4.6 Article

TMPRSS4 upregulates uPA gene expression through JNK signaling activation to induce cancer cell invasion

Journal

CELLULAR SIGNALLING
Volume 26, Issue 2, Pages 398-408

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cellsig.2013.08.002

Keywords

TMPRSS4; uPA; Invasion; Transcription

Categories

Funding

  1. National R&D Program for Cancer Control, Ministry for Health and Welfare [1320050]
  2. Basic Science Research Program through the National Research Foundation of Korea
  3. Ministry of Education, Science and Technology [2012R1A1A2002242, 2012K001395]
  4. Converging Research Center Program of the National Research Foundation of Korea
  5. Tumor Microenvironment Global Core Research Center
  6. Ministry of Science, ICT & Future Planning (GCRC) [2011-0030001]
  7. KRIBB Research Initiative Program, Republic of Korea [KCM2021312]
  8. National Research Council of Science & Technology (NST), Republic of Korea [KCM2021312] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  9. National Research Foundation of Korea [2012R1A1A2002242] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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TMPRSS4 is a novel type II transmembrane serine protease that is highly expressed in pancreatic, thyroid, colon, and other cancer tissues. Previously, we demonstrated that TMPRSS4 mediates tumor cell invasion, migration, and metastasis. However, the mechanisms by which TMPRSS4 contributes to invasion are not fully understood. Here, we demonstrated that TMPRSS4 induced the transcription of the urokinase-type plasminogen activator (uPA) gene through activating the transcription factors Sp1, Sp3, and AP-1 in mainly a JNK-dependent manner and that the induction of uPA was required for TMPRSS4-mediated cancer cell invasion and signaling events. In addition, the uPA receptor was involved in TMPRSS4-induced signaling activation and subsequent uPA expression probably through its association with TMPRSS4 on the cell surface. Immunohistochemical analysis showed that uPA expression was significantly correlated with TMPRSS4 expression in human lung and prostate cancers. These observations suggest that TMPRSS4 is an important regulator of uPA gene expression; the upregulation of uPA by TMPRSS4 contributes to invasion and may represent a novel mechanism for the control of invasion. (C) 2013 Elsevier Inc. All rights reserved.

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