溶血磷脂酸
磷脂酸
脂质信号
PLD2型
磷脂酶D
磷脂酶
信号转导
二酰甘油激酶
细胞生物学
细胞信号
花生四烯酸
生物
磷脂酶C
磷脂酶A2
癌症
癌细胞
血管生成
化学
生物化学
癌症研究
酶
磷脂
蛋白激酶C
受体
膜
遗传学
作者
Yu Jin Lee,Kyeong Jin Shin,Hyun‐Jun Jang,Dong‐Young Noh,Sung Ho Ryu,Pann‐Ghill Suh
标识
DOI:10.1007/978-981-32-9620-6_2
摘要
Breast cancer progression results from subversion of multiple intra- or intercellular signaling pathways in normal mammary tissues and their microenvironment, which have an impact on cell differentiation, proliferation, migration, and angiogenesis. Phospholipases (PLC, PLD and PLA) are essential mediators of intra- and intercellular signaling. They hydrolyze phospholipids, which are major components of cell membrane that can generate many bioactive lipid mediators, such as diacylglycerol, phosphatidic acid, lysophosphatidic acid, and arachidonic acid. Enzymatic processing of phospholipids by phospholipases converts these molecules into lipid mediators that regulate multiple cellular processes, which in turn can promote breast cancer progression. Thus, dysregulation of phospholipases contributes to a number of human diseases, including cancer. This review describes how phospholipases regulate multiple cancer-associated cellular processes, and the interplay among different phospholipases in breast cancer. A thorough understanding of the breast cancer–associated signaling networks of phospholipases is necessary to determine whether these enzymes are potential targets for innovative therapeutic strategies.
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