Desai Rhea H, Zandvakili Niloofar, Bohlander Stefan K
Leukaemia & Blood Cancer Research Unit, Department of Molecular Medicine and Pathology, University of Auckland, Auckland 1023, New Zealand.
Cancers (Basel). 2022 Apr 27;14(9):2182. doi: 10.3390/cancers14092182.
Acute myeloid leukemia (AML) is an extremely aggressive and heterogeneous disorder that results from the transformation of hematopoietic stem cells. Although our understanding of the molecular pathology of AML has greatly improved in the last few decades, the overall and relapse free survival rates among AML patients remain quite poor. This is largely due to evolution of the disease and selection of the fittest, treatment-resistant leukemic clones. There is increasing evidence that most AMLs possess a highly complex clonal architecture and individual leukemias are comprised of genetically, phenotypically and epigenetically distinct clones, which are continually evolving. Advances in sequencing technologies as well as studies using murine AML models have provided further insights into the heterogeneity of leukemias. We will review recent advances in the field of genetic and non-genetic heterogeneity in AML.
急性髓系白血病(AML)是一种极具侵袭性且异质性的疾病,由造血干细胞转化所致。尽管在过去几十年里,我们对AML分子病理学的理解有了很大提高,但AML患者的总体生存率和无复发生存率仍然很低。这主要是由于疾病的演变以及最适应环境、具有治疗抗性的白血病克隆的选择。越来越多的证据表明,大多数AML具有高度复杂的克隆结构,个体白血病由基因、表型和表观遗传上不同的克隆组成,这些克隆在不断演变。测序技术的进步以及使用小鼠AML模型的研究,为白血病的异质性提供了进一步的见解。我们将综述AML领域中遗传和非遗传异质性方面的最新进展。