The anti-proliferative and apoptotic effects of curcumin on feline mammary gland tumor cells in vitro


Ozkan D. A., Eskiler G. G., Turna Ö., Kazan N., Kucukkara S. E., Baykal A., ...Daha Fazla

IRANIAN JOURNAL OF VETERINARY RESEARCH, cilt.22, sa.3, ss.222-229, 2021 (SCI-Expanded, Scopus) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 22 Sayı: 3
  • Basım Tarihi: 2021
  • Doi Numarası: 10.22099/ijvr.2021.40452.5866
  • Dergi Adı: IRANIAN JOURNAL OF VETERINARY RESEARCH
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, CAB Abstracts, EMBASE, Veterinary Science Database
  • Sayfa Sayıları: ss.222-229
  • Anahtar Kelimeler: Apoptosis, Cell cycle, Curcumin, Feline mammary gland tumor, CANCER, CANINE, CARCINOMA, PCNA
  • İstanbul Üniversitesi-Cerrahpaşa Adresli: Evet

Özet

Background: Feline mammary gland tumors (FMGTs) are the third most diagnosed tumors in cats. Feline mammary gland tumors have aggressive biological behavior and poor response to both surgical and medical treatments, thus, new therapeutic approaches are essential to improve. Curcumin (CUR) is a polyphenol component exhibiting anti-cancer effects and induces apoptosis through different mechanisms especially in human breast cancer. However, there is no study investigating the effects of CUR on FMGTs. Aims: The aim of this study was to determine the anti-proliferative and apoptotic effects of CUR on primary cell lines from FMGT tissue samples of two cases classified as carcinoma-simple, tubular type (grade III). Methods: The cytotoxic effect of CUR was determined by water-soluble tetrazolium salt-1 (WST-1) assay. Annexin V, cell cycle, and acridine orange (AO) analyses were performed to determine the apoptotic effect of CUR. Results: Our results showed that CUR had an anti-proliferative and apoptotic effect through induction of apoptosis and cell cycle arrest (G0/G1) on FMGT cells. Conclusion: Therefore, this is the first study that shows the effects of CUR on FMGTs. However, further molecular studies are required to compare the effects of CUR on different histopathological phenotypes and to determine the further molecular mechanisms including the potential apoptotic and cellular pathways affected by CUR.