肿瘤微环境
CXCR3型
癌症研究
细胞生物学
肿瘤进展
单因子
CXCL9型
免疫系统
生物
癌症
化学
趋化因子
趋化因子受体
免疫学
遗传学
作者
Shiyong Neo,Andreas Lundqvist
标识
DOI:10.1007/978-3-030-36667-4_5
摘要
Chemokines are soluble proteins that orchestrate cell migration in a regulated concentration gradient. During early stages of tumor development, chemokines shape the immune landscape of tumor microenvironment. CXCL9, also known as monokine induced by gamma-interferon (MIG), can be produced during inflammatory conditions by myeloid cells within the tumor microenvironment. It attracts cells expressing the CXCR3 receptor including activated T and NK cells and has been shown to play a role in responses to immune checkpoint therapy. Overexpression of CXCL9 has also shown to reduce tumor progression and metastasis via the inhibition of angiogenesis. Conversely, CXCL9 can act directly on tumor cells expressing the CXCR3 receptor to promote cell migration and epithelial mesenchymal transition. In this chapter we discuss the anti- and pro-tumoral features of CXCL9 within the tumor microenvironment.
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