Sinnett Daniel, N'Diaye Nina, St-Onge Pascal, Healy Jasmine
Service d'Hématologie-Oncologie, Centre de Cancérologie Charles-Bruneau, Centre de Recherche, Hôpital Sainte-Justine, Québec, Canada.
Med Sci (Paris). 2007 Nov;23(11):968-74. doi: 10.1051/medsci/20072311968.
Cancer affects 1 in every 500 children before the age of 14. Little is known about the etiology of this heterogeneous group of diseases despite the fact that they constitute the major cause of death by disease among this population. Because of its relatively higher prevalence, most of the work done in pediatric oncogenetics has been focused on leukemias, particularly acute lymphoblastic leukemia (ALL). Although it is now well accepted that genetic variations play a significant role in determining individual's cancer susceptibility, few studies have explored genetic susceptibility to childhood leukemia with respect to polymorphisms. The main biological mechanisms contributing to cancer susceptibility can be grouped into broad categories : (1) cellular growth and differentiation, (2) DNA replication and repair, (3) xenobiotic metabolism, (4) apoptosis, (5) oxidative stress response and (6) cell cycle. To evaluate whether candidate genes in these pathways are involved in childhood leukemogenesis, we conducted association studies. We showed that leukemogenesis in children may be associated with genetic variants and that the combination of genotypes seems to be more predictive of risk than either of them independently. These results indicate that the genetic investigation of several enzymes (or metabolic pathways) is needed to explain the physiopathology of childhood leukemia because of the complexity of the environment and that of the inter-individual variability in cancer susceptibility.
在14岁之前,每500名儿童中就有1人受癌症影响。尽管这类异质性疾病是该人群中因病死亡的主要原因,但人们对其病因却知之甚少。由于其发病率相对较高,儿科肿瘤遗传学领域的大部分研究都集中在白血病上,尤其是急性淋巴细胞白血病(ALL)。尽管现在人们普遍认为基因变异在决定个体患癌易感性方面起着重要作用,但很少有研究探讨多态性与儿童白血病遗传易感性的关系。导致癌症易感性的主要生物学机制可大致分为几大类:(1)细胞生长与分化;(2)DNA复制与修复;(3)外源性物质代谢;(4)细胞凋亡;(5)氧化应激反应;(6)细胞周期。为了评估这些途径中的候选基因是否参与儿童白血病的发生,我们进行了关联研究。我们发现儿童白血病的发生可能与基因变异有关,而且基因型的组合似乎比单一基因型更能预测患病风险。这些结果表明,由于环境的复杂性以及个体间癌症易感性的差异,需要对几种酶(或代谢途径)进行遗传学研究,以解释儿童白血病的生理病理学机制。