Aboody Karen S, Najbauer Joseph, Schmidt Nils Ole, Yang Wendy, Wu Julian K, Zhuge Yuzheng, Przylecki Wojciech, Carroll Rona, Black Peter M, Perides George
Divisions of Hematology and Hematopoietic Cell Transplantation and Neurosciences and Beckman Research Institute, City of Hope National Medical Center, Duarte, CA 91010-3000, USA.
Neuro Oncol. 2006 Apr;8(2):119-26. doi: 10.1215/15228517-2005-012. Epub 2006 Mar 8.
Brain metastases are an increasingly frequent and serious clinical problem for cancer patients, especially those with advanced melanoma. Given the extensive tropism of neural stem/progenitor cells (NSPCs) for pathological areas in the central nervous system, we expanded investigations to determine whether NSPCs could also target multiple sites of brain metastases in a syngeneic experimental melanoma model. Using cytosine deaminase-expressing NSPCs (CD-NSPCs) and systemic 5-fluorocytosine (5-FC) pro-drug administration, we explored their potential as a cell-based targeted drug delivery system to disseminated brain metastases. Our results indicate a strong tropism of NSPCs for intracerebral melanoma metastases. Furthermore, in our therapeutic paradigm, animals with established melanoma brain metastasis received intracranial implantation of CD-NSPCs followed by systemic 5-FC treatment, resulting in a significant (71%) reduction in tumor burden. These data provide proof of principle for the use of NSPCs for targeted delivery of therapeutic gene products to melanoma brain metastases.
脑转移瘤对癌症患者来说是一个日益常见且严重的临床问题,尤其是对于晚期黑色素瘤患者。鉴于神经干细胞/祖细胞(NSPCs)对中枢神经系统病理区域具有广泛的嗜性,我们展开了研究,以确定在同基因实验性黑色素瘤模型中,NSPCs是否也能靶向脑转移瘤的多个部位。我们使用表达胞嘧啶脱氨酶的NSPCs(CD-NSPCs)并进行全身性5-氟胞嘧啶(5-FC)前药给药,探索它们作为基于细胞的靶向药物递送系统用于播散性脑转移瘤的潜力。我们的结果表明NSPCs对脑内黑色素瘤转移灶具有强烈的嗜性。此外,在我们的治疗模式中,已发生黑色素瘤脑转移的动物接受了CD-NSPCs的颅内植入,随后进行全身性5-FC治疗,肿瘤负荷显著降低(71%)。这些数据为使用NSPCs将治疗性基因产物靶向递送至黑色素瘤脑转移瘤提供了原理证明。