TY - JOUR A1 - Windisch, Roland A1 - Pirschtat, Nina A1 - Kellner, Christian A1 - Chen-Wichmann, Linping A1 - Lausen, Jörn A1 - Humpe, Andreas A1 - Krause, Daniela Sandra A1 - Wichmann, Christian T1 - Oncogenic deregulation of cell adhesion molecules in leukemia T2 - Cancers N2 - Numerous cell–cell and cell–matrix interactions within the bone marrow microenvironment enable the controlled lifelong self-renewal and progeny of hematopoietic stem and progenitor cells (HSPCs). On the cellular level, this highly mutual interaction is granted by cell adhesion molecules (CAMs) integrating differentiation, proliferation, and pro-survival signals from the surrounding microenvironment to the inner cell. However, cell–cell and cell–matrix interactions are also critically involved during malignant transformation of hematopoietic stem/progenitor cells. It has become increasingly apparent that leukemia-associated gene products, such as activated tyrosine kinases and fusion proteins resulting from chromosomal translocations, directly regulate the activation status of adhesion molecules, thereby directing the leukemic phenotype. These observations imply that interference with adhesion molecule function represents a promising treatment strategy to target pre-leukemic and leukemic lesions within the bone marrow niche. Focusing on myeloid leukemia, we provide a current overview of the mechanisms by which leukemogenic gene products hijack control of cellular adhesion to subsequently disturb normal hematopoiesis and promote leukemia development. KW - adhesion KW - leukemia KW - oncogene KW - integrin KW - CAM Y1 - 2019 UR - http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/48874 UR - https://nbn-resolving.org/urn:nbn:de:hebis:30:3-488740 SN - 2072-6694 N1 - This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0). VL - 11 IS - 3, Art. 311 SP - 1 EP - 18 PB - MDPI CY - Basel ER -