Evidence map›Paper›PMID 31868996›Full record

ArticleThe Kaohsiung journal of medical sciences2020

FKBP10 functioned as a cancer-promoting factor mediates cell proliferation, invasion, and migration via regulating PI3K signaling pathway in stomach adenocarcinoma.

Ruo-Gu Wang, Dan Zhang, Chun-Hong Zhao, Qi-Long Wang, Hui Qu, Qing-Si He

Open access · goldAbstract read
In one paragraph

Article in The Kaohsiung journal of medical sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

23 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  20. A tumour-resident Lgr5Nature cell biology · 2021
    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

6 authors at 3 institutions in 1 country.

Ruo-Gu WangDepartment of Gastrointestinal Surgery, Affiliated Hospital of Shandong Academy of Medical Sciences, Jinan, Shandong, China.
Dan ZhangDepartment of Gastrointestinal Surgery, Affiliated Hospital of Shandong Academy of Medical Sciences, Jinan, Shandong, China.
Chun-Hong ZhaoCentral Lab, Affiliated Hospital of Shandong Academy of Medical Sciences, Jinan, Shandong, China.
Qi-Long WangDepartment of Gastrointestinal Surgery, Affiliated Hospital of Shandong Academy of Medical Sciences, Jinan, Shandong, China.
Hui QuDepartment of Gastrointestinal Surgery, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Qing-Si HeDepartment of Gastrointestinal Surgery, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Affiliated Hospital of Shandong Academy of Medical Sciences · CNQilu Hospital of Shandong University · CNShandong First Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As documented, the expression, biological roles, and prognostic significance of FKBP10 in stomach adenocarcinoma (STAD) have not been investigated till now. This drives us to detect the biological roles and clinical significance of FKBP10 in STAD. The expression level of FKBP10 was measured based on the data obtained from the TCGA, ONCOMINE, and GEPIA databases, and STAD cell lines. Through in vitro experiments, cell behaviors were investigated to evaluate the effects of FKBP10 on STAD. Moreover, the PI3K-AKT signaling pathway was measured. Relying on the data of TCGA, ONCOMINE, and GEPIA databases, and cancer cell lines, FKBP10 was up-regulated in STAD when compared with normals. The patients with low expression of FKBP10 had higher survival rate than those with high FKBP10 expression. After knockdown of FKBP10 in AGS cells, cell vitality, colony formation ability, and the migratory and invasive potential were inhibited. Western blotting analysis exhibited that knockdown of FKBP10 significantly reduced the expression level of p-AKT, and p-PI3K, but it did not influence the total expression level of AKT, and PI3K. FKBP10 might serve as a crucial player in gastric cancer, and targeting FKBP10 might provide clinical utility in gastric cancer in future.

Indexed as

Signal TransductionAdenocarcinomaCell Line, TumorCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedNeoplasm InvasivenessPhosphatidylinositol 3-KinasesPhosphorylationPrognosisRNA, Small InterferingStomach NeoplasmsFKBP10 protein, humanPhosphatidylinositol 3-KinasesRNA, Small InterferingTacrolimus Binding ProteinsFKBP10invasionmigrationprognosisstomach adenocarcinoma

Identifiers

PMID31868996
PMCPMC11896317
OpenAlexW2997218512

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.