|Publication Type||Journal Article|
|Year of Publication||2002|
|Authors||Armstrong, SA, Staunton, JE, Silverman, LB, Pieters, R, den Boer, ML, Minden, MD, Sallan, SE, Lander, ES, Golub, TR, Korsmeyer, SJ|
|Pages||41 - 7|
|Keywords||Acute Disease, Cancer, Cell Lineage, DNA-Binding Proteins, Gene Expression Profiling, Gene Expression Regulation, Genes, Hematopoietic Stem Cells, Homeobox, Homeodomain Proteins, Humans, Immunophenotyping, Leukemia, Leukemic, Myeloid, Myeloid-Lymphoid Leukemia Pr|
Acute lymphoblastic leukemias carrying a chromosomal translocation involving the mixed-lineage leukemia gene (MLL, ALL1, HRX) have a particularly poor prognosis. Here we show that they have a characteristic, highly distinct gene expression profile that is consistent with an early hematopoietic progenitor expressing select multilineage markers and individual HOX genes. Clustering algorithms reveal that lymphoblastic leukemias with MLL translocations can clearly be separated from conventional acute lymphoblastic and acute myelogenous leukemias. We propose that they constitute a distinct disease, denoted here as MLL, and show that the differences in gene expression are robust enough to classify leukemias correctly as MLL, acute lymphoblastic leukemia or acute myelogenous leukemia. Establishing that MLL is a unique entity is critical, as it mandates the examination of selectively expressed genes for urgently needed molecular targets.