Evidence map›Paper›PMID 31338708›Full record

ArticleHuman cell2019

The clinical and prognostic significance of paraoxonase-2 in gastric cancer patients: immunohistochemical analysis.

Xiaohua Wang, Guifang Xu, Jingyuan Zhang, Shuaiyu Wang, Min Ji, Lei Mo, Mengxia Zhu, Jun Li, Guoren Zhou, Jianwei Lu and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Human cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.0field-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

17 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  14. Article
  15. Human Paraoxonase-2 (PON2): Protein Functions and Modulation.Antioxidants (Basel, Switzerland) · 2021
    Review
  16. Article
  17. Article
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 4 institutions in 1 country.

Xiaohua Wang *Department of Oncology, Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research & The Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, 210009, Jiangsu, China.
Guifang Xu *Department of Gastroenterology, Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, 210008, Jiangsu, China.
Jingyuan Zhang *Department of Pathology, Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research & The Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, 210009, Jiangsu, China.
Shuaiyu WangDepartment of Pharmacy, China Pharmaceutical University, Nanjing, 210029, Jiangsu, China.
Min JiDepartment of Clinical Medicine, Nanjing Medical University, Nanjing, 210029, Jiangsu, China.
Lei MoDepartment of Clinical Medicine, Nanjing Medical University, Nanjing, 210029, Jiangsu, China.
Mengxia ZhuDepartment of Clinical Medicine, Nanjing Medical University, Nanjing, 210029, Jiangsu, China.
Jun LiDepartment of Clinical Medicine, Nanjing Medical University, Nanjing, 210029, Jiangsu, China.
Guoren ZhouDepartment of Oncology, Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research & The Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, 210009, Jiangsu, China. groupeight@163.com.
Jianwei LuDepartment of Oncology, Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research & The Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, 210009, Jiangsu, China. jsszhope@163.com.
Cheng ChenDepartment of Radiotherapy, Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research & The Affiliated Cancer Hospital of Nanjing Medical University, No. 42 Baiziting Road, Nanjing, 210009, Jiangsu, China. chencheng_nj@126.com.
Nanjing Medical University · CNChina Pharmaceutical University · CNJiangsu Cancer Hospital · CNNanjing Drum Tower Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Paraoxonase-2 (PON2) belongs to the paraoxonase (PON) protein family. Unlike paraoxonase-1 (PON1), the expression and significance of PON2 remained largely unknown in gastric cancer (GC). Thus, the purpose of our study was to investigate the role of PON2 in GC. First, we found PON2 expression was obviously increased in GC samples compared with paired normal tissue samples at The Cancer Genome Atlas (TCGA) database. Then the high expression status of PON2 mRNA and protein in GC tissues was confirmed by RT-qPCR and immunohistochemistry. Furthermore, we performed the immunohistochemical analysis to study the correlation between PON2 expression and clinicopathological parameters of GC patients, and found high PON2 expression had significantly positive association with diffuse type, clinical stage, tumor invasion, lymph node metastasis and distant metastasis in GC patients. Moreover, survival analysis suggested GC patients with high PON2 expression resulted in a remarkably shorter overall survival compared with GC patients with low PON2 expression, and high expression of PON2 acted as an unfavorable predictor for overall survival. The in vitro studies indicated that silencing of PON2 expression inhibited GC cell proliferation, migration and invasion. In conclusion, our findings give first evidence that PON2 serves as oncogene in GC.

Indexed as

OncogenesAryldialkylphosphataseCell Line, TumorCell MovementCell ProliferationFemaleGene ExpressionGene SilencingHumansImmunohistochemistryMaleMiddle AgedNeoplasm InvasivenessPrognosisStomach NeoplasmsSurvival RateAryldialkylphosphatasePON2 protein, humanBiomarkerGastric cancerParaoxonase-2PON2

Identifiers

PMID31338708
OpenAlexW2962676943

What OpenQuestion holds

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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.