Journal
CANCER LETTERS
Volume 277, Issue 1, Pages 114-120Publisher
ELSEVIER IRELAND LTD
DOI: 10.1016/j.canlet.2008.11.035
Keywords
TGF-beta; Colon cancer; Liver metastasis; LY2109761; Bioluminescence
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Funding
- Flight Attendant Medical Research Institute [R01 CA95195, CA113519, 5P50CA90949]
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Despite a primary tumor suppressor role, there is compelling evidence suggesting that TGF-beta can promote tumor growth, invasion and metastasis in advanced stages of colorectal cancer. Blocking these tumor-promoting effects of TGF-beta provides a potentially important therapeutic strategy for the treatment of colorectal cancer. However, little is known about how the inhibitors of TGF-beta receptor kinases affect colorectal carcinogenesis in vivo. Here, we have observed that a novel dual kinase inhibitor of TGF-beta type I and type 11 receptors, LY2109761, inhibits TGF-beta-mediated activation of Smad and non-Smad pathways in CT26 colon adenocarcinoma cells having K-Ras mutation. The inhibitor attenuates the oncogenic effects of TGF-beta on cell migration, invasion and tumorigenicity of CT26 cells. Furthermore, LY2109761 decreases liver metastases and prolongs survival in an experimental metastasis model. These findings suggest that the dual kinase inhibitor LY2109761 has potential therapeutic value for metastatic colorectal cancer. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
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