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首页> 外文期刊>Integrative cancer therapies. >Onbaekwon Suppresses Colon Cancer Cell Invasion by Inhibiting Expression of the CXC Chemokine Receptor 4
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Onbaekwon Suppresses Colon Cancer Cell Invasion by Inhibiting Expression of the CXC Chemokine Receptor 4

机译:Onbaekwon通过抑制CXC趋化因子受体4的表达抑制结肠癌细胞的侵袭。

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Cysteine X cysteine (CXC) chemokine receptor 4 (CXCR4) and C-X-C motif chemokine 12 (CXCL12) were originally identified as chemoattractants between immune cells and sites of inflammation. Since studies have validated an increased level of CXCL12 and its receptor in patients with colorectal cancers, CXCL12/CXCR4 axis has been considered as a valuable marker of cancer metastasis. Therefore, identification of CXCR4 inhibitors has great potential to abrogate tumor metastasis. Onbaekwon (OBW) is a complex herbal formula that is derived from the literature of traditional Korean medicine Dongeuibogam. In this study, we demonstrated that OBW suppressed CXCR4 expression in various cancer cell types in a concentration- and time-dependent manner. Both proteasomal and lysosomal inhibitors had no effect to prevent the OBW-induced suppression of CXCR4, suggesting that the inhibitory effect of OBW was not due to proteolytic degradation but occurred at the transcriptional level. Electrophoretic mobility shift assay further confirmed that OBW could block endogenous activation of nuclear factor kappa B, a key transcription factor that regulates the expression of CXCR4 in colon cancer cells. Consistent with the aforementioned molecular basis, OBW abolished cell invasion induced by CXCL12 in colon cancer cells. Together, our results suggest that OBW, as a novel inhibitor of CXCR4, could be a promising therapeutic agent contributing to cancer treatment.
机译:半胱氨酸X半胱氨酸(CXC)趋化因子受体4(CXCR4)和C-X-C基序趋化因子12(CXCL12)最初被确定为免疫细胞和炎症部位之间的趋化因子。由于研究已证实在结直肠癌患者中CXCL12及其受体水平升高,因此CXCL12 / CXCR4轴被认为是癌症转移的重要标志。因此,鉴定CXCR4抑制剂具有消除肿瘤转移的巨大潜力。 Onbaekwon(OBW)是一种复杂的草药配方,它源自韩国传统医学Dongeuibogam的文献。在这项研究中,我们证明了OBW以浓度和时间依赖性方式抑制了各种癌细胞类型中CXCR4的表达。蛋白酶体和溶酶体抑制剂都没有阻止OBW诱导的CXCR4抑制的作用,这表明OBW的抑制作用不是由于蛋白水解降解,而是在转录水平上发生。电泳迁移率迁移分析进一步证实,OBW可以阻断核因子κB的内源性活化,核转录因子κB是调节结肠癌细胞中CXCR4表达的关键转录因子。与上述分子基础一致,OBW消除了CXCL12在结肠癌细胞中诱导的细胞侵袭。总之,我们的结果表明,OBW作为CXCR4的新型抑制剂,可能是有助于癌症治疗的有前途的治疗剂。

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