Jin Fengshuo, Xie Zhihui, Kuo Calvin J, Chung Leland W K, Hsieh Chia-Ling
Department of Urology, Molecular Urology and Therapeutic Program, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
Cancer Gene Ther. 2005 Mar;12(3):257-67. doi: 10.1038/sj.cgt.7700790.
Tumor-endothelial interaction contributes to local prostate tumor growth and distant metastasis. In this communication, we designed a novel approach to target both cancer cells and their "crosstalk" with surrounding microvascular endothelium in an experimental hormone refractory human prostate cancer model. We evaluated the in vitro and in vivo synergistic and/or additive effects of a combination of conditional oncolytic adenovirus plus an adenoviral-mediated antiangiogenic therapy. In the in vitro study, we demonstrated that human umbilical vein endothelial cells (HUVEC) and human C4-2 androgen-independent (AI) prostate cancer cells, when infected with an antiangiogenic adenoviral (Ad)-Flk1-Fc vector secreting a soluble form of Flk1, showed dramatically inhibited proliferation, migration and tubular formation of HUVEC endothelial cells. C4-2 cells showed maximal growth inhibition when coinfected with Ad-Flk1-Fc and Ad-hOC-E1, a conditional replication-competent Ad vector with viral replication driven by a human osteocalcin (hOC) promoter targeting both prostate cancer epithelial and stromal cells. Using a three-dimensional (3D) coculture model, we found that targeting C4-2 cells with Ad-hOC-E1 markedly decreased tubular formation in HUVEC, as visualized by confocal microscopy. In a subcutaneous C4-2 tumor xenograft model, tumor volume was decreased by 40-60% in animals treated with Ad-Flk1-Fc or Ad-hOC-E1 plus vitamin D3 alone and by 90% in a combined treatment group, compared to untreated animals in an 8-week treatment period. Moreover, three of 10 (30%) pre-established tumors completely regressed when animals received combination therapy. Cotargeting tumor and tumor endothelium could be a promising gene therapy strategy for the treatment of both localized and metastatic human prostate cancer.
肿瘤-内皮细胞相互作用促进局部前列腺肿瘤生长和远处转移。在本报告中,我们设计了一种新方法,在实验性激素难治性人前列腺癌模型中靶向癌细胞及其与周围微血管内皮细胞的“串扰”。我们评估了条件性溶瘤腺病毒联合腺病毒介导的抗血管生成疗法的体外和体内协同和/或相加作用。在体外研究中,我们证明,人脐静脉内皮细胞(HUVEC)和人C4-2雄激素非依赖性(AI)前列腺癌细胞在感染分泌可溶性形式Flk1的抗血管生成腺病毒(Ad)-Flk1-Fc载体后,HUVEC内皮细胞的增殖、迁移和管状形成受到显著抑制。当与Ad-Flk1-Fc和Ad-hOC-E1共感染时,C4-2细胞显示出最大程度的生长抑制,Ad-hOC-E1是一种条件性复制能力的Ad载体,其病毒复制由靶向前列腺癌上皮和基质细胞的人骨钙素(hOC)启动子驱动。使用三维(3D)共培养模型,我们发现用Ad-hOC-E1靶向C4-2细胞可显著减少HUVEC中的管状形成,这通过共聚焦显微镜观察可见。在皮下C4-2肿瘤异种移植模型中,与8周治疗期内未治疗的动物相比,单独用Ad-Flk1-Fc或Ad-hOC-E1加维生素D3治疗的动物肿瘤体积减少了40%-60%,联合治疗组减少了90%。此外,当动物接受联合治疗时,10个预先建立的肿瘤中有3个(30%)完全消退。同时靶向肿瘤和肿瘤内皮细胞可能是治疗局限性和转移性人前列腺癌的一种有前景的基因治疗策略。