Evidence map›Paper›PMID 28230774›Full record

ArticleInternational journal of molecular sciences2017

Inhibition of CCAR1, a Coactivator of β-Catenin, Suppresses the Proliferation and Migration of Gastric Cancer Cells.

Te-Sheng Chang, Kuo-Liang Wei, Chung-Kuang Lu, Yi-Hsing Chen, Ying-Tung Cheng, Shui-Yi Tung, Cheng-Shyong Wu, Ming-Ko Chiang

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

21 citing papers in PubMed, 29 citations in OpenAlex.

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  4. Circular RNAs in Cell Cycle Regulation of Cancers.International journal of molecular sciences · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Te-Sheng ChangDepartment of Gastroenterology and Hepatology, Chang Gung Memorial Hospital, Chiayi 61303, Taiwan. cgmh3621@adm.cgmh.org.tw.
Kuo-Liang WeiDepartment of Gastroenterology and Hepatology, Chang Gung Memorial Hospital, Chiayi 61303, Taiwan. wkliang@adm.cgmh.org.tw.
Chung-Kuang LuDepartment of Gastroenterology and Hepatology, Chang Gung Memorial Hospital, Chiayi 61303, Taiwan. cmusickimo@yahoo.com.tw.
Yi-Hsing ChenDepartment of Gastroenterology and Hepatology, Chang Gung Memorial Hospital, Chiayi 61303, Taiwan. a12509@cgmh.org.tw.
Ying-Tung ChengDepartment of Life Science, National Chung Cheng University, Chiayi 62102, Taiwan. s26136282@livemail.tw.
Shui-Yi TungDepartment of Gastroenterology and Hepatology, Chang Gung Memorial Hospital, Chiayi 61303, Taiwan. ma1898@adm.cgmh.org.tw.
Cheng-Shyong WuDepartment of Gastroenterology and Hepatology, Chang Gung Memorial Hospital, Chiayi 61303, Taiwan. gi0005@adm.cgmh.org.tw.
Ming-Ko ChiangDepartment of Life Science, National Chung Cheng University, Chiayi 62102, Taiwan. biomkc@ccu.edu.tw.
Chiayi Chang Gung Memorial Hospital · TWNational Chung Cheng University · TWChang Gung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aberrant activation of Wnt signaling has been implicated in a variety of human cancers, including gastric cancer. Given the current hypothesis that cancer arises from cancer stem cells (CSCs), targeting the critical signaling pathways that support CSC self-renewal appears to be a useful approach for cancer therapy. Cell cycle and apoptosis regulator 1 (CCAR1) is a transcriptional coactivator which has been shown to be a component of Wnt/β-catenin signaling, and which plays an important role in transcriptional regulation by β-catenin. However, the function and clinical significance of CCAR1 in gastric cancer have not been elucidated. Here, we show that elevated CCAR1 nuclear expression correlates with the occurrence of gastric cancer. In addition, RNAi-mediated CCAR1 reduction not only suppressed the cell growth and increased apoptosis in AGS and MKN28 cells, but also reduced the migration and invasion ability of these cells. Furthermore, an in vivo xenograft assay revealed that the expression level of CCAR1 was critical for tumorigenesis. Our data demonstrates that CCAR1 contributes to carcinogenesis in gastric cancer and is required for the survival of gastric cancer cells. Moreover, CCAR1 may serve as a diagnostic marker and a potential therapeutic target.

Indexed as

AgedAnimalsApoptosisApoptosis Regulatory Proteinsbeta CateninCell CycleCell Cycle ProteinsCell Line, TumorCell MovementCell ProliferationDisease Models, AnimalGene Expression Regulation, NeoplasticHeterograftsHumansKaplan-Meier EstimateMaleApoptosis Regulatory Proteinsbeta CateninCCAR1 protein, humanCell Cycle ProteinsRNA, Small InterferingCCAR1gastric cancermetastasisWnt signalingβ-catenin

Identifiers

PMID28230774
PMCPMC5343993
OpenAlexW2589317690

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.