ARHGAP21 is a RhoGAP for RhoA and RhoC with a role in proliferation and migration of prostate adenocarcinoma cells

Mariana Lazarini, Fabiola Traina, João A Machado-Neto, Karin S A Barcellos, Yuri B Moreira, Marcelo M Brandão, Sergio Verjovski-Almeida, Anne J Ridley, Sara T Olalla Saad

Research output: Contribution to journalArticle (Academic Journal)peer-review

Abstract

BACKGROUND: Several Rho GTPase-activating proteins (RhoGAPs) are implicated in tumor progression through their effects on Rho GTPase activity. ARHGAP21 is a RhoGAP with increased expression in head and neck squamous cell carcinoma and with a possible role in glioblastoma tumor progression, yet little is known about the function of ARHGAP21 in cancer cells. Here we studied the role of ARHGAP21 in two prostate adenocarcinoma cell lines, LNCaP and PC3, which respectively represent initial and advanced stages of prostate carcinogenesis.

RESULTS: ARHGAP21 is located in the nucleus and cytoplasm of both cell lines and its depletion resulted in decreased proliferation and increased migration of PC3 cells but not LNCaP cells. In PC3 cells, ARHGAP21 presented GAP activity for RhoA and RhoC and induced changes in cell morphology. Moreover, its silencing altered the expression of genes involved in cell proliferation and cytoskeleton organization, as well as the endothelin-1 canonical pathway.

CONCLUSIONS: Our results reveal new functions and signaling pathways regulated by ARHGAP21, and indicate that it could contribute to prostate cancer progression.

Original languageEnglish
Pages (from-to)365-74
Number of pages10
JournalBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
Volume1832
Issue number2
DOIs
Publication statusPublished - Feb 2013

Keywords

  • Adenocarcinoma
  • Base Sequence
  • Cell Line, Tumor
  • Cell Movement
  • Cell Proliferation
  • DNA Primers
  • GTPase-Activating Proteins
  • Gene Silencing
  • Humans
  • In Situ Nick-End Labeling
  • Male
  • Prostatic Neoplasms
  • Reverse Transcriptase Polymerase Chain Reaction
  • Journal Article
  • Research Support, Non-U.S. Gov't

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