肝细胞生长因子
癌症研究
血管内皮生长因子
MAPK/ERK通路
蛋白激酶B
血管内皮生长因子A
PI3K/AKT/mTOR通路
肝细胞生长因子受体
激酶
血管内皮生长因子B
血管内皮生长因子C
生物
信号转导
蛋白激酶A
细胞生物学
受体
C-Met公司
血管内皮生长因子受体
遗传学
作者
Angela Queisser,Emmanuel Seront,Laurence M. Boon,Miikka Vikkula
出处
期刊:Circulation Research
[Ovid Technologies (Wolters Kluwer)]
日期:2021-06-24
卷期号:129 (1): 155-173
被引量:138
标识
DOI:10.1161/circresaha.121.318145
摘要
Vascular and lymphatic malformations represent a challenge for clinicians. The identification of inherited and somatic mutations in important signaling pathways, including the PI3K (phosphoinositide 3-kinase)/AKT (protein kinase B)/mTOR (mammalian target of rapamycin), RAS (rat sarcoma)/RAF (rapidly accelerated fibrosarcoma)/MEK (mitogen-activated protein kinase kinase)/ERK (extracellular signal-regulated kinases), HGF (hepatocyte growth factor)/c-Met (hepatocyte growth factor receptor), and VEGF (vascular endothelial growth factor) A/VEGFR (vascular endothelial growth factor receptor) 2 cascades has led to the evaluation of tailored strategies with preexisting cancer drugs that interfere with these signaling pathways. The era of theranostics has started for the treatment of vascular anomalies. Registration: URL: https://www.clinicaltrialsregister.eu ; Unique identifier: 2015-001703-32.
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