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CATS (FAM64A) abnormal expression reduces clonogenicity of hematopoietic cells
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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356563/ https://www.ncbi.nlm.nih.gov/pubmed/27588395 http://dx.doi.org/10.18632/oncotarget.11724 |
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author | Barbutti, Isabella Xavier, Juliana M. Machado-Neto, João Agostinho Ricon, Lauremilia Traina, Fabiola Bohlander, Stefan K. Saad, Sara Teresinha Olalla Archangelo, Leticia Fröhlich |
author_facet | Barbutti, Isabella Xavier, Juliana M. Machado-Neto, João Agostinho Ricon, Lauremilia Traina, Fabiola Bohlander, Stefan K. Saad, Sara Teresinha Olalla Archangelo, Leticia Fröhlich |
author_sort | Barbutti, Isabella |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5356563 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53565632017-03-24 CATS (FAM64A) abnormal expression reduces clonogenicity of hematopoietic cells Barbutti, Isabella Xavier, Juliana M. Machado-Neto, João Agostinho Ricon, Lauremilia Traina, Fabiola Bohlander, Stefan K. Saad, Sara Teresinha Olalla Archangelo, Leticia Fröhlich Oncotarget Research Paper 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. Impact Journals LLC 2016-08-31 /pmc/articles/PMC5356563/ /pubmed/27588395 http://dx.doi.org/10.18632/oncotarget.11724 Text en Copyright: © 2016 Barbutti et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Barbutti, Isabella Xavier, Juliana M. Machado-Neto, João Agostinho Ricon, Lauremilia Traina, Fabiola Bohlander, Stefan K. Saad, Sara Teresinha Olalla Archangelo, Leticia Fröhlich CATS (FAM64A) abnormal expression reduces clonogenicity of hematopoietic cells |
title | CATS (FAM64A) abnormal expression reduces clonogenicity of hematopoietic cells |
title_full | CATS (FAM64A) abnormal expression reduces clonogenicity of hematopoietic cells |
title_fullStr | CATS (FAM64A) abnormal expression reduces clonogenicity of hematopoietic cells |
title_full_unstemmed | CATS (FAM64A) abnormal expression reduces clonogenicity of hematopoietic cells |
title_short | CATS (FAM64A) abnormal expression reduces clonogenicity of hematopoietic cells |
title_sort | cats (fam64a) abnormal expression reduces clonogenicity of hematopoietic cells |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356563/ https://www.ncbi.nlm.nih.gov/pubmed/27588395 http://dx.doi.org/10.18632/oncotarget.11724 |
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