Johnson Jeremy J, Syed Deeba N, Heren Chenelle R, Suh Yewseok, Adhami Vaqar M, Mukhtar Hasan
Center for Women's Health Research, University of Wisconsin, School of Medicine and Public Health, Madison, Wisconsin, USA.
Pharm Res. 2008 Sep;25(9):2125-34. doi: 10.1007/s11095-008-9552-0. Epub 2008 Feb 21.
This study examines the anti-cancer effect of carnosol in human prostate cancer PC3 cells and its role in modulating multiple signaling pathways associated with carcinogenesis.
PC3 cells were treated with carnosol and were evaluated using a flow cytometry, a protein array and Western blot analysis to identify signaling pathways targeted by carnosol.
Using an MTT assay we found that carnosol (10-70 microM) decreases cell viability in a time and dose-dependent manner. Further analysis using flow cytometry as well as biochemical analysis identified G2-phase cell cycle arrest. To establish a more precise mechanism, we performed a protein array that evaluated 638 proteins involved in cell signaling pathways. The protein array identified 5'-AMP-activated protein kinase (AMPK), a serine/threonine protein kinase involved in the regulation of cellular energy balance as a potential target. Further downstream effects consistent with cancer inhibition included the modulation of the mTOR/HSP70S6k/4E-BP1 pathway. Additionally, we found that carnosol targeted the PI3K/Akt pathway in a dose dependent manner.
These results suggest that carnosol targets multiple signaling pathways that include the AMPK pathway. The ability of carnosol to inhibit prostate cancer in vitro suggests carnosol may be a novel agent for the management of PCa.
本研究考察了鼠尾草酸对人前列腺癌PC3细胞的抗癌作用及其在调节与致癌作用相关的多种信号通路中的作用。
用鼠尾草酸处理PC3细胞,并通过流式细胞术、蛋白质芯片和蛋白质免疫印迹分析进行评估,以确定鼠尾草酸靶向的信号通路。
使用MTT法,我们发现鼠尾草酸(10 - 70微摩尔)以时间和剂量依赖性方式降低细胞活力。使用流式细胞术以及生化分析进一步分析确定了G2期细胞周期阻滞。为了建立更精确的机制,我们进行了蛋白质芯片分析,评估了参与细胞信号通路的638种蛋白质。蛋白质芯片分析确定5'-AMP激活蛋白激酶(AMPK),一种参与调节细胞能量平衡的丝氨酸/苏氨酸蛋白激酶,为潜在靶点。与癌症抑制一致的进一步下游效应包括对mTOR/HSP70S6k/4E-BP1通路的调节。此外,我们发现鼠尾草酸以剂量依赖性方式靶向PI3K/Akt通路。
这些结果表明鼠尾草酸靶向包括AMPK通路在内的多种信号通路。鼠尾草酸在体外抑制前列腺癌的能力表明其可能是一种用于治疗前列腺癌的新型药物。