Lu Zhi Hong, Kaliberov Sergey, Sohn Rebecca E, Kaliberova Lyudmila, Du Yingqiu, Prior Julie L, Leib Daniel J, Chauchereau Anne, Sehn Jennifer K, Curiel David T, Arbeit Jeffrey M
Urology Division and Department of Surgery, Washington University in St. Louis School of Medicine, St. Louis, MO 63110, USA.
Siteman Cancer Center, Washington University in St. Louis School of Medicine, St. Louis, MO 63110, USA.
Oncotarget. 2017 Feb 14;8(7):12272-12289. doi: 10.18632/oncotarget.14699.
While modern therapies for metastatic prostate cancer (PCa) have improved survival they are associated with an increasingly prevalent entity, aggressive variant PCa (AVPCa), lacking androgen receptor (AR) expression, enriched for cancer stem cells (CSCs), and evidencing epithelial-mesenchymal plasticity with a varying extent of neuroendocrine transdifferentiation. Parallel work revealed that endothelial cells (ECs) create a perivascular CSC niche mediated by juxtacrine and membrane tethered signaling. There is increasing interest in pharmacological metastatic niche targeting, however, targeted access has been impossible. Here, we discovered that the Gleason 7 derived, androgen receptor negative, IGR-CaP1 cell line possessed some but not all of the molecular features of AVPCa. Intracardiac injection into NOD/SCID/IL2Rg -/- (NSG) mice produced a completely penetrant bone, liver, adrenal, and brain metastatic phenotype; noninvasively and histologically detectable at 2 weeks, and necessitating sacrifice 4-5 weeks post injection. Bone metastases were osteoblastic, and osteolytic. IGR-CaP1 cells expressed the neuroendocrine marker synaptophysin, near equivalent levels of vimentin and e-cadherin, all of the EMT transcription factors, and activation of NOTCH and WNT pathways. In parallel, we created a new triple-targeted adenoviral vector containing a fiber knob RGD peptide, a hexon mutation, and an EC specific ROBO4 promoter (Ad.RGD.H5/3.ROBO4). This vector was expressed in metastatic microvessels tightly juxtaposed to IGR-CaP1 cells in bone and visceral niches. Thus, the combination of IGR-CaP1 cells and NSG mice produces a completely penetrant metastatic PCa model emulating end-stage human disease. In addition, the metastatic niche access provided by our novel Ad vector could be therapeutically leveraged for future disease control or cure.
虽然转移性前列腺癌(PCa)的现代疗法提高了生存率,但它们与一种日益普遍的实体——侵袭性变异型PCa(AVPCa)相关,这种癌症缺乏雄激素受体(AR)表达,富含癌症干细胞(CSCs),并表现出上皮-间质可塑性以及不同程度的神经内分泌转分化。并行研究表明,内皮细胞(ECs)通过旁分泌和膜结合信号介导形成血管周围CSC微环境。人们对药理学转移性微环境靶向的兴趣日益浓厚,然而,靶向进入一直无法实现。在这里,我们发现源自Gleason 7、雄激素受体阴性的IGR-CaP1细胞系具有AVPCa的一些但并非全部分子特征。向NOD/SCID/IL2Rg -/-(NSG)小鼠进行心内注射产生了完全穿透性的骨、肝、肾上腺和脑转移表型;在2周时可通过非侵入性和组织学检测到,注射后4 - 5周需要处死小鼠。骨转移既有成骨的,也有溶骨的。IGR-CaP1细胞表达神经内分泌标志物突触素,波形蛋白和E-钙黏蛋白水平相近,所有EMT转录因子,以及NOTCH和WNT信号通路的激活。同时,我们构建了一种新的三靶向腺病毒载体,其包含纤维结RGD肽、六邻体突变和EC特异性ROBO4启动子(Ad.RGD.H5/3.ROBO4)。该载体在骨和内脏微环境中与IGR-CaP1细胞紧密相邻的转移性微血管中表达。因此,IGR-CaP1细胞和NSG小鼠的组合产生了一个完全穿透性的转移性PCa模型,模拟终末期人类疾病。此外,我们新型腺病毒载体提供的转移性微环境进入途径可用于未来疾病控制或治愈的治疗手段。