Imprinted genes in myeloid lineage commitment in normal and malignant hematopoiesis

被引:5
作者
Benetatos, L. [1 ]
Vartholomatos, G. [2 ]
机构
[1] Preveza Gen Hosp, Blood Bank, Preveza 48100, Greece
[2] Ioannina Univ Hosp, Mol Biol Lab, Ioannina, Greece
关键词
TUMOR-SUPPRESSOR GENE; LONG NONCODING RNA; CHRONIC MYELOGENOUS LEUKEMIA; BONE-MARROW-CELLS; CANCER STEM-CELLS; GROWTH-FACTOR; DNA METHYLATION; HIGH EXPRESSION; WT1; MUTATIONS; DISEASE;
D O I
10.1038/leu.2015.47
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Genomic imprinting is characterized by the parent-of-origin monoallelic expression of several diploid genes because of epigenetic regulation. Imprinted genes (IGs) are key factors in development, supporting the ability of a genotype to produce phenotypes in response to environmental stimuli. IGs are highly expressed during prenatal stages but are downregulated after birth. They also affect aspects of life other than growth such as cognition, behavior, adaption to novel environments, social dominance and memory consolidation. Deregulated genomic imprinting leads to developmental disorders and is associated with solid and blood cancer as well. Several data have been published highlighting the involvement of IGs in as early as the very small embryonic-like stem cells stage and further during myeloid lineage commitment in normal and malignant hematopoiesis. Therefore, we have assembled the current knowledge on the topic, based mainly on recent findings, trying not to focus on a particular cluster but rather to have a global view of several different IGs in hematopoiesis.
引用
收藏
页码:1233 / 1242
页数:10
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