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Institution

Dalian Medical University

EducationDalian, China
About: Dalian Medical University is a education organization based out in Dalian, China. It is known for research contribution in the topics: Cancer & Apoptosis. The organization has 15623 authors who have published 9993 publications receiving 164145 citations.


Papers
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Journal ArticleDOI
TL;DR: Increased scarring in fmod(-/-) mice indicates that TGF-β3's antimotility effects predominate over its antifibrotic effects when high TGF -β3 levels disrupt early fibroblastic wound ingress.

63 citations

Journal ArticleDOI
Zi Wang1, Jialei Hu1, Yue Pan1, Yujia Shan1, Liqun Jiang1, Xia Qi1, Li Jia1 
TL;DR: MiR-140-5p and miR-149 could mediate the development of OA, which was regulated by FUT1, and might serve as a predictive biomarker and a potential therapeutic target in OA treatment.
Abstract: Osteoarthritis (OA), the most prevalent chronic and degenerative joint disease, is characterized by articular cartilage degradation and chondrocyte injury. Increased cell apoptosis and defective cell autophagy in chondrocytes are a feature of degenerative cartilage. MicroRNAs (miRNAs) have been identified as potential regulators of OA. This study aimed to determine the potential role of miR-140-5p and miR-149 in apoptosis, autophagy, and proliferation in human primary chondrocytes and investigate the underlying mechanism. We revealed the differential expressional profiles of miR-140-5p/149 and fucosyltransferase 1 (FUT1) in the articular cartilage tissues of OA patients and normal people and validated FUT1 was a direct target of miR-140-5p/149. The overexpression of miR-140-5p/149 inhibited apoptosis and promoted proliferation and autophagy of human primary chondrocytes via downregulating FUT1. On the contrary, the downregulation of miR-140-5p/149 inhibited chondrocyte proliferation and autophagy, whereas the effect was reversed by FUT1 knockdown. Taken together, our data suggested that miR-140-5p and miR-149 could mediate the development of OA, which was regulated by FUT1. miR-140-5p/miR-149/FUT1 axis might serve as a predictive biomarker and a potential therapeutic target in OA treatment.

63 citations

Journal ArticleDOI
TL;DR: AB23A produces protective effect against ANIT-induced hepatotoxity and cholestasis, due to FXR-mediated regulation of transporters and enzymes.

63 citations

Journal ArticleDOI
TL;DR: It is shown that repeat administration of bone marrow mononuclear cells can improve left ventricular function compared with a single infusion in patients with large acute myocardial infarction.
Abstract: Aims We sought to determine whether repeat administration of bone marrow mononuclear cells (BMC) can improve left ventricular function compared with a single infusion in patients with large acute myocardial infarction (AMI). Methods and results Thirty-nine patients with a ST-elevation AMI of the anterior wall and a significantly decreased left ventricular ejection fraction (LVEF 20–39%) were randomly assigned to three groups following primary percutaneous coronary intervention: Group A (n = 12) received a single intracoronary infusion of BMC (1.9 ± 1.2 × 108) at 3–7 days after AMI; Group B (n = 15) received BMC administration both at 3–7 days (2.0 ± 1.4 × 108) and at 3 months (2.1 ± 1.7 × 108); and the control group (CON, n = 12) received one placebo injection at 3–7 days. We noted no severe complications associated with the BMC transfer. The increase in LVEF evaluated by magnetic resonance imaging (MRI) after 12 months in Group B (11.7 ± 2.6%) was significantly greater than that in Group A (7.2 ± 1.6%, P < 0.001) or in CON (2.9 ± 2.0%, P < 0.001). Magnetic resonance imaging-derived myocardial infarct size decreased significantly in Group B compared with Group A (11.3 ± 2.7% vs. 6.3 ± 1.6%, P < 0.001). Conclusion Data from this preliminary study suggest that repeated BMC administration might be a safe and feasible therapeutic strategy for patients with large AMI.

63 citations


Authors

Showing all 15657 results

NameH-indexPapersCitations
Jing Wang1844046202769
Jan-Åke Gustafsson147105898804
Melitta Schachner13586167304
Yan Zhang107241057758
Jau-Shyong Hong9347437172
Li Zhang9291835648
Charles G. Eberhart8444429920
Ying Lu8334324913
You-Lin Qiao7859523919
Wei Wei75106829415
Weidong Le7428722551
Jin-Tai Yu6643920020
Wei Jiang6566018932
Lan Tan6238713828
Hua Li6284917933
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202318
202252
20211,433
20201,251
20191,075
2018911