Institute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan.
Institute of Molecular and Genomic Medicine, National Health Research Institutes, Miaoli, Taiwan.
Cell Death Dis. 2021 Nov 17;12(12):1090. doi: 10.1038/s41419-021-04231-4.
Certain immune cells and inflammatory cytokines are essential components in the tumor microenvironment to promote breast cancer progression. To identify key immune players in the tumor microenvironment, we applied highly invasive MDA-MB-231 breast cancer cell lines to co-culture with human monocyte THP-1 cells and identified CXCL7 by cytokine array as one of the increasingly secreted cytokines by THP-1 cells. Further investigations indicated that upon co-culturing, breast cancer cells secreted CSF1 to induce expression and release of CXCL7 from monocytes, which in turn acted on cancer cells to promote FAK activation, MMP13 expression, migration, and invasion. In a xenograft mouse model, administration of CXCL7 antibodies significantly reduced abundance of M2 macrophages in tumor microenvironment, as well as decreased tumor growth and distant metastasis. Clinical investigation further suggested that high CXCL7 expression is correlated with breast cancer progression and poor overall survival of patients. Overall, our study unveils an important immune cytokine, CXCL7, which is secreted by tumor infiltrating monocytes, to stimulate cancer cell migration, invasion, and metastasis, contributing to the promotion of breast cancer progression.
某些免疫细胞和炎症细胞因子是肿瘤微环境中促进乳腺癌进展的重要组成部分。为了鉴定肿瘤微环境中的关键免疫细胞,我们应用高侵袭性的 MDA-MB-231 乳腺癌细胞系与人类单核细胞 THP-1 细胞共培养,并通过细胞因子阵列鉴定出 CXCL7 是 THP-1 细胞不断分泌的细胞因子之一。进一步的研究表明,在共培养时,乳腺癌细胞分泌 CSF1 诱导单核细胞表达和释放 CXCL7,CXCL7 反过来作用于癌细胞促进 FAK 激活、MMP13 表达、迁移和侵袭。在异种移植小鼠模型中,CXCL7 抗体的给药显著减少了肿瘤微环境中 M2 巨噬细胞的丰度,并降低了肿瘤生长和远处转移。临床研究进一步表明,高 CXCL7 表达与乳腺癌进展和患者总体生存率降低相关。总的来说,我们的研究揭示了一种重要的免疫细胞因子 CXCL7,它由肿瘤浸润的单核细胞分泌,刺激癌细胞迁移、侵袭和转移,促进乳腺癌的进展。