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通过钙循环基因疗法治疗心力衰竭。

Treatment of heart failure by calcium cycling gene therapy.

作者信息

Lipskaia Larissa, Ly Hung, Kawase Yoshiaki, Hajjar Roger J, Lompre Anne-Marie

机构信息

INSERM U621, Université Pierre et Marie Curie-CHU Pitié-Salpétriêre, Paris, France.

出版信息

Future Cardiol. 2007 Jul;3(4):413-23. doi: 10.2217/14796678.3.4.413.

DOI:10.2217/14796678.3.4.413
PMID:19804232
Abstract

Heart failure is a major cause of morbidity and mortality in Western countries. While progress in conventional treatment modalities is making steady and incremental gains to reduce this disease burden, there remains a need to explore new and potentially therapeutic approaches. Gene therapy, for example, was initially envisioned as a treatment strategy for inherited monogenic disorders. It is now apparent that gene therapy has broader potential, which also includes acquired polygenic diseases such as heart failure. Advances in the understanding of the molecular basis of conditions such as these, together with the evolution of increasingly efficient gene transfer technology, has placed congestive heart failure within the reach of gene-based therapy.

摘要

心力衰竭是西方国家发病和死亡的主要原因。虽然传统治疗方式的进展正在稳步且逐步地减轻这种疾病负担,但仍有必要探索新的潜在治疗方法。例如,基因治疗最初被设想为一种治疗遗传性单基因疾病的策略。现在很明显,基因治疗具有更广泛的潜力,这也包括诸如心力衰竭等获得性多基因疾病。对这类疾病分子基础认识的进展,以及日益高效的基因转移技术的发展,使充血性心力衰竭有望通过基因治疗来攻克。

相似文献

1
Treatment of heart failure by calcium cycling gene therapy.通过钙循环基因疗法治疗心力衰竭。
Future Cardiol. 2007 Jul;3(4):413-23. doi: 10.2217/14796678.3.4.413.
2
Gene therapy in the treatment of heart failure.基因治疗在心力衰竭治疗中的应用。
Physiology (Bethesda). 2007 Apr;22:81-96. doi: 10.1152/physiol.00037.2006.
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Targeted gene transfer in heart failure: implications for novel gene identification.心力衰竭中的靶向基因转移:对新基因识别的意义
Curr Opin Mol Ther. 2004 Aug;6(4):381-94.
4
Rescuing the failing heart by targeted gene transfer.通过靶向基因转移拯救衰竭心脏。
J Am Coll Cardiol. 2011 Mar 8;57(10):1169-80. doi: 10.1016/j.jacc.2010.11.023.
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Method of gene delivery in large animal models of cardiovascular diseases.心血管疾病大型动物模型中的基因递送方法。
Methods Mol Biol. 2011;709:355-67. doi: 10.1007/978-1-61737-982-6_23.
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Therapeutic prospects of cardiac gene transfer.心脏基因转移的治疗前景。
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Cardiac gene therapy: therapeutic potential and current progress.心脏基因治疗:治疗潜力与当前进展
Curr Gene Ther. 2003 Oct;3(5):418-51. doi: 10.2174/1566523034578249.
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Advances in gene-based therapy for heart failure.心力衰竭的基因治疗进展。
J Cardiovasc Transl Res. 2008 Jun;1(2):127-36. doi: 10.1007/s12265-008-9022-4. Epub 2008 May 29.
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Cardiac gene therapy with SERCA2a: from bench to bedside.心脏基因治疗中的 SERCA2a:从实验室到临床。
J Mol Cell Cardiol. 2011 May;50(5):803-12. doi: 10.1016/j.yjmcc.2010.11.011. Epub 2010 Nov 18.
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Sarcoplasmic reticulum and calcium cycling targeting by gene therapy.基因治疗靶向肌浆网和钙循环。
Gene Ther. 2012 Jun;19(6):596-9. doi: 10.1038/gt.2012.34. Epub 2012 May 17.

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High-throughput FRET assay yields allosteric SERCA activators.高通量荧光共振能量转移分析产生变构肌浆网Ca2+-ATP酶激活剂。
J Biomol Screen. 2013 Jan;18(1):97-107. doi: 10.1177/1087057112456878. Epub 2012 Aug 24.
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Molecular targets in heart failure gene therapy: current controversies and translational perspectives.心力衰竭基因治疗的分子靶点:当前的争议和转化观点。
Ann N Y Acad Sci. 2012 Apr;1254:42-50. doi: 10.1111/j.1749-6632.2012.06520.x.
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Sarcoplasmic reticulum Ca(2+) ATPase as a therapeutic target for heart failure.肌浆网 Ca(2+)ATP 酶作为心力衰竭的治疗靶点。
Expert Opin Biol Ther. 2010 Jan;10(1):29-41. doi: 10.1517/14712590903321462.
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Role of sarco/endoplasmic reticulum calcium content and calcium ATPase activity in the control of cell growth and proliferation.肌浆网/内质网钙含量及钙ATP酶活性在细胞生长与增殖调控中的作用
Pflugers Arch. 2009 Jan;457(3):673-85. doi: 10.1007/s00424-007-0428-7. Epub 2008 Jan 11.