Wahab Shadma, Alsayari Abdulrhman, Muhsinah Abdullatif Bin, Ahmad Irfan, Hussain Md Sarfaraj, Mallick Jewel
Department of Pharmacognosy, College of Pharmacy, King Khalid University, Abha 61421, Saudi Arabia.
Complementary and Alternative Medicine Unit, College of Pharmacy, King Khalid University, Abha 6142, Saudi Arabia.
Evid Based Complement Alternat Med. 2022 Jul 9;2022:7975664. doi: 10.1155/2022/7975664. eCollection 2022.
Cirsilineol has been reported to exhibit anticancer effects against several human cancer cell lines. The present study was designed to evaluate the anticancer effects of cirsilineol against the human DU-145 prostate cancer cells. The results showed that cirsilineol suppressed the proliferation of DU-145 cancer cells in a dose-dependent manner with minimal cytotoxic effects against the normal cells. The IC of cirsilineol was found to be 7 M and 110 M against prostate cancer DU-145 and normal HPrEC prostate cells, respectively. Acridine orange and ethidium bromide (AO/EB) staining showed that cirsilineol induced apoptosis in DU-145 prostate cancer cells. The Annexin V/PI staining further confirmed the induction of apoptosis in DU-145 cells. The western blot analysis showed that cirsilineol suppressed the expression of Bax and upregulated the expression of Bcl-2 in prostate cancer DU-145 cells. Moreover, cirsilineol caused a dose-dependent increase in reactive oxygen species (ROS) levels in prostate cancer. Wound healing and Transwell assays showed that cirsilineol inhibits migration and invasion of DU-145 prostate cancer cells. Summing up, the results suggest that cirsilineol suppresses the proliferation of prostate cancer cells and may prove to be a beneficial lead molecule for the development of chemotherapy for prostate cancer.
据报道,cirsilineol对多种人类癌细胞系具有抗癌作用。本研究旨在评估cirsilineol对人DU - 145前列腺癌细胞的抗癌作用。结果表明,cirsilineol以剂量依赖的方式抑制DU - 145癌细胞的增殖,对正常细胞的细胞毒性作用最小。cirsilineol对前列腺癌DU - 145细胞和正常HPrEC前列腺细胞的半数抑制浓度分别为7μM和110μM。吖啶橙和溴化乙锭(AO/EB)染色显示cirsilineol诱导DU - 145前列腺癌细胞凋亡。膜联蛋白V/碘化丙啶(Annexin V/PI)染色进一步证实了DU - 145细胞凋亡的诱导。蛋白质印迹分析表明,cirsilineol抑制前列腺癌DU - 145细胞中Bax的表达并上调Bcl - 2的表达。此外,cirsilineol导致前列腺癌中活性氧(ROS)水平呈剂量依赖性增加。伤口愈合和Transwell实验表明,cirsilineol抑制DU - 145前列腺癌细胞的迁移和侵袭。综上所述,结果表明cirsilineol抑制前列腺癌细胞的增殖,可能被证明是前列腺癌化疗开发中有价值的先导分子。