Cell Line Derived Xenograft Mouse Models Are a Suitable in vivo Model for Studying Tumor Budding in Colorectal Cancer

Frontiers in Medicine

article

Laurent M. C. Georges¹  Olivier De Wever²  José A. Galván³  Heather Dawson³  Alessandro Lugli³  Pieter Demetter¹  Inti Zlobec³ 

[1] Department of Pathology, Hôpital Erasme, Université Libre de Bruxelles;Laboratory of Experimental Cancer Research, Ghent University;Institute of Pathology, University of Bern

关键词: colorectal cancer;    tumor budding;    mouse model;    xenograft;    cell line;    epithelial-mesenchymal transition;   

DOI  :  10.3389/fmed.2019.00139

学科分类：社会科学、人文和艺术（综合）

来源: Frontiers

【 摘 要 】

Tumor budding (TB) is an important prognostic parameter in colorectal cancer (CRC) and associated with metastasis. However, the mechanisms of TB have not been fully elucidated and a major limitation is the absence of in vivo models. Here, we determine the suitability of human cell line derived xenografts (CDX) as models of TB in CRC. Pan-cytokeratin (CK)-stained next-generation Tissue Microarrays (ngTMA) of two CDX models (HT-29, n = 12 and HCT-8, n = 8) and human CRC ( n = 27 high-grade and 25 low-grade budding tumors, each) were evaluated for TB. Immunohistochemistry for E-cadherin, β-catenin, Ki-67, ZEB1, and TWIST1 was performed. HT-29 and HCT-8 were predominantly high-grade and no/low-grade TB tumors, respectively. TB counts in the tumor center (intratumoral budding, ITB) were significantly higher in HT-29 CDX tumors compared to human CRC ( p = 0.0099). No difference was found in TB counts at the invasion front (peritumoral budding, PTB; p =0.07). ITB and PTB were strongly correlated ( r = 0.438 and r = 0.62 in CDX and human CRC, respectively). Immunohistochemistry profiles were comparable in CDX and human CRC tissues. TB in the CDX mouse models is phenotypically similar to human CRCs and highlights comparable protein profiles. The HT-29 CDX could be a suitable model for the in vivo assessment of TB.

【 授权许可】

CC BY