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中国基因治疗的最新进展。

An update on gene therapy in China.

作者信息

Shi Juan, Zheng Dexian

机构信息

National Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100005, China.

出版信息

Curr Opin Mol Ther. 2009 Oct;11(5):547-53.

PMID:19806503
Abstract

Gene therapy has made significant progress in the past decade, and has strong promise for the treatment of chronic diseases. China has emerged as a pioneer in some fields of gene therapy and, in 2003, became the first country to commercialize a gene therapy product, Gendicine. H-101 (Ocorine), the second gene therapy-based medicine, was approved in China in 2005. Commercialization of these two gene therapy products provides China with worldwide recognition in the field of gene therapy. The progress of gene therapy in China has resulted in the establishment of several companies pursuing gene therapy technology for commercial purposes. This review summarizes the recent advances in gene therapy in China, including preclinical studies, clinical trials and product commercialization.

摘要

在过去十年中,基因治疗取得了重大进展,对慢性病的治疗具有巨大潜力。中国已成为基因治疗某些领域的先驱,并于2003年成为首个将基因治疗产品“今又生”商业化的国家。第二种基于基因治疗的药物“安柯瑞”于2005年在中国获批。这两种基因治疗产品的商业化使中国在基因治疗领域获得了全球认可。中国基因治疗的进展促使几家公司为商业目的而追求基因治疗技术。本综述总结了中国基因治疗的最新进展,包括临床前研究、临床试验和产品商业化。

相似文献

1
An update on gene therapy in China.中国基因治疗的最新进展。
Curr Opin Mol Ther. 2009 Oct;11(5):547-53.
2
The application of gene therapy in China.基因疗法在中国的应用。
IDrugs. 2008 May;11(5):346-50.
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Gene therapy of cancer in the clinic: good news in sight from Asia?临床癌症基因治疗:亚洲有望传来好消息?
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Clinical trial design for adenoviral gene therapy products.腺病毒基因治疗产品的临床试验设计
Drug News Perspect. 2009 Apr;22(3):140-5. doi: 10.1358/dnp.2009.22.3.1354090.
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Gene therapy progress and prospects cancer: oncolytic viruses.基因治疗在癌症领域的进展与前景:溶瘤病毒
Gene Ther. 2008 Jun;15(12):877-84. doi: 10.1038/gt.2008.72. Epub 2008 Apr 17.
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China's gene therapy drug: do Shenzen SiBiono Gen-Tech's claims hold up?中国的基因治疗药物:深圳赛百诺基因技术公司的说法站得住脚吗?
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[The advances of gene therapy in this quarter century].[这四分之一个世纪里基因治疗的进展]
Gan To Kagaku Ryoho. 1999 Jun;26 Suppl 1:51-9.
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Gene therapy clinical trials worldwide to 2007--an update.截至2007年全球基因治疗临床试验——最新情况
J Gene Med. 2007 Oct;9(10):833-42. doi: 10.1002/jgm.1100.
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Lentiviral vectors in clinical trials: Current status.临床试验中的慢病毒载体:现状
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Current status and prospects for gene therapy.基因治疗的现状与前景
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Oncolytic viruses-modulated immunogenic cell death, apoptosis and autophagy linking to virotherapy and cancer immune response.溶瘤病毒调节的免疫原性细胞死亡、细胞凋亡和自噬与病毒疗法和癌症免疫反应的关联。
Front Cell Infect Microbiol. 2023 Mar 15;13:1142172. doi: 10.3389/fcimb.2023.1142172. eCollection 2023.
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Senescence of Tumor Cells in Anticancer Therapy-Beneficial and Detrimental Effects.肿瘤细胞衰老在抗癌治疗中的有益和有害影响。
Int J Mol Sci. 2022 Sep 21;23(19):11082. doi: 10.3390/ijms231911082.
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Gene therapy for Mucopolysaccharidoses.
黏多糖贮积症的基因治疗。
Mol Genet Metab. 2018 Feb;123(2):59-68. doi: 10.1016/j.ymgme.2017.12.434. Epub 2017 Dec 26.
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Adenovirus-Mediated Gene Delivery: Potential Applications for Gene and Cell-Based Therapies in the New Era of Personalized Medicine.腺病毒介导的基因递送:个性化医疗新时代中基于基因和细胞疗法的潜在应用。
Genes Dis. 2017 Jun;4(2):43-63. doi: 10.1016/j.gendis.2017.04.001. Epub 2017 Apr 27.
5
Expression of the fusogenic p14 FAST protein from a replication-defective adenovirus vector does not provide a therapeutic benefit in an immunocompetent mouse model of cancer.来自复制缺陷型腺病毒载体的融合性p14 FAST蛋白在免疫健全的癌症小鼠模型中未显示出治疗益处。
Cancer Gene Ther. 2016 Oct;23(10):355-364. doi: 10.1038/cgt.2016.41. Epub 2016 Oct 14.
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Autoregulated expression of p53 from an adenoviral vector confers superior tumor inhibition in a model of prostate carcinoma gene therapy.来自腺病毒载体的p53自调控表达在前列腺癌基因治疗模型中赋予了卓越的肿瘤抑制能力。
Cancer Biol Ther. 2016 Dec;17(12):1221-1230. doi: 10.1080/15384047.2016.1235655. Epub 2016 Sep 19.
7
Recombinant Newcastle disease virus expressing P53 demonstrates promising antitumor efficiency in hepatoma model.表达P53的重组新城疫病毒在肝癌模型中显示出有前景的抗肿瘤效果。
J Biomed Sci. 2016 Jul 28;23(1):55. doi: 10.1186/s12929-016-0273-0.
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Transduction of Recombinant M3-p53-R12 Protein Enhances Human Leukemia Cell Apoptosis.重组M3-p53-R12蛋白的转导增强人白血病细胞凋亡。
J Cancer. 2016 Jun 28;7(10):1360-73. doi: 10.7150/jca.15155. eCollection 2016.
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Has the Human Genome Project Delivered for Healthcare?人类基因组计划对医疗保健产生了实际影响吗?
Ann Med Surg (Lond). 2012 Oct 24;1:19-20. doi: 10.1016/S2049-0801(12)70006-7. eCollection 2012.
10
Ad-REIC Gene Therapy: Promising Results in a Patient with Metastatic CRPC Following Chemotherapy.Ad-REIC 基因治疗:化疗后转移性 CRPC 患者的可喜结果。
Clin Med Insights Oncol. 2015 Mar 23;9:31-8. doi: 10.4137/CMO.S23252. eCollection 2015.