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前列腺癌的原位基因治疗:免疫调节方法。

In situ gene therapy for prostate cancer: immunomodulatory approaches.

作者信息

Thompson T C, Timme T L, Ebara S, Satoh T, Yang G, Wang J, Miles B J, Ayala G, Wheeler T M, Kadmon D

机构信息

Baylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USA.

出版信息

Expert Opin Biol Ther. 2001 May;1(3):481-95. doi: 10.1517/14712598.1.3.481.

DOI:10.1517/14712598.1.3.481
PMID:11727520
Abstract

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.

摘要

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。

相似文献

1
In situ gene therapy for prostate cancer: immunomodulatory approaches.前列腺癌的原位基因治疗:免疫调节方法。
Expert Opin Biol Ther. 2001 May;1(3):481-95. doi: 10.1517/14712598.1.3.481.
2
In situ gene therapy for prostate cancer.前列腺癌的原位基因治疗。
Oncol Res. 1999;11(1):1-8.
3
In situ gene therapy for prostate cancer.前列腺癌的原位基因治疗。
Curr Gene Ther. 2005 Feb;5(1):111-9. doi: 10.2174/1566523052997523.
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Therapeutic targets for metastatic prostate cancer.转移性前列腺癌的治疗靶点。
Curr Drug Targets. 2003 Apr;4(3):251-61. doi: 10.2174/1389450033491127.
5
Management of localised prostate cancer: watchful waiting, surgery or radiation therapy, depending on the natural course, which is often relatively slow.局限性前列腺癌的治疗:根据其自然病程(通常进展相对缓慢),可选择观察等待、手术或放射治疗。
Prescrire Int. 2012 Oct;21(131):242-8.
6
Gene therapy for prostate cancer: current status and future prospects.前列腺癌的基因治疗:现状与未来前景
J Urol. 2001 Oct;166(4):1220-33. doi: 10.1016/s0022-5347(05)65742-4.
7
Cryotherapy for localised prostate cancer.局部前列腺癌的冷冻疗法。
Cochrane Database Syst Rev. 2007 Jul 18(3):CD005010. doi: 10.1002/14651858.CD005010.pub2.
8
Advances in preclinical investigation of prostate cancer gene therapy.前列腺癌基因治疗的临床前研究进展
Mol Ther. 2007 Jun;15(6):1053-64. doi: 10.1038/sj.mt.6300181. Epub 2007 Apr 24.
9
Gene delivery and gene therapy of prostate cancer.前列腺癌的基因递送与基因治疗
Expert Opin Drug Deliv. 2006 Jan;3(1):37-51. doi: 10.1517/17425247.3.1.37.
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Adenovirus-mediated suicide-gene therapy using the herpes simplex virus thymidine kinase gene in cell and animal models of human prostate cancer: changes in tumour cell proliferative activity.在人前列腺癌的细胞和动物模型中使用单纯疱疹病毒胸苷激酶基因进行腺病毒介导的自杀基因治疗:肿瘤细胞增殖活性的变化
BJU Int. 2000 Apr;85(6):759-66. doi: 10.1046/j.1464-410x.2000.00516.x.

引用本文的文献

1
Considering the potential for gene-based therapy in prostate cancer.考虑在前列腺癌中应用基于基因的治疗方法。
Nat Rev Urol. 2021 Mar;18(3):170-184. doi: 10.1038/s41585-021-00431-x. Epub 2021 Feb 26.