Zimra Y, Wasserman L, Maron L, Shaklai M, Nudelman A, Rephaeli A
Division of Hematology, Rabin Medical Center, Petach Tikava, Israel.
J Cancer Res Clin Oncol. 1997;123(3):152-60. doi: 10.1007/BF01214667.
A novel butyric acid derivative, pivaloyloxymethyl butyrate, AN-9, was previously shown to be a potent differentiating agent. AN-9 exerts a significant anticancer activity in vitro and in vivo. In all the activities examined, AN-9 was more potent than butyric acid. Here we show that AN-9 and butyric acid induce cell death by apoptosis. Exposure of HL-60 cells to butyric acid and AN-9 decreased cell numbers and induced cell differentiation and the appearance of typical apoptotic features. Induction of apoptosis and/or differentiation by AN-9 and butyric acid was dependent on the concentration and the time of exposure to the drugs. The advantage of AN-9 over butyric acid was further confirmed. Apoptosis induced by AN-9 occurred after a shorter exposure and at lower drug concentrations than that induced by butyric acid. Apoptosis by AN-9 was accompanied by reduction in Bcl-2 expression. Preincubation with antioxidants did not protect HL-60 cells from apoptosis induced by AN-9. HL-60 cells that were induced to differentiate by preincubation with retinoic acid or low AN-9 concentrations were more resistant to apoptosis, induced later by high concentrations of AN-9, than were undifferentiated cells.
一种新型丁酸衍生物,特戊酰氧基甲基丁酸酯(AN-9),先前已被证明是一种有效的分化剂。AN-9在体外和体内均具有显著的抗癌活性。在所有检测的活性中,AN-9比丁酸更有效。在此我们表明,AN-9和丁酸通过凋亡诱导细胞死亡。将HL-60细胞暴露于丁酸和AN-9会减少细胞数量,并诱导细胞分化以及出现典型的凋亡特征。AN-9和丁酸诱导凋亡和/或分化取决于药物暴露的浓度和时间。AN-9相对于丁酸的优势得到了进一步证实。与丁酸诱导的凋亡相比,AN-9诱导的凋亡在更短的暴露时间和更低的药物浓度下发生。AN-9诱导的凋亡伴随着Bcl-2表达的降低。用抗氧化剂预孵育不能保护HL-60细胞免受AN-9诱导的凋亡。与未分化细胞相比,用视黄酸或低浓度AN-9预孵育诱导分化的HL-60细胞对高浓度AN-9随后诱导的凋亡更具抗性。