Publication:
Targeting ovarian cancer with chalcone derivatives: cytotoxicity and apoptosis induction in HGSOC Cells

dc.contributor.coauthorColombo, Eleonora
dc.contributor.coauthorPrinciotto, Salvatore
dc.contributor.coauthorPassarella, Daniele
dc.contributor.coauthorDallavalle, Sabrina
dc.contributor.coauthorChristodoulou, Michael S.
dc.contributor.coauthorDurmaz Şahin, Irem
dc.contributor.departmentKUTTAM (Koç University Research Center for Translational Medicine)
dc.contributor.departmentGraduate School of Health Sciences
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorAydın, Elif Merve
dc.contributor.kuauthorŞahin, İrem Durmaz
dc.contributor.schoolcollegeinstituteGRADUATE SCHOOL OF HEALTH SCIENCES
dc.contributor.schoolcollegeinstituteResearch Center
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2025-01-19T10:32:59Z
dc.date.issued2023
dc.description.abstractOvarian cancer ranks as the eighth most prevalent form of cancer in women across the globe and stands as the third most frequent gynecological cancer, following cervical and endometrial cancers. Given its resistance to standard chemotherapy and high recurrence rates, there is an urgent imperative to discover novel compounds with potential as chemotherapeutic agents for treating ovarian cancer. Chalcones exhibit a wide array of biological properties, with a particular focus on their anti-cancer activities. In this research, we documented the synthesis and in vitro study of a small library of chalcone derivatives designed for use against high-grade serous ovarian cancer (HGSOC) cell lines, specifically OVCAR-3, OVSAHO, and KURAMOCHI. Our findings revealed that three of these compounds exhibited cytotoxic and anti-proliferative effects against all the tested HGSOC cell lines, achieving IC50 concentrations lower than 25 µM. Further investigations disclosed that these chalcones prompted an increase in the subG1 phase cell cycle and induced apoptosis in OVCAR-3 cells. In summary, our study underscores the potential of chalcones as promising agents for the treatment of ovarian cancer. © 2023 by the authors.
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue23
dc.description.openaccessAll Open Access; Gold Open Access
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.volume28
dc.identifier.doi10.3390/molecules28237777
dc.identifier.eissn1420-3049
dc.identifier.issn14203049
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85179351670
dc.identifier.urihttps://doi.org/10.3390/molecules28237777
dc.identifier.urihttps://hdl.handle.net/20.500.14288/26522
dc.identifier.wos1116217700001
dc.keywordsChalcones
dc.keywordsKURAMOCHI
dc.keywordsOvarian cancer
dc.keywordsOVCAR-3
dc.keywordsOVSAHO
dc.language.isoeng
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)
dc.relation.ispartofMolecules
dc.subjectMedicine
dc.titleTargeting ovarian cancer with chalcone derivatives: cytotoxicity and apoptosis induction in HGSOC Cells
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorAydın, Elif Merve
local.contributor.kuauthorCanıtez, İdil Su
local.contributor.kuauthorŞahin, İrem Durmaz
local.publication.orgunit1GRADUATE SCHOOL OF HEALTH SCIENCES
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit1Research Center
local.publication.orgunit2KUTTAM (Koç University Research Center for Translational Medicine)
local.publication.orgunit2School of Medicine
local.publication.orgunit2Graduate School of Health Sciences
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