Cancer letters · 2016
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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Mikami Yoshikazu, Fukushima Atsushi, Komiyama Yusuke, Iwase Takashi, Tsuda Hiromasa, Higuchi Yasuhiko, Hayakawa Satoshi, Kuyama Kayo, Komiyama Kazuo
Аннотация
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 SLPI-mediated tumor invasion.
Предметные рубрики MeSH
Cell Line, TumorCell MovementCoculture TechniquesComputational BiologyDatabases, GeneticFemaleGene Expression ProfilingGene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticHigh-Throughput Nucleotide SequencingHumansLeiomyomaMatrix Metalloproteinase 2Matrix Metalloproteinase 9Mouth NeoplasmsNeoplasm InvasivenessOligonucleotide Array Sequence AnalysisSecretory Leukocyte Peptidase InhibitorSignal TransductionTime FactorsTissue Culture TechniquesTransfectionTumor MicroenvironmentUterine Neoplasms