Oncology Research Center, Federal University of Pará, Belém 66073, PA, Brazil.
Laboratory of Human and Medical Genetics, Institute of Biological Science, Federal University of Pará, Belém 66077-830, PA, Brazil.
Genes (Basel). 2022 Mar 29;13(4):610. doi: 10.3390/genes13040610.
In Brazil, Acute lymphoid leukemia (ALL) is the leading cause of cancer deaths in children and adolescents. Treatment toxicity is one of the reasons for stopping chemotherapy. Amerindian genomic ancestry is an important factor for this event due to fluctuations in frequencies of genetic variants, as in the and genes, which make up the pharmacokinetic and pharmacodynamic pathways of chemotherapy. This study aimed to investigate possible associations between (rs1272632214) and (rs202220802) gene polymorphism and genomic ancestry as a risk of treatment toxicities in patients with childhood ALL in the Amazon region of Brazil. The studied population consisted of 51 patients with a recent diagnosis of ALL when experiencing induction therapy relative to the BFM 2009 protocol. Our results evidenced a significant association of risk of severe infectious toxicity for the variant of the gene (OR: 3.18, = 0.031). Genetic ancestry analyses demonstrated that patients who had a high contribution of African ancestry had a significant protective effect for the development of toxicity (OR: 0.174; = 0.010), possibly due to risk effects of the Amerindian contribution. Our results indicate that mixed populations with a high degree of African ancestry have a lower risk of developing general toxicity during induction therapy for ALL. In addition, individuals with the variant have a higher risk of developing severe infectious toxicity while undergoing the same therapy.
在巴西,急性淋巴细胞白血病(ALL)是儿童和青少年癌症死亡的主要原因。治疗毒性是停止化疗的原因之一。由于遗传变异频率的波动,美洲印第安人基因组的遗传背景是导致这种情况的一个重要因素,这些遗传变异存在于化疗的药代动力学和药效学途径的 和 基因中。本研究旨在调查巴西亚马逊地区儿童 ALL 患者治疗毒性的 (rs1272632214)和 (rs202220802)基因多态性与基因组遗传背景之间可能存在的关联。研究人群包括 51 名近期诊断为 ALL 的患者,他们正在接受 BFM 2009 方案诱导治疗。我们的结果表明, 基因变异与严重感染毒性风险显著相关(OR:3.18, = 0.031)。遗传背景分析表明,具有高非洲遗传背景的患者对毒性的发展具有显著的保护作用(OR:0.174; = 0.010),这可能是由于美洲印第安人遗传背景的风险效应。我们的结果表明,具有高度非洲遗传背景的混合人群在接受 ALL 诱导治疗时发生一般毒性的风险较低。此外,在接受相同治疗的个体中,携带 变异的个体发生严重感染毒性的风险更高。