A new three-dimensional ultrasound microimaging technology for preclinical studies using a transgenic prostate cancer mouse model

被引:65
作者
Wirtzfeld, LA
Wu, GJ
Bygrave, M
Yamasaki, Y
Sakai, H
Moussa, M
Izawa, JI
Downey, DB
Greenberg, NM
Fenster, A
Xuan, JW
Lacefield, JC
机构
[1] Univ Western Ontario, Biomed Engn Grad Program, London, ON N6A 3K7, Canada
[2] Univ Western Ontario, Dept Surg, London, ON N6A 3K7, Canada
[3] Univ Western Ontario, Dept Pathol, London, ON N6A 3K7, Canada
[4] Univ Western Ontario, Dept Diagnost Radiol & Nucl Med, London, ON N6A 3K7, Canada
[5] Univ Western Ontario, Dept Med Biophys, London, ON N6A 3K7, Canada
[6] Univ Western Ontario, Dept Elect & Comp Engn, London, ON N6A 3K7, Canada
[7] Robarts Res Inst, Imaging Res Labs, London, ON N6A 5C1, Canada
[8] Nagasaki Univ, Sch Med, Dept Urol, Nagasaki 852, Japan
[9] Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98104 USA
关键词
D O I
10.1158/0008-5472.CAN-05-0414
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Prostate cancer is the most common cancer in adult men in North America. Preclinical studies of prostate cancer employ genetically engineered mouse models, because prostate cancer does not occur naturally in rodents. Widespread application of these models has been limited because autopsy was the only reliable method to evaluate treatment efficacy in longitudinal studies. This article reports the first use of three-dimensional ultrasound microimaging for measuring tumor progression in a genetically engineered mouse model, the 94-amino acid prostate secretory protein gene-directed transgenic prostate cancer model. Qualitative comparisons of three-dimensional ultrasound images with serial histology sections of prostate tumors show the ability of ultrasound to accurately depict the size and shape of malignant masses in live mice. Ultrasound imaging identified tumors ranging from 2.4 to 14 mm maximum diameter. The correlation coefficient of tumor diameter measurements done in vivo with three-dimensional ultrasound and at autopsy was 0.998. Prospective tumor detection sensitivity and specificity were both > 90% when diagnoses were based on repeated ultrasound examinations done on separate days. Representative exponential growth curves constructed via longitudinal ultrasound imaging indicated volume doubling times of 5 and 13 days for two prostate tumors. Compared with other microimaging and molecular imaging modalities, the application of three-dimensional ultrasound imaging to prostate cancer in mice showed advantages, such as high spatial resolution and contrast in soft tissue, fast and uncomplicated protocols, and portable and economical equipment that will likely enable ultrasound to become a new microimaging modality for mouse preclinical trial studies.
引用
收藏
页码:6337 / 6345
页数:9
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