结直肠癌原位转移小鼠模型的建立与验证。

ISRN hepatology Pub Date : 2013-04-21 eCollection Date: 2013-01-01 DOI:10.1155/2013/206875
Ashwani Rajput, Ekta Agarwal, Premila Leiphrakpam, Michael G Brattain, Sanjib Chowdhury
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引用次数: 17

摘要

由于缺乏针对播散性疾病的有效治疗,转移在很大程度上导致了实体肿瘤的癌症死亡,迫切需要填补这一空白。本研究证明了原位结直肠癌(CRC)小鼠模型系统在体内发生自发转移,并比较了其与人类结直肠癌的可重复性。igf1r依赖性GEO人CRC细胞被用于原位移植程序研究转移定植,并显示出强劲的肝转移。在原位结肠原发瘤和肝转移瘤中均进行细胞增殖试验,在原位产生的原发性和肝转移瘤和人CRC标本中观察到人CRC患者标本的H&E和Ki67染色相似。通过微阵列分析生成基因标记,并与Oncomine分析的人类CRC基因表达数据集进行比较,发现基因标记与原位产生的肝转移中与CRC相关的侵袭性标记表达增加具有相似性。因此,我们建立了一种复制人类结直肠癌转移的原位小鼠模型。该模型系统可以有效地开发针对播散性疾病的新治疗策略,并可用于识别调节已建立转移的发展和/或维持的基因。
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Establishment and Validation of an Orthotopic Metastatic Mouse Model of Colorectal Cancer.

Metastases are largely responsible for cancer deaths in solid tumors due to the lack of effective therapies against disseminated disease, and there is an urgent need to fill this gap. This study demonstrates an orthotopic colorectal cancer (CRC) mouse model system to develop spontaneous metastasis in vivo and compare its reproducibility against human CRC. IGF1R-dependent GEO human CRC cells were used to study metastatic colonization using orthotopic transplantation procedures and demonstrated robust liver metastasis. Cell proliferation assays were performed both in the orthotopic primary colon and liver metastatic tumors, and human CRC patient's specimen and similar patterns in H&E and Ki67 staining were observed between the orthotopically generated primary and liver metastatic tumors and human CRC specimens. Microarray analysis was performed to generate gene signatures, compared with deposited human CRC gene expression data sets, analyzed by Oncomine, and revealed similarity in gene signatures with increased aggressive markers expression associated with CRC in orthotopically generated liver metastasis. Thus, we have developed an orthotopic mouse model that reproduces human CRC metastasis. This model system can be effective in developing new therapeutic strategies against disseminated disease and could be implemented for identifying genes that regulate the development and/or maintenance of established metastasis.

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