作者: Shanfeng Tan , Kai Wang , Fuguang Sun , Yang Li , Yisheng Gao
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摘要: Chemokines have been demonstrated to serve an important role in a variety of diseases, particularly tumor progression. There numerous studies that reported T cells major roles However, the function CXC motif chemokine ligand 9 (CXCL9) prostate cancer remains unknown. The present study aimed investigate CXCL9 cancer. A mouse model was generated by treating C57/BL-6 and B6.Cg-Selplgtm1Fur/J mice with 3,2′-dimethyl 4-aminobiphenyl (DMAB). Hematoxylin eosin staining detected histopathological alterations tissues. Immunohistochemistry (IHC) determined cell proliferation mice. Flow cytometry used detect C57+DMAB or CXCL9+DMAB Immunofluorescence revealed there positive expression interleukin-6 (IL-6) transforming growth factor (TGF)-β survival rates analyzed. association clinical stages also evaluated. Results pathology were significantly greater compared Compared mice, number peripheral blood spleen reduced. IHC IL-6 TGF-β downregulated rate decreased In addition, reverse transcription-quantitative polymerase chain reaction analysis mRNA samples positively associated pathological conclusion, may promote progression via inhibition cytokines from cells.