Evidence map›Paper›PMID 32922038›Full record

ArticleOncoTargets and therapy2020

GCNT4 is Associated with Prognosis and Suppress Cell Proliferation in Gastric Cancer.

Hui Sun, Jinjia Chang, Min Ye, Weiwei Weng, Meng Zhang, Shujuan Ni, Cong Tan, Dan Huang, Lei Wang, Xiang Du and 2 more

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 13 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

12 authors at 2 institutions in 1 country.

Hui Sun *Department of Pathology, Fudan University Shanghai Cancer Center, Shanghai 200032, People's Republic of China.ORCID 0000-0002-7145-6991
Jinjia Chang *Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, People's Republic of China.ORCID 0000-0002-9105-8691
Min Ye *Department of Pathology, Fudan University Shanghai Cancer Center, Shanghai 200032, People's Republic of China.
Weiwei WengDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai 200032, People's Republic of China.
Meng ZhangDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai 200032, People's Republic of China.
Shujuan NiDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai 200032, People's Republic of China.ORCID 0000-0002-8030-0294
Cong TanDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai 200032, People's Republic of China.
Dan HuangDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai 200032, People's Republic of China.
Lei WangDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai 200032, People's Republic of China.
Xiang DuDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai 200032, People's Republic of China.
Mi-Die XuDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai 200032, People's Republic of China.ORCID 0000-0003-1775-6608
Weiqi ShengDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai 200032, People's Republic of China.
Shanghai Medical College of Fudan University · CNFudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGCNT4 is a member of the glucosaminyl (N-acetyl) transferases family that has been implicated in multiple human malignancies. However, the role of GCNT4 in gastric cancer (GC) is unknown. In this present study, we aimed to explore the role and clinicopathological correlation of GCNT4 in GC. MATERIALS AND

methodsWe first evaluated the dysregulation of GCNT4 in The Cancer Genome Atlas (TCGA) and then we performed RT-qPCR and immunohistochemistry to validate the results in a cohort of in-house patients. The clinicopathological correlation and function of GCNT4 in GC were also analysed.

resultsGCNT4 was found to be significantly downregulated in GC. In addition, GCNT4 expression correlated with tumour depth, nervous invasion and pathological tumor-node-metastasis (pTNM) stage. Moreover, lower GCNT4 levels conferred poor overall survival (OS) and disease-free survival (DFS) to GC patients. Multivariate Cox regression analysis revealed that GCNT4 protein expression is an independent prognostic factor for OS in patients with GC. Further functional experimental results revealed that overexpression of GCNT4 appears to halt GC cell proliferation and the cell cycle.

conclusionAltogether, these findings indicated that GCNT4 regulates the GC cell cycle and have important implications for the selection of therapeutic targets to prevent tumour proliferation.

Indexed as

cell cycledysregulationgastric cancerGCNT4prognosis

Identifiers

PMID32922038
PMCPMC7457769
OpenAlexW3080550574

What OpenQuestion holds

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LicenceCC BY-NC
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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.