Evidence map›Paper›PMID 25922553›Full record

ArticleDisease markers2015

Overexpression of FRAT1 is associated with malignant phenotype and poor prognosis in human gliomas.

Geng Guo, Cheng-liang Zhong, Yang Liu, Xing-gang Mao, Zheng Zhang, Ji Jin, Jing Liu, Liu Yang, Jin-ming Mao, Yu-hong Guo and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Disease markers, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
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  5. Article
  6. Regulation of GSK3 cellular location by FRAT modulates mTORC1-dependent cell growth and sensitivity to rapamycin.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
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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 6 institutions in 1 country.

Geng GuoDepartment of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing 100050, China ; Department of Neurosurgery, The First Hospital, Shanxi Medical University, Taiyuan, Shanxi 030001, China.
Cheng-liang ZhongGCP Center, The First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin 300192, China ; Postdoctoral Programme, China Academy of Chinese Medical Sciences, Beijing 100700, China.
Yang LiuDepartment of Neurosurgery, The Third Hospital of Mianyang, Mianyang, Sichuan 621000, China.
Xing-gang MaoDepartment of Neurosurgery, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710032, China.
Zheng ZhangDepartment of Neurology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325000, China.
Ji JinShanxi Medical University, Taiyuan, Shanxi 030001, China.
Jing LiuDepartment of Neurosurgery, The First Hospital, Shanxi Medical University, Taiyuan, Shanxi 030001, China.
Liu YangDepartment of Neurology, The First Hospital, Shanxi Medical University, Taiyuan, Shanxi 030001, China.
Jin-ming MaoDepartment of Neurology, The First Hospital, Shanxi Medical University, Taiyuan, Shanxi 030001, China.
Yu-hong GuoDepartment of Neurosurgery, The First Hospital, Shanxi Medical University, Taiyuan, Shanxi 030001, China.
Yuan-li ZhaoDepartment of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing 100050, China.
Shanxi Medical University · CNCapital Medical University · CNMianyang Third People's Hospital · CNTianjin University of Traditional Chinese Medicine · CNWenzhou Medical University · CNXijing Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioma is the most common malignancy of the central nervous system. Approximately 40 percent of intracranial tumors are diagnosed as gliomas. Difficulties in treatment are associated closely with the malignant phenotype, which is characterized by excessive proliferation, relentless invasion, and angiogenesis. Although the comprehensive treatment level of brain glioma is continuously progressing, the outcome of this malignancy has not been improved drastically. Therefore, the identification of new biomarkers for diagnosis and therapy of this malignancy is of significant scientific and clinical value. FRAT1 is a positive regulator of the Wnt/β-catenin signaling pathway and is overexpressed in many human tumors. In the present study, we investigated the expression status of FRAT1 in 68 patients with human gliomas and its correlation with the pathologic grade, proliferation, invasion, angiogenesis, and prognostic significance. These findings suggest that FRAT1 may be an important factor in the tumorigenesis and progression of glioma and could be explored as a potential biomarker for pathological diagnosis, an indicator for prognosis, and a target for biological therapy of malignancy.

Indexed as

Adaptor Proteins, Signal TransducingAdolescentAdultAgedBiomarkers, TumorBrain NeoplasmsCase-Control StudiesChildFemaleGene Expression Regulation, NeoplasticGliomaHumansIntracellular Signaling Peptides and ProteinsMaleMiddle AgedProto-Oncogene ProteinsAdaptor Proteins, Signal TransducingBiomarkers, TumorFRAT1 protein, humanIntracellular Signaling Peptides and ProteinsProto-Oncogene Proteins

Identifiers

PMID25922553
PMCPMC4398933
OpenAlexW2047575155

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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.