Thompson T C, Timme T L, Ebara S, Satoh T, Yang G, Wang J, Miles B J, Ayala G, Wheeler T M, Kadmon D
Baylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USA.
Expert Opin Biol Ther. 2001 May;1(3):481-95. doi: 10.1517/14712598.1.3.481.
The development of effective treatments for prostate cancer is thwarted by the natural history of the disease. The biological and clinical potential of most individual cancers is uncertain. In many cases the disease will not progress to clinical significance but experimental and clinical studies indicate that prostate cancer can and may metastasis early in the course of the disease from relatively small foci (i.e., not necessarily the largest or index cancer). Localised prostate cancer is potentially curable with localised therapies (radical prostatectomy or irradiation therapy). However, there are no curative therapies for metastatic prostate cancer. Gene therapy, especially those approaches with an immunomodulatory component, may provide additional therapeutic options with the potential to affect both localised and systemic disease. We have pioneered the development and application of in situ gene therapy protocols using adenoviral vectors to transduce specific genes that generate cytotoxic activity and/or a systemic antitumour immune response. In addition we have completed initial studies that demonstrate the therapeutic potential of adenoviral vector-mediated gene modified cell-based vaccines. Our review discusses preclinical studies focused on the development of immunostimulatory in situ gene therapy approaches that hopefully will provide novel and effective treatments for localised and metastatic prostate cancer.
前列腺癌有效治疗方法的研发因该疾病的自然病程而受阻。大多数个体癌症的生物学和临床潜力尚不确定。在许多情况下,该疾病不会发展到具有临床意义的程度,但实验和临床研究表明,前列腺癌在疾病进程早期就可能从相对较小的病灶(即不一定是最大的或原发癌)发生转移。局限性前列腺癌通过局部治疗(根治性前列腺切除术或放射治疗)有治愈的可能。然而,转移性前列腺癌没有治愈性疗法。基因治疗,尤其是那些具有免疫调节成分的方法,可能会提供额外的治疗选择,有可能影响局限性和全身性疾病。我们率先开发并应用了原位基因治疗方案,使用腺病毒载体转导产生细胞毒性活性和/或全身性抗肿瘤免疫反应的特定基因。此外,我们已经完成了初步研究,证明了腺病毒载体介导的基因修饰细胞疫苗的治疗潜力。我们的综述讨论了专注于免疫刺激原位基因治疗方法开发的临床前研究,有望为局限性和转移性前列腺癌提供新颖有效的治疗方法。