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首页> 外文期刊>Oncology letters >4-Methylumbelliferone inhibits enhanced hyaluronan synthesis and cell migration in pancreatic cancer cells in response to tumor-stromal interactions
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4-Methylumbelliferone inhibits enhanced hyaluronan synthesis and cell migration in pancreatic cancer cells in response to tumor-stromal interactions

机译:4-甲基纤维酮抑制胰腺癌细胞中增强的透明质酸合成和细胞迁移,响应肿瘤 - 基质相互作用

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摘要

Hyaluronic acid (HA) in tumor stroma promotes tumor invasion and progression. 4-Methylumbelliferone (4-MU) is a potent HA synthesis inhibitor. In the present study, the effects of 4-MU on enhanced HA synthesis and cell migration in pancreatic ductal adenocarcinoma (PDAC) cells, in response to co-culture with stromal fibroblasts, was investigated. The HA concentration was determined using ELISA and a Transwell migration assay was used to analyze cell migratory capability. The mRNA expression levels of hyaluronan synthases (HAS1, HAS2 and HAS3) were determined using the quantitative polymerase chain reaction. Co-culture between Panc-1 cells and stromal fibroblasts markedly increased cell migration in association with increasing HA production, which was markedly associated with an increase in HAS3 mRNA expression. Treatment with 4-MU markedly decreased the HA production and cell migration of Panc-1 cells in the co-culture system. The results of the present study suggested that interactions between PDAC cells and stromal fibroblasts increased HA production, resulting in a marked increase in migration of PDAC cells, and 4-MU may be used as a chemotherapeutic agent to inhibit the enhanced migration of PDAC cells in response to tumor-stromal interactions.
机译:透明质酸(HA)在肿瘤基质中促进肿瘤侵袭和进展。 4-甲基ZHEMLIFERONE(4-MU)是一种有效的HA合成抑制剂。在本研究中,研究了4-Mu对增强的HA合成和细胞迁移在胰腺导管腺癌(PDAC)细胞中的影响,响应于具有基质成纤维细胞的共培养物。使用ELISA测定HA浓度,并使用Transwell迁移测定来分析细胞迁移能力。使用定量聚合酶链反应测定透明质酸合酶的mRNA表达水平(HAS1,HAS2和HAS3)。 Panc-1细胞和基质成纤维细胞之间的共同培养明显增加了与增加的HA生产相关的细胞迁移,这与HAS3 mRNA表达的增加显着相关。用4-mu治疗显着降低了共培养系统中Panc-1细胞的HA生产和细胞迁移。本研究的结果表明,PDAC细胞和基质成纤维细胞之间的相互作用增加了HA生产,导致PDAC细胞的迁移显着增加,并且4-MU可以用作化学治疗剂以抑制PDAC细胞的增强迁移反应肿瘤 - 基质相互作用。

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