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二烯丙基二硫化物诱导人结肠肿瘤细胞中ERK磷酸化并改变基因表达谱。

Diallyl disulfide induces ERK phosphorylation and alters gene expression profiles in human colon tumor cells.

作者信息

Knowles L M, Milner J A

机构信息

Graduate Program in Nutrition and the Nutrition Department, The Pennsylvania State University, University Park, PA 16802, USA.

出版信息

J Nutr. 2003 Sep;133(9):2901-6. doi: 10.1093/jn/133.9.2901.

Abstract

Diallyl disulfide (DADS), a compound found in processed garlic, has been shown to arrest unsynchronized human colon tumor cells (HCT-15) in the G(2)/M phase of the cell cycle. The present studies were designed to examine whether this cell cycle block related to alterations in protein kinase C (PKC), Ca(2+)/calmodulin-dependent protein kinase II (CAMK II) or extracellular signal-regulated kinase (ERK) activity. Exposing double thymidine synchronized HCT-15 cells to DADS (25, 50 and 100 micromol/L) for 4 h increased the G(2)/M population by 30, 31 and 63%, respectively, compared with controls (P < 0.05). PKC and CAM KII activities were not influenced by increasing DADS exposure and thus did not correlate with the block of cells in the G(2)/M phase. Although ERK activity increased by 44 and 60% after treatment with 100 and 500 micromol/L DADS (P < 0.05), it was not influenced by exposure to 25 or 50 micromol/L DADS. Western blot analysis revealed that although DADS (25, 50, 100 and 500 micromol/L) did not influence the quantity of ERK protein expressed, it did increase its phosphorylation by 39, 52, 73 and 61%, respectively, compared with controls (P < 0.05). These studies provide evidence that early alterations in ERK pathway signaling may contribute to the G(2)/M arrest observed after DADS exposure. Preliminary data generated using the Clonetech Atlas Human Cancer cDNA Expression Array suggest that alterations in cell cycle, DNA repair and cellular adhesion factors accompany DADS exposure and may also be involved in mediating the block in G(2)/M progression.

摘要

二烯丙基二硫化物(DADS)是一种在加工大蒜中发现的化合物,已被证明可使未同步化的人结肠肿瘤细胞(HCT - 15)停滞于细胞周期的G(2)/M期。本研究旨在检验这种细胞周期阻滞是否与蛋白激酶C(PKC)、钙/钙调蛋白依赖性蛋白激酶II(CAMK II)或细胞外信号调节激酶(ERK)活性的改变有关。将经双胸腺嘧啶同步化的HCT - 15细胞暴露于DADS(25、50和100 μmol/L)4小时后,与对照组相比,G(2)/M期细胞群体分别增加了30%、31%和63%(P < 0.05)。PKC和CAM KII活性不受DADS暴露增加的影响,因此与G(2)/M期细胞阻滞无关。虽然用100和500 μmol/L DADS处理后ERK活性分别增加了44%和60%(P < 0.05),但暴露于25或50 μmol/L DADS时不受影响。蛋白质印迹分析显示,虽然DADS(25、50、100和500 μmol/L)不影响ERK蛋白表达量,但与对照组相比,其磷酸化水平分别增加了39%、52%、73%和61%(P < 0.05)。这些研究提供了证据,表明ERK信号通路的早期改变可能导致DADS暴露后观察到的G(2)/M期阻滞。使用Clonetech Atlas Human Cancer cDNA表达阵列生成的初步数据表明,细胞周期、DNA修复和细胞黏附因子的改变伴随DADS暴露,也可能参与介导G(2)/M期进程的阻滞。

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