Department of Oncology, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Biosci Biotechnol Biochem. 2021 Mar 24;85(4):786-797. doi: 10.1093/bbb/zbaa108.
Prostate cancer (PCa) is one of the important factors of cancer deaths especially in the western countries. Hispidulin (4',5,7-trihydroxy-6-methoxyflavone) is a phenolic flavonoid compound proved to possess anticancer properties, but its effects on PCa are left to be released. The aims of this study were to investigate the effects and the relative mechanisms of Hispidulin on PCa development. Hispidulin administration inhibited proliferation, invasion, and migration, while accelerated apoptosis in Du145 and VCaP cells, which was accompanied by PPARγ activation and autophagy enhancement. The beneficial effects of Hispidulin could be diminished by PPARγ inhibition. Besides, Hispidulin administration suppressed PCa tumorigenicity in Xenograft models, indicating the anticancer properties in vivo. Therefore, our work revealed that the anticancer properties of Hispidulin might be conferred by its activation on PPARγ and autophagy.
前列腺癌(PCa)是癌症死亡的重要因素之一,尤其是在西方国家。山柰素(4',5,7-三羟基-6-甲氧基黄酮)是一种酚类黄酮类化合物,已被证明具有抗癌特性,但它对 PCa 的影响尚待揭示。本研究旨在探讨山柰素对 PCa 发展的影响及其相关机制。山柰素给药可抑制 Du145 和 VCaP 细胞的增殖、侵袭和迁移,同时促进细胞凋亡,这伴随着 PPARγ 的激活和自噬的增强。PPARγ 抑制可减弱山柰素的有益作用。此外,山柰素给药抑制了异种移植模型中的 PCa 致瘤性,表明其具有体内抗癌特性。因此,我们的工作表明,山柰素的抗癌特性可能与其对 PPARγ 和自噬的激活有关。