| Literature DB >> 26940138 |
Zhang Zhang1, Xiaomei Ren2, Xiaoyun Lu2, Deping Wang2, Xianjing Hu3, Yi Zheng2, Liyan Song3, Hongwen Pang2, Rongmin Yu4, Ke Ding5.
Abstract
Platelet-derived growth factor receptors (PDGFRα/β) play critical roles in the autocrine-stimulated growth and recruitment of cancer-associated fibroblasts (CAFs) of human lung cancer cells. We have identified GZD856 as a new PDGFR inhibitor that potently inhibits PDGFRα/β kinase activity and blocks this signaling pathway in lung cancer cells both in vitro and in vivo. GZD856 strongly suppresses the proliferation of PDGFRα-amplified H1703 (PDGFRβ(-)) human lung cancer cells and demonstrates significant in vivo antitumor efficacy in a xenograft mouse model. Although GZD856 displays only limited in vitro antiproliferative efficiency against PDGFRα(-)/PDGFRβ(+) A549 lung cancer cells, it efficiently inhibits the in vivo growth and metastasis of A549 cancer cells in xenograft and orthotopic models, respectively. The promising in vivo antitumor activity of GZD856 in A549 models may result from its suppression of PDGFR-related microenvironment factors, such as recruitment of CAFs and collagen content in stromal cells. GZD856 may be considered as a promising new candidate for anti-lung cancer drug development.Entities:
Keywords: GZD856; Lung cancer; Metastasis; PDGFRα/β inhibitor; Stromal
Mesh:
Substances:
Year: 2016 PMID: 26940138 DOI: 10.1016/j.canlet.2016.02.017
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679