Punicalagin Induces Apoptosis in A549 Cell Line Through Mitochondria-Mediated Pathway

dc.authorscopusid 12801030200
dc.authorscopusid 6602345446
dc.contributor.author Berkoz, Mehmet
dc.contributor.author Krosniak, Miroslaw
dc.date.accessioned 2025-05-10T17:34:28Z
dc.date.available 2025-05-10T17:34:28Z
dc.date.issued 2020
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp [Berkoz, Mehmet] Van Yuzuncu Yil Univ, Fac Pharm, Dept Biochem, Zeve Campus, TR-65080 Van, Turkey; [Krosniak, Miroslaw] Jagiellonian Univ, Med Coll, Dept Food Chem & Nutr, Krakow, Poland en_US
dc.description.abstract Lung cancer is the most common cause of cancer-related deaths worldwide. Punicalagin is an ellagitannin mostly found in pomegranate husk and shows very strong antitumoral activity. The purpose of this study was to investigate the mechanism in which punicalagin acts as an antiproliferative agent on A549 cell line (adenocarcinomic human alveolar basal epithelial cells) and MRC-5 cell line (normal lung fibroblast cells). The cultured cells were treated with punicalagin at concentrations of 1-100 mu M for 24 h. For this aim, cell growth inhibition, percentage of apoptotic cells, cell cycle distribution, morphological changes, cellular and mitochondrial reactive oxygen species (ROS) production, and expression of apoptotic proteins were evaluated. Cell viability test and morphological examinations showed that punicalagin at 50 and 75 mu M concentrations exhibited toxic effect against lung cancer cells but not toxic against normal lung cells. Cytoplasmic ROS production decreased with the application of punicalagin, while the level of ROS released from mitochondria increased due to mitochondrial dysfunction. Studies of apoptosis indicated that both punicalagin concentrations induced apoptotic process in A549 cells. However, cell cycle was arrested in the G(1)/S phase after punicalagin treatment. These findings suggest that punicalagin has antiproliferative and apoptotic properties in these concentrations. en_US
dc.description.sponsorship Office of Scientific Research Projects of Mersin University [2016-2-TP3-1891] en_US
dc.description.sponsorship The author sincerely thanks the laboratory technicians and assistants in Jagiellonian University, Medical Collage, Department of Food Chemistry and Nutrition. This research was financially supported in part by the Office of Scientific Research Projects of Mersin University under Grant number (2016-2-TP3-1891). en_US
dc.description.woscitationindex Science Citation Index Expanded
dc.identifier.doi 10.4149/gpb_2020024
dc.identifier.endpage 567 en_US
dc.identifier.issn 0231-5882
dc.identifier.issn 1338-4325
dc.identifier.issue 6 en_US
dc.identifier.pmid 33226364
dc.identifier.scopus 2-s2.0-85096813630
dc.identifier.scopusquality Q4
dc.identifier.startpage 557 en_US
dc.identifier.uri https://doi.org/10.4149/gpb_2020024
dc.identifier.uri https://hdl.handle.net/20.500.14720/13811
dc.identifier.volume 39 en_US
dc.identifier.wos WOS:000599164200005
dc.identifier.wosquality Q4
dc.language.iso en en_US
dc.publisher General Physiol and Biophysics 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 Cell Line en_US
dc.subject Mrc-5 Cell Line en_US
dc.subject Punicalagin en_US
dc.subject Cell Proliferation en_US
dc.subject Apoptosis en_US
dc.title Punicalagin Induces Apoptosis in A549 Cell Line Through Mitochondria-Mediated Pathway en_US
dc.type Article en_US
dspace.entity.type Publication

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