| Literature DB >> 28854359 |
Kazuhiro Takara1, Daisuke Eino2, Koji Ando3, Daisuke Yasuda4, Hisamichi Naito5, Yohei Tsukada5, Tomohiro Iba5, Taku Wakabayashi5, Fumitaka Muramatsu5, Hiroyasu Kidoya5, Shigetomo Fukuhara3, Naoki Mochizuki3, Satoshi Ishii4, Haruhiko Kishima6, Nobuyuki Takakura7.
Abstract
Vascular normalization in tumors may improve drug delivery and anti-tumor immunity. Angiogenesis inhibitors induce hypoxia, which may facilitate malignant progression; therefore, we investigated other methods to promote vascular maturation. Here, we show that lysophosphatidic acid (LPA) enhances blood flow by promoting fine vascular networks, thereby improving vascular permeability and suppressing tumor growth when combined with anti-cancer drug treatment. Six different G protein-coupled receptors have been identified as LPA receptors (LPA1-6). In studies using mutant mice, we found that LPA4 is involved in vascular network formation. LPA4 activation induces circumferential actin bundling beneath the cell membrane and enhances linear adherens junction formation by VE-cadherin in endothelial cells. Therefore, we conclude that activation of LPA4 is a promising approach for vascular regulation.Entities:
Keywords: LPA; LPA4; VE-cadherin; angiogenesis; drug delivery
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Year: 2017 PMID: 28854359 DOI: 10.1016/j.celrep.2017.07.080
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423