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Ethacrynic Acid Inhibits Sphingosylphosphorylcholine-Induced Keratin 8 Phosphorylation and Reorganization via Transglutaminase-2 Inhibitionopen access

Authors
Byun, Hyun JungKang, Kyung JinPark, Mi KyungLee, Hye JaKang, June HeeLee, Eun JiKim, You RiKim, Hyun JiKim, Young WooJung, Kyung ChaeKim, Soo YoulLee, Chang Hoon
Issue Date
30-Sep-2013
Publisher
KOREAN SOC APPLIED PHARMACOLOGY
Keywords
Sphingosylphosphorylcholine; Transglutaminase-2; Keratin-8 phosphorylation and reorganization; Ethacrynic acid; Migration; Invasion
Citation
BIOMOLECULES & THERAPEUTICS, v.21, no.5, pp 338 - 342
Pages
5
Indexed
SCIE
SCOPUS
KCI
Journal Title
BIOMOLECULES & THERAPEUTICS
Volume
21
Number
5
Start Page
338
End Page
342
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/15372
DOI
10.4062/biomolther.2013.066
ISSN
1976-9148
2005-4483
Abstract
Sphingosylphosphorylcholine (SPC) is significantly increased in the malicious ascites of tumor patients and induces perinuclear reorganization of keratin 8 (K8) filaments 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.
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