| Literature DB >> 27728807 |
Phuong-Hien Nguyen1, Oleg Fedorchenko1, Natascha Rosen1, Maximilian Koch1, Romy Barthel1, Tomasz Winarski1, Alexandra Florin2, F Thomas Wunderlich3, Nina Reinart1, Michael Hallek4.
Abstract
Survival of chronic lymphocytic leukemia (CLL) cells strictly depends on the support of an appropriate tumor microenvironment. Here, we demonstrate that LYN kinase is essential for CLL progression. Lyn deficiency results in a significantly reduced CLL burden in vivo. Loss of Lyn within leukemic cells reduces B cell receptor (BCR) signaling including BTK phosphorylation, but surprisingly does not affect leukemic cell expansion. Instead, syngeneic CLL transplantation of CLL cells into Lyn- or Btk-deficient recipients results in a strongly delayed leukemic progression and prolonged survival. Moreover, Lyn deficiency in macrophages hinders nursing functions for CLL cells, which is mediated by direct contact rather than secretion of soluble factors. Taken together, LYN and BTK seem essential for the formation of a microenvironment supporting leukemic growth.Entities:
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Year: 2016 PMID: 27728807 DOI: 10.1016/j.ccell.2016.09.007
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743