Evidence map›Paper›PMID 30863180›Full record

ArticleCancer management and research2019

C14orf159 suppresses gastric cancer cells' invasion and proliferation by inactivating ERK signaling.

Yan-Mei Zhu, Qiang Li, Xiao-Zhuo Gao, Xiao Meng, Li-Li Sun, Yu Shi, En-Tian Lu, Yong Zhang

Open access · goldAbstract read
In one paragraph

Article in Cancer management and research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

6 citing papers in PubMed, 8 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

8 authors at 3 institutions in 1 country.

Yan-Mei ZhuDepartment of Pathology, Cancer Hospital of China Medical University, Liaoning Cancer Hospital and Institute, Shenyang, Liaoning 110042, P.R. China, zhangyong@cancerhosp-ln-cmu.com.
Qiang LiDepartment of Pathology, Cancer Hospital of China Medical University, Liaoning Cancer Hospital and Institute, Shenyang, Liaoning 110042, P.R. China, zhangyong@cancerhosp-ln-cmu.com.
Xiao-Zhuo GaoDepartment of Pathology, Cancer Hospital of China Medical University, Liaoning Cancer Hospital and Institute, Shenyang, Liaoning 110042, P.R. China, zhangyong@cancerhosp-ln-cmu.com.
Xiao MengDepartment of Pathology, Cancer Hospital of China Medical University, Liaoning Cancer Hospital and Institute, Shenyang, Liaoning 110042, P.R. China, zhangyong@cancerhosp-ln-cmu.com.
Li-Li SunDepartment of Pathology, Cancer Hospital of China Medical University, Liaoning Cancer Hospital and Institute, Shenyang, Liaoning 110042, P.R. China, zhangyong@cancerhosp-ln-cmu.com.
Yu ShiDepartment of Pathology, People's Hospital of Dawa District, Panjin, Liaoning 124200, P.R. China.
En-Tian LuDepartment of Pathology, Central Hospital of Pulandian District, Dalian, Liaoning 116200, P.R. China.
Yong ZhangDepartment of Pathology, Cancer Hospital of China Medical University, Liaoning Cancer Hospital and Institute, Shenyang, Liaoning 110042, P.R. China, zhangyong@cancerhosp-ln-cmu.com.
China Medical University · CNDalian Municipal Central Hospital · CNLiaoning Cancer Hospital & Institute · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundC14orf159, a new protein, has been identified recently. But its expression in tissues and clinicopathologic correlation is still unknown. PATIENTS AND

methodsWe carried out immunohistochemistry staining in 144 gastric cancer cases in this study. Then Western blot was used to detect the expression of protein. MTT and matrigel invasion assay were used to assess the biological effects.

resultsThe immunohistochemical results indicated that the expression of C14orf159 in normal gastric mucosa close to cancer tissue was remarkably higher than that in stomach carcinoma samples (63.9% and 34.7%, respectively,

conclusionIn other words, loss of C14orf159 is associated with the progression of gastric cancer. The role of C14orf159 in repression of proliferation and invasion may be due to resuming E-cadherin and abolishing Snail and Cyclin D1 expression through inactivating ERK-P90RSK pathway.

Indexed as

C14orf159ERKgastric cancerinvasionproliferation

Identifiers

PMID30863180
PMCPMC6388960
OpenAlexW2914841401

What OpenQuestion holds

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Registered trials

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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.