Evidence map›Paper›PMID 30348936›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2018

High Expression of PTPN3 Predicts Progression and Unfavorable Prognosis of Glioblastoma.

Yu Wang, Yan Su, Zhiling Ji, Zhonghua Lv

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Frontiers in immunology · 2022
    Article
  3. Review
  4. Comprehensive analysis ofFrontiers in genetics · 2022
    Article
  5. Article
  6. Tivantinib Hampers the Proliferation of Glioblastoma Cells via PI3K/Akt/Mammalian Target of Rapamycin (mTOR) Signaling.Medical science monitor : international medical journal of experimental and clinical research · 2019
    Article
  7. Identification of SEC61G as a Novel Prognostic Marker for Predicting Survival and Response to Therapies in Patients with Glioblastoma.Medical science monitor : international medical journal of experimental and clinical research · 2019
    Article
  8. 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

4 authors at 2 institutions in 1 country.

Yu WangDepartment of Cardiology, Yidu Central Hospital of Qingzhou, Weifang, Shandong, China (mainland).
Yan SuDepartment of Intensive Care, Yidu Central Hospital of Qingzhou, Weifang, Shandong, China (mainland).
Zhiling JiDepartment of Neurology, Yidu Central Hospital of Qingzhou, Weifang, Shandong, China (mainland).
Zhonghua LvDepartment of Neurosurgery, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China (mainland).
Yidu Central Hospital of Weifang · CNHarbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND PTPN3 was demonstrated to be involved in the progression of several types of cancers, such as gastric adenocarcinoma, lung cancer, and intrahepatic cholangiocarcinoma. However, its clinical significance in glioblastoma (GBM) has not been elucidated. MATERIAL AND METHODS We investigated the expression of PTPN3 in 95 cases of GBM with immunohistochemistry and in 8 pairs of fresh GBMs and their adjacent tissues with qualitative polymerase chain reaction. Moreover, the correlation between PTPN3 and clinicopathological factors was evaluated by chi-square test. The prognostic value of PTPN3 was investigated with univariate analysis and multivariate analysis. With MTT assay and Transwell assay, the oncogenic functions of PTPN3 in GBM proliferation and invasion were further investigated. RESULTS Expression of PTPN3 in GBM tissues was significantly higher than in their corresponding adjacent tissues. High expression of PTPN3 was significantly associated with unfavorable prognosis of GBM. Moreover, in GBM cell lines, PTPN3 promoted cell proliferation and invasion, and the PTP common inhibitor pervanadate suppressed GBM proliferation and invasion. CONCLUSIONS Our experiments show that PTPN3 is an independent prognostic factor in GBM and indicated that postoperative detection of PTPN3 can be used to identify high-risk patients and guide individual treatment.

Indexed as

AdultAgedBrain NeoplasmsCell Line, TumorCell ProliferationDisease ProgressionFemaleGlioblastomaHumansImmunohistochemistryKaplan-Meier EstimateMaleMiddle AgedPrognosisProtein Tyrosine Phosphatase, Non-Receptor Type 3RNA InterferenceProtein Tyrosine Phosphatase, Non-Receptor Type 3PTPN3 protein, human

Identifiers

PMID30348936
PMCPMC6354633
OpenAlexW2895997476

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.