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首页> 外文期刊>International Journal of Molecular Sciences >Secreted Protein Acidic and Rich in Cysteine (SPARC) Enhances Cell Proliferation, Migration, and Epithelial Mesenchymal Transition, and SPARC Expression is Associated with Tumor Grade in Head and Neck Cancer
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Secreted Protein Acidic and Rich in Cysteine (SPARC) Enhances Cell Proliferation, Migration, and Epithelial Mesenchymal Transition, and SPARC Expression is Associated with Tumor Grade in Head and Neck Cancer

机译:酸性且富含半胱氨酸的分泌蛋白(SPARC)增强细胞增殖,迁移和上皮间充质转化,并且SPARC的表达与头颈癌的肿瘤分级有关

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Secreted protein acidic and rich in cysteine (SPARC) is a secreted protein which is involved in various biological processes. SPARC expression is associated with tumor metastasis and poor prognosis in several types of cancer. However, the SPARC-induced signaling pathway was not fully understood in head and neck cancer. In this study, our results showed that SPARC treatment promoted cell proliferation and migration in head and neck cancer cell lines FaDu and Detroit 562. In addition, SPARC induced expression of epithelial mesenchymal transition (EMT) regulators, including Slug, Snail, and Twist in Detroit 562. The results of phospho-kinase array analysis showed that SPARC treatment increased phosphorylation of some molecules including protein kinase B (PKB/AKT), ribosomal S6 kinase (RSK), and extracellular signal–regulated kinases (ERK). The expression of SPARC-induced EMT regulator Slug was suppressed by AKT inhibitor, but not ERK and RSK inhibitors. The SPARC expression in grade IV tumor samples is higher when compared to that in grade I–III tumor samples. Our results suggest that SPARC treatment enhances the EMT signaling pathway via activation of AKT, and exogenous SPARC and tumor expressing SPARC might be associated with tumor progression in head and neck cancers.
机译:分泌的蛋白质呈酸性,富含半胱氨酸(SPARC)是一种分泌的蛋白质,与各种生物过程有关。在多种类型的癌症中,SPARC表达与肿瘤转移和不良预后有关。但是,SPARC诱导的信号通路在头颈癌中尚未完全了解。在这项研究中,我们的结果表明SPARC处理可促进头颈部癌细胞FaDu和底特律562细胞增殖和迁移。此外,SPARC诱导上皮间质转化(EMT)调节剂的表达,包括Slug,Snail和Twist。底特律562.磷酸激酶阵列分析的结果表明,SPARC处理增加了某些分子的磷酸化,包括蛋白激酶B(PKB / AKT),核糖体S6激酶(RSK)和细胞外信号调节激酶(ERK)。 SPARC诱导的EMT调节剂Slug的表达被AKT抑制剂抑制,但未抑制ERK和RSK抑制剂。与I–III级肿瘤样品相比,IV级肿瘤样品中的SPARC表达更高。我们的结果表明,SPARC治疗可通过激活AKT增强EMT信号通路,而外源性SPARC和表达SPARC的肿瘤可能与头颈癌的肿瘤进展有关。

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