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https://hdl.handle.net/11499/37094
Title: | Evaluation of antioxidant and anticancer effects of Thymbra sintenisii subsp. isaurica extract | Authors: | Hepokur, C. Misir, S. Çiçek, Mehmet Yaylim, I. Zeybek, U. |
Keywords: | Antioxidant apoptosis cancer Thymbra sintenisii subsp. isaurica antineoplastic agent antioxidant ascorbic acid cisplatin phytochemical plant extract polyphenol Thymbra sintenisii subsp. isaurica extract unclassified drug antineoplastic activity antioxidant activity Article cell growth cell viability concentration (parameter) controlled study DPPH radical scavenging assay drug cytotoxicity drug design drug efficacy endemic species flow cytometry human human cell IC50 Lamiaceae mass fragmentography MCF-7 cell line NCTC clone 929 cell line plant leaf breast tumor cell survival chemistry drug effect female metabolism Antioxidants Breast Neoplasms Cell Survival Female Humans MCF-7 Cells Plant Extracts Plant Leaves Polyphenols |
Publisher: | Wolters Kluwer Medknow Publications | Abstract: | Background: The purpose of this study was to investigate the phenolic composition and antioxidant activity of Thymbra sintenisii subsp. isaurica extract (TSIE) and, to evaluate, for the first time, anticancer effect on human MCF-7 (breast carcinoma) cells. Materials and Methods: The antioxidant capacity of TSIE was evaluated using 2,2-diphenyl-1-picrylhydrazyl (DPPH) and total polyphenol assays. The anticancer activities of TSIE were tested on MCF-7 (breast carcinoma) cells. Results: Total polyphenol value of extracts TSIE was found as 73.02 mg gallic acid /g powder. DPPH result of IC50 value of TSIE was found to be 27.15 µg/mL. To examine anticancer effect of TSIE at different concentrations were given on MCF-7 cells. TSIE was observed to reduce the cell viability in a dose-dependent manner. This anticancer property of the TSIE provides a highlights the importance of plant research for drug design. Conclusion: In this study, anticancer effects and antioxidant level of endemic species, that is TSIE, are evaluated on MCF-7 cells. Thus, an effective therapeutic agent for cancer treatment is aimed to develop. Further studies are needed to better understand the molecular mechanisms underlying this effect of TSIE. © 2020 Wolters Kluwer Medknow Publications. All rights reserved. | URI: | https://hdl.handle.net/11499/37094 https://doi.org/10.4103/jcrt.JCRT_355_17 |
ISSN: | 0973-1482 |
Appears in Collections: | Fen-Edebiyat Fakültesi Koleksiyonu PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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