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Genetic pathways in the pathogenesis of therapy-related myelodysplasia and acute myeloid leukemia Pedersen-Bjergaard J; Andersen MT; Andersen MKHematology Am Soc Hematol Educ Program 2007[]; ä (ä): 392-7In therapy-related myelodysplasia (t-MDS) and acute myeloid leukemia (t-AML), at least eight alternative genetic pathways have been defined based on characteristic recurrent chromosome abnormalities. Patients presenting as t-MDS and patients presenting as overt t-AML cluster differently in these pathways. The cytogenetic pattern depends on the type of leukemogenic therapy received: alkylating agents, topoisomerase II inhibitors, or radiotherapy. Three types of gene mutations are observed in MDS and AML: (1) Activating mutations of genes in the tyrosine kinase-RAS/BRAF signal transduction pathway, leading to increased cell proliferation (Class I mutations); (2) Inactivating mutations of genes encoding hematopoietic transcription factors, resulting in disturbed cell differentiation (Class II mutations); and (3) Inactivating mutations of the tumor suppressor gene p53. At least 14 different genes have been identified as mutated in t-MDS and t-AML, clustering differently and characteristically in the eight genetic pathways. Class I and Class II mutations are significantly associated, indicating their cooperation in leukemogenesis The chromosome aberrations and gene mutations detected in the therapy-related and in the de novo subsets of MDS and AML are identical, although the frequencies with which they are observed may differ. Hence, therapy-related and de novo MDS and AML are identical diseases and should be subclassified and treated similarly.|Antineoplastic Agents/*adverse effects[MESH]|Chromosome Aberrations[MESH]|Epigenesis, Genetic[MESH]|Humans[MESH]|Leukemia, Myeloid, Acute/etiology/*genetics[MESH]|Mutation[MESH]|Myelodysplastic Syndromes/etiology/*genetics[MESH]|Radiotherapy/*adverse effects[MESH] |
