原癌基因酪氨酸蛋白激酶Src
蛋白激酶A
癌症研究
酪氨酸激酶
生物
脂肪酸结合蛋白
血管内皮生长因子A
细胞生物学
激酶
MAPK/ERK通路
血管内皮生长因子
化学
信号转导
生物化学
基因
血管内皮生长因子受体
作者
W. G. Warren,Myles Osborn,Andrew Yates,Saoirse E. O’Sullivan
标识
DOI:10.1016/j.drudis.2024.103980
摘要
Fatty acid binding protein 7 (FABP7) is an intracellular protein involved in the uptake, transportation, metabolism, and storage of fatty acids (FAs). FABP7 is upregulated up to 20-fold in multiple cancers, usually correlated with poor prognosis. FABP7 silencing or pharmacological inhibition suggest FABP7 promotes cell growth, migration, invasion, colony and spheroid formation/increased size, lipid uptake, and lipid droplet formation. Xenograft studies show that suppression of FABP7 inhibits tumour formation and tumour growth, and improves host survival. The molecular mechanisms involve promotion of FA uptake, lipid droplets, signalling [focal adhesion kinase (FAK), proto-oncogene tyrosine-protein kinase Src (Src), mitogen-activated protein kinase kinase/p-extracellular signal-regulated kinase (MEK/ERK), and Wnt/β-catenin], hypoxia-inducible factor 1-alpha (Hif1α), vascular endothelial growth factor A/prolyl 4-hydroxylase subunit alpha-1 (VEGFA/P4HA1), snail family zinc finger 1 (Snail1), and twist-related protein 1 (Twist1). The oncogenic capacity of FABP7 makes it a promising pharmacological target for future cancer treatments.
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