PAR-1 and thrombin: The ties that bind the microenvironment to melanoma metastasis

Maya Zigler, Takafumi Kamiya, Emily C. Brantley, Gabriel J. Villares, Menashe Bar-Eli

Research output: Contribution to journalReview articlepeer-review

73 Scopus citations

Abstract

Progression of melanoma is dependent on cross-talk between tumor cells and the adjacent microenvironment. The thrombin receptor, protease-activated receptor-1 (PAR-1), plays a key role in exerting this function during melanoma progression. PAR-1 and its activating factors, which are expressed on tumor cells and the surrounding stroma, induce not only coagulation but also cell signaling, which promotes the metastatic phenotype. Several adhesion molecules, cytokines, growth factors, and proteases have recently been identified as downstream targets of PAR-1 and have been shown to modulate interactions between tumor cells and the microenvironment in the process of melanoma growth and metastasis. Inhibiting such interactions by targeting PAR-1 could potentially be a useful therapeutic modality for melanoma patients.

Original languageEnglish (US)
Pages (from-to)6561-6566
Number of pages6
JournalCancer Research
Volume71
Issue number21
DOIs
StatePublished - Nov 1 2011

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

MD Anderson CCSG core facilities

  • Flow Cytometry and Cellular Imaging Facility

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