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小鼠乳腺肿瘤生物学:简史

Mouse mammary tumor biology: a short history.

作者信息

Cardiff Robert D, Kenney Nicholas

机构信息

Center for Comparative Medicine, Department of Pathology and Laboratory Medicine, School of Medicine, University of California, Davis, California 95616, USA.

出版信息

Adv Cancer Res. 2007;98:53-116. doi: 10.1016/S0065-230X(06)98003-8.

Abstract

For over a century, mouse mammary tumor biology and the associated Mouse mammary tumor virus (MMTV) have served as the foundation for experimental cancer research, in general, and, in particular, experimental breast cancer research. Spontaneous mouse mammary tumors were the basis for studies of the natural history of neoplasia, oncogenic viruses, host responses, endocrinology, and neoplastic progression. However, lacking formal proof of a human mammary tumor virus, the preeminence of the mouse model faded in the 1980s. Since the late 1980s, genetically engineered mice (GEM) have proven extremely useful for studying breast cancer and have become the animal model for human breast cancer. Hundreds of mouse models of human breast cancer have been developed since the first demonstration, in 1984, that the mouse mammary gland could be molecularly targeted and used to test the oncogenicity of candidate human genes. Now, very few scientists can avoid using a mouse model to test the biology of their favorite gene. The GEM have attracted a new generation of molecular and cellular biologists eager to apply their skills to these surrogates of the human disease. Newcomers often enter the field without an appreciation of the origins of mouse mammary tumor biology and the basis for many of the prevailing concepts. Our purpose in writing this short history of mouse mammary tumor biology is to provide a historical perspective for the benefit of the newcomers. If Einstein was correct in that "we stand on the shoulders of giants," the neophytes should meet their giants.

摘要

一个多世纪以来,小鼠乳腺肿瘤生物学以及相关的小鼠乳腺肿瘤病毒(MMTV)一直是实验性癌症研究的基础,总体而言,尤其是实验性乳腺癌研究的基础。自发性小鼠乳腺肿瘤是肿瘤自然史、致癌病毒、宿主反应、内分泌学和肿瘤进展研究的基础。然而,由于缺乏人类乳腺肿瘤病毒的正式证据,小鼠模型的卓越地位在20世纪80年代逐渐衰落。自20世纪80年代末以来,基因工程小鼠(GEM)已被证明在研究乳腺癌方面极为有用,并已成为人类乳腺癌的动物模型。自1984年首次证明小鼠乳腺可进行分子靶向并用于测试候选人类基因的致癌性以来,已经开发了数百种人类乳腺癌小鼠模型。如今,很少有科学家能够避免使用小鼠模型来测试他们感兴趣基因的生物学特性。基因工程小鼠吸引了新一代分子和细胞生物学家,他们渴望将自己的技能应用于这些人类疾病的替代模型。新进入该领域的人往往在不了解小鼠乳腺肿瘤生物学起源以及许多主流概念基础的情况下就进入了这个领域。我们撰写这篇小鼠乳腺肿瘤生物学简史的目的是为新手提供一个历史视角,以资借鉴。如果爱因斯坦所说的“我们站在巨人的肩膀上”是正确的,那么新手应该结识他们的巨人。

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