Transient strong reduction of PTEN expression by specific RNAi induces loss of adhesion of the cells

Setsuko Mise-Omata, Yuichi Obata, Shigeru Iwase, Nathan Mise, Takahiro S. Doi

Research output: Contribution to journalArticlepeer-review

20 Citations (Scopus)


The tumor suppressor gene pten encodes a lipid phosphatase that dephosphorylates D3 of phosphatidylinositol(3,4,5)trisphosphate, producing phosphatidylinositol(4,5)bisphosphate. Although PTEN has been implicated in cell adhesion and migration, the underlying molecular mechanism is unknown. To investigate the role of PTEN in cell adhesion, we designed three different siRNAs (siRNA PTEN-a, siRNA PTEN-b, and siRNA PTEN-c) and transfected into 293T cells. Two days later, only the cells transfected with siRNA PTEN-b became round and detached from the culture dishes, whereas cells transfected with a control siRNA against GFP or the two other siRNAs against PTEN did not. Evaluation of the RNAi effect revealed that siRNA PTEN-b inhibited >95% of PTEN expression, the most effective among the three siRNAs. To check for non-specific effects such as interferon response and inhibition of off-target genes, we then used quantitative PCR analysis and DNA microarray analysis. None was detected, indicating that the RNAi system was highly specific. Immunofluorescence studies using PTEN-knockdown HeLa cells revealed that the loss of adhesion was accompanied by a reduction in the number of focal adhesion plaques and disorganization of the actin cytoskeleton. Transient and near-complete loss of PTEN expression induces loss of adhesion of the cells.

Original languageEnglish
Pages (from-to)1034-1042
Number of pages9
JournalBiochemical and Biophysical Research Communications
Issue number4
Publication statusPublished - 2005 Mar 25
Externally publishedYes


  • Actin cytoskeleton
  • Cell adhesion
  • Interferon response
  • PTEN
  • RNA interference
  • Specificity of RNAi

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Molecular Biology
  • Cell Biology


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