Cancer Research UK Stem Cell Biology Group, Cancer Research UK Manchester Institute, The University of Manchester, Macclesfield, SK10 4TG, UK.
These authors contributed equally to this work.
Mol Cells. 2020 Feb 29;43(2):126-138. doi: 10.14348/molcells.2019.0301.
The transcription factor RUNX1 first came to prominence due to its involvement in the t(8;21) translocation in acute myeloid leukemia (AML). Since this discovery, RUNX1 has been shown to play important roles not only in leukemia but also in the ontogeny of the normal hematopoietic system. Although it is currently still challenging to fully assess the different parameters regulating RUNX1 dosage, it has become clear that the dose of RUNX1 can greatly affect both leukemia and normal hematopoietic development. It is also becoming evident that varying levels of RUNX1 expression can be used as markers of tumor progression not only in the hematopoietic system, but also in non-hematopoietic cancers. Here, we provide an overview of the current knowledge of the effects of RUNX1 dosage in normal development of both hematopoietic and epithelial tissues and their associated cancers.
转录因子 RUNX1 最初因其参与急性髓系白血病(AML)中的 t(8;21)易位而受到关注。自这一发现以来,RUNX1 不仅在白血病中,而且在正常造血系统的发生中都发挥着重要作用。尽管目前仍然难以全面评估调节 RUNX1 剂量的不同参数,但很明显,RUNX1 的剂量会极大地影响白血病和正常造血的发展。越来越明显的是,RUNX1 表达水平的变化不仅可以作为造血系统,而且可以作为非造血系统癌症中肿瘤进展的标志物。在这里,我们概述了 RUNX1 剂量在造血和上皮组织正常发育及其相关癌症中的作用的现有知识。