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首页> 外文期刊>Journal of Agricultural and Food Chemistry >Apple polyphenols affect protein kinase c activity and the onset of apoptosis in human colon carcinoma cells
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Apple polyphenols affect protein kinase c activity and the onset of apoptosis in human colon carcinoma cells

机译:苹果多酚影响人结肠癌细胞中蛋白激酶c的活性和凋亡的开始

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Polyphenol-rich apple extracts have been reported to suppress human colon cancer cell growth in vitro. The protein kinase C (PKC) is among the signaling elements known to play an important role in colon carcinogenesis. In the present study, we investigated whether apple polyphenols affect PKC activity and induce apoptosis in the human colon carcinoma cell line HT29. A polyphenol-rich apple juice extract (AE02) was shown to inhibit cytosolic PKC activity in a cell-free system. In contrast, incubation of HT29 cells for 1 or 3 h with AE02 up to 2 mg/mL did not affect the cytosolic PKC activity. After prolonged incubation (24 h), cytosolic PKC activity was modulated, albeit a u-shaped curve of effectiveness was observed, with an initial inhibitory effect followed by the recurrence and even induction of enzyme activity. Concomitantly, in the cytosol, a significant decrease of the protein levels of PKC alpha, PKC beta(II), and PKC gamma together with a significant increase of a proapoptotic PKC delta fragment was observed. However, the effects on the protein levels of these PKC isoforms in the cytosol were not associated with translocation between the different cellular compartments but might instead result from the onset of apoptosis. Indeed, the treatment with AE02 was shown to induce apoptosis by the activation of caspase-3, DNA fragmentation, and cleavage of poly(ADP ribose) polymerase. So far, identified and available constituents of the apple extract did not contribute substantially to the observed effects on PKC and apoptosis induction. In summary, apple polyphenols were found to inhibit PKC activity in a cell-free system. However, our results indicate that within intact cells PKC does not represent the primary target of apple polyphenols but appears to be affected in the course of apoptosis induction.
机译:据报道,富含多酚的苹果提取物可在体外抑制人结肠癌细胞的生长。蛋白激酶C(PKC)是已知在结肠癌发生中起重要作用的信号传导元件之一。在本研究中,我们调查了苹果多酚是否会影响人结肠癌细胞株HT29的PKC活性并诱导细胞凋亡。富含多酚的苹果汁提取物(AE02)在无细胞系统中显示出抑制胞浆PKC活性的作用。相反,HT29细胞与AE02孵育2到2 mg / mL的时间为1或3 h不会影响胞浆PKC活性。延长孵育时间(24小时)后,虽然观察到了U型曲线,但调节了胞浆PKC活性,具有初步的抑制作用,其后是酶活性的复发甚至诱导。同时,在细胞质中,观察到PKCα,PKC beta(II)和PKCγ的蛋白质水平显着下降,同时凋亡前PKCδ片段也显着上升。但是,对这些PKC亚型在细胞质中的蛋白质水平的影响与不同细胞区室之间的易位无关,而可能是细胞凋亡的开始。实际上,已证明用AE02的处理通过激活caspase-3,DNA片段化和聚(ADP核糖)聚合酶的裂解来诱导凋亡。到目前为止,苹果提取物中已确定和可用的成分对观察到的对PKC和细胞凋亡诱导的影响没有实质性贡献。总之,发现苹果多酚在无细胞系统中抑制PKC活性。然而,我们的结果表明,在完整细胞中,PKC并不代表苹果多酚的主要靶点,但似乎在凋亡诱导过程中受到影响。

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