Department of Chemical Biology, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, USA.
Department of Cancer Biology, MD Anderson Cancer Center, Houston, USA.
Carcinogenesis. 2018 Feb 9;39(2):158-169. doi: 10.1093/carcin/bgx128.
The PTEN/PI3K/AKT axis plays a critical role in regulating cell growth, differentiation and survival. Activation of this signaling pathway is frequently found in human cancers. Our previous studies demonstrated that δ-tocopherol (δ-T) attenuates the activation of AKT by growth factor in prostate cancer cell lines, leading to inhibition of proliferation and induction of apoptosis. Herein, we investigated whether δ-T inhibits the development of prostate adenocarcinoma in prostate-specific Pten-/- (Ptenp-/-) mice in which the activation of AKT is the major driving force for tumorigenesis. By feeding Ptenp-/- mice with AIN93M or 0.2% δ-T supplemented diet starting at the age of 6 or 12 weeks, we found that δ-T treatment reduced prostate adenocarcinoma multiplicity at the age of 40 weeks by 53.3 and 42.7%, respectively. Immunohistochemical (IHC) analysis demonstrated that the phosphorylation of AKT (T308) was reduced in the prostate of the mice administered the δ-T diet. Consistently, proliferation was reduced and apoptosis was increased in prostate lesions of mice on the δ-T diet. Oxidative stress, as determined by IHC staining of 8-OH-dG, was not altered during prostate tumorigenesis, nor was it affected by administration of δ-T. In contrast, α-tocopherol (α-T) at 0.2% in the diet did not affect prostate adenocarcinoma multiplicity in the Ptenp-/- mice. This finding is consistent with data from our previous study that δ-T, but not α-T, inhibits the activation of AKT and the growth of prostate cancer cells. Together, these results demonstrate that δ-T inhibits the development of prostate adenocarcinoma in Ptenp-/- mice, mainly through inhibition of AKT activation.
PTEN/PI3K/AKT 轴在调节细胞生长、分化和存活方面起着关键作用。该信号通路的激活在人类癌症中经常被发现。我们之前的研究表明,δ-生育酚(δ-T)通过生长因子减弱前列腺癌细胞系中 AKT 的激活,导致增殖抑制和凋亡诱导。在此,我们研究了 δ-T 是否抑制了 AKT 激活是肿瘤发生主要驱动力的前列腺特异性 Pten-/-(Ptenp-/-)小鼠中前列腺腺癌的发展。通过从 6 或 12 周龄开始用 AIN93M 或 0.2%δ-T 补充饮食喂养 Ptenp-/-小鼠,我们发现,δ-T 处理分别将 40 周龄时的前列腺腺癌多发性降低了 53.3%和 42.7%。免疫组织化学(IHC)分析表明,给予 δ-T 饮食的小鼠前列腺中 AKT(T308)的磷酸化减少。一致地,在 δ-T 饮食的小鼠前列腺病变中,增殖减少,凋亡增加。氧化应激,如 8-OH-dG 的 IHC 染色所示,在前列腺肿瘤发生过程中没有改变,也不受 δ-T 给药的影响。相比之下,饮食中 0.2%的α-生育酚(α-T)并未影响 Ptenp-/-小鼠的前列腺腺癌多发性。这一发现与我们之前的研究数据一致,即δ-T 而不是 α-T 抑制 AKT 的激活和前列腺癌细胞的生长。总之,这些结果表明,δ-T 主要通过抑制 AKT 激活抑制 Ptenp-/-小鼠前列腺腺癌的发展。