affiliated Hospital of GuangXi Medical University, NanNing.
Liu JiayiDepartment of Pathology, The First Affiliated Hospital of Guang, Xi Medical University, NanNing, GuangXi, China.
Liang QiumeiDepartment of Urology, The First Affiliated Hospital of GuangXi Medical University, NanNing.
Chen YilongDepartment of Urology, The First Affiliated Hospital of GuangXi Medical University, NanNing.
Mi HuaDepartment of Urology, The First Affiliated Hospital of GuangXi Medical University, NanNing.
Liu DeyunDepartment of Urology, The First Affiliated Hospital of GuangXi Medical University, NanNing.
Cheng JiwenDepartment of Urology, The First Affiliated Hospital of GuangXi Medical University, NanNing.
First Affiliated Hospital of GuangXi Medical University · CNGuilin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pyrroline-5-carboxylate reductase 1 (PYCR1) is an enzyme involved in cell metabolism and is upregulated in cancer. However, the correlations of PYCR1 expression with the clinicopathological features and prognosis of renal cell carcinoma (RCC) remain unclear. The purpose of this study was to identify the expression of PYCR1 and its clinical relevance in RCC patients.PYCR1 mRNA expression differences between RCC and the adjacent normal renal tissues were assessed using the Cancer Genome Atlas database (TCGA). Subsequently, the expression of PYCR1 mRNA and protein were evaluated by quantitative real-time polymerase chain reaction, Western blot, and immunochemistry using 30 paired frozen samples of RCC and the adjacent normal renal tissues. The protein expression of PYCR1 was evaluated by immunostaining formalin-fixed, paraffin-embedded sections of RCC samples from 96 patients who underwent radical nephrectomy, and its relationship with clinical features were analyzed. Nonpaired t tests were used to statistically analyze the differences between the 2 groups. Cox univariable and multivariable analyses of overall survival (OS) among RCC patients were performed.The expression of PYCR1 mRNA was significantly upregulated in RCC tissues compared to adjacent normal renal tissues in the TCGA database (P < .01). The area under the receiver operating characteristic curve value was 0.748. The expression of PYCR1 mRNA and protein was significantly upregulated in RCC compared with that in paired normal renal tissues (P < .01). Higher PYCR1 levels were associated with metastasis (P < .01). Kaplan-Meier survival curves indicated that higher PYCR1 expression was correlated with poorer OS. Therefore, PYCR1 may act as a novel prognostic marker and therapeutic target in the diagnosis and treatment of RCC.

Indexed as

Biomarkers, TumorCarcinoma, Renal Celldelta-1-Pyrroline-5-Carboxylate ReductaseFemaleGene Expression Regulation, NeoplasticHumansKidneyKidney NeoplasmsMaleMiddle AgedPrognosisPyrroline Carboxylate ReductasesRNA, MessengerSurvival AnalysisBiomarkers, Tumordelta-1-Pyrroline-5-Carboxylate ReductasePyrroline Carboxylate ReductasesRNA, Messenger

Identifiers

PMID31305441
PMCPMC6641676
OpenAlexW2959164548

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.