血管生成拟态
血管生成
瘦素
脂肪因子
PI3K/AKT/mTOR通路
癌症研究
转移
生物
癌症
肿瘤微环境
内科学
内分泌学
医学
信号转导
细胞生物学
肿瘤细胞
肥胖
作者
Ana K. Herrera-Vargas,Eduardo García-Rodríguez,Monserrat Olea‐Flores,Miguel A. Mendoza‐Catalán,Eugenia Flores‐Alfaro,Napoleón Navarro‐Tito
标识
DOI:10.1016/j.cytogfr.2021.10.006
摘要
The acquired ability to induce the formation of a functional vasculature is a hallmark of cancer. Blood vessels in tumors are formed through various mechanisms, among the most important in cancer biology, angiogenesis, and vasculogenic mimicry have been described. Leptin is one of the main adipokines secreted by adipocytes in normal breast tissue and the tumor microenvironment. Here, we provide information on the relationship between leptin and the development of angiogenesis and vasculogenic mimicry in different types of cancer. Here, we report that leptin activates different pathways such as JAK-STAT3, MAPK/ERK, PKC, JNK, p38, and PI3K-Akt to induce the expression of various angiogenic factors and vasculogenic mimicry. In vivo models, leptin induces blood vessel formation through the PI3K-Akt-mTOR pathway. Interestingly, the relationship between leptin and vasculogenic mimicry was more significant in breast cancer. The information obtained suggests that leptin could be playing an essential role in tumor survival and metastasis through the induction of vascular mechanisms such as angiogenesis and vasculogenic mimicry; thus, leptin-induced pathways could be suggested as a promising therapeutic target.
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