Department of Pathology, University of Arizona College of Medicine Tucson, AZ 85724, USA.
University of Arizona Cancer Center Tucson, AZ 85724, USA.
Am J Transl Res. 2015 Feb 15;7(2):348-55. eCollection 2015.
Bone is a favored site for solid tumor metastasis, especially among patients with breast, lung or prostate carcinomas. Micro CT is a powerful and inexpensive tool that can be used to investigate tumor progression in xenograft models of human disease. Many previous studies have relied on terminal analysis of harvested bones to document metastatic tumor activity. The current protocol uses live animals and combines sequential micro CT evaluation of lesion development with matched histopathology at the end of the study. The approach allows for both rapid detection and evaluation of bone lesion progression in live animals. Bone resident tumors are established either by direct (intraosseous) or arterial (intracardiac) injection, and lesion development is evaluated for up to eight weeks. This protocol provides a clinically relevant method for investigating bone metastasis progression and the development of osteotropic therapeutic strategies for the treatment of bone metastases.
骨骼是实体瘤转移的理想部位,尤其是在乳腺癌、肺癌或前列腺癌患者中。微 CT 是一种强大且廉价的工具,可用于研究人类疾病异种移植模型中的肿瘤进展。许多先前的研究依赖于对收获的骨骼进行终端分析来记录转移性肿瘤的活性。本方案使用活体动物,将病变发展的连续微 CT 评估与研究结束时的匹配组织病理学相结合。该方法允许在活体动物中快速检测和评估骨病变的进展。骨内肿瘤通过直接(骨内)或动脉(心内)注射建立,病变发展评估长达 8 周。该方案为研究骨转移进展和开发用于治疗骨转移的亲骨性治疗策略提供了一种具有临床相关性的方法。