Investigation of New Benzimidazole Derivative Compounds' Effects on A549 Cell Line
dc.authorid | Terzi, Menderes Yusuf/0000-0001-8478-0451 | |
dc.contributor.author | Duran, Gulay Gulbol | |
dc.contributor.author | Kucuk, Meral Urhan | |
dc.contributor.author | Algul, Oztekin | |
dc.contributor.author | Terzi, Menderes Yusuf | |
dc.date.accessioned | 2024-09-18T19:47:58Z | |
dc.date.available | 2024-09-18T19:47:58Z | |
dc.date.issued | 2020 | |
dc.department | Hatay Mustafa Kemal Üniversitesi | en_US |
dc.description.abstract | Chronic inflammation is a common indication of several diseases, e.g. asthma, chronic obstructive pulmonary disease (COPD), atherosclerosis, etc. Benzimidazole derivatives are preferable compounds to design new analgesic and anti-inflammatory substances due to their unique biological features. We aimed to investigate the effect of a newly synthesized benzimidazole derivative, ORT-83, on A549 human lung adenocarcinoma cell line. ORT-83 was synthesized, and a non-cytotoxic concentration of ORT-83 on A549 cells was detected with MTT assay. To analyze the anti-inflammatory effect of ORT-83, an inflammatory cell culture model was established by stimulating A549 cell line with IL1-beta (10 ng/ml). After 2 hours of treatment with IL1-beta to induce inflammation, A549 cells were exposed to ORT-83 (0.78 mu g/ml) for 24 hours. Thereafter gene expression analyses were performed with qRT-PCR. We found that ORT-83 significantly suppressed the gene expression levels of the proinflammatory cytokines; IL-6, NFkB, and TNF-alpha. However, the increased levels of IL-10 (2.8 folds) by IL-1 beta induction did not change after ORT-83 and/or dexamethasone (Dex: positive control) treatments. While Dex; a COX-2 inhibitor, reduced the COX-2 expression level in inflammatory cells from 10.03 folds to 0.71 folds, ORT-83 reduced its level to 4.37 folds. iNOS expression levels did not change in any experimental groups. In conclusion, we showed that ORT-83 exerted its anti-inflammatory effects by repressing the gene expression of proinflammatory cytokines in the inflammation-induced A549 cell line. Although ORT-83 had a weaker COX-2 inhibitory effect compared to Dex, it was shown to be still a strong anti-inflammatory compound. | en_US |
dc.description.sponsorship | Hatay Mustafa Kemal University [15704] | en_US |
dc.description.sponsorship | This project was supported by Hatay Mustafa Kemal University Scientific Research Projects Funding with project number 15704. | en_US |
dc.identifier.doi | 10.1590/1678-4324-2020190364 | |
dc.identifier.issn | 1516-8913 | |
dc.identifier.issn | 1678-4324 | |
dc.identifier.scopus | 2-s2.0-85090269549 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.uri | https://doi.org/10.1590/1678-4324-2020190364 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12483/7265 | |
dc.identifier.volume | 63 | en_US |
dc.identifier.wos | WOS:000568669100001 | en_US |
dc.identifier.wosquality | Q4 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | Inst Tecnologia Parana | en_US |
dc.relation.ispartof | Brazilian Archives of Biology and Technology | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | A549 | en_US |
dc.subject | benzimidazole | en_US |
dc.subject | inflammation | en_US |
dc.subject | anti-inflammatory | en_US |
dc.title | Investigation of New Benzimidazole Derivative Compounds' Effects on A549 Cell Line | en_US |
dc.type | Article | en_US |
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