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A3 adenosine receptor mediates apoptosis in in vitro RCC4-VHL human renal cancer cells by up-regulating AMID expression

机译:A3腺苷受体通过上调AMID表达介导体外RCC4-VHL人肾癌细胞的凋亡

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Purpose: Accumulating studies have shown that extracellular adenosine induces apoptosis in various cancer cells via diverse signaling pathways. We sought to understand adenosine induced apoptosis in human renal cancer cells and the underlying pathway. Materials and Methods: RCC4-VHL (European Collection of Animal Cell Cultures, Salisbury, United Kingdom), ACHN (Cell Resource Center for Biomedical Research, Institute of Development, Aging and Cancer, Tohuku University, Aoba-ku, Sendai, Japan) and 786-O (ATCC?) human renal cancer cells were cultured. MTT assay, TUNEL staining, reverse transcriptase-polymerase chain reaction and Western blot were done in cells untransfected and transfected with siRNA silencing the A3 adenosine receptor targeted gene or the AMID targeted gene. Results: Adenosine induced apoptosis in all cell types used in a concentration (1 to 10 mM) dependent manner. A similar effect was obtained with the A3 adenosine receptor agonist 2-Cl-IB-MECA. Adenosine induced RCC4-VHL cell death was inhibited by the A3 adenosine receptor inhibitor MRS1191 or by knocking down A3 adenosine receptor or AMID. Adenosine up-regulated the expression of AMID mRNA and protein in RCC4-VHL cells, which was suppressed by A3 adenosine receptor knockdown. Moreover, adenosine promoted AMID translocation from cytosol to nucleus. Conclusions: Adenosine induces RCC4-VHL cell apoptosis by up-regulating AMID expression and accumulating AMID in the nucleus via A 3 adenosine receptor. ? 2013 American Urological Association Education and Research, Inc.
机译:目的:越来越多的研究表明,细胞外腺苷通过多种信号传导途径诱导各种癌细胞的凋亡。我们试图了解腺苷诱导人肾癌细胞的凋亡及其潜在途径。材料和方法:RCC4-VHL(英国索尔兹伯里的欧洲动物细胞培养物收藏),ACHN(日本仙台市青叶区东北大学发育,衰老和癌症研究所生物医学研究细胞资源中心)和培养了786-O(ATCC 3)人肾癌细胞。在未转染的细胞中进行MTT测定,TUNEL染色,逆转录酶-聚合酶链反应和Western印迹,并用siRNA沉默A3腺苷受体靶基因或AMID靶基因。结果:腺苷以浓度依赖性(1至10 mM)诱导所有细胞类型的凋亡。用A3腺苷受体激动剂2-Cl-IB-MECA获得了类似的效果。 A3腺苷受体抑制剂MRS1191或敲低A3腺苷受体或AMID抑制了腺苷诱导的RCC4-VHL细胞死亡。腺苷上调RCC4-VHL细胞中AMID mRNA和蛋白的表达,这被A3腺苷受体敲低所抑制。此外,腺苷促进了AMID从胞质溶胶到细胞核的转运。结论:腺苷通过上调AMID的表达并通过A 3腺苷受体在细胞核中积累AMID来诱导RCC4-VHL细胞凋亡。 ? 2013美国泌尿科协会教育与研究公司

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