Evidence map›Paper›PMID 27725906›Full record

ArticleAmerican journal of cancer research2016

MicroRNA-17-5p promotes gastric cancer proliferation, migration and invasion by directly targeting early growth response 2.

Peng Chen, Huasi Zhao, Jingjing Huang, Xizhong Yan, Yunfei Zhang, Yongshun Gao

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 32 citations in OpenAlex.

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  15. Autophagy-Regulating microRNAs and Cancer.Frontiers in oncology · 2017
    Review
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

6 authors at 1 institution in 1 country.

Peng ChenDepartment of Gastrointestinal Surgery, The First Affiliated Hospital of Zhengzhou University Zhengzhou, China.
Huasi ZhaoDepartment of Respiration, The First Affiliated Hospital of Zhengzhou University Zhengzhou, China.
Jingjing HuangDepartment of Gastrointestinal Surgery, The First Affiliated Hospital of Zhengzhou University Zhengzhou, China.
Xizhong YanDepartment of Gastrointestinal Surgery, The First Affiliated Hospital of Zhengzhou University Zhengzhou, China.
Yunfei ZhangDepartment of Gastrointestinal Surgery, The First Affiliated Hospital of Zhengzhou University Zhengzhou, China.
Yongshun GaoDepartment of Gastrointestinal Surgery, The First Affiliated Hospital of Zhengzhou University Zhengzhou, China.
First Affiliated Hospital of Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNA-17-5p (miR-17-5p) has previously been reported to play an important role in tumor development and progression. However, it functions differently regarding different kinds of malignant tumor, and its role and mechanism in gastric cancer (GC) still lacks investigation. In this study, we detected the relationship between miR-17-5p and the development of GC by qRT-PCR, and it turned out that the level of miR-17-5p was significantly higher in GC patients than that in normal controls, and the aberrant expression of miR-17-5p was correlated with lymph node metastasis. After that, we examined the effect of miR-17-5p taking on the proliferation, apoptosis, migration and invasion of GC cells and the underlying mechanism. Experiments indicated that knockdown of miR-17-5p inhibited the proliferation, invasion and migration, while promoting apoptosis of SGC7901 cells. Early Growth Response 2 (EGR2) protein or mRNA levels were downregulated or upregulated after overexpression or knockdown of miR-17-5p, respectively. By using dual luciferase assay and Western blot, we identified EGR2 as a functional target of miR-17-5p. As far as we know, this could be the first study to demonstrate that miR-17-5p is associated with tumor stage of GC and that it could possibly become a new therapeutic method for the treatment of GC.

Indexed as

early growth response 2Gastric cancermiR-17-5pSGC7901tumor

Identifiers

PMID27725906
PMCPMC5043110
OpenAlexW2533700114

What OpenQuestion holds

Textmetadata
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.