Majumder Mousumi, Xin Xiping, Liu Ling, Girish Gannareddy V, Lala Peeyush K
Department of Anatomy and Cell Biology, Schulich School of Medicine and Dentistry, University of Western Ontario, London, Ontario, Canada.
Cancer Sci. 2014 Sep;105(9):1142-51. doi: 10.1111/cas.12475. Epub 2014 Sep 11.
We previously established that COX-2 overexpression promotes breast cancer progression and metastasis. As long-term use of COX-2 inhibitors (COX-2i) can promote thrombo-embolic events, we tested an alternative target, prostaglandin E2 receptor EP4 subtype (EP4), downstream of COX-2. Here we used the highly metastatic syngeneic murine C3L5 breast cancer model to test the role of EP4-expressing macrophages in vascular endothelial growth factor (VEGF)-C/D production, angiogenesis, and lymphangiogenesis in situ, the role of EP4 in stem-like cell (SLC) functions of tumor cells, and therapeutic effects of an EP4 antagonist RQ-15986 (EP4A). C3L5 cells expressed all EP receptors, produced VEGF-C/D, and showed high clonogenic tumorsphere forming ability in vitro, functions inhibited with COX-2i or EP4A. Treating murine macrophage RAW 264.7 cell line with COX-2i celecoxib and EP4A significantly reduced VEGF-A/C/D production in vitro, measured with quantitative PCR and Western blots. Orthotopic implants of C3L5 cells in C3H/HeJ mice showed rapid tumor growth, angiogenesis, lymphangiogenesis (CD31/LYVE-1 and CD31/PROX1 immunostaining), and metastasis to lymph nodes and lungs. Tumors revealed high incidence of EP4-expressing, VEGF-C/D producing macrophages identified with dual immunostaining of F4/80 and EP4 or VEGF-C/D. Celecoxib or EP4A therapy at non-toxic doses abrogated tumor growth, lymphangiogenesis, and metastasis to lymph nodes and lungs. Residual tumors in treated mice revealed markedly reduced VEGF-A/C/D and phosphorylated Akt/ERK proteins, VEGF-C/D positive macrophage infiltration, and proliferative/apoptotic cell ratios. Knocking down COX-2 or EP4 in C3L5 cells or treating cells in vitro with celecoxib or EP4A and treating tumor-bearing mice in vivo with the same drug reduced SLC properties of tumor cells including preferential co-expression of COX-2 and SLC markers ALDH1A, CD44, OCT-3/4, β-catenin, and SOX-2. Thus, EP4 is an excellent therapeutic target to block stem-like properties, angiogenesis, and lymphangiogenesis induced by VEGF-A/C/D secreted by cancer cells and tumor infiltrating macrophages.
我们之前证实,COX-2的过表达会促进乳腺癌的进展和转移。由于长期使用COX-2抑制剂(COX-2i)会增加血栓栓塞事件的发生风险,我们测试了COX-2下游的另一个靶点——前列腺素E2受体EP4亚型(EP4)。在此,我们使用高转移性同基因小鼠C3L5乳腺癌模型,来测试表达EP4的巨噬细胞在血管内皮生长因子(VEGF)-C/D产生、原位血管生成和淋巴管生成中的作用,EP4在肿瘤细胞的干细胞样细胞(SLC)功能中的作用,以及EP4拮抗剂RQ-15986(EP4A)的治疗效果。C3L5细胞表达所有EP受体,产生VEGF-C/D,并在体外表现出较高的克隆形成肿瘤球能力,这些功能可被COX-2i或EP4A抑制。用COX-2i塞来昔布和EP4A处理小鼠巨噬细胞RAW 264.7细胞系,通过定量PCR和蛋白质免疫印迹法检测发现,体外VEGF-A/C/D的产生显著减少。将C3L5细胞原位植入C3H/HeJ小鼠体内,结果显示肿瘤生长迅速,伴有血管生成、淋巴管生成(CD31/LYVE-1和CD31/PROX1免疫染色),并转移至淋巴结和肺部。通过F4/80与EP4或VEGF-C/D的双重免疫染色鉴定发现,肿瘤中表达EP4、产生VEGF-C/D的巨噬细胞发生率很高。无毒剂量的塞来昔布或EP4A治疗可消除肿瘤生长、淋巴管生成以及向淋巴结和肺部的转移。经治疗小鼠体内的残留肿瘤显示,VEGF-A/C/D和磷酸化Akt/ERK蛋白明显减少,VEGF-C/D阳性巨噬细胞浸润以及增殖/凋亡细胞比例降低。在C3L5细胞中敲低COX-2或EP4,或在体外使用塞来昔布或EP4A处理细胞,并在体内用相同药物治疗荷瘤小鼠,均可降低肿瘤细胞的SLC特性,包括COX-2与SLC标志物ALDH1A、CD44、OCT-3/4、β-连环蛋白和SOX-2的共表达。因此,EP4是一个很好的治疗靶点,可阻断癌细胞和肿瘤浸润巨噬细胞分泌的VEGF-A/C/D诱导的干细胞样特性、血管生成和淋巴管生成。