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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Cellular Migration Ability Is Modulated by Extracellular Purines in Ovarian Carcinoma SKOV-3 Cells

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Author(s):
Martinez-Ramirez, A. S. [1] ; Diaz-Munoz, M. [1] ; Battastini, A. M. [2] ; Campos-Contreras, A. [1] ; Olvera, A. [1] ; Bergamin, L. [3] ; Glaser, T. [3] ; Moritz, C. E. Jacintho [2] ; Ulrich, H. [3] ; Vazquez-Cuevas, F. G. [1]
Total Authors: 10
Affiliation:
[1] Univ Nacl Autonoma Mexico, Inst Neurobiol, Dept Neurobiol Celular & Mol, Blvd Juriquilla 3001, Juriquilla Queretaro 76230, Queretaro - Mexico
[2] Univ Fed Rio Grande do Sul, Dept Bioquim, Inst Ciencias Basicas & Saude, Porto Alegre, RS - Brazil
[3] Univ Sao Paulo, Inst Quim, Dept Bioquim, Ave Prof Lineu Prestes 748, BR-05508900 Sao Paulo - Brazil
Total Affiliations: 3
Document type: Journal article
Source: Journal of Cellular Biochemistry; v. 118, n. 12, p. 4468-4478, DEC 2017.
Web of Science Citations: 1
Abstract

Extracellular nucleotides and nucleosides have emerged as important elements regulating tissue homeostasis. Acting through specific receptors, have the ability to control gene expression patterns to direct cellular fate. We observed that SKOV-3 cells express the ectonucleotidases: ectonucleotide pyrophosphatase 1 (ENPP1), ecto-5-nucleotidase (NT5E), and liver alkaline phosphatase (ALPL). Strikingly, in pulse and chase experiments supplemented with ATP, SKOV-3 cells exhibited low catabolic efficiency in the conversion of ADP into AMP, but they were efficient in converting AMP into adenosine. Since these cells release ATP, we proposed that the conversion of ADP into AMP is a regulatory node associated with the migratory ability and the mesenchymal characteristics shown by SKOV-3 cells under basal conditions. The landscape of gene expression profiles of SKOV-3 cell cultures treated with apyrase or adenosine demonstrated similarities (e.g., decrease FGF16 transcript) and differences (e.g., the negative regulation of Wnt 2, and 10B by adenosine). Thus, in SKOV-3 we analyzed the migratory ability and the expression of epithelium to mesenchymal transition (EMT) markers in response to apyrase. Apyrase-treatment favored the epithelial-like phenotype, as revealed by the re-location of E-cadherin to the cell to cell junctions. Pharmacological approaches strongly suggested that the effect of Apyrase involved the accumulation of extracellular adenosine; this notion was strengthened when the incubation of the SKOV-3 cell with ,-methylene ADP (CD73 inhibitor) or adenosine deaminase was sufficient to abolish the effect of apyrase on cell migration. Overall, adenosine signaling is a fine tune mechanism in the control of cell phenotype in cancer. J. Cell. Biochem. 118: 4468-4478, 2017. (c) 2017 Wiley Periodicals, Inc. (AU)

FAPESP's process: 15/13345-1 - Huntington's disease: Huntingtin roles during cell fate decision
Grantee:Talita Glaser
Support type: Scholarships in Brazil - Post-Doctorate
FAPESP's process: 16/07659-6 - Huntingtin's Roles in Fate Decision of GABAergic Neurons Derived from iPSCs of HD Patients
Grantee:Talita Glaser
Support type: Scholarships abroad - Research Internship - Post-doctor
FAPESP's process: 12/50880-4 - Stem cells: from basic studies of kinin and purinergic receptor roles towards therapeutical applications
Grantee:Alexander Henning Ulrich
Support type: Research Projects - Thematic Grants