Kavianpour Maria, Ahmadzadeh Ahmad, Shahrabi Saeid, Saki Najmaldin
Health research institute, Thalassemia & Hemoglobinopathy Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Department of Biochemistry and Hematology, Faculty of Medicine, Semnan University of Medical Sciences, Semnan, Iran.
Tumour Biol. 2016 Aug;37(8):10041-52. doi: 10.1007/s13277-016-5067-1. Epub 2016 May 14.
Acute myeloid leukemia (AML) is a heterogeneous disorder among hematologic malignancies. Several genetic alterations occur in this disease, which cause proliferative progression, reducing differentiation and apoptosis in leukemic cells as well as increasing their survival. In the genetic study of AML, genetic translocations, gene overexpression, and mutations effective upon biology and pathogenesis of this disease have been recognized. Proto-oncogenes and tumor suppressor genes, which are important in normal development of myeloid cells, are involved in the regulation of cell cycle and apoptosis, undergo mutation in this type of leukemia, and are effective in prognosis of AML subtypes. This review deals with these genes, the assessment of which can be important in the diagnosis and prognosis of patients as well as therapeutic outcome.
急性髓系白血病(AML)是血液系统恶性肿瘤中的一种异质性疾病。该疾病会发生多种基因改变,这些改变导致白血病细胞增殖进展、分化和凋亡减少以及存活期延长。在AML的遗传学研究中,已经识别出对该疾病生物学特性和发病机制有影响的基因易位、基因过表达及突变。原癌基因和肿瘤抑制基因在髓系细胞的正常发育中起重要作用,参与细胞周期调控和凋亡过程,在这类白血病中会发生突变,并且对AML各亚型的预后有影响。本文综述这些基因,对它们的评估在患者的诊断、预后以及治疗结果方面可能具有重要意义。