首页> 外文期刊>Journal of Agricultural and Food Chemistry >Phenethyl Isothiocyanate Inhibited Tumor Migration and Invasion via Suppressing Multiple Signal Transduction Pathways in Human Colon Cancer HT29 Cells
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Phenethyl Isothiocyanate Inhibited Tumor Migration and Invasion via Suppressing Multiple Signal Transduction Pathways in Human Colon Cancer HT29 Cells

机译:异硫氰酸苯乙酯通过抑制人类结肠癌HT29细胞中的多种信号转导途径来抑制肿瘤的迁移和侵袭。

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Phenethyl isothiocyanate (PEITC), one of the major compounds from dietary cruciferous vegetables, has been found to have antitumor properties and therefore could generate special interest for the development of chemopreventive and/or chemotherapeutic agent for human cancers. In the primary studies, we found that PEITC induced cytotoxic effect (decreased the percentage of viable cells) in human colon cancer HT29 cells. Here, in this study, we are the first to report the antimetastatic effect of PEITC in HT29 human colon cancer cells. The results show that PEITC exhibited an inhibitory effect on the abilities of adhesion, migration, and invasion by Boyden chamber assay. Western blotting examination indicated that PEITC exerted an inhibitory effect on the SOS-1, PKC, ERK1/2 and Rho A for causing the inhibitions of MMP-2 and -9 then followed by the inhibition of invasion and migration of HT29 cells in vitro. PEITC also affected Ras, FAK, PI3K or inhibited GRB2, NF-κB, iNOS and COX-2 for causing the inhibition of cell proliferation in HT29 cells. Realtime PCR also showed that PEITC inhibited the gene expressions of MMP-2, -7, -9, FAK and Rho A after PEITC treatment for 48 h in HT29 cells. PEITC also inhibited the activities of AKT, ERK, JNK and PKC. Our results provide a new insight into the mechanisms and functions of PEITC which inhibit migration and invasion of HT29 human colon cancer cells. These results suggest that molecular targeting of NF-κB led to the inhibition of MMP-2, -7, and -9 and it might be a useful strategy for the inhibition of migration and invasion on human colon cancer.
机译:膳食十字花科蔬菜中的主要化合物之一异硫氰酸苯乙基酯(PEITC)具有抗肿瘤特性,因此对于开发用于人类癌症的化学预防剂和/或化学治疗剂可能引起特殊兴趣。在初步研究中,我们发现PEITC在人结肠癌HT29细胞中诱导了细胞毒性作用(降低了存活细胞的百分比)。在本研究中,我们是第一个报道PEITC在HT29人结肠癌细胞中的抗转移作用的药物。结果表明,通过博登室测定法,PEITC对粘附,迁移和侵袭能力表现出抑制作用。 Western blotting检测结果表明,PEITC对SOS-1,PKC,ERK1 / 2和Rho A均具有抑制作用,可抑制MMP-2和-9,进而抑制HT29细胞的侵袭和迁移。 PEITC还影响Ras,FAK,PI3K或抑制GRB2,NF-κB,iNOS和COX-2,从而抑制HT29细胞的细胞增殖。实时荧光定量PCR还显示PEITC抑制HT29细胞中PEITC处理48h后MMP-2,-7,-9,FAK和Rho A的基因表达。 PEITC还抑制AKT,ERK,JNK和PKC的活性。我们的结果为抑制PEITC抑制HT29人结肠癌细胞的迁移和侵袭的机制和功能提供了新的见解。这些结果表明,NF-κB的分子靶向导致MMP-2,-7和-9的抑制,这可能是抑制人类结肠癌迁移和侵袭的有用策略。

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