4.6 Article

G Cryptotanshinone, a Novel Tumor Angiogenesis Inhibitor, Destabilizes Tumor Necrosis Factor-α mRNA Via Decreasing Nuclear-Cytoplasmic Translocation of RNA-Binding Protein HuR

Journal

MOLECULAR CARCINOGENESIS
Volume 55, Issue 10, Pages 1399-1410

Publisher

WILEY
DOI: 10.1002/mc.22383

Keywords

cryptotanshinone; angiogenesis; tumor necrosis factor-alpha; mRNA stability; HuR

Funding

  1. National Natural Science Foundation of China [81173174, 81202655]
  2. National Key Technology R and D Program [2008BAI51B02]
  3. Programs Foundation of Ministry of Education of China [20113237110008]
  4. Chinese Postdoctoral Science Foundation [2014M551639]
  5. Postdoctoral Science Foundation of Jiangsu province [1401138C]
  6. National Science Foundation [81403260]
  7. Priority Academic Program Development of Jiangsu Higher Education Institutions
  8. Program for Technological Innovation Team of Jiangsu Higher Education

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Cryptotanshinone (CT), one major lipophilic component isolated from Salvia miltiorrhiza Bunge, has shown to possess chemopreventive properties against various types of cancer cells. In this study, CT was shown to be a potent antiangiogenic agent in zebrafish, and mouse models and could limit tumor growth by inhibiting tumor angiogenesis. We further found that CT could inhibit the proliferation, migration, angiogenic sprouting, and tube formation of HUVECs. In addition, we demonstrated that CT could lower the level of TNF-alpha due to the destabilization of TNF-alpha mRNA, which associated with regulating 3'-untranslated region (3'-UTR) of TNF-alpha and preventing the translocation of RNA binding protein, HuR, from the nucleus to the cytoplasm. Moreover, the underlying mechanism responsible for the regulation in angiogenesis by CT was partially related to the suppression of NF-kappa B, and STAT3 activity. Based on the abilities of CT in targeting tumor cells, inhibiting angiogenesis, and destroying tumor vasculature, CT is worthy of further investigation for preventive, and therapeutic purposes in cancer. (C) 2015 Wiley Periodicals, Inc.

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