在评估暴露于环境致癌物的人的癌症风险时早期健康影响的生物标志物。

J A Indulski, W Lutz, B Krajewska
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引用次数: 0

摘要

早期健康影响的生物标志物代表癌变过程的中间阶段,介于起始和转化阶段和临床明显的肿瘤疾病之间。因此,由这些标记所指示的细胞过程与促进过程相对应。检测这些细胞过程是非常重要的,因为促进过程持续多年,并且有一些可逆的迹象。促进过程包括一系列连续的细胞变化,其中包括原癌原的激活及其向癌原的转化,以及抑制基因的失活。因此,通过监测容易获得的物质(血液、尿液)中致癌基因和抑制基因的蛋白质产物来观察这些变化趋势的可能性是非常有用的。细胞间通讯的抑制似乎在正常细胞向肿瘤细胞转化的复杂机制中起着极其重要的作用。在致癌过程促进阶段,这种抑制作用与形成细胞间连接并参与细胞粘附的蛋白质有关。这组蛋白质包括癌胚抗原(CEA)和组织多肽抗原(TPA),这两种肿瘤抗原已被发现多年。TPA和CEA浓度增加之间可能存在的关系不仅得到了肿瘤学数据的支持,也得到了暴露于已知会增加肿瘤疾病风险的物质的人群研究数据的支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biological markers of early health effects in the assessment of the risk of cancer in people exposed to environmental carcinogens.

Biomarkers of early health effects represent the intermediate stages of the carcinogenesis process, between the initiation and conversion stage and the clinically overt neoplastic disease. The cellular processes indicated by those markers correspond, therefore, to the promotion process. Detection of those cellular processes is extremely important, as the promotion process lasts for many years and bears some signs of being reversible. The promotion process, consisting of a range of consecutive cellular changes involves, among others, activation of proto-oncogens and their transformation into oncogens, and inactivation of the suppressor genes. Therefore, the possibility of observing the trends of those changes by monitoring protein products of the oncogens and suppressor genes in the easily available material (blood, urine) is very useful. Inhibition of intercellular communication seems to play an extremely important role in the complex mechanism of transformation of a normal cell into a neoplastic one. During the carcinogenic process promotion stage, the inhibition is associated with the proteins which form the intercellular junctions and participate in cellular adhesion. That group of proteins includes carcinoembryonal antigen (CEA) and tissue polypeptide antigen (TPA), the tumour antigens which have been known for years. The possible relationship between increased TPA and CEA concentrations is supported not only by the data from the oncology but also by the data from the studies on populations exposed to agents known to increase the risk of neoplastic disease.

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