血管生成
肿瘤微环境
1-磷酸鞘氨醇
细胞信号
细胞生物学
癌症研究
信号转导
免疫系统
肿瘤进展
转移
细胞内
鞘氨醇
化学
生物
癌症
肿瘤细胞
免疫学
受体
生物化学
遗传学
标识
DOI:10.1007/978-3-030-35582-1_7
摘要
Sphingosine-1-phosphate (S1P), together with other phosphosphingolipids, has been found to regulate complex cellular function in the tumor microenvironment (TME) where it acts as a signaling molecule that participates in cell–cell communication. S1P, through intracellular and extracellular signaling, was found to promote tumor growth, angiogenesis, chemoresistance, and metastasis; it also regulates anticancer immune response, modulates inflammation, and promotes angiogenesis. Interestingly, cancer cells are capable of releasing S1P and thus modifying the behavior of the TME components in a way that contributes to tumor growth and progression. Therefore, S1P is considered an important therapeutic target, and several anticancer therapies targeting S1P signaling are being developed and tested in clinics.
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