Wang Peiqi, Deng Yun, Yan Xinyu, Zhu Jianhui, Yin Yuanyuan, Shu Yang, Bai Ding, Zhang Shouyue, Xu Heng, Lu Xiaoxi
Department of Pediatric Hematology/Oncology, West China Second University Hospital, Sichuan University, Chengdu, China.
State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Front Genet. 2020 Jun 12;11:598. doi: 10.3389/fgene.2020.00598. eCollection 2020.
Acute lymphoblastic leukemia (ALL) is the most common malignancy in children with distinct characteristics among different subtypes. Although the etiology of ALL has not been fully unveiled, initiation of ALL has been demonstrated to partly depend on genetic factors. As indicated by several genome wide association studies (GWASs) and candidate gene analyses, ARID5B, a member of AT-rich interactive domain (ARID) protein family, is associated with the occurrence and prognosis of ALL. However, the mechanisms by which genotype impact on the susceptibility and treatment outcome remain vague. In this review, we outline developments in the understanding of in the susceptibility of ALL and its therapeutic perspectives, and summarize the underlying mechanisms based on the limited functional studies, hoping to illustrate the possible mechanisms of ARID5B impact and highlight the potential treatment regimens.
急性淋巴细胞白血病(ALL)是儿童中最常见的恶性肿瘤,不同亚型具有不同特征。尽管ALL的病因尚未完全明确,但已证明ALL的发病部分取决于遗传因素。几项全基因组关联研究(GWAS)和候选基因分析表明,富含AT交互结构域(ARID)蛋白家族成员ARID5B与ALL的发生和预后相关。然而,基因型影响易感性和治疗结果的机制仍不明确。在本综述中,我们概述了对ALL易感性及其治疗前景的认识进展,并基于有限的功能研究总结了潜在机制,希望阐明ARID5B影响的可能机制并突出潜在的治疗方案。