Evidence map›Paper›PMID 26996552›Full record

ArticleYonsei medical journal2016

Isoprenaline Induces Periostin Expression in Gastric Cancer.

Guo-Xiao Liu, Hong-Qing Xi, Xiao-Yan Sun, Zhi-Jun Geng, Shao-Wei Yang, Yan-Jie Lu, Bo Wei, Lin Chen

Open access · goldAbstract read
In one paragraph

Article in Yonsei medical journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Effect of chronic stress on tumorigenesis and development.Cellular and molecular life sciences : CMLS · 2022
    Review
  2. Assessment of Epinephrine and Norepinephrine in Gastric Carcinoma.International journal of molecular sciences · 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

8 authors at 2 institutions in 1 country.

Guo-Xiao LiuDepartment of General Surgery, Chinese PLA General Hospital, Beijing, China.
Hong-Qing XiDepartment of General Surgery, Chinese PLA General Hospital, Beijing, China.
Xiao-Yan SunWound Healing and Cell Biology Laboratory, Institute of Basic Medical Science, Trauma Center of Postgraduate Medical School, Chinese PLA General Hospital, Beijing, China.
Zhi-Jun GengWound Healing and Cell Biology Laboratory, Institute of Basic Medical Science, Trauma Center of Postgraduate Medical School, Chinese PLA General Hospital, Beijing, China.
Shao-Wei YangWound Healing and Cell Biology Laboratory, Institute of Basic Medical Science, Trauma Center of Postgraduate Medical School, Chinese PLA General Hospital, Beijing, China.
Yan-Jie LuDepartment of Pathology, Chengde Medical College, Chengde, Hebei Province, China.
Bo WeiDepartment of General Surgery, Chinese PLA General Hospital, Beijing, China. weibo@vip.163.com.
Lin ChenDepartment of General Surgery, Chinese PLA General Hospital, Beijing, China. 13381326128@163.com.
Chinese PLA General Hospital · CNAffiliated Hospital of Chengde Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePeriostin mediates critical steps in gastric cancer and is involved in various signaling pathways. However, the roles of periostin in promoting gastric cancer metastasis are not clear. The aim of this study was to investigate the relevance between periostin expression and gastric cancer progression and the role of stress-related hormones in the regulation of cancer development and progression. MATERIALS AND

methodsNormal, cancerous and metastatic gastric tissues were collected from patients diagnosed with advanced gastric cancer. The in vivo expression of periostin was evaluated by in situ hybridization and immunofluorescent staining. Meanwhile, human gastric adenocarcinoma cell lines MKN-45 and BGC-803 were used to detect the in vitro expression of periostin by using quantitative real-time polymerase chain reaction (PCR) and western blotting.

resultsPeriostin is expressed in the stroma of the primary gastric tumors and metastases, but not in normal gastric tissue. In addition, we observed that periostin is located mainly in pericryptal fibroblasts, but not in the tumor cells, and strongly correlated to the expression of α-smooth muscle actin (SMA). Furthermore, the distribution patterns of periostin were broader as the clinical staging of tumors progressed. We also identified a role of stress-related signaling in promoting cancer development and progression, and found that isoprenaline upregulated expression levels of periostin in gastric cancer cells.

conclusionThese findings suggest that the distribution pattern of periostin was broader as the clinical staging of the tumor progressed and found that isoprenaline upregulated expression levels of periostin in gastric cancer cells.

Indexed as

AdenocarcinomaAdrenergic beta-AgonistsAgedBlotting, WesternCell Adhesion MoleculesCell Line, TumorFibroblastsGastric MucosaGene Expression Regulation, NeoplasticHumansIsoproterenolMaleNeoplasm StagingReal-Time Polymerase Chain ReactionRNA, MessengerSignal TransductionAdrenergic beta-AgonistsCell Adhesion MoleculesIsoproterenolPOSTN protein, humanRNA, Messengerextracellular matrixGastric cancermetastasisnichperiostinstress

Identifiers

PMID26996552
PMCPMC4800342
OpenAlexW2299904739

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.