LncRNA-SNHG1 promotes macrophage M2-like polarization and contributes to breast cancer growth and metastasis

被引:0
作者
Zong, Shoukai [1 ]
Dai, Wei [2 ]
Guo, Xiangting [3 ]
Wang, Kai [4 ]
机构
[1] Peoples Hosp Rizhao, Dept Breast Surg, Rizhao, Shandong, Peoples R China
[2] TCM Hosp Rizhao, Dept Breast & Thyroid Surg, Rizhao, Shandong, Peoples R China
[3] Peoples Hosp Rizhao, Dept Rheumatol & Immunol, Rizhao, Shandong, Peoples R China
[4] Peoples Hosp Rizhao, Dept Oncol, Rizhao, Shandong, Peoples R China
来源
AGING-US | 2021年 / 13卷 / 19期
关键词
breast cancer; macrophage; polarization; lncRNA; tumor associated macrophages; LONG NONCODING RNA; CELL LUNG-CANCER; TUMOR; PROGRESSION; CLASSIFICATION; ANGIOGENESIS;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Breast cancer is one of the most common malignant cancers among women. Cancer cells and adjacent cells determine the development of the disease. Tumor associated macrophages (TAMs) are involved in the regulation of different stages of cancer progression. LncRNAs play an important role in tumor growth and metastasis. However, the function of lncRNA in macrophage and tumor cell interaction is poorly described. Here we reported that lncRNA SNHG1 functioned as a modulator of M2 macrophage polarization and regulated tumor growth and angiogenesis. We indicated that knockdown of SNHG1 inhibited M2 macrophage polarization by suppression of STAT6 phosphorylation. SNHG1 silencing significantly alleviated migration of MCF-7 cells and tube formation of Human Umbilical Vein Endothelial Cells (HUVEC). Furthermore, we found that implantation of cell mixture of MCF-7 cells and macrophages promoted tumor growth and angiogenesis. However, knockdown of SNHG1 in macrophages reversed that effect. Collectively, we demonstrated the important role of lncRNA SNHG1 in macrophages and breast cancer cells interaction. We highlight the essential effect of lncRNA in tumor progression and provide a new method for the prevention and treatment of breast tumor metastasis.
引用
收藏
页码:23169 / 23181
页数:13
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