Please use this identifier to cite or link to this item: 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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