共 139 条
An emergent Wnt5a/YAP/TAZ regulatory circuit and its possible role in cancer
被引:11
作者:

Astudillo, Pablo
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Autonoma Chile, Fac Ciencias Salud, Inst Ciencias Biomed, Santiago, Chile
Llano Subercaseaux 2801, Santiago, Chile Univ Autonoma Chile, Fac Ciencias Salud, Inst Ciencias Biomed, Santiago, Chile
机构:
[1] Univ Autonoma Chile, Fac Ciencias Salud, Inst Ciencias Biomed, Santiago, Chile
[2] Llano Subercaseaux 2801, Santiago, Chile
关键词:
Wnt5a;
YAP;
TAZ;
beta-catenin;
Cancer;
Regulatory networks;
EMT;
WNT SIGNALING PATHWAYS;
WNT/BETA-CATENIN;
HIPPO PATHWAY;
BETA-CATENIN;
NEGATIVE REGULATOR;
TUMOR-SUPPRESSOR;
GASTRIC-CANCER;
STEM-CELLS;
INTESTINAL REGENERATION;
PROMOTER METHYLATION;
D O I:
10.1016/j.semcdb.2021.10.001
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Wnt5a is a ligand that plays several roles in development, homeostasis, and disease. A growing body of evidence indicates that Wnt5a is involved in cancer progression. Despite extensive research in this field, our knowledge about how Wnt5a is precisely involved in cancer is still incomplete. It is usually thought that certain combinations of Frizzled receptors and co-receptors might explain the observed effects of Wnt5a either as a tumor suppressor or by promoting migration and invasion. While accepting this 'receptor context' model, this review proposes that Wnt5a is integrated within a larger regulatory circuit involving beta-catenin, YAP/TAZ, and LATS1/2. Remarkably, WNT5A and YAP1 are transcriptionally regulated by the Hippo and Wnt pathways, respectively, and might form a regulatory circuit acting through LATS kinases and secreted Wnt/beta-catenin inhibitors, including Wnt5a itself. Therefore, understanding the precise role of Wnt5a and YAP in cancer requires a systems biology perspective.
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收藏
页码:45 / 54
页数:10
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