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https://hdl.handle.net/11499/10946
Title: | Potential anticancer activity of the parasol mushroom, macrolepiota rocera(Agaricomycetes), against the A549 human lung cancer cell line | Authors: | Seçme, Mücahit Kaygusuz, Oğuzhan Eroğlu, C. Dodurga, Yavuz Çolak, Ö.F. Atmaca, P. |
Keywords: | A549 cells Anticancer activity Apoptosis Macrolepiota procera Medicinal mushrooms caspase 3 caspase 9 cyclin D1 cyclin dependent kinase 4 cyclin dependent kinase 6 fungal extract Macrolepiota procera extract messenger RNA phosphatidylinositol 3,4,5 trisphosphate 3 phosphatase protein Bax protein bcl 2 protein kinase B protein Noxa protein p21 protein p53 PUMA protein unclassified drug antineoplastic agent A-549 cell line antineoplastic activity antiproliferative activity apoptosis Article Basidiomycetes basidiospore cell culture cell cycle arrest cell invasion assay cell migration controlled study cytotoxicity down regulation fluorescence microscopy gene expression human human cell inhibitory concentration matrigel chamber assay morphology nonhuman protein expression real time polymerase chain reaction reverse transcription polymerase chain reaction RNA isolation TUNEL assay upregulation Western blotting XTT assay Agaricales cell motion cell survival chemistry drug effect tumor invasion A549 Cells Antineoplastic Agents Basidiomycota Cell Movement Cell Survival Humans Neoplasm Invasiveness |
Publisher: | Begell House Inc. | Abstract: | Mushrooms comprise an unlimited source of active compounds that have beneficial health effects without known negative side effects and can potentially be used as important therapeutic products against cancer, which is the leading cause of death worldwide. In this study we investigated the cytotoxic, antiproliferative, apoptotic, and anti-invasion effects of Macrolepiota procera, which is valued as an edible and medicinal mushroom, on A549 lung cancer cells. The cytotoxic effect of the M. procera extract was determined by using the XTT method. Total RNA was isolated from cells with TRI Reagent to determine the apoptotic effect of the extract, after which complementary DNA was synthesized. Expression profiles of the target genes were determined by quantitative reverse-transcriptase polymerase chain reaction, and protein changes were determined by using Western blotting. We used the TUNEL assay to evaluate the apoptotic effects of the M. procera extract. Effects of M. procera on cell invasion were investigated by using a Matrigel chamber assay. The half-maximal inhibitory concentration of the M. procera extract was determined to be 2 mg/mL against A549 lung cancer cells at 72 hours. According to our results, expression of Cyclin Dl, CDK4, CDK6, Bcl-2, Akt, and NOXA genes significantly decreased and that of Bax, Caspase-3, Caspase-9, PTEN, PUMA, p21, and p53 increased in cells from the dose group compared with their expression in control cells. According to the results of the TUNEL assay, 28 ± 3.6% of cells were apoptotic in the dose group. The M. procera extract also reduced invasion in A549 cancer cells. The results suggest that M. procera has an antiproliferative effect in a dose- and time-dependent manner. © 2018 Begell House, Inc. | URI: | https://hdl.handle.net/11499/10946 https://doi.org/10.1615/IntJMedMushrooms.2018028589 |
ISSN: | 1521-9437 |
Appears in Collections: | Fen-Edebiyat Fakültesi Koleksiyonu PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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