Effect of Turkish propolis extracts on proteome of prostate cancer cell line

MakaleAçık Erişim
  • SDG 3 · Sağlık ve Kaliteli Yaşam

Özet

Background: Propolis is a natural, resinous hive product that has several pharmacological activities. Its composition varies depending on the vegetation, climate, season and environmental conditions of the area from where it was collected. Surface enhanced laser desorption ionization time of flight mass spectrometry (SELDI-TOF MS) is a proteomic approach which has been used in cancer proteomics studies. Prostate cancer is one of the most commonly diagnosed cancers in men. It has shown that nutritional supplements rich in polyphenolic compounds such as propolis play a significant role in prostate cancer chemoprevention. The aim of this study is to evaluate if protein expression profile in PC-3 prostate cancer cell lines could be differentiated when incubated with dimethyl sulfoxide and water extracts of Turkish propolis.Results: The antioxidant potentials of dimethyl sulfoxide and water extracts of propolis were found in correlation with the amount of total phenolic compounds of them. Dimethyl sulfoxide and water extracts of propolis of 20 μg/mL reduced the cell viability to 24.5% and 17.7%, respectively. Statistically significant discriminatory peaks between control PC-3 cells and dimethyl sulfoxide extract of propolis-treated PC-3 cells were found to be the proteomic features at m/z 5143, 8703, 12661, 20184 and 32794, detected by CM10 ProteinChip, and the peak at m/z 3772, detected by Q10 ProteinChip. Between control PC-3 cells and water extract of propolis-treated PC-3 cells, statistically significant discriminatory peaks were found to be the proteomic features at m/z 15846, 16052 and 24658, detected by CM10 ProteinChip and the peaks at m/z 10348, 10899 and 11603, detected by Q10 ProteinChip.Conclusions: It was concluded that dimethyl sulfoxide and water extracts of Turkish propolis may have anti-proliferative activity through differentiating protein expression profile in PC-3 prostate cancer cell lines along with their antioxidant capacity.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/gumushane/15533Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1186/1477-5956-9-74Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorBarlak, Yaşam
dc.contributor.authorDeǧer, Orhan
dc.contributor.authorÇolak, Meltem
dc.contributor.authorKaratayli, Senem C.
dc.contributor.authorBozdayi, Abdurrahman M.
dc.contributor.authorYücesan, Fulya
dc.date.accessioned2026-10-22T10:24:09.367034140Z
dc.date.available2026-10-22T10:24:09.367034140Z
dc.date.issued2011
dc.description.abstractBackground: Propolis is a natural, resinous hive product that has several pharmacological activities. Its composition varies depending on the vegetation, climate, season and environmental conditions of the area from where it was collected. Surface enhanced laser desorption ionization time of flight mass spectrometry (SELDI-TOF MS) is a proteomic approach which has been used in cancer proteomics studies. Prostate cancer is one of the most commonly diagnosed cancers in men. It has shown that nutritional supplements rich in polyphenolic compounds such as propolis play a significant role in prostate cancer chemoprevention. The aim of this study is to evaluate if protein expression profile in PC-3 prostate cancer cell lines could be differentiated when incubated with dimethyl sulfoxide and water extracts of Turkish propolis.Results: The antioxidant potentials of dimethyl sulfoxide and water extracts of propolis were found in correlation with the amount of total phenolic compounds of them. Dimethyl sulfoxide and water extracts of propolis of 20 μg/mL reduced the cell viability to 24.5% and 17.7%, respectively. Statistically significant discriminatory peaks between control PC-3 cells and dimethyl sulfoxide extract of propolis-treated PC-3 cells were found to be the proteomic features at m/z 5143, 8703, 12661, 20184 and 32794, detected by CM10 ProteinChip, and the peak at m/z 3772, detected by Q10 ProteinChip. Between control PC-3 cells and water extract of propolis-treated PC-3 cells, statistically significant discriminatory peaks were found to be the proteomic features at m/z 15846, 16052 and 24658, detected by CM10 ProteinChip and the peaks at m/z 10348, 10899 and 11603, detected by Q10 ProteinChip.Conclusions: It was concluded that dimethyl sulfoxide and water extracts of Turkish propolis may have anti-proliferative activity through differentiating protein expression profile in PC-3 prostate cancer cell lines along with their antioxidant capacity.
dc.description.sponsorshipFoundation of Karadeniz Technical University, (2007.114.001.3)
dc.identifier.articlenumber74
dc.identifier.doi10.1186/1477-5956-9-74
dc.identifier.eissn1477-5956
dc.identifier.issn1477-5956
dc.identifier.pmid22152088
dc.identifier.scopus2-s2.0-82755162471
dc.identifier.startpage74
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/gumushane/15533
dc.identifier.volume9
dc.identifier.wosWOS:000301708700001
dc.language.isoen
dc.publisherBMC
dc.relation.ispartofProteome Science
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectPc-3 prostate cancer cell line
dc.subjectPropolis
dc.subjectProteome
dc.subjectSELDI-TOF MS
dc.subject.classificationBiochemical Research Methods
dc.subject.classificationBiochemistry & Molecular Biology
dc.subject.otherantioxidant
dc.subject.otherdimethyl sulfoxide
dc.subject.otherphenol derivative
dc.subject.otherpropolis
dc.subject.otherproteome
dc.subject.otherarticle
dc.subject.othercancer cell
dc.subject.othercell differentiation
dc.subject.othercell viability
dc.subject.otherhuman
dc.subject.otherhuman cell
dc.subject.otherprostate cancer
dc.subject.otherprotein expression
dc.subject.otherprotein microarray
dc.subject.othersurface enhanced laser desorption ionization time of flight mass spectrometry
dc.titleEffect of Turkish propolis extracts on proteome of prostate cancer cell line
dc.typeArticle
dspace.entity.typePublication
rdl.citation.openalex61
rdl.citation.scopus57
rdl.citation.wos50
rdl.departmentSchool of Health Sciences, Gümüşhane University, Gümüşhane, 29100, Turkey
rdl.oa.statushybrid
rdl.oa.urlhttps://proteomesci.biomedcentral.com/counter/pdf/10.1186/1477-5956-9-74
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)