CATS (FAM64A) abnormal expression reduces clonogenicity of hematopoietic cells
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Isabella Barbutti1, Juliana M. Xavier-Ferrucio1,*, João Agostinho Machado-Neto1,#, Lauremilia Ricon1, Fabiola Traina2, Stefan K. Bohlander3, Sara Teresinha Olalla Saad1, Leticia Fröhlich Archangelo1,4
1Hematology and Hemotherapy Center, State University of Campinas (UNICAMP), Carlos Chagas 480, Campinas-SP, Brazil
2Department of Internal Medicine, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil
3Department of Molecular Medicine and Pathology, The University of Auckland, Auckland, New Zealand
4Department of Cellular and Molecular Biology and Pathogenic Bioagents, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil
*Present address: Department of Laboratory Medicine, Yale Stem Cell Center
#Present address: Department of Internal Medicine, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil
Leticia Fröhlich Archangelo, email: email@example.com
Keywords: CATS (FAM64A), proliferation, clonogenicity, CALM/AF10, leukemogenesis
Received: November 10, 2015 Accepted: August 21, 2016 Published: August 31, 2016
The CATS (FAM64A) protein interacts with CALM (PICALM) and the leukemic fusion protein CALM/AF10. CATS is highly expressed in leukemia, lymphoma and tumor cell lines and its protein levels strongly correlates with cellular proliferation in both malignant and normal cells. In order to obtain further insight into CATS function we performed an extensive analysis of CATS expression during differentiation of leukemia cell lines. While CATS expression decreased during erythroid, megakaryocytic and monocytic differentiation, a markedly increase was observed in the ATRA induced granulocytic differentiation. Lentivirus mediated silencing of CATS in U937 cell line resulted in somewhat reduced proliferation, altered cell cycle progression and lower migratory ability in vitro; however was not sufficient to inhibit tumor growth in xenotransplant model. Of note, CATS knockdown resulted in reduced clonogenicity of CATS-silenced cells and reduced expression of the self-renewal gene, GLI-1. Moreover, retroviral mediated overexpression of the murine Cats in primary bone marrow cells lead to decreased colony formation. Although our in vitro data suggests that CATS play a role in cellular processes important for tumorigenesis, such as cell cycle control and clonogenicity, these effects were not observed in vivo.
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