Department of Pharmacognosy, College of Pharmacy, Third Military Medical University, Chongqing, China.
Graduate Center for Toxicology, College of Medicine, University of Kentucky, Lexington, KY, USA.
Cell Death Dis. 2014 Jan 16;5(1):e998. doi: 10.1038/cddis.2013.519.
R-(-)-gossypol acetic acid (AT-101) is a natural cottonseed product that exhibits anticancer activity. However, the molecular mechanism behind the antileukemic activity of AT-101 has not been well characterized. In this study, we investigated how AT-101 induces apoptosis in human leukemia cells. Exposure to AT-101 significantly increased apoptosis in both human leukemia cell lines and primary human leukemia cells. This increase was accompanied by the activation of caspases, cytochrome c release, Bcl2-associated X protein (Bax) translocation, myeloid cell leukemia-1 (Mcl-1) downregulation, Bcl-2-associated death promoter (Bad) dephosphorylation, Akt inactivation, and RhoA/Rho-associated coiled-coil containing protein kinase 1/phosphatase and tensin homolog (RhoA/ROCK1/PTEN) activation. RhoA, rather than caspase-3 cleavage, mediated the cleavage/activation of ROCK1 that AT-101 induced. Inhibiting RhoA and ROCK1 activation by C3 exoenzyme (C3) and Y27632, respectively, attenuated the ROCK1 cleavage/activation, PTEN activity, Akt inactivation, Mcl-1 downregulation, Bad dephosphorylation, and apoptosis mediated by AT-101. Knocking down ROCK1 expression using a ROCK1-specific siRNA also significantly abrogated AT-101-mediated apoptosis. Constitutively active Akt prevented the AT-101-induced Mcl-1 downregulation, Bad dephosphorylation, and apoptosis. Conversely, AT-101 lethality was potentiated by the phosphatidylinositol 3-kinase inhibitor LY294002. In vivo, the tumor growth inhibition caused by AT-101 was also associated with RhoA/ROCK1/PTEN activation and Akt inactivation in a mouse leukemia xenograft model. Collectively, these findings suggest that AT-101 may preferentially induce apoptosis in leukemia cells by interrupting the RhoA/ROCK1/PTEN pathway, leading to Akt inactivation, Mcl-1 downregulation, Bad dephosphorylation, and Bax translocation, which culminate in mitochondrial injury and apoptosis.
R-(-)-棉酚乙酸(AT-101)是一种天然的棉籽产物,具有抗癌活性。然而,AT-101 的抗白血病活性的分子机制尚未得到很好的描述。在这项研究中,我们研究了 AT-101 如何诱导人白血病细胞凋亡。暴露于 AT-101 显著增加了人白血病细胞系和原代人白血病细胞的凋亡。这种增加伴随着半胱天冬酶的激活、细胞色素 c 的释放、Bcl2 相关 X 蛋白(Bax)易位、髓样细胞白血病-1(Mcl-1)下调、Bcl-2 相关死亡促进剂(Bad)去磷酸化、Akt 失活以及 RhoA/Rho 相关卷曲螺旋蛋白激酶 1/磷酸酶和张力蛋白同源物(RhoA/ROCK1/PTEN)的激活。RhoA,而不是半胱天冬酶-3 切割,介导了 AT-101 诱导的 ROCK1 的切割/激活。用 C3 外切酶(C3)和 Y27632 分别抑制 RhoA 和 ROCK1 的激活,减弱了 AT-101 介导的 ROCK1 切割/激活、PTEN 活性、Akt 失活、Mcl-1 下调、Bad 去磷酸化和凋亡。用 ROCK1 特异性 siRNA 敲低 ROCK1 表达也显著阻断了 AT-101 介导的凋亡。组成型激活的 Akt 阻止了 AT-101 诱导的 Mcl-1 下调、Bad 去磷酸化和凋亡。相反,PI3K 抑制剂 LY294002 增强了 AT-101 的致死性。在体内,在小鼠白血病异种移植模型中,AT-101 引起的肿瘤生长抑制也与 RhoA/ROCK1/PTEN 激活和 Akt 失活有关。总的来说,这些发现表明,AT-101 可能通过中断 RhoA/ROCK1/PTEN 途径,导致 Akt 失活、Mcl-1 下调、Bad 去磷酸化和 Bax 易位,从而导致线粒体损伤和凋亡,从而优先诱导白血病细胞凋亡。