4.5 Article

Delivery of curcumin within emulsome nanoparticles enhances the anti-cancer activity in androgen-dependent prostate cancer cell

Journal

MOLECULAR BIOLOGY REPORTS
Volume -, Issue -, Pages -

Publisher

SPRINGER
DOI: 10.1007/s11033-022-08208-0

Keywords

Androgen dependent prostate cancer; Curcumin; Emulsome; Anti-cancer; Phytochemical

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This study evaluated the therapeutic potential of a new type of curcumin-loaded emulsome nanoparticular system, CurcuEmulsomes, in androgen dependent prostate cancer cell line LNCaP. The results showed that CurcuEmulsomes had a more effective inhibitory effect on the proliferation of LNCaP cells compared to free curcumin. CurcuEmulsomes not only prolonged the biological activity of curcumin but also induced apoptotic cell death and cell cycle arrest. This highlights the potential of CurcuEmulsomes to enhance the intrinsic anticancer activities of curcumin in androgen dependent prostate cancer therapy.
Background Curcumin, a dietary polyphenol isolated from turmeric, is a potent phytochemical possessing intrinsic anticancer activities against various cancer types including prostate cancer. However, low water solubility and bioavailability of the compound are major challenges against its medical use. The objective of this study is to evaluate the therapeutic potential of curcumin-loaded emulsome nanoparticular system, i.e. CurcuEmulsomes, for the treatment of androgen dependent LNCaP prostate cancer cell line. Methods and results The antiproliferative effect of both free curcumin and CurcuEmulsome were investigated comparatively on LNCaP and PNT1A cells. Cell viability data indicates that the inhibition in proliferation of LNCaP cells becomes more effective when curcumin is provided with its emulsome formulation rather than its free form. Corresponding to a therapeutic index of 2.25, Half maximal inhibitory (IC50) and cytotoxic (CC50) concentrations of CurcuEmulsomes for LNCaP and PNT1A cells were estimated as 17.1 mu M and 38.6 mu M, respectively. The fluorescence signal of autofluorescence curcumin was preserved within the CurcuEmulsomes at 72 h after the treatment. Thus, CurcuEmulsomes prolonged biological activity of curcumin. Induced apoptotic cell death and stimulated cell cycle arrest at G2/M phase were attributed to antiproliferative activity of CurcuEmulsomes. Treatment of LNCaP cells with CurcuEmulsomes increased expression of caspase-3 significantly by 11.76-fold, whereas decreased cyclin D1, Bcl-2 and AR expression levels significantly by of 0.18, 0.06 and 0.46-fold, respectively. Conclusions Presented safety and anticancer activity of CurcuEmulsomes on LNCaP cell line highlights the potential of CurcuEmulsomes to benefit intrinsic anticancer activities of curcumin in androgen dependent prostate cancer therapy.

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