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本文引用的文献

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Ethanol-induced mast cell-mediated inflammation leads to increased susceptibility of intestinal tumorigenesis in the APC Δ468 min mouse model of colon cancer.乙醇诱导的肥大细胞介导的炎症导致 APC Δ468 min 结肠癌小鼠模型中肠道肿瘤易感性增加。
Alcohol Clin Exp Res. 2013 Jan;37 Suppl 1(0 1):E199-208. doi: 10.1111/j.1530-0277.2012.01894.x.
2
MAP kinase genes and colon and rectal cancer.MAP 激酶基因与结肠和直肠癌。
Carcinogenesis. 2012 Dec;33(12):2398-408. doi: 10.1093/carcin/bgs305. Epub 2012 Oct 1.
3
RETRACTED: Obesity-induced increase in tumor necrosis factor-α leads to development of colon cancer in mice.撤回:肥胖诱导的肿瘤坏死因子-α增加导致小鼠结肠癌的发生。
Gastroenterology. 2012 Sep;143(3):741-753.e4. doi: 10.1053/j.gastro.2012.05.045. Epub 2012 Jun 4.
4
Gut stem cells in tissue renewal and disease: methods, markers, and myths.肠道干细胞在组织更新和疾病中的作用:方法、标记物和误区。
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5
Identification of five novel modifier loci of Apc(Min) harbored in the BXH14 recombinant inbred strain.鉴定 BXH14 重组近交系中存在的五个新型 Apc(Min) 修饰基因座。
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Mice expressing activated PI3K rapidly develop advanced colon cancer.表达激活的 PI3K 的小鼠迅速发展为晚期结肠癌。
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In vivo imaging of colorectal cancer growth and metastasis by targeting MACC1 with shRNA in xenografted mice.利用靶向 MACC1 的 shRNA 在异种移植小鼠中对结直肠癌生长和转移进行体内成像。
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P53 gene mutation increases progastrin dependent colonic proliferation and colon cancer formation in mice.P53 基因突变增加了胃泌素依赖性结肠增殖和小鼠结肠癌的形成。
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Post-translational modifications of nuclear receptors and human disease.核受体的翻译后修饰与人类疾病
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Utilization of murine colonoscopy for orthotopic implantation of colorectal cancer.利用鼠结肠镜进行结直肠癌的原位种植。
PLoS One. 2011;6(12):e28858. doi: 10.1371/journal.pone.0028858. Epub 2011 Dec 12.

结直肠癌的小鼠模型。

Mouse models for colorectal cancer.

机构信息

Department of Molecular and Comparative Pathobiology, The Johns Hopkins University Baltimore, MD 21205, USA.

出版信息

Am J Cancer Res. 2013 Jun 20;3(3):240-50. Print 2013.

PMID:23841024
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3696531/
Abstract

Colorectal cancer (CRC) is the third leading cause of cancer-related death in the United States, with the number of affected people increasing. There are many risk factors that increase CRC risk, including family or personal history of CRC, smoking, consumption of red meat, obesity, and alcohol consumption. Conversely, increased screening, maintaining healthy body weight, not smoking, and limiting intake of red meat are all associated with reduced CRC morbidity and mortality. Mouse models of CRC were first used in 1928 and have played an important role in understanding CRC biology and treatment and have long been instrumental in clarifying the pathobiology of CRC formation and inhibition. This review focuses on advancements in modeling CRC in mice.

摘要

结直肠癌(CRC)是美国癌症相关死亡的第三大主要原因,且患病人数呈上升趋势。许多危险因素会增加 CRC 的风险,包括结直肠癌家族史或个人史、吸烟、食用红肉、肥胖和饮酒。相反,增加筛查、保持健康的体重、不吸烟和限制摄入红肉都与降低 CRC 的发病率和死亡率有关。1928 年首次在小鼠中使用 CRC 模型,这些模型在了解 CRC 生物学和治疗方面发挥了重要作用,并长期以来一直有助于阐明 CRC 形成和抑制的病理生物学。本综述重点介绍了在小鼠中建立 CRC 模型的进展。