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癌症的条件性基因敲除小鼠模型。

Conditional knockout mouse models of cancer.

作者信息

Deng Chu-Xia

机构信息

Genetics of Development and Disease Branch, National Institute of Diabetes, Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

Cold Spring Harb Protoc. 2014 Dec 1;2014(12):1217-33. doi: 10.1101/pdb.top074393.

Abstract

In 2007, three scientists, Drs. Mario R. Capecchi, Martin J. Evans, and Oliver Smithies, received the Nobel Prize in Physiology or Medicine for their contributions of introducing specific gene modifications into mice. This technology, commonly referred to as gene targeting or knockout, has proven to be a powerful means for precisely manipulating the mammalian genome and has generated great impacts on virtually all phases of mammalian biology and basic biomedical research. Of note, germline mutations of many genes, especially tumor suppressors, often result in lethality during embryonic development or at developmental stages before tumor formation. This obstacle has been effectively overcome by the use of conditional knockout technology in conjunction with Cre-LoxP- or Flp-Frt-mediated temporal and/or spatial systems to generate genetic switches for precise DNA recombination. Currently, numerous conditional knockout mouse models have been successfully generated and applied in studying tumor initiation, progression, and metastasis. This review summarizes some conditional mutant mouse models that are widely used in cancer research and our understanding of the possible mechanisms underlying tumorigenesis.

摘要

2007年,马里奥·R·卡佩奇博士、马丁·J·埃文斯博士和奥利弗·史密斯博士三位科学家因在小鼠中引入特定基因修饰的贡献而获得诺贝尔生理学或医学奖。这项技术,通常称为基因靶向或基因敲除,已被证明是精确操纵哺乳动物基因组的有力手段,并对哺乳动物生物学和基础生物医学研究的几乎所有阶段都产生了重大影响。值得注意的是,许多基因的种系突变,尤其是肿瘤抑制基因,常常在胚胎发育期间或肿瘤形成前的发育阶段导致致死性。通过使用条件性基因敲除技术结合Cre-LoxP或Flp-Frt介导的时间和/或空间系统来产生精确DNA重组的遗传开关,有效克服了这一障碍。目前,许多条件性基因敲除小鼠模型已成功构建并应用于肿瘤起始、进展和转移的研究。本综述总结了一些在癌症研究中广泛使用的条件性突变小鼠模型以及我们对肿瘤发生潜在机制的理解。

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