Evidence map›Paper›PMID 32725378›Full record

ArticleMedical oncology (Northwood, London, England)2020

Suppression of PTTG1 inhibits cell angiogenesis, migration and invasion in glioma cells.

Lishan Cui, Tong Ren, Haitao Zhao, Shuide Chen, Mingcheng Zheng, Xuemin Gao, Dingrui Feng, Lichao Yang, Xin Jin, Rengong Zhuo

Abstract read
PubMed Publisher
In one paragraph

Article in Medical oncology (Northwood, London, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Lishan CuiXiang'an Branch, The First Affiliated Hospital of Xiamen University, Xiamen University, Xiamen, 361005, China.
Tong RenXiamen Key Laboratory of Chiral Drugs, School of Medicine, Xiamen University, Xiamen, China.
Haitao ZhaoXiang'an Branch, The First Affiliated Hospital of Xiamen University, Xiamen University, Xiamen, 361005, China.
Shuide ChenXiang'an Branch, The First Affiliated Hospital of Xiamen University, Xiamen University, Xiamen, 361005, China.
Mingcheng ZhengXiang'an Branch, The First Affiliated Hospital of Xiamen University, Xiamen University, Xiamen, 361005, China.
Xuemin GaoSchool of Pharmacy, Xiamen University, Xiamen, China.
Dingrui FengSchool of Medicine, Xiamen University, Xiang'an District, Xiamen, 361102, China.
Lichao YangSchool of Medicine, Xiamen University, Xiang'an District, Xiamen, 361102, China. yanglc116@xmu.edu.cn.ORCID http://orcid.org/0000-0001-9945-2338
Xin JinSchool of Medicine, Xiamen University, Xiang'an District, Xiamen, 361102, China. xinjin@xmu.edu.cn.
Rengong ZhuoSchool of Medicine, Xiamen University, Xiang'an District, Xiamen, 361102, China. zrg870322@xmu.edu.cn.
Xiamen University · CNFirst Affiliated Hospital of Xiamen University · CN

Funding

Fundamental Research Funds for the Central Universities 20720180042Health Science Research Personnel Training Program of Fujian Province 2016-CXB-12
6 · The paper itself

Abstract

Pituitary tumor-transforming gene 1 (PTTG1) has been identified as an oncogene and is overexpressed in many tumor types. However, the role of PTTG1 in glioblastoma (GBM) has not been well characterized, especially in relation to angiogenesis, migration, and invasion. In the present study, our results showed that the expression of PTTG1 was significantly higher in patients with GBM. Bioinformatic analysis showed that angiogenesis and the cell migration-related process were increased in patients with high PTTG1 expression levels; meanwhile, PTTG1 was positively correlated with marker genes of angiogenesis, migration and the evasion of apoptosis. In vitro assays showed that PTTG1 knockdown dramatically suppressed angiogenesis, migration and invasion, and increased the apoptosis of GBM cells. Moreover, our results also showed that silencing PTTG1 suppressed the activity of the TGF-β/PI3K-AKT-mTOR pathway, which induced tumor deterioration in multiple organs. Overall, our findings indicate that PTTG1 is a glioma malignant factor that promotes angiogenesis, migration, invasion, and the evasion of apoptosis, and these roles may be related to the TGF-β/PI3K-AKT-mTOR pathway. Thus, the targeted inhibition of PTTG1 might be a novel therapeutic strategy and a potential diagnostic biomarker for GBM-targeted therapies.

Indexed as

Cell Line, TumorCell MovementCell ProliferationComputational BiologyDatabases, GeneticGliomaHumansNeoplasm InvasivenessNeovascularization, PathologicRNA, Small InterferingSecurinSignal TransductionSurvival RateTOR Serine-Threonine KinasesMTOR protein, humanpituitary tumor-transforming protein 1, humanRNA, Small InterferingSecurinTOR Serine-Threonine KinasesAngiogenesisGlioblastomaInvasionPituitary tumor-transforming gene 1

Identifiers

PMID32725378
OpenAlexW3045761055

What OpenQuestion holds

Textmetadata
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.