Hensley Harvey H, Merkel Carrie E, Chang Wen-Chi L, Devarajan Karthik, Cooper Harry S, Clapper Margie L
Divisions of Basic Science, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111, USA.
Gastrointest Endosc. 2009 Mar;69(3 Pt 2):742-9. doi: 10.1016/j.gie.2008.09.054.
The scientific potential of animal models of carcinogenesis has not been fully realized because of our limited ability to monitor tumor growth in vivo.
To develop an endoscopy-based protocol for the accurate estimation of adenoma size in vivo from images obtained during colonoscopy.
To compare estimates of lesion size acquired during endoscopy with those obtained from magnetic resonance imaging (MRI) and at necropsy.
A small-animal imaging facility.
Adenomatous polyposis coli multiple intestinal metaplasia Fox Chase Cancer Center mice that develop multiple colorectal adenomas.
The mice received colonoscopic examination by using a rigid endoscope, and high-resolution images of colon adenomas were captured by using a charge-coupled-device camera. Lesion size was estimated by comparing the dimensions of the adenoma relative to a reference rod by using a novel geometric construction. The resulting areas were compared with estimates from MRIs and validated at necropsy.
Cross-sectional area of colon adenomas.
The cross-sectional area of 20 adenomas was measured in vivo during colonoscopy and compared with the size as measured at necropsy, which yielded a Pearson correlation coefficient of 0.94 (P = 6.52 x 10(-9)). Assessment of interoperator variability, when using measurements from 11 adenomas, yielded a Pearson correlation coefficient of 0.85 (P = 4.35 x 10(-3)) and demonstrated excellent reproducibility.
Only the distal colon could be viewed, and endoscopic measurements were 2-dimensional.
An endoscopic method for the reliable measurement of colorectal adenomas in vivo was established. The application of this technique to mouse models of colon carcinogenesis will provide unique insight into the dynamics of adenoma growth.
由于我们在体内监测肿瘤生长的能力有限,致癌作用动物模型的科学潜力尚未得到充分发挥。
制定一种基于内镜检查的方案,以便根据结肠镜检查期间获得的图像在体内准确估计腺瘤大小。
比较内镜检查期间获得的病变大小估计值与磁共振成像(MRI)和尸检时获得的估计值。
一个小动物成像设施。
携带多发性结肠直肠腺瘤的腺瘤性息肉病大肠杆菌多重肠化生福克斯蔡斯癌症中心小鼠。
使用硬式内窥镜对小鼠进行结肠镜检查,并使用电荷耦合器件相机拍摄结肠腺瘤的高分辨率图像。通过使用一种新颖的几何结构,将腺瘤的尺寸与参考杆进行比较来估计病变大小。将所得面积与MRI的估计值进行比较,并在尸检时进行验证。
结肠腺瘤的横截面积。
在结肠镜检查期间对20个腺瘤的横截面积进行了体内测量,并与尸检时测量的大小进行比较,得到的Pearson相关系数为0.94(P = 6.52×10⁻⁹)。使用11个腺瘤的测量值评估操作者间的变异性,得到的Pearson相关系数为0.85(P = 4.35×10⁻³),并显示出极好的可重复性。
只能观察到结肠远端,且内镜测量为二维的。
建立了一种在体内可靠测量结肠直肠腺瘤的内镜方法。将该技术应用于结肠癌发生的小鼠模型将为腺瘤生长动力学提供独特的见解。