Department of Oral Pathology, School of Dentistry, Institute of Oral Bioscience, Brain Korea 21, Chonbuk National University, Jeonju, Republic of Korea.
J Agric Food Chem. 2011 Aug 10;59(15):8124-31. doi: 10.1021/jf2006358. Epub 2011 Jul 6.
Cruciferous vegetables have been shown to have the possibility to protect against multistep carcinogenesis. β-Phenylethyl isothiocyanate (PEITC) is one component of these vegetables demonstrated to help fight many types of cancer. The present study examined the apoptotic effects of PEITC and its molecular mechanism in human cervical cancer cell lines (HEp-2 and KB). PEITC induced apoptosis to inhibit cell proliferation. According to the protein chip assay, PEITC increased the expression of the death receptors (DR4 and DR5) and cleaved caspase-3 compared to the DMSO treatment group. PEITC also induced caspase-8 and truncated BID. PEITC down-regulated the phosphorylation of extracellular-related kinase (ERK)1/2, whereas neither phospho-c-Jun NH(2)-terminal kinases (JNK) nor phospho-p38 MAPK was changed. The role of ERK in PEITC-induced apoptosis was also investigated using MEK inhibitor (PD98059). PD98059 increased the expression of DR4 and DR5, activated caspase-3, and cleaved PARP. In addition, PEITC decreased the phosphorylation of MEK. Therefore, the apoptotic mechanism of PEITC in cervical cancer cells involves the induction of DR4 and DR5 through the inactivation of ERK and MEK.
十字花科蔬菜已被证明具有多步骤致癌作用的保护潜力。β-苯乙基异硫氰酸酯(PEITC)是这些蔬菜中的一种成分,已被证明有助于对抗多种类型的癌症。本研究探讨了 PEITC 及其在人宫颈癌细胞系(HEp-2 和 KB)中的分子机制对细胞凋亡的影响。PEITC 通过诱导细胞凋亡来抑制细胞增殖。根据蛋白芯片检测,与 DMSO 处理组相比,PEITC 增加了死亡受体(DR4 和 DR5)和裂解的 caspase-3 的表达。PEITC 还诱导了 caspase-8 和截断的 BID。PEITC 下调了细胞外相关激酶(ERK)1/2 的磷酸化,而磷酸化 c-Jun NH(2)-末端激酶(JNK)和磷酸化 p38 MAPK 均未改变。还使用 MEK 抑制剂(PD98059)研究了 ERK 在 PEITC 诱导的细胞凋亡中的作用。PD98059 增加了 DR4 和 DR5 的表达,激活了 caspase-3,并切割了 PARP。此外,PEITC 降低了 MEK 的磷酸化。因此,PEITC 在宫颈癌细胞中的凋亡机制涉及通过失活 ERK 和 MEK 诱导 DR4 和 DR5 的表达。