Evidence map›Paper›PMID 30349300›Full record

ArticleOncoTargets and therapy2018

Construction of a recombinant eukaryotic expression vector containing

Liang Jiang, Qi-Lian Liang, Wei-Ming Liang, Hui-Jie Zhang, Jie Huang, Gao-Le Yuan, Xiao-Xia Peng, Shao-Ang Cheng, Zhi-Gang Huang, Xiang-Ning Zhang

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 46% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. In vivo (Athens, Greece)
    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

10 authors at 1 institution in 2 countries.

Liang JiangInterventional Ward, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524001, China, 13600389991@139.com.
Qi-Lian LiangOncology Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524001, China, lianqilian@gdmu.edu.cn.
Wei-Ming LiangInterventional Ward, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524001, China, 13600389991@139.com.
Hui-Jie ZhangOncology Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524001, China, lianqilian@gdmu.edu.cn.
Jie HuangOncology Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524001, China, lianqilian@gdmu.edu.cn.
Gao-Le YuanOncology Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524001, China, lianqilian@gdmu.edu.cn.
Xiao-Xia PengOncology Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524001, China, lianqilian@gdmu.edu.cn.
Shao-Ang ChengOncology Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524001, China, lianqilian@gdmu.edu.cn.
Zhi-Gang HuangDepartment of Epidemiology, School of Public Health, Guangdong Medical University, Dongguan 523808, China.
Xiang-Ning ZhangDepartment of Pathophysiology, School of Basic Medical Science, Guangdong Medical University, Dongguan 523808, China.
Guangdong Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDynamin 3 (DNM3) is a large GTPase that possesses mechanochemical properties and has been shown to be involved in malignancies. However, most studies about DNM3 are observational, and knowledge of the precise molecular mechanism of DNM3 remains limited. MATERIALS AND

methodsWe constructed a PCDH-CMV-MCS-EF1a-GFP-Puro-DNM3 recombinant eukaryotic expression vector, which was then transfected into SW620 and LoVo cells. One cell line was divided into three groups. DNM3 mRNA and protein expression was analyzed by quantitative real-time PCR and Western blot assay. To investigate DNM3 biological activity in colon cancer SW620 and LoVo cell line, we performed cell proliferation, transwell migration, and invasion assay. Matrix metalloproteinase (MMP)-2 and MMP-9 protein expressions were detected by Western blot.

resultWe successfully constructed a PCDH-CMV-MCS-EF1a-GFP-Puro-DNM3 recombinant eukaryotic expression vector, and stable DNM3 expression was observed in SW620 and LoVo cell lines. The vector overexpressing DNM3 inhibited the proliferation, weak invasion, and migration ability of colon cancer SW620 and LoVo cells relative to those in the control group (all

conclusionDNM3 may weaken the malignant behavior of colon cancer and may have promoted the invasion and migration of colon cancer by regulating the expression of MMP-2 and MMP-9.

Indexed as

colon cancerdynamin 3invasionmigrationproliferation

Identifiers

PMID30349300
PMCPMC6186302
OpenAlexW2894784701

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.