Suckow Mark A, Wolter William R, Duffield Giles E
Department of Veterinary Population Medicine, University of Minnesota, St. Paul, MN, U.S.A.
Freimann Life Science Center, University of Notre Dame, Notre Dame, IN, U.S.A.
Anticancer Res. 2017 Sep;37(9):4967-4971. doi: 10.21873/anticanres.11907.
BACKGROUND/AIM: Cancer research requires for consistent models that minimize environmental variables. Within the typical laboratory animal housing facility, animals may be exposed to varying intensities of light as a result of cage type, cage position, light source, and other factors; however, studies evaluating the differential effect of light intensity during the light phase on tumor growth are lacking.
The effect of cage face light intensity, as determined by cage rack position was evaluated with two tumor models using the C57Bl/6NHsd mouse and transplantable B16F10 melanoma cells or Lewis lung carcinoma (LLC) cells. Animals were housed in individually-ventilated cages placed at the top, middle, or bottom of the rack in a diagonal pattern so that the top cage was closest to the ceiling light source, and cage face light intensity was measured. Following a two-week acclimation period at the assigned cage position, animals were subcutaneously administered either 1.3×10 B16F10 melanoma cells or 2.5×10 Lewis lung carcinoma cells. Weights of excised tumors were measured following euthanasia 18 days (melanoma) or 21 days (LCC) after tumor cell administration.
Cage face light intensity was significantly different depending on the location of the cage, with cages closest to the light source have the greatest intensity. Mean tumor weights were significantly less (p<0.001 for melanoma; p≤0.01 for LCC) in middle light intensity mice compared to high and low light intensity mice.
The environmental light intensity to which experimental animals are exposed may vary markedly with cage location and can significantly influence experimental tumor growth, thus supporting the idea that light intensity should be controlled as an experimental variable for animals used in cancer research.
背景/目的:癌症研究需要一致的模型,以尽量减少环境变量。在典型的实验动物饲养设施中,由于笼子类型、笼子位置、光源和其他因素,动物可能会暴露于不同强度的光照下;然而,缺乏评估光照阶段光强度差异对肿瘤生长影响的研究。
使用C57Bl/6NHsd小鼠和可移植的B16F10黑色素瘤细胞或Lewis肺癌(LLC)细胞的两种肿瘤模型,评估由笼子架位置决定的笼子正面光强度的影响。将动物饲养在单独通风的笼子里,笼子以对角线模式放置在架子的顶部、中间或底部,使得顶部的笼子最靠近天花板光源,并测量笼子正面的光强度。在指定的笼子位置经过两周的适应期后,给动物皮下注射1.3×10个B16F10黑色素瘤细胞或2.5×10个Lewis肺癌细胞。在注射肿瘤细胞后18天(黑色素瘤)或21天(LCC)安乐死后,测量切除肿瘤的重量。
笼子正面的光强度根据笼子的位置有显著差异,离光源最近的笼子光强度最大。与高光强度和低光强度的小鼠相比,中等光强度的小鼠的平均肿瘤重量显著更小(黑色素瘤p<0.001;LCC p≤0.01)。
实验动物所暴露的环境光强度可能因笼子位置而有显著差异,并可显著影响实验性肿瘤生长,从而支持将光强度作为癌症研究中所用动物的实验变量进行控制的观点。