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引用本文的文献

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本文引用的文献

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2
Cancer-prone mice expressing the Ki-rasG12C gene show increased lung carcinogenesis after CT screening exposures.表达 Ki-rasG12C 基因的易患癌小鼠在 CT 筛查暴露后肺癌发生增加。
Radiat Res. 2011 Dec;176(6):842-8. doi: 10.1667/rr2649.1. Epub 2011 Sep 30.
3
Cancer statistics, 2010.癌症统计数据,2010 年。
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4
Projected cancer risks from computed tomographic scans performed in the United States in 2007.2007年美国计算机断层扫描所预测的癌症风险。
Arch Intern Med. 2009 Dec 14;169(22):2071-7. doi: 10.1001/archinternmed.2009.440.
5
Lung tumor promotion by curcumin.姜黄素对肺部肿瘤的促进作用。
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6
Conditional expression of the mutant Ki-rasG12C allele results in formation of benign lung adenomas: development of a novel mouse lung tumor model.突变型Ki-rasG12C等位基因的条件性表达导致良性肺腺瘤的形成:一种新型小鼠肺肿瘤模型的建立。
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7
Radiation risks potentially associated with low-dose CT screening of adult smokers for lung cancer.成人吸烟者低剂量CT肺癌筛查可能存在的辐射风险。
Radiology. 2004 May;231(2):440-5. doi: 10.1148/radiol.2312030880.
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K-ras oncogene activation in atypical alveolar hyperplasias of the human lung.人肺非典型肺泡增生中的K-ras癌基因激活
Cancer Res. 1996 May 1;56(9):2224-8.
9
K-ras oncogene activation in lung adenocarcinomas from former smokers. Evidence that K-ras mutations are an early and irreversible event in the development of adenocarcinoma of the lung.既往吸烟者肺腺癌中的K-ras癌基因激活。K-ras突变是肺腺癌发生过程中早期且不可逆事件的证据。
Cancer. 1993 Jul 15;72(2):432-8. doi: 10.1002/1097-0142(19930715)72:2<432::aid-cncr2820720219>3.0.co;2-#.
10
c-k-ras and p53 mutations occur very early in adenocarcinoma of the lung.c-k-ras和p53突变在肺腺癌发生的早期就会出现。
Am J Pathol. 1994 Feb;144(2):303-9.

一种在可控气体环境中对小鼠进行辐照的技术。

A technique for murine irradiation in a controlled gas environment.

作者信息

Walb M C, Moore J E, Attia A, Wheeler K T, Miller M S, Munley M T

机构信息

Wake Forest School of Medicine.

出版信息

Biomed Sci Instrum. 2012;48:470-7.

PMID:22846321
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3709974/
Abstract

NASA’s extra-vehicular activities (EVAs) involve exposure to high energy photons while breathing 100% oxygen. Using previously verified mouse models, our laboratory is studying whether low dose irradiation under these hyperoxic conditions could lead to an increase in carcinogenic potential. To simulate the environment astronauts encounter during an EVA, enclosed chambers were constructed that allowed for mouse movement, controlled gas conditions, and uniform radiation dose delivery. Custom-built gas chambers with input/output gas valves and dividers that allowed for uniform gas flow were used to keep 6 unanesthetized mice separated while they were irradiated. The chambers were supplied with 100% oxygen or air using ball valves linked together with T-splitters. A calibrated ion chamber was used to verify the radiation dose distribution across an entire chamber. Mice were placed in the gas environments for 0.5 h, irradiated with a 10 or 18 MV photon beam from a medical linear accelerator, and left in their gas environment for 2 h post-irradiation. We irradiated 200 mice (5 different doses between 0-1000 mGy) under normoxic or 100% oxygen conditions. For the next step of this research, these mice will be euthanized 9 months post-irradiation, and lung tumors will be counted and sized to determine if hyperoxia increases the carcinogenic effect for this model.

摘要

美国国家航空航天局(NASA)的舱外活动(EVA)涉及在呼吸100%氧气的同时暴露于高能光子。利用先前验证过的小鼠模型,我们的实验室正在研究在这些高氧条件下低剂量辐射是否会导致致癌潜力增加。为了模拟宇航员在舱外活动期间遇到的环境,构建了封闭舱室,该舱室允许小鼠活动、控制气体条件并实现均匀的辐射剂量传递。使用定制的带有输入/输出气阀和隔板以实现均匀气流的气室,在照射6只未麻醉的小鼠时将它们隔开。通过与T形分流器相连的球阀向舱室供应100%氧气或空气。使用校准过的电离室来验证整个舱室内的辐射剂量分布。将小鼠置于气体环境中0.5小时,用医用直线加速器产生的10或18兆伏光子束进行照射,并在照射后将它们留在气体环境中2小时。我们在常氧或100%氧气条件下对200只小鼠(0至1000毫戈瑞之间的5种不同剂量)进行了照射。对于本研究的下一步,这些小鼠将在照射后9个月实施安乐死,然后对肺部肿瘤进行计数和测量大小,以确定高氧是否会增加该模型的致癌作用。