Evidence map›Paper›PMID 31758636›Full record

ArticleJournal of cellular and molecular medicine2020

Production of bioactive recombinant human myeloid-derived growth factor in Escherichia coli and its mechanism on vascular endothelial cell proliferation.

Longwei Zhao, Shuang Feng, Shen Wang, Miaojuan Fan, Wei Jin, Xianjing Li, Chen Wang, Yong Yang

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 28% 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

9 citing papers in PubMed, 14 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 2 institutions in 1 country.

Longwei ZhaoSchool of Life Science and Technology, China Pharmaceutical University, Nanjing, China.
Shuang FengCenter for New Drug Safety Evaluation and Research, China Pharmaceutical University, Nanjing, China.
Shen WangSchool of Life Science and Technology, China Pharmaceutical University, Nanjing, China.
Miaojuan FanSchool of Pharmaceutical Sciences & Center for Structural Biology, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Wei JinSchool of Pharmaceutical Sciences & Center for Structural Biology, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Xianjing LiSchool of Life Science and Technology, China Pharmaceutical University, Nanjing, China.
Chen WangSchool of Life Science and Technology, China Pharmaceutical University, Nanjing, China.
Yong YangSchool of Life Science and Technology, China Pharmaceutical University, Nanjing, China.ORCID 0000-0002-2841-8420
China Pharmaceutical University · CNWenzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myeloid-derived growth factor (MYDGF) is a novel protein secreted by bone marrow cells that features important physiological functions. In recent years, MYDGF has gained considerable interest due to their extensive beneficial effect on cardiac repair and protects cardiomyocytes from cell death. However, its precise molecular mechanisms have not been well elucidated. The purpose of this study was to produce sufficient amount of biologically active recombinant human (rh) MYDGF more economically and effectively by using in vitro molecular cloning techniques to study its clinical application. The prokaryotic expression system of Escherichia coli was established for the preparation of rhMYDGF. Finally, a large amount of high biologically active and purified form of recombinant protein was obtained. Moreover, we investigated the potential mechanism of rhMYDGF-mediated proliferation and survival in human coronary artery endothelial cells (HCAECs). Mechanistically, the results suggested that MAPK/STAT3 and the cyclin D1 signalling pathways are indispensable for rhMYDGF-mediated HCAEC proliferation and survival. Therefore, this study successfully established a preparation protocol for biologically active rhMYDGF and it may be a most economical way to produce high-quality active rhMYDGF for future clinical application.

Indexed as

Cell ProliferationSignal TransductionCells, CulturedEndothelium, VascularEscherichia coliHumansInterleukinsRecombinant ProteinsInterleukinsMYDGF protein, humanRecombinant ProteinsE coli expression systemhuman coronary artery endothelial cellsmitogen activityrecombinant human MYDGFsignal mechanism

Identifiers

PMID31758636
PMCPMC6991672
OpenAlexW2991184353

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.