Author/Authors :
Mousavi, Nadia Department of Molecular Medicine - Cancer biomedical center, Tehran, Iran , Rahimi, Shahrzad Department of Biology - North Tehran Branch - Islamic Azad University, Tehran, Iran , Yavari, Saeede Department of Biology - Science and Research Branch - Islamic Azad University, Tehran, Iran , Kazemi, Amir Hossein Department of Biochemistry - School of Medicine - Zanjan university of medical sciences, Zanjan, Iran , Mohammad Taghi Kashi, Rana Department of Molecular Medicine - Cancer biomedical center, Tehran, Iran , Heidarian, Ronak Department of Genetic - Tonekabon Branch - Islamic Azad University, Tehran, Iran , Emami, Hanane Department of Developmental Biology - School of Biological Sciences - Kharazmi University, Tehran, Iran
Abstract :
Background: Prostate cancer (PCa) is the second leading cause of cancer death in American population.
In this manner, novel therapeutic approaches for identification of therapeutic targets for PCa has
significant clinical implications. Quercetin is a potent cancer therapeutic agent and dietary antioxidant
present in fruit and vegetables.
Methods: To investigate the underlying mechanism by which the PCa was regulated, nanoparticles of
quercetin were administrated to cells. For in vitro experiments, human PCa cell line LNCaP were involved.
Cell viability assay and quantitative RT-PCR (qRT-PCR) for hedgehog signaling pathway genes were used to
determine the key signaling pathway regulated for PCa progression.
Results: The cell viability gradually decreased with increased concentration of quercetin nanoparticles.
At 48 h, 40 mM concentration of quercetin treatment showed near 50% of viable cells. Quercetin
nanoparticles upregulates Su(Fu) mRNA expressions and downregulates gli mRNA expressions in the
LNCaP cells.
Conclusions: The results showed that the hedgehog signaling targeted inhibition may have important
implications of PCa therapeutics. Additionally, the outcomes provided new mechanistic basis for further
examination of quercetin nanoparticles to discover potential treatment strategies and new targets for PCa
inhibition.
Keywords :
Hedgehog , Prostate cancer , Proliferation , Quercetin nanoparticles , Signaling pathway