Inactivation of the NHEJ activity of DNA-PKcs prevents fanconi anemia pre-leukemic HSC expansion

3Citations
Citations of this article
7Readers
Mendeley users who have this article in their library.

Abstract

Fanconi anemia (FA) is a genetic disorder characterized by bone marrow failure and high risk of cancer particularly leukemia. Here we show that inactivation of the non-homologous end-joining (NHEJ) activity of DNA-PKcs prevented DNA damage-induced expansion of FA pre-leukemic hematopoietic stem cells (HSCs). Furthermore, we performed serial BM transplantation to demonstrate that the DNA damage-induced expanded FA HSC compartment contained pre-leukemic stem cells that required the NHEJ activity of DNA-PKcs to induce leukemia in the secondary recipients. These results suggest that NHEJ may collaborate with FA deficiency to promote DNA damage-induced expansion of pre-leukemic HSCs.

Cite

CITATION STYLE

APA

Chatla, S., Wilson, A. F., & Pang, Q. (2019). Inactivation of the NHEJ activity of DNA-PKcs prevents fanconi anemia pre-leukemic HSC expansion. International Journal of Stem Cells, 12(3), 457–462. https://doi.org/10.15283/ijsc19074

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free