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PMID: 27588395 Published · ppublish English Journal Article

CATS (FAM64A) abnormal expression reduces clonogenicity of hematopoietic cells.

Oncotarget ·Vol. 7 ·No. 42 ·2016-10-18 ·页码 68385-68396

Barbutti I, Xavier-Ferrucio JM, Machado-Neto JA, Ricon L, Traina F, Bohlander SK, Saad ST, Archangelo LF

Abstract

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.

Keywords
CALM/AF10 CATS (FAM64A) clonogenicity leukemogenesis proliferation
MeSH 主题词
Animals Carrier Proteins/genetics,metabolism Cell Cycle/drug effects,genetics Cell Differentiation/drug effects,genetics Cell Line, Tumor Cell Movement/drug effects,genetics Cell Proliferation/genetics Gene Expression Regulation, Neoplastic Humans Intracellular Signaling Peptides and Proteins K562 Cells Leukemia/genetics,pathology,therapy Mice, Inbred NOD Mice, SCID Nuclear Proteins RNA Interference RNAi Therapeutics/methods Tretinoin/pharmacology U937 Cells Xenograft Model Antitumor Assays/methods
化学物质
Carrier Proteins Intracellular Signaling Peptides and Proteins Nuclear Proteins PIMREG protein, human Tretinoin
作者与单位
共 8 位作者,点击展开单位 / ORCID
Barbutti Isabella
Hematology and Hemotherapy Center, State University of Campinas (UNICAMP), Carlos Chagas 480, Campinas-SP, Brazil.
Xavier-Ferrucio Juliana M
Hematology and Hemotherapy Center, State University of Campinas (UNICAMP), Carlos Chagas 480, Campinas-SP, Brazil.
Machado-Neto João Agostinho
Hematology and Hemotherapy Center, State University of Campinas (UNICAMP), Carlos Chagas 480, Campinas-SP, Brazil.
Ricon Lauremilia
Hematology and Hemotherapy Center, State University of Campinas (UNICAMP), Carlos Chagas 480, Campinas-SP, Brazil.
Traina Fabiola
Department of Internal Medicine, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Bohlander Stefan K
Department of Molecular Medicine and Pathology, The University of Auckland, Auckland, New Zealand.
Saad Sara Teresinha Olalla
Hematology and Hemotherapy Center, State University of Campinas (UNICAMP), Carlos Chagas 480, Campinas-SP, Brazil.
Archangelo Leticia Fröhlich
Hematology and Hemotherapy Center, State University of Campinas (UNICAMP), Carlos Chagas 480, Campinas-SP, Brazil. | Department of Cellular and Molecular Biology and Pathogenic Bioagents, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Article Info
Journal
Oncotarget
Abbr.
Oncotarget
ISSN
1949-2553
Published
2016-10-18
页码
68385-68396
Language
English
Country/Region
United States
NLM ID
101532965
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