Pathogenesis of Acute Lymphoblastic Leukemia

Shahin Aghamiri, Farhad Hajializadeh, A. Jafarpour, Shiva Bayat, Soodeh Namjoo, F. Zaker
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Abstract

Acute lymphoblastic leukemia (ALL) is a hematological malignant disease characterized by an enhanced self-renewal ability of precursor lymphoid cells whose cell division takes more time than their normal counterparts.  ALL occurs most between 2 to 5 years of age and during the sixth decade of life. There is a strong relationship between the time ALL occurs in children and the genetic abnormalities which are identified by the rate of leukemic concordance between identical twins. About 90% of ALL cases do not have a clear etiological mechanism. Genetic syndromes, polymorphic variants genes, germline mutations, and some environmental factors are responsible for less than 10% of ALL predisposition but the pathogenesis mechanism of ALL is not identified precisely. Here we review the recent findings and earlier studies about the pathogenesis of acute lymphoblastic leukemia and its incidence. This article also summarizes the identification of predictive factors for ALL and options available to predict disease recurrence.
急性淋巴细胞白血病的发病机制
急性淋巴细胞白血病(ALL)是一种血液系统恶性疾病,其特征是前体淋巴样细胞的自我更新能力增强,其细胞分裂比正常细胞需要更多的时间。ALL多发生在2至5岁之间和生命的第六个十年。儿童罹患ALL的时间与同卵双胞胎之间的白血病一致性率所确定的遗传异常之间有很强的关系。大约90%的ALL病例没有明确的病因机制。遗传综合征、多态变异基因、种系突变和一些环境因素占ALL易感性的不到10%,但ALL的发病机制尚不明确。本文就急性淋巴细胞白血病发病机制及其发病率的最新发现和早期研究进行综述。本文还总结了ALL的预测因素的识别和预测疾病复发的可用选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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