Wnt1 inducible signalling pathway protein-2 (WISP-2/CCN5): Roles and regulation in human cancers (Review)
doi: 10.3892/or.2013.2909
pmid: 24337439
Wnt1 inducible signalling pathway protein-2 (WISP-2/CCN5): Roles and regulation in human cancers (Review)
Wnt1 inducible signalling pathway protein-2 (WISP‑2), also known as CCN5, CT58, CTGF-L, CTGF-3, HICP and Cop1, is one of the 3 WNT1 inducible proteins that belongs to the CCN family. This family of members has been shown to play multiple roles in a number of pathophysiological processes, including cell proliferation, adhesion, wound healing, extracellular matrix regulation, epithelial-mesenchymal transition, angiogenesis, fibrosis, skeletal development and embryo implantation. Recent results suggest that WISP-2 is relevant to tumorigenesis and malignant transformation, particularly in breast cancer, colorectal cancer and hepatocarcinoma. Notably, its roles in cancer appear to vary depending on cell/tumour type and the microenvironment. The striking difference in the structure of WISP-2 in comparison with the other 2 family members may contribute to its difference in functions, which leads to the hypothesis that WISP-2 may act as a dominant-negative regulator of other CCN family members. In the present review, we summarise the roles, regulation and underlying mechanism of WISP-2 in human cancers.
- Cardiff University United Kingdom
- Peking University China (People's Republic of)
- Inner Mongolia Medical College China (People's Republic of)
- Peking University China (People's Republic of)
- Peking University Cancer Hospital China (People's Republic of)
Epithelial-Mesenchymal Transition, Carcinogenesis, CCN Intercellular Signaling Proteins, Gene Expression Regulation, Neoplastic, Repressor Proteins, Cell Movement, Cell Line, Tumor, Neoplasms, Cell Adhesion, Humans, Neoplasm Invasiveness, Cell Proliferation, Signal Transduction
Epithelial-Mesenchymal Transition, Carcinogenesis, CCN Intercellular Signaling Proteins, Gene Expression Regulation, Neoplastic, Repressor Proteins, Cell Movement, Cell Line, Tumor, Neoplasms, Cell Adhesion, Humans, Neoplasm Invasiveness, Cell Proliferation, Signal Transduction
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