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首页> 外文期刊>Medicina (Buenos Aires) >In vivo effects of adenosine 5′-triphosphate on rat preneoplastic liver
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In vivo effects of adenosine 5′-triphosphate on rat preneoplastic liver

机译:5'-三磷酸腺苷对大鼠肿瘤前肝的体内作用

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The utilization of adenosine 5′-triphosphate (ATP ) infusions to inhibit the growth of some human and animals tumors was based on the anticancer activity observed in in vitro and in vivo experiments, but contradictory results make the use of ATP in clinical practice rather controversial. Moreover, there is no literature regarding the use of ATP infusions to treat hepatocarcinomas. The purpose of this study was to investigate whether ATP prevents in vivo oncogenesis in very-early-stage cancer cells in a well characterized two-stage model of hepatocarcinogenesis in the rat. As we could not preclude the possible effect due to the intrinsic properties of adenosine, a known tumorigenic product of ATP hydrolysis, the effect of the administration of adenosine was also studied. Animals were divided in groups: rats submitted to the two stage preneoplasia initiation/promotion model of hepatocarcinogenesis, rats treated with intraperitoneal ATP or adenosine during the two phases of the model and appropriate control groups. The number and volume of preneoplastic foci per liver identified by the expression of glutathione S-transferase placental type and the number of proliferating nuclear antigen positive cells significantly increased in ATP and adenosine treated groups. Taken together, these results indicate that in this preneoplastic liver model, ATP as well as adenosine disturb the balance between apoptosis and proliferation contributing to malignant transformation.
机译:利用5'-三磷酸腺苷(ATP)输注来抑制某些人和动物肿瘤的生长是基于在体内和体外实验中观察到的抗癌活性,但是矛盾的结果使ATP在临床实践中的使用颇具争议。此外,没有关于使用ATP输注治疗肝癌的文献。这项研究的目的是在特征明确的大鼠肝癌发生的两阶段模型中研究ATP是否能阻止非常早期阶段的癌细胞体内的肿瘤发生。由于腺苷(一种已知的ATP水解致瘤产物)的内在特性无法阻止可能的作用,因此也研究了腺苷给药的作用。将动物分为几组:将大鼠置于肝癌发生的两期新肿瘤形成前/促进模型,在模型的两个阶段中用腹膜内ATP或腺苷治疗的大鼠和适当的对照组。在ATP和腺苷治疗组中,通过谷胱甘肽S-转移酶胎盘类型的表达确定的每个肝脏的肿瘤前病灶的数量和体积以及增殖的核抗原阳性细胞的数量显着增加。综上所述,这些结果表明,在这种肿瘤前肝模型中,ATP和腺苷会干扰细胞凋亡与增殖之间的平衡,从而导致恶性转化。

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