Microenvironment-dependent phenotypic changes in a SCID mouse model for malignant mesothelioma

Frontiers in Oncology

Eva eDarai-Ramqvist¹  Carmen eFlores-Staino¹  Katalin eDobra¹  Anders eHjerpe¹  Gustav eNilsonne² 

[1] Karolinska Institutet;Stockholm University;

关键词: Mesothelioma;    differentiation;    SCID mice;    epithelioid;    sarcomatoid;    chromosome 3;   

DOI  :  10.3389/fonc.2013.00203

来源: DOAJ

【 摘 要 】

Background and Aims: Malignant mesothelioma is an aggressive, therapy-resistant tumor. Mesothelioma cells may assume an epithelioid or a sarcomatoid phenotype, and presence of sarcomatoid cells predicts poor prognosis. In this study, we investigated differentiation of mesothelioma cells in a xenograft model, where mesothelioma cells of both phenotypes were induced to form tumors in SCID mice. Methods: Xenografts were established and thoroughly characterized using a comprehensive immunohistochemical panel, array comparative genomic hybridization of chromosome 3, fluorescent in situ hybridization and electron microscopy.Results: Epithelioid and sarcomatoid cells gave rise to xenografts of similar epithelioid morphology. While sarcomatoid-derived xenografts had higher growth rates, the morphology and expression of differentiation-related markers was similar between xenografts derived from both phenotypes. Array comparative genomic hybridization showed a convergent genotype for both xenografts, resembling the original aggressive sarcomatoid cell sub-line.Conclusions: Human mesothelioma xenografts from sarcomatoid and epithelioid phenotypes converged to a similar differentiation state, and genetic analyses suggested that clonal selection in the mouse microenvironment was a major contributing factor. This thoroughly characterized animal model can be used for further studies of molecular events underlying tumor cell differentiation.

【 授权许可】

Unknown