Evidence map›Paper›PMID 30126387›Full record

ArticleBMC cancer2018

Expression of oxidized protein tyrosine phosphatase and γH2AX predicts poor survival of gastric carcinoma patients.

Usama Khamis Hussein, Ho Sung Park, Jun Sang Bae, Kyoung Min Kim, Yun Jo Chong, Chan Young Kim, Keun Sang Kwon, Myoung Ja Chung, Ho Lee, Myoung Jae Kang and 2 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Expression of DNA Damage Response Markers in Early-Onset or Familial Gastric CancersAsian Pacific journal of cancer prevention : APJCP · 2019
    Article
  4. 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

12 authors at 3 institutions in 2 countries.

Usama Khamis HusseinDepartment of Pathology, Chonbuk National University Medical School, Research Institute of Clinical Medicine of Chonbuk, National University-Biomedical Research Institute of Chonbuk National University Hospital, Jeonju, Republic of Korea.
Ho Sung ParkDepartment of Pathology, Chonbuk National University Medical School, Research Institute of Clinical Medicine of Chonbuk, National University-Biomedical Research Institute of Chonbuk National University Hospital, Jeonju, Republic of Korea.
Jun Sang BaeDepartment of Pathology, Chonbuk National University Medical School, Research Institute of Clinical Medicine of Chonbuk, National University-Biomedical Research Institute of Chonbuk National University Hospital, Jeonju, Republic of Korea.
Kyoung Min KimDepartment of Pathology, Chonbuk National University Medical School, Research Institute of Clinical Medicine of Chonbuk, National University-Biomedical Research Institute of Chonbuk National University Hospital, Jeonju, Republic of Korea.
Yun Jo ChongCenter for University-wide Research Facilities, Chonbuk National University, Jeonju, Republic of Korea.
Chan Young KimDepartment of Surgery, Chonbuk National University Medical School, Jeonju, Republic of Korea.
Keun Sang KwonDepartment of Preventive Medicine, Chonbuk National University Medical School, Jeonju, Republic of Korea.
Myoung Ja ChungDepartment of Pathology, Chonbuk National University Medical School, Research Institute of Clinical Medicine of Chonbuk, National University-Biomedical Research Institute of Chonbuk National University Hospital, Jeonju, Republic of Korea.
Ho LeeDepartment of Forensic Medicine, Chonbuk National University Medical School, Jeonju, Republic of Korea.
Myoung Jae KangDepartment of Pathology, Chonbuk National University Medical School, Research Institute of Clinical Medicine of Chonbuk, National University-Biomedical Research Institute of Chonbuk National University Hospital, Jeonju, Republic of Korea.
Woo Sung MoonDepartment of Pathology, Chonbuk National University Medical School, Research Institute of Clinical Medicine of Chonbuk, National University-Biomedical Research Institute of Chonbuk National University Hospital, Jeonju, Republic of Korea.
Kyu Yun JangDepartment of Pathology, Chonbuk National University Medical School, Research Institute of Clinical Medicine of Chonbuk, National University-Biomedical Research Institute of Chonbuk National University Hospital, Jeonju, Republic of Korea. kyjang@chonbuk.ac.kr.ORCID http://orcid.org/0000-0002-5276-4446
Jeonbuk National University Hospital · KRJeonbuk National University · KRBeni-Suef University · EG

Funding

National Research Foundation of Korea 2017R1A2B2005730National Research Foundation of Korea NRF-2017K2A9A1A09062912
6 · The paper itself

Abstract

backgroundOxidative stress induces various intracellular damage, which might be correlated with tumorigenesis. Accumulated oxidative stresses might inactivate protein tyrosine phosphatase (PTP) by oxidizing it, and inducing the phosphorylation of H2AX (γH2AX) in response to DNA damage.

methodsWe evaluated the clinical significance of the expression of oxidized-PTP and γH2AX in 169 gastric carcinomas.

resultsImmunohistochemical expression of nuclear oxidized-PTP, cytoplasmic oxidized-PTP, and γH2AX expression were significantly associated with each other, and their expressions predicted shorter survival of gastric carcinoma patients. In multivariate analysis, nuclear oxidized-PTP (overall survival; p <  0.001, relapse-free survival; P <  0.001) was an independent indicator of poor prognosis of gastric carcinoma patients. In addition, co-expression patterns of nuclear oxidized-PTP and γH2AX were independent indicators of poor prognosis of gastric carcinoma patients (overall survival; P <  0.001, relapse-free survival; P <  0.001).

conclusionsThis study suggests that oxidative stress-mediated oxidation of PTP might be involved in the progression of gastric carcinomas. In addition, this study suggests that individual and co-expression pattern of nuclear oxidized-PTP and γH2AX might be used as a prognostic marker of gastric carcinomas.

Indexed as

AdultAgedCarcinogenesisCarcinomaDisease-Free SurvivalDisease ProgressionDNA DamageFemaleGene Expression Regulation, NeoplasticHistonesHumansMaleMiddle AgedOxidative StressPrognosisProtein Tyrosine PhosphatasesH2AX protein, humanHistonesProtein Tyrosine PhosphatasesCarcinomaOxidative stressProtein tyrosine phosphataseStomachγH2AX

Identifiers

PMID30126387
PMCPMC6102926
OpenAlexW2888133647

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.