Tower Richard L, Spector Logan G
Department of Pediatrics, University of Minnesota, Minneapolis, Minnesota 55455, USA.
Crit Rev Clin Lab Sci. 2007;44(3):203-42. doi: 10.1080/10408360601147536.
Leukemia is the most common childhood cancer and a major source of morbidity and mortality. The etiology of childhood leukemia remains largely unknown. Cytogenetic abnormalities determine disease subtypes, prognosis, clinical presentation, and course and may help in discovering etiological factors. Epidemiologic investigations of leukemia are complicated by many factors, including the rarity of the disease, necessitating careful study design. Two emerging areas of interest in leukemia etiology are birth weight and diet. High birth weight has been associated with increased risk of childhood leukemia. The biological mechanism behind this association may involve insulin-like growth factor I (IGF-I), which is associated with high birth weight. IGF-I may act by increasing the absolute number of stem cells available for transformation, stimulating the growth of cells that are already transformed, or a combination of effects. Diet has been linked with leukemia. Maternal dietary DNA topoisomerase II (DNAt2) inhibitor intake is associated with infant acute myeloid leukemia (AML) with the MLL gene translocation. Increased intake of fruits and vegetables has been associated with decreased leukemia risk and, relatedly, lack of maternal folate supplementation has been associated with increased childhood leukemia risk, possibly by causing DNA hypomethylation and increased DNA strand breaks. Methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms modify this risk.
白血病是儿童期最常见的癌症,也是发病和死亡的主要原因。儿童白血病的病因在很大程度上仍不清楚。细胞遗传学异常决定疾病亚型、预后、临床表现和病程,并可能有助于发现病因。白血病的流行病学调查因多种因素而变得复杂,包括该疾病的罕见性,这就需要精心设计研究。白血病病因学中两个新出现的研究热点是出生体重和饮食。高出生体重与儿童白血病风险增加有关。这种关联背后的生物学机制可能涉及胰岛素样生长因子I(IGF-I),它与高出生体重有关。IGF-I可能通过增加可用于转化的干细胞绝对数量、刺激已转化细胞的生长或两种作用的组合来发挥作用。饮食与白血病有关。母亲摄入膳食DNA拓扑异构酶II(DNAt2)抑制剂与婴儿急性髓系白血病(AML)伴MLL基因易位有关。水果和蔬菜摄入量增加与白血病风险降低有关,与此相关的是,母亲缺乏叶酸补充与儿童白血病风险增加有关,可能是通过导致DNA低甲基化和DNA链断裂增加。亚甲基四氢叶酸还原酶(MTHFR)基因多态性会改变这种风险。