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沃克256肿瘤中NTPD酶和5'外核苷酸酶的表达谱以及细胞外ATP代谢模式

NTPDase and 5' ecto-nucleotidase expression profiles and the pattern of extracellular ATP metabolism in the Walker 256 tumor.

作者信息

Buffon A, Wink M R, Ribeiro B V, Casali E A, Libermann T A, Zerbini L F, Robson S C, Sarkis J J F

机构信息

Departamento de Bioquímica, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul, ICBS, Rua Ramiro Barcelos, Porto Alegre, RS, Brazil.

出版信息

Biochim Biophys Acta. 2007 Aug;1770(8):1259-65. doi: 10.1016/j.bbagen.2007.05.004. Epub 2007 May 21.

Abstract

In this study, we evaluated the NTPDases and ecto-5'-nucleotidase (CD73) expression profiles and the pattern of adenine nucleotide hydrolysis in rats submitted to the Walker 256 tumor model, 6, 10 and 15 days after the subcutaneous inoculation. Using RT-PCR analysis, we identified mRNA for all of the members of the ecto-nucleoside triphosphate diphosphohydrolase family investigated and a 5'-nucleotidase. By quantitative real-time PCR, Entpd1 (Cd39) and Entpd2 (Cd39L1) and CD73 were identified as the dominant genes expressed by the Walker 256 tumor, at all times studied. Extracellular adenine nucleotide hydrolysis by the Walker 256 tumor was estimated by HPLC analysis. Rapid hydrolysis of extracellular ATP by the tumor cells was observed, leading to the formation of adenosine and inosine in cells obtained from solid tumors at 6 and 10 days after inoculation. Cells obtained from solid tumors at 15 days of growth presented high levels of AMP and presented adenosine as a final product after 90 min of incubation. Results demonstrate that the presence of NTPDases and 5'-nucleotidase enzymes in Walker 256 tumor cells may be important for regulation of the extracellular adenine nucleotides/adenine nucleoside ratio, therefore leading to tumor growth.

摘要

在本研究中,我们评估了皮下接种Walker 256肿瘤模型6天、10天和15天后大鼠的NTPD酶和胞外5'-核苷酸酶(CD73)表达谱以及腺嘌呤核苷酸水解模式。通过逆转录-聚合酶链反应(RT-PCR)分析,我们鉴定出了所研究的胞外核苷三磷酸二磷酸水解酶家族所有成员以及一种5'-核苷酸酶的信使核糖核酸(mRNA)。通过定量实时聚合酶链反应(qRT-PCR),在所有研究时间点,Entpd1(Cd39)、Entpd2(Cd39L1)和CD73被确定为Walker 256肿瘤表达的主要基因。通过高效液相色谱(HPLC)分析估计Walker 256肿瘤的胞外腺嘌呤核苷酸水解情况。观察到肿瘤细胞对胞外三磷酸腺苷(ATP)的快速水解,在接种后6天和10天从实体瘤获得的细胞中导致了腺苷和肌苷的形成。生长15天的实体瘤获得的细胞呈现高水平的一磷酸腺苷(AMP),孵育90分钟后以腺苷作为最终产物。结果表明,Walker 256肿瘤细胞中NTPD酶和5'-核苷酸酶的存在可能对调节胞外腺嘌呤核苷酸/腺嘌呤核苷比例很重要,因此导致肿瘤生长。

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