Researching New Drug Combinations with Senolytic Activity Using Senescent Human Lung Fibroblasts MRC-5 Cell Line
-
Published:2024-01-04
Issue:1
Volume:17
Page:70
-
ISSN:1424-8247
-
Container-title:Pharmaceuticals
-
language:en
-
Short-container-title:Pharmaceuticals
Author:
de Godoy Maria Carolina Ximenes1, Macedo Juliana Alves2, Gambero Alessandra12
Affiliation:
1. School for Life Sciences, Pontifical Catholic University of Campinas (PUC-Campinas), Av. John Boyd Dunlop, s/n, Campinas 13034-685, SP, Brazil 2. Department of Food and Nutrition, School of Food Engineering, State University of Campinas, Campinas 13083-862, SP, Brazil
Abstract
Therapeutically targeting senescent cells seems to be an interesting perspective in treating chronic lung diseases, which are often associated with human aging. The combination of the drug dasatinib and the polyphenol quercetin is used in clinical trials as a senolytic, and the first results point to the relief of physical dysfunction in patients with idiopathic pulmonary fibrosis. In this work, we tested new combinations of drugs and polyphenols, looking for senolytic activity using human lung fibroblasts (MRC-5 cell line) with induced senescence. We researched drugs, such as azithromycin, rapamycin, metformin, FK-506, aspirin, and dasatinib combined with nine natural polyphenols, namely caffeic acid, chlorogenic acid, ellagic acid, ferulic acid, gallic acid, epicatechin, hesperidin, quercetin, and resveratrol. We found new effective senolytic combinations with dasatinib and ellagic acid and dasatinib and resveratrol. Both drug combinations increased apoptosis, reduced BCL-2 expression, and increased caspase activity in senescent MRC-5 cells. Ellagic acid senolytic activity was more potent than quercetin, and resveratrol counteracted inflammatory cytokine release during senolysis in vitro. In conclusion, dasatinib and ellagic acid and dasatinib and resveratrol present in vitro senolytic potential like that observed for the combination in clinical trials of dasatinib and quercetin, and maybe they could be future alternatives in the senotherapeutic field.
Funder
Fundação de Amparo à Pesquisa do Estado de São Paulo—FAPESP, Brazil Conselho Nacional de Desenvolvimento Científico e Tecnológico
Reference55 articles.
1. Ruiz, A., Flores-Gonzalez, J., Buendia-Roldan, I., and Chavez-Galan, L. (2021). Telomere Shortening and Its Association with Cell Dysfunction in Lung Diseases. Int. J. Mol. Sci., 23. 2. Waters, D.W., Schuliga, M., Pathinayake, P.S., Wei, L., Tan, H.Y., Blokland, K.E.C., Jaffar, J., Westall, G.P., Burgess, J.K., and Prele, C.M. (2021). A Senescence Bystander Effect in Human Lung Fibroblasts. Biomedicines, 9. 3. Cellular senescence: When bad things happen to good cells;Campisi;Nat. Rev. Mol. Cell Biol.,2007 4. Kumari, R., and Jat, P. (2021). Mechanisms of Cellular Senescence: Cell Cycle Arrest and Senescence Associated Secretory Phenotype. Front. Cell Dev. Biol., 9. 5. Hu, L., Li, H., Zi, M., Li, W., Liu, J., Yang, Y., Zhou, D., Kong, Q.P., Zhang, Y., and He, Y. (2022). Why Senescent Cells Are Resistant to Apoptosis: An Insight for Senolytic Development. Front. Cell Dev. Biol., 10.
Cited by
2 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|