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抗癌基因与肿瘤抑制基因治疗——来自肺癌动物模型的实例

Anti-oncogene and tumor suppressor gene therapy--examples from a lung cancer animal model.

作者信息

Zhang W W, Roth J A

机构信息

Department of Thoracic and Cardiovascular Surgery, University of Texas M.D. Anderson Cancer Center, Houston 77030, USA.

出版信息

In Vivo. 1994 Nov-Dec;8(5):755-69.

PMID:7727723
Abstract

Rapid advances in cancer gene therapy are driven by an explosive development of gene transfer technology and a strong demand for effective alternatives to unsatisfactory conventional cancer therapies. Discovery of the genetic basis of cancer has indicated that cancer is a disease of genes. Among a variety of approaches to gene therapy of cancer, anti-oncogene and tumor suppressor gene therapy of cancer are the two strategies that aim at correcting genetic disorders of cancer. The potential effectiveness of these approaches is promised by their precise targeting at the mechanisms of the disease. Successful examples of human lung cancer animal models by applying anti-K-ras retrovirus and recombinant p53 adenovirus are reviewed. Future development of these approaches towards clinical application is also discussed.

摘要

癌症基因治疗的快速进展是由基因转移技术的迅猛发展以及对不尽人意的传统癌症治疗方法的有效替代方案的强烈需求所推动的。癌症遗传基础的发现表明癌症是一种基因疾病。在多种癌症基因治疗方法中,癌症的抗癌基因和肿瘤抑制基因治疗是旨在纠正癌症基因紊乱的两种策略。这些方法的潜在有效性因其对疾病机制的精确靶向而得到保证。本文综述了应用抗K-ras逆转录病毒和重组p53腺病毒建立人肺癌动物模型的成功实例。还讨论了这些方法在临床应用方面的未来发展。

相似文献

1
Anti-oncogene and tumor suppressor gene therapy--examples from a lung cancer animal model.抗癌基因与肿瘤抑制基因治疗——来自肺癌动物模型的实例
In Vivo. 1994 Nov-Dec;8(5):755-69.
2
[Gene therapy in oncology: applications to lung cancer].
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Biological principles and clinical development of prostate cancer gene therapy.前列腺癌基因治疗的生物学原理与临床进展
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Antisense approaches to cancer gene therapy.癌症基因治疗的反义方法。
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Delivery of the p53 tumor suppressor gene into lung cancer cells by an adenovirus/DNA complex.通过腺病毒/DNA复合物将p53肿瘤抑制基因导入肺癌细胞。
Cancer Gene Ther. 1997 May-Jun;4(3):191-8.
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Gene replacement strategies for cancer.
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Antisense oncogene and tumor suppressor gene therapy of cancer.癌症的反义癌基因与肿瘤抑制基因治疗
J Mol Med (Berl). 1996 Apr;74(4):191-204. doi: 10.1007/BF00204749.
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Retrovirus vectors designed for efficient transduction of cytotoxic or cytostatic genes.为有效转导细胞毒性或细胞生长抑制基因而设计的逆转录病毒载体。
Gene Ther. 1999 Oct;6(10):1670-8. doi: 10.1038/sj.gt.3301009.

引用本文的文献

1
Perspective on Adenoviruses: Epidemiology, Pathogenicity, and Gene Therapy.腺病毒视角:流行病学、致病性与基因治疗
Biomedicines. 2019 Aug 19;7(3):61. doi: 10.3390/biomedicines7030061.
2
[Gene therapy with p53 tumor suppressors].[使用p53肿瘤抑制因子的基因治疗]
HNO. 2003 May;51(5):365-8. doi: 10.1007/s00106-003-0850-x. Epub 2003 Apr 15.
3
Adenoviral vector-mediated gene transfer: timing of wild-type p53 gene expression in vivo and effect of tumor transduction on survival in a rat glioma brachytherapy model.腺病毒载体介导的基因转移:大鼠胶质瘤近距离治疗模型中野生型p53基因在体内的表达时机及肿瘤转导对生存的影响。
J Neurooncol. 2000 Aug;49(1):27-39. doi: 10.1023/a:1006476608036.
4
Anti-tumor gene therapy.抗肿瘤基因治疗。
J Neurooncol. 1997 Jan;31(1-2):217-23. doi: 10.1023/a:1005791012205.