101. Long non‐coding RNA cox‐2 prevents immune evasion and metastasis of hepatocellular carcinoma by altering M1/M2 macrophage polarization
- Author
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Wenguang He, Yunxiuxiu Xu, Yanshan Li, Ruomei Wang, Xinxi Luo, Yu Lai, Rufu Chen, Tao Chen, and Yibiao Ye
- Subjects
0301 basic medicine ,Carcinoma, Hepatocellular ,Angiogenesis ,Cell ,Macrophage polarization ,Biology ,Biochemistry ,Mice ,03 medical and health sciences ,0302 clinical medicine ,Immune system ,medicine ,Animals ,RNA, Neoplasm ,Epithelial–mesenchymal transition ,Neoplasm Metastasis ,Molecular Biology ,Cell growth ,Macrophages ,Liver Neoplasms ,Cell Biology ,M2 Macrophage ,RAW 264.7 Cells ,030104 developmental biology ,medicine.anatomical_structure ,Apoptosis ,030220 oncology & carcinogenesis ,Immunology ,Cancer research ,RNA, Long Noncoding ,Tumor Escape - Abstract
Objective: Macrophages have been shown to demonstrate a high level of plasticity, with the ability to undergo dynamic transition between M1 and M2 polarized phenotypes. We investigate long non-coding RNA (lncRNA) cox-2 in macrophage polarization and the regulatory mechanism functions in hepatocellular carcinoma (HCC). Methods: Lipopolysaccharide (LPS) was used to induce RAW264.7 macrophages into M1 type, and IL-4 was to induce RAW264.7 macrophages into M2 type. We selected mouse hepatic cell line Hepal-6 and hepatoma cell line HepG2 for co-incubation with M1 or M2 macrophages. Quantitative real-time PCR was used to detect the expressions of lncRNA cox-2and mRNAs. ELISA was conducted for testing IL-12 and IL-10 expressions; western blotting for epithelial mesenchymal transition related factors (E-cadherin and Vimentin). An MTT, colony formation assay, flow cytometry, transwell assay and stretch test were conducted to test cell abilities. Results: The M1 macrophages had higher lncRNA cox-2 expression than that in the non-polarized macrophages and M2 macrophages. The lncRNA cox-2 siRNA decreased the expression levels of IL-12, iNOS, and TNF-α in M1 macrophages, increased the expression levels of IL-10, Arg-1, and Fizz-1 in M2 macrophages (all P < 0.05). The lncRNA cox-2 siRNA reduces the ability of M1 macrophages to inhibit HCC cell proliferation, invasion, migration, EMT, angiogenesis and facilitate apoptosis while strengthening the ability of M2 macrophages to promote proliferation HCC cell growth and inhibit apoptosis. Conclusion: These findings indicate that lncRNA cox-2 inhibits HCC immune evasion and tumor growth by inhibiting the polarization of M2 macrophages. This article is protected by copyright. All rights reserved
- Published
- 2017