一种具有免疫应答的外科原位异种移植入路用于结直肠癌的研究。

IF 3.4 Q1 Health Professions Animal models and experimental medicine Pub Date : 2025-01-24 DOI:10.1002/ame2.12560
Xiaoying Hou, Xiaoxuan Li, Qian Fang, Yufei Deng, Haiping Wang, Binlian Sun, Chengliang Zhang, Hongzhi Du, Yuchen Liu
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引用次数: 0

摘要

结直肠癌(CRC)的高发病率和高死亡率是临床实践中的一个重大挑战。虽然已经建立了一系列CRC的替代研究模型,但仍然缺乏适当的原位动物模型来再现CRC的特定临床反应和病理生理免疫特征。在本研究中,我们通过在小鼠结肠直肠植入肿瘤管构建了CRC原位异种移植模型,并利用生物发光成像技术监测模型的发育。该模型成功地总结了CRC一线化疗方案(FOLFOX:奥沙利铂和5-氟尿嘧啶/亚叶酸钙)治疗后的临床化疗疗效,包括总通量、肿瘤重量和Ki67的表达。该模型还再现了FOLFOX的免疫抑制作用,表现为肿瘤中巨噬细胞浸润减少,Treg细胞增加。此外,原位异种移植物方法可用于免疫缺陷NCG/NSG小鼠构建患者源性异种移植物,并可用于临床精准医学和药物评价。我们认为目前的模型是一种成功的外科原位异种移植癌症研究方法,值得推广,为深入探讨结直肠癌的机制和临床前药物评价提供一个方便高效的平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A surgical orthotopic xenograft approach with immune response for colorectal cancer research

The high morbidity and mortality of colorectal cancer (CRC) is a major challenge in clinical practice. Although a series of alternative research models of CRC have been developed, appropriate orthotopic animal models that reproduce the specific clinical response as well as pathophysiological immune features of CRC are still lacking. In the current study, we constructed a CRC orthotopic xenograft model by implanting the tumor tubes at the colorectum of mice and monitored the model development using bioluminescence imaging. This model successfully recapitulates the clinical chemotherapy efficacy, including reduced total flux, tumor weight, and the expression of Ki67 after treatment of the first-line chemotherapy regime of CRC (FOLFOX: oxaliplatin and 5-fluorouracil/calcium folinate). The model also reproduced the immunosuppressive effect of FOLFOX, indicated by decreased infiltration of macrophages and increased Treg cells in tumor. Additionally, the orthotopic xenograft approach may be applied in immunodeficient NCG/NSG mice for constructing patient-derived xenografts, and being used in clinical precision medicine and drug evaluation. We believe the current model is a successful surgical orthotopic xenograft approach for cancer research and deserves to be popularized, which will provide a convenient and efficient platform for in-depth mechanism exploration of CRC and preclinical drug evaluation.

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来源期刊
CiteScore
5.50
自引率
0.00%
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0
审稿时长
12 weeks
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