Edderkaoui Mouad, Odinokova Irina, Ohno Izumi, Gukovsky Ilya, Go Vay Liang W, Pandol Stephen J, Gukovskaya Anna S
Department of Medicine, Veterans Affairs Greater Los Angeles Healthcare System and University of California, Los Angeles, CA 90073, California, United States.
World J Gastroenterol. 2008 Jun 21;14(23):3672-80. doi: 10.3748/wjg.14.3672.
To determine the effect of ellagic acid on apoptosis and proliferation in pancreatic cancer cells and to determine the mechanism of the pro-survival effects of ellagic acid.
The effect of ellagic acid on apoptosis was assessed by measuring phosphatidylserine externalization, caspase activity, mitochondrial membrane potential and DNA fragmentation; and proliferation by measuring DNA thymidine incorporation. Mitochondrial membrane potential was measured in permeabilized cells, and in isolated mitochondria. Nuclear factor kappa B (NF-kappa B) activity was measured by electromobility shift assay (EMSA).
We show that ellagic acid, a polyphenolic compound in fruits and berries, at concentrations 10 to 50 mmol/L stimulates apoptosis in human pancreatic adenocarcinoma cells. Further, ellagic acid decreases proliferation by up to 20-fold at 50 mmol/L. Ellagic acid stimulates the mitochondrial pathway of apoptosis associated with mitochondrial depolarization, cytochrome C release, and the downstream caspase activation. Ellagic acid does not directly affect mitochondria. Ellagic acid dose-dependently decreased NF-kappa B binding activity. Furthermore, inhibition of NF-kappa B activity using IkB wild type plasmid prevented the effect of ellagic acid on apoptosis.
Our data indicate that ellagic acid stimulates apoptosis through inhibition of the prosurvival transcription factor NF-kappa B.
确定鞣花酸对胰腺癌细胞凋亡和增殖的影响,并确定鞣花酸促生存作用的机制。
通过检测磷脂酰丝氨酸外翻、半胱天冬酶活性、线粒体膜电位和DNA片段化来评估鞣花酸对凋亡的影响;通过检测DNA胸苷掺入来评估增殖。在通透细胞和分离的线粒体中测量线粒体膜电位。通过电泳迁移率变动分析(EMSA)测量核因子κB(NF-κB)活性。
我们发现,水果和浆果中的一种多酚化合物鞣花酸,在浓度为10至50 mmol/L时可刺激人胰腺腺癌细胞凋亡。此外,鞣花酸在50 mmol/L时可使增殖降低多达20倍。鞣花酸刺激与线粒体去极化、细胞色素C释放及下游半胱天冬酶激活相关的凋亡线粒体途径。鞣花酸不直接影响线粒体。鞣花酸剂量依赖性地降低NF-κB结合活性。此外,使用IkB野生型质粒抑制NF-κB活性可阻止鞣花酸对凋亡的影响。
我们的数据表明,鞣花酸通过抑制促生存转录因子NF-κB来刺激凋亡。