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Ethacrynic acid inhibits sphingosylphosphorylcholine-induced keratin 8 phosphorylation and reorganization via transglutaminase-2 inhibition

  • Hyun Jung Byun
  • , Kyung Jin Kang
  • , Mi Kyung Park
  • , Hye Ja Lee
  • , June Hee Kang
  • , Eun Ji Lee
  • , You Ri Kim
  • , Hyun Ji Kim
  • , Young Woo Kim
  • , Kyung Chae Jung
  • , Soo Youl Kim
  • , Chang Hoon Lee

Research output: Contribution to journalArticlepeer-review

20 Scopus citations

Abstract

Sphingosylphosphorylcholine (SPC) is significantly increased in the malicious ascites of tumor patients and induces perinuclear reorganization of keratin 8 (K8) fi laments in PANC-1 cells. The reorganization contributes to the viscoelasticity of metastatic cancer cells resulting in increased migration. Recently, we reported that transglutaminase-2 (Tgase-2) is involved in SPC-induced K8 phosphorylation and reorganization. However, effects of Tgase-2 inhibitors on SPC-induced K8 phosphorylation and reorganization were not clearly studied. We found that ethacrynic acid (ECA) concentration-dependently inhibited Tgase-2. Therefore, we examined the effects of ECA on SPC-induced K8 phosphorylation and reorganization. ECA concentration-dependently suppressed the SPC-induced phosphorylation and perinuclear reorganization of K8. ECA also suppressed the SPC-induced migration and invasion. SPC induced JNK activation through Tgase-2 expression and ECA suppressed the activation and expression of JNK in PANC-1 cells. These results suggested that ECA might be useful to control Tgase-2 dependent metastasis of cancer cells such as pancreatic cancer and lung cancers.

Original languageEnglish
Pages (from-to)338-342
Number of pages5
JournalBiomolecules and Therapeutics
Volume21
Issue number5
DOIs
StatePublished - 2013

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Ethacrynic acid
  • Invasion
  • Keratin-8 phosphorylation and reorganization
  • Migration
  • Sphingosylphosphorylcholine
  • Transglutaminase-2

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