Modulatory effect of curcumin analogs on the activation of metalloproteinases in human periodontal stem cells-Reference-Cited by-同舟云学术

Modulatory effect of curcumin analogs on the activation of metalloproteinases in human periodontal stem cells

Published:2019-07-03 Issue:4 Volume:127 Page:304-312
ISSN:0909-8836
Container-title:European Journal of Oral Sciences
language:en
Short-container-title:Eur J Oral Sci

Author:

Boșca Adina B.¹^ORCID,Ilea Aranka²^ORCID,Sorițău Olga³,Tatomir Corina³,Miklášová Natalia⁴,Pârvu Alina E.⁵,Mihu Carmen M.¹,Melincovici Carmen S.¹,Fischer‐Fodor Eva³⁶

Affiliation:

1. Department of Histology Faculty of Medicine University of Medicine and Pharmacy ‘Iuliu Hatieganu’ Cluj‐Napoca Cluj‐NapocaRomania

2. Department of Oral Rehabilitation, Oral Health and Dental Office Management Faculty of Dental Medicine University of Medicine and Pharmacy ‘Iuliu Hatieganu’ Cluj‐Napoca Cluj‐NapocaRomania

3. Radiotherapy, Tumor and Radiobiology Laboratory ‘Ion Chiricuță’ Institute of Oncology Cluj‐Napoca Romania

4. Department of Chemical Theory of Drugs Faculty of Pharmacy Comenius University Bratislava Slovakia

5. Department of Physiopathology Faculty of Medicine University of Medicine and Pharmacy ‘Iuliu Hatieganu’ Cluj‐Napoca Cluj‐NapocaRomania

6. Medfuture Research Center University of Medicine and Pharmacy ‘Iuliu Hatieganu’ Cluj Napoca Cluj Napoca Romania

Publisher

Wiley

Subject

General Dentistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/eos.12625

Reference42 articles.

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2. In vitro effect of caffeic acid phenethyl ester on matrix metalloproteinases (MMP-1 and MMP-9) and their inhibitor (TIMP-1) in lipopolysaccharide-activated human monocytes

3. Regulation of Matrix Metalloproteinases, Tissue Inhibitor of Matrix Metalloproteinase-1, and Extracellular Metalloproteinase Inducer by Interleukin-17 in Human Periodontal Ligament Fibroblasts

4. Heterogeneity in the collagen-degrading ability ofPorphyromonas gingivalis-stimulated human gingival fibroblasts

5. Porphyromonas gingivalis affects host collagen degradation by affecting expression, activation, and inhibition of matrix metalloproteinases

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