Altered Biological Potential and Radioresponse of Murine Tumors in Different Microenvironments.
- Author:
Ik Jae LEE
1
;
Eun Jeong LEE
;
Hyojin PARK
;
Wonwoo KIM
;
Sang Jun HA
;
You Keun SHIN
;
Jinsil SEONG
Author Information
- Publication Type:Original Article
- Keywords: Tumor microenvironment; Hepatocarcinoma; Radiation
- MeSH: Angiogenesis Inducing Agents; Animals; Cyclooxygenase 2; Humans; Interleukin-6; Liver; Lung; Male; Mice; Neoplasm Metastasis; Radiation Effects; T-Lymphocytes, Regulatory; Thigh; Transforming Growth Factor beta1; Translational Medical Research; Tumor Burden; Tumor Microenvironment; Vascular Endothelial Growth Factor A
- From:Cancer Research and Treatment 2016;48(2):727-737
- CountryRepublic of Korea
- Language:English
- Abstract: PURPOSE: This study was conducted to evaluate the biological features of murine hepatocarcinoma according to different tumor microenvironmental models and to determine the change in molecular and immunologic responses after radiation. MATERIALS AND METHODS: Tumor models were established in the liver (orthotopic) and thigh (heterotopic) of male C3H/HeN mice. Tumor growth and lung metastasis were assessed in these models. To evaluate the radiation effect, the tumors were irradiated with 10 Gy. Factors associated with tumor microenvironment including vascular endothelial growth factor (VEGF), cyclooxygenase-2 (COX-2), transforming growth factor beta1 (TGF-β1), CD31, and serum interleukin-6 (IL-6) were evaluated. Tumor-infiltrating regulatory immune cells, regulatory T cells (Tregs), and myeloid-derived suppressor cells (MDSCs) were also analyzed. RESULTS: A higher number of lung metastases were observed in the orthotopic tumor model than in the heterotopic tumor model. VEGF, CD31, COX-2, and TGF-β1 expression was more prominent in the orthotopic tumor model than in the heterotopic tumor model. Expression of the angiogenic factor VEGF and key regulatory molecules (TGF-β1 and COX-2) decreased following radiation in the orthotopic tumor model, while the serum IL-6 level increased after radiation. In the orthotopic tumor model, the number of both Tregs and MDSCs in the tumor burden decreased after radiation. CONCLUSION: The orthotopic tumor model showed higher metastatic potential and more aggressive molecular features than the heterotopic tumor model. These findings suggest that the orthotopic tumor mouse model may be more reflective of the tumor microenvironment and suitable for use in the translational research of radiation treatment.
