Dual targeting of vascular endothelial growth factor and bone morphogenetic protein‐9/10 impairs tumor growth through inhibition of angiogenesis. Issue 1 (January 2017)

• Record Type: Journal Article
• Authors: Akatsu, Yuichi; Yoshimatsu, Yasuhiro; Tomizawa, Taishi; Takahashi, Kazuki; Katsura, Akihiro; Miyazono, Kohei; Watabe, Tetsuro
• Is Part Of: Cancer science. Volume 108:Issue 1(2017)
• Page Start: 151
• Page End: 155
• Publication Date: 2017-01
• Subjects: ALK1 -- angiogenesis -- BMP‐9/10 -- Fc‐chimera -- vascular endothelial growth factor; Cancer -- Periodicals; Neoplasms -- Periodicals; Research -- Periodicals; Electronic journals; 616.994005
• DOI: 10.1111/cas.13103
• Languages: English
• ISSNs: 1347-9032

Abstract

Abstract : Clinical development of anti‐angiogenic agents has been a major landmark in cancer therapy for several types of cancers. Signals mediated by both vascular endothelial growth factor (VEGF) and bone morphogenetic protein (BMP)‐9 and 10 have been implicated in tumor angiogenesis. However, previous studies have shown that targeting the individual signals was not sufficiently effective in retarding tumor growth in certain preclinical and clinical conditions. In the present study, we developed a novel decoy chimeric receptor that traps both VEGF and BMP‐9/10. Single targeting of either VEGF or BMP‐9/10 signals significantly reduced the formation of tumor vessels in a mouse xenograft model of human pancreatic cancer; however, it did not show significant therapeutic effects on tumor growth. In contrast, dual targeting of the angiogenic signals resulted in more significant inhibition of tumor angiogenesis, leading to delay of tumor growth. Our findings suggest that simultaneous blockade of VEGF and BMP‐9/10 signals is a promising therapeutic strategy for the cancers that are resistant to anti‐VEGF and BMP‐9/10 therapies. Abstract : Dual targeting of the VEGF and BMP‐9/10 signals impairs tumor growth via inhibition of angiogenesis in a mouse xenograft model of human pancreatic cancer.