Evidence map›Paper›PMID 26987289›Full record

ArticleCancer gene therapy2016

Adenovirus-directed expression of TIPE2 suppresses gastric cancer growth via induction of apoptosis and inhibition of AKT and ERK1/2 signaling.

Y Zhu, M Tao, J Wu, Y Meng, C Xu, Y Tian, X Zhou, J Xiang, H Zhang, Y Xie

Abstract read
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Article in Cancer gene therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

26 citing papers in PubMed, 39 citations in OpenAlex.

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  12. Tumor Necrosis Factor-α-Induced Protein 8-like 2 Downregulation Reduces CD4⁺ T Lymphocyte Apoptosis in Mice with Thermal Injury.Medical science monitor : international medical journal of experimental and clinical research · 2019
    Article
  13. Article
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  15. Review
  16. TIPE Family of Proteins and Its Implications in Different Chronic Diseases.International journal of molecular sciences · 2018
    Review
  17. 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

10 authors at 3 institutions in 2 countries.

Y ZhuDepartment of Oncology, The First Affiliated Hospital of Soochow University, Suzhou, China.
M TaoDepartment of Oncology, The First Affiliated Hospital of Soochow University, Suzhou, China.
J WuDepartment of Oncology, The First Affiliated Hospital of Soochow University, Suzhou, China.
Y MengDepartment of Oncology, The First Affiliated Hospital of Soochow University, Suzhou, China.
C XuDepartment of Oncology, The First Affiliated Hospital of Soochow University, Suzhou, China.
Y TianDepartment of Oncology, Suzhou Xiangcheng People's Hospital, Suzhou, China.
X ZhouDepartment of Oncology, The First Affiliated Hospital of Soochow University, Suzhou, China.
J XiangCancer Research Unit, Saskatchewan Cancer Agency, Saskatoon, Saskatchewan, Canada.
H ZhangDepartment of General Surgery, The First Affiliated Hospital of Soochow University, Suzhou, China.
Y XieDepartment of Oncology, The First Affiliated Hospital of Soochow University, Suzhou, China.
Soochow University · CNFirst Affiliated Hospital of Soochow University · CNSaskatchewan Cancer Agency · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor necrosis factor (TNF)-α-induced protein 8-like 2 (TNFAIP8L2/TIPE2) as a novel anti-inflammatory factor plays an important role in maintaining immune homeostasis. Recently, TIPE2 has been shown to inhibit hepatocarcinoma growth and metastasis through targeting Ras and Rac1. However, its effects in human cancers are poorly understood. In the present study, we analyzed TIPE2 mRNA expression in a panel of human gastric cancer cells (AGS, HGC-27 and SGC-7901) and then examined the cell-autonomous effects of adenovirus-mediated human TIPE2 gene transfer (AdVTIPE2) on AGS and HGC-27 human gastric cancer cells. We found that compared with the GES-1 normal human gastric mucous epithelial cells, human TIPE2 was lost in the AGS, HGC-27 and SGC-7901 gastric cancer cells. Adenovirus-mediated human TIPE2 overexpression significantly inhibited AGS and HGC-27 gastric cancer cell growth and induced AGS and HGC-27 tumor cell apoptosis in vitro. Furthermore, AdVTIPE2 treatment obviously suppressed the growth of AGS gastric cancer subcutaneously xenografted tumors implanted in athymic BALB/c nude mice in vivo. Mechanistically, AdVTIPE2 exhibited marked effects on the upregulation of Bax, cleaved Caspase-9, cleaved Caspase-3, cleaved poly ADP ribose polymerase as well as the downregulation of B-cell lymphoma (Bcl)-XL, phosphorylated-protein kinase B (p-PKB/AKT), phosphorylated-extracellular signal-regulated kinase 1/2 (p-ERK1/2) in AGS gastric cancer cells in vitro and in vivo. Collectively, AdVTIPE2 suppressed gastric cancer growth very possibly by the activation of intrinsic apoptotic pathway and the attenuation of AKT and ERK1/2 signaling. Thus, our data indicated that TIPE2 may be a novel potential therapeutic target for human gastric cancer.

Indexed as

Gene ExpressionMAP Kinase Signaling SystemAdenoviridaeAnimalsApoptosisCell Line, TumorDisease Models, AnimalFemaleGene OrderGenetic VectorsHumansIntracellular Signaling Peptides and ProteinsMiceProto-Oncogene Proteins c-aktStomach NeoplasmsTransduction, GeneticIntracellular Signaling Peptides and ProteinsProto-Oncogene Proteins c-aktTNFAIP8L2 protein, human

Identifiers

PMID26987289
OpenAlexW2301050709

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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.