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首页> 外文期刊>International journal of clinical pharmacology and therapeutics >Reduction in human melanoma cell adhesion receptor activity by lysophosphatidylcholine (LPC) treatment - functional characterization and signal pathway analyses.
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Reduction in human melanoma cell adhesion receptor activity by lysophosphatidylcholine (LPC) treatment - functional characterization and signal pathway analyses.

机译:溶血磷脂酰胆碱(LPC)处理可降低人黑素瘤细胞粘附受体的活性-功能表征和信号通路分析。

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摘要

Tumor cell metastasis is the most fatal complication of cancer. Cell adhesion receptors, such as P- and L-selectin, and the inte-grin VLA-4 are closely involved in the course of hematogenous metastasis, mediating manifold interactions of tumor cells with platelets and leukocytes. Recent data on the antimetas-tatic effects of empty liposomes of saturated phosphatidylcholine have been reported [2]. It might be assumed that lysophosphati-dylcholine (LPC) is the active agent for this effect since, (i) we could detect a rapid uptake of LPC by different tumor cells, and (ii) this is in line with clinical findings on reduced levels of LPC in tumor patients suffering from cachexia. However, the mechanisms remain to be elucidated.
机译:肿瘤细胞转移是癌症最致命的并发症。细胞粘附受体,例如P-和L-选择素,以及整联蛋白VLA-4与血行转移过程密切相关,介导肿瘤细胞与血小板和白细胞的多种相互作用。关于饱和磷脂酰胆碱空脂质体的抗代谢作用的最新数据已有报道[2]。可以假设溶血磷脂酰胆碱(LPC)是此作用的活性剂,因为(i)我们可以检测到不同肿瘤细胞对LPC的快速摄取,并且(ii)与降低水平的临床发现相符恶病质的肿瘤患者中LPC的变化。但是,机制尚待阐明。

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