Article

RECK-mediated inhibition of glioma migration and invasion

  1. Tatiana C. Silveira Corrêa1,‡,
  2. Renato Ramos Massaro1,‡,
  3. Carla Abdo Brohem1,
  4. Sebastião Roberto Taboga2,
  5. Marcelo Lazzaron Lamers3,†,
  6. Marinilce Fagundes Santos3,
  7. Silvya Stuchi Maria-Engler1,*

Article first published online: 1 FEB 2010

DOI: 10.1002/jcb.22472

Issue

Journal of Cellular Biochemistry

Journal of Cellular Biochemistry

Volume 110, Issue 1, pages 52–61, 1 May 2010

Additional Information

How to Cite

Silveira Corrêa, T. C., Massaro, R. R., Brohem, C. A., Taboga, S. R., Lamers, M. L., Santos, M. F. and Maria-Engler, S. S. (2010), RECK-mediated inhibition of glioma migration and invasion. J. Cell. Biochem., 110: 52–61. doi: 10.1002/jcb.22472

Author Information

  1. 1

    Department of Clinical Chemistry & Toxicology, School of Pharmaceutical Sciences, University of São Paulo, São Paulo, SP, Brazil

  2. 2

    Department of Biology, IBILCE—University State of São Paulo, São José do Rio Preto, SP, Brazil

  3. 3

    Department of Cell and Developmental Biology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil

  1. †

    Department of Morphological Sciences, Institute of Basic Health Sciences, Federal University of Rio Grande do Sul.

  1. ‡

    Tatiana C. Silveira Corrêa and Renato Ramos Massaro contributed equally to this work.

*580 Lineu Prestes Ave, 17 Bldg 22 Room, São Paulo 05508-900, SP, Brazil.

  1. ‡

    Tatiana C. Silveira Corrêa and Renato Ramos Massaro contributed equally to this work.

Publication History

  1. Issue published online: 16 APR 2010
  2. Article first published online: 1 FEB 2010
  3. Manuscript Accepted: 25 NOV 2009
  4. Manuscript Received: 15 SEP 2009

Funded by

  • FAPESP. Grant Numbers: 06/50915-1, 05/51194-3
  • CNPq
  • CAPES
  • PRP-USP

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FilenameFormatSizeDescription
JCB_22472_sm_SupplData.doc22KSupplemental Data
JCB_22472_sm_SupplFig1.tif314KSupplementry Figure 1. Validation of RECK Clones. (A) Eleven G418-resistent cell colonies were screened for the expression of RECK by real time PCR. (B) Immunohistochemistry showing the RECK expression in RECK+ cells overexpressing RECK.
JCB_22472_sm_SupplFig2.tif649KSupplementry Figure 2. Senescence-associated β-galactosidase assay, BrdU and cell cycle progression were performed in order to characterize cell proliferation cells overexpressing RECK. No alteration of proliferation rates was observed in RECK+ cells compared to the controls:T98G and Mock.

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