Department of Pathology and the Hematological Malignancy Program, St Jude Children's Research Hospital, Memphis, TN 38105, USA.
Cell Stem Cell. 2018 Nov 1;23(5):632-633. doi: 10.1016/j.stem.2018.10.022.
Hematopoietic progenitors undergo marked shifts during transition from fetal to postnatal life, and the implication of these changes for the cell-of-origin of childhood leukemia are unclear. In this issue of Cell Stem Cell, Giambra et al. (2018) show that epigenetically regulated IGF1 signaling regulates the ability of fetal-liver- or bone-marrow-derived cells to initiate T-ALL.
造血祖细胞在从胎儿到出生后的过渡过程中经历明显的转变,这些变化对儿童白血病的起源细胞意味着什么尚不清楚。在本期《Cell Stem Cell》杂志上,Giambra 等人(2018)表明,受表观遗传调控的 IGF1 信号调节了胎肝或骨髓来源的细胞引发 T-ALL 的能力。