4.8 Article

Vascular RhoJ Is an Effective and Selective Target for Tumor Angiogenesis and Vascular Disruption

期刊

CANCER CELL
卷 25, 期 1, 页码 102-117

出版社

CELL PRESS
DOI: 10.1016/j.ccr.2013.12.010

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资金

  1. National Research Foundation of Korea
  2. Ministry of Science, ICT, and Future Planning [NRF-2009-0079390, NRF-2013M3A9B6046565, NRF-2012M3A9C 4048758]
  3. Ministry of Health and Welfare [A110076]
  4. JSPS KAKENHI [25293078]
  5. Takeda Science Foundation
  6. Korea Health Promotion Institute [HI11C0069010013] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  7. National Research Foundation of Korea [2013M3A9B6046565, 2009-0079390, KIB01, 2012M3A9C4048758] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  8. Grants-in-Aid for Scientific Research [25293078] Funding Source: KAKEN

向作者/读者索取更多资源

Current antiangiogenic therapy is limited by its cytostatic nature and systemic side effects. To address these limitations, we have unveiled the role of RhoJ, an endothelial-enriched Rho GTPase, during tumor progression. RhoJ blockade provides a double assault on tumor vessels by both inhibiting tumor angiogenesis and disrupting the preformed tumor vessels through the activation of the RhoA-ROCK (Rho kinase) signaling pathway in tumor endothelial cells, consequently resulting in a functional failure Of tumor vasculatures. Moreover, enhanced anticancer effects were observed when RhoJ blockade was employed in concert with a cytotoxic chemotherapeutic agent, angiogenesis-inhibiting agent, or vascular-disrupting agent. These results identify RhoJ blockade as a selective and effective therapeutic strategy for targeting tumor vasculature with minimal side effects.

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