Tight junction protein 1 is regulated by transforming growth factor-ß and contributes to cell motility in NSCLC cells

So Hee Lee, A. Rome Paek, Kyungsil Yoon, Seok Hyun Kim, Soo Young Lee, Hye Jin You

Research output: Contribution to journalArticlepeer-review

20 Scopus citations

Abstract

Tight junction protein 1 (TJP1), a component of tight junction, has been reported to play a role in protein networks as an adaptor protein, and TJP1 expression is altered during tumor development. Here, we found that TJP1 expression was increased at the RNA and protein levels in TGF-ß-stimulated lung cancer cells, A549. SB431542, a type-I TGF-ß receptor inhibitor, as well as SB203580, a p38 kinase inhibitor, significantly abrogated the effect of TGF-ß on TJP1 expression. Diphenyleneiodonium, an NADPH oxidase inhibitor, also attenuated TJP1 expression in response to TGF-ß in lung cancer cells. When TJP1 expression was reduced by shRNA lentiviral particles in A549 cells (A549-sh TJP1), wound healing was much lower than in cells infected with control viral particles. Taken together, these data suggest that TGF-ß enhances TJP1 expression, which may play a role beyond structural support in tight junctions during cancer development.

Original languageEnglish
Pages (from-to)115-120
Number of pages6
JournalBMB Reports
Volume48
Issue number2
DOIs
StatePublished - 2015

Bibliographical note

Publisher Copyright:
© 2015 by the The Korean Society for Biochemistry and Molecular Biology.

Keywords

  • EMT
  • Motility
  • ROS
  • TGF-ß
  • TJP1

Fingerprint

Dive into the research topics of 'Tight junction protein 1 is regulated by transforming growth factor-ß and contributes to cell motility in NSCLC cells'. Together they form a unique fingerprint.

Cite this