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首页> 外文期刊>Cancer science. >The expression of dipeptidyl peptidase IV (DPPIV/CD26) is associated with enhanced chemosensitivity to paclitaxel in epithelial ovarian carcinoma cells
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The expression of dipeptidyl peptidase IV (DPPIV/CD26) is associated with enhanced chemosensitivity to paclitaxel in epithelial ovarian carcinoma cells

机译:二肽基肽酶IV(DPPIV / CD26)的表达与上皮性卵巢癌细胞对紫杉醇的化学敏感性增强有关

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Dipeptidyl peptidase IV (DPPIV/CD26) is a multifunctional cell surface aminopeptidase that is widely expressed in different cell types. Recent studies have suggested that DPPIV plays an important role in tumor progression in several human malignancies. In the current study, we investigated the role of DPPIV in paclitaxel resistance in epithelial ovarian carcinoma (EOC) cells. We first examined the correlation between expression levels of DPPIV and sensitivity to paclitaxel in various EOC cell lines. Subsequently, to clarify the cellular functions of DPPIV, we investigated the role of this molecule in the sensitivity of EOC to paclitaxel in vitro and in vivo using stably DPPIV-transfected EOC cells. We identified a positive correlation between DPPIV expression and paclitaxel sensitivity in various EOC cell lines. In addition, we observed a significant increase in the paclitaxel sensitivity of DPPIV-overexpressing EOC cells. Furthermore, no apparent alteration in paclitaxel sensitivity was noted by the addition of a specific inhibitor of DPPIV activity in DPPIV-transfected or natively DPPIV-overexpressing EOC cells. In a subcutaneous murine model treated with paclitaxel, on Day 39, the tumor size of the DPPIV-transfected cell-inoculated group was as large as that of the vector-transfected cell-inoculated group. In contrast, on Day 61, the former was smaller than the latter. The present findings show that DPPIV may be involved in the increased sensitivity to paclitaxel of EOC cells regardless of the involvement of DPPIV activity. ( Cancer Sci 2009)
机译:二肽基肽酶IV(DPPIV / CD26)是一种多功能的细胞表面氨基肽酶,在不同的细胞类型中广泛表达。最近的研究表明,DPPIV在几种人类恶性肿瘤的肿瘤进展中起着重要作用。在当前的研究中,我们调查了DPPIV在上皮性卵巢癌(EOC)细胞中对紫杉醇耐药性中的作用。我们首先检查了在各种EOC细胞系中DPPIV表达水平与对紫杉醇敏感性之间的相关性。随后,为了阐明DPPIV的细胞功能,我们使用稳定的DPPIV转染的EOC细胞在体外和体内研究了该分子在EOC对紫杉醇敏感性中的作用。我们在各种EOC细胞系中确定了DPPIV表达与紫杉醇敏感性之间的正相关。此外,我们观察到过表达DPPIV的EOC细胞的紫杉醇敏感性显着增加。此外,在DPPIV转染的或天然表达DPPIV的EOC细胞中添加DPPIV活性的特异性抑制剂,未发现紫杉醇敏感性的明显改变。在用紫杉醇处理的皮下鼠模型中,在第39天,DPPIV转染的细胞接种组的肿瘤大小与载体转染的细胞接种组的肿瘤大小一样大。相反,在第61天,前者要小于后者。目前的发现表明,DPPIV可能参与了EOC细胞对紫杉醇敏感性的提高,而与DPPIV活性无关。 (癌症科学2009)

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