Mechanism of Antitumor Effects of Saffron in Human Prostate Cancer Cells.
Mohammad KhanKaitlyn HearnChristian ParryMudasir RasidHassan BrimHassan AshktorabBernard Kwabi-AddoPublished in: Nutrients (2023)
Prostate cancer is the most common cancer and the second leading cause of cancer deaths among men in the USA. Several studies have demonstrated the antitumor properties of saffron in different types of cancers, including prostate cancer. The oral administration of saffron extract has been reported to have antitumor effects on aggressive prostate-cancer-cell-line-derived xenografts in nude male mice. The objective of this study was to carry out in vitro studies of saffron-treated prostate cancer cells to ascertain the effects of saffron on key intermediates in prostate carcinogenesis. Our studies demonstrated the significant inhibition of cell proliferation for androgen-sensitive prostate cancer cell lines via apoptotic pathways. We also demonstrate the statistically significant down-regulation of DNA methyltransferases (COMT, MGMT, EHMT2, and SIRT1 deacetylase) in saffron-treated prostate cancer cells. In addition, saffron-treated prostate cancer cells displayed a statistically significant dysregulation of DNA repair intermediates (WRN, p53, RECQ5, MST1R, and WDR70) in a time-dependent manner. Furthermore, Western blot analysis demonstrated that saffron treatment induced changes in the expression of other key genes (DNMT1, DNMT3b, MBD2, CD44, HDAC3, c-Myc, NF-kB, TNFα, AR, N-RAS, and PTEN) in prostate cancer cells. Collectively, our findings demonstrate the important mechanisms by which saffron mediates anti-tumor properties in prostate cancer. These findings suggest that the use of saffron supplements alongside standard treatment protocols may yield beneficial effects for individuals with prostate cancer.
Keyphrases
- prostate cancer
- radical prostatectomy
- dna repair
- cell proliferation
- oxidative stress
- dna methylation
- dna damage
- rheumatoid arthritis
- endothelial cells
- papillary thyroid
- immune response
- signaling pathway
- cell death
- case control
- squamous cell carcinoma
- gene expression
- cell cycle
- pi k akt
- combination therapy
- ischemia reperfusion injury
- genome wide
- squamous cell
- lps induced
- replacement therapy
- nuclear factor
- nk cells
- histone deacetylase
- benign prostatic hyperplasia
- bioinformatics analysis