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首页> 外文期刊>Cancer letters >Human uterus myoma and gene expression profiling: A novel in vitro model for studying secretory leukocyte protease inhibitor-mediated tumor invasion
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Human uterus myoma and gene expression profiling: A novel in vitro model for studying secretory leukocyte protease inhibitor-mediated tumor invasion

机译:人子宫肌瘤和基因表达谱:研究分泌性白细胞蛋白酶抑制剂介导的肿瘤侵袭的新型体外模型

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摘要

Secretory leukocyte protease inhibitor (SLPI) is a serine protease inhibitor that diminishes tissue destruction during inflammation. A recent report revealed high levels of SLPI expression in the oral carcinoma cell. In addition, overexpression of SLPI up-regulates metastasis in lung carcinoma cells. On the other hand, matrix metalloproteinases (MMPs) are proteinases that participate in extracellular matrix degradation. SLPI and MMPs are involved as accelerators of the tumor invasion process; however, their exact roles are not fully understood. Understanding the mechanism of tumor invasion requires models that take the effect of microenvironmental factors into account. In one such in vitro model, different carcinoma cells have been shown to invade myoma tissue in highly distinct patterns. We have used this myoma model, as it provides a more natural stroma-like environment, to investigate the role of SLPI in tumor invasion. Our results indicate that the model provides a relevant matrix for tumor invasion studies, and that SLPI is important for the invasion of oral carcinoma Ca9-22 cells in conjunction with MMPs. Furthermore, using bioinformatics analysis, we have identified candidates as key molecules involved in SLPImediated tumor invasion. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
机译:分泌型白细胞蛋白酶抑制剂(SLPI)是一种丝氨酸蛋白酶抑制剂,可减少炎症过程中的组织破坏。最近的报告显示口腔癌细胞中SLPI表达高水平。另外,SLPI的过表达上调了肺癌细胞的转移。另一方面,基质金属蛋白酶(MMP)是参与细胞外基质降解的蛋白酶。 SLPI和MMP作为肿瘤侵袭过程的促进剂。但是,它们的确切作用尚不完全清楚。要了解肿瘤的侵袭机制,就需要考虑微环境因素影响的模型。在一种这样的体外模型中,已经显示出不同的癌细胞以高度不同的模式侵入肌瘤组织。我们使用了这种肌瘤模型,因为它提供了更自然的基质样环境,以研究SLPI在肿瘤侵袭中的作用。我们的结果表明,该模型为肿瘤侵袭研究提供了相关的矩阵,并且SLPI与MMP一起对于口腔癌Ca9-22细胞的侵袭很重要。此外,使用生物信息学分析,我们已确定候选物为参与SLPI介导的肿瘤侵袭的关键分子。 (C)2016 Elsevier Ireland Ltd.保留所有权利。

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