Wnt1 inducible signalling pathway protein-2 (WISP-2/CCN5): Roles and regulation in human cancers (Review)

被引:29
作者
Ji, Jiafu [1 ,2 ,3 ]
Jia, Shuqin [1 ,3 ,4 ]
Ji, Ke [1 ,4 ]
Jiang, Wen G. [1 ,4 ]
机构
[1] Peking Univ, Joint Canc Inst, Cardiff Univ, Beijing 100871, Peoples R China
[2] Peking Univ, Canc Hosp, Dept Gastroenterol Canc, Beijing 100871, Peoples R China
[3] Inner Mongolia Med Univ, Affiliated Hosp, Surg Lab, Hohhot, Peoples R China
[4] Cardiff Univ, Sch Med, Metastasis & Angiogenesis Res Grp, Cardiff CF14 4XN, S Glam, Wales
关键词
Wnt1 inducible signalling pathway protein-2; CCN5; epithelial-mesenchymal transition; angiogenesis; cellular migration; metastasis; HUMAN BREAST-CANCER; TISSUE GROWTH-FACTOR; TUMOR-CELL-PROLIFERATION; MOLECULAR CROSS-TALKS; ARREST-SPECIFIC GENE; CCN FAMILY; DIFFERENTIAL EXPRESSION; HEPATOCELLULAR-CARCINOMA; PROGNOSTIC IMPLICATIONS; CCN5/WISP-2; EXPRESSION;
D O I
10.3892/or.2013.2909
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:533 / 539
页数:7
相关论文
共 56 条
[1]   Epidermal growth factor induces WISP-2/CCN5 expression in estrogen receptor-α-positive breast tumor cells through multiple molecular cross-talks [J].
Banerjee, S ;
Sengupta, K ;
Saxena, NK ;
Dhar, K ;
Banerjee, SK .
MOLECULAR CANCER RESEARCH, 2005, 3 (03) :151-162
[2]   WISP-2 gene in human breast cancer: Estrogen and progesterone inducible expression and regulation of tumor cell proliferation [J].
Banerjee, S ;
Saxena, N ;
Sengupta, K ;
Tawfik, O ;
Mayor, MS ;
Banerjee, SK .
NEOPLASIA, 2003, 5 (01) :63-73
[3]   CCN5/WISP-2 expression in breast adenocarcinoma is associated with less frequent progression of the disease and suppresses the invasive phenotypes of tumor cells [J].
Banerjee, Snigdha ;
Dhar, Gopal ;
Haque, Inamul ;
Kambhampati, Suman ;
Mehta, Smita ;
Sengupta, Krishanu ;
Tawfik, Ossama ;
Phillips, Teresa A. ;
Banerjee, Sushanta K. .
CANCER RESEARCH, 2008, 68 (18) :7606-7612
[4]   CCN5/WISP-2: A micromanager of breast cancer progression [J].
Banerjee, Sushanta K. ;
Banerjee, Snigdha .
JOURNAL OF CELL COMMUNICATION AND SIGNALING, 2012, 6 (02) :63-71
[5]   Wnt pathway activation: New relations and locations [J].
Bejsovec, A .
CELL, 2005, 120 (01) :11-14
[6]   A homologue of Drosophila aurora kinase is oncogenic and amplified in human colorectal cancers [J].
Bischoff, JR ;
Anderson, L ;
Zhu, YF ;
Mossie, K ;
Ng, L ;
Souza, B ;
Schryver, B ;
Flanagan, P ;
Clairvoyant, F ;
Ginther, C ;
Chan, CSM ;
Novotny, M ;
Slamon, DJ ;
Plowman, GD .
EMBO JOURNAL, 1998, 17 (11) :3052-3065
[7]   THE MODULAR ARCHITECTURE OF A NEW FAMILY OF GROWTH-REGULATORS RELATED TO CONNECTIVE-TISSUE GROWTH-FACTOR [J].
BORK, P .
FEBS LETTERS, 1993, 327 (02) :125-130
[8]   Gene array analysis of macronodular adrenal hyperplasia confirms clinical heterogeneity and identifies several candidate genes as molecular mediators [J].
Bourdeau, I ;
Antonini, SR ;
Lacroix, A ;
Kirschner, LS ;
Matyakhina, L ;
Lorang, D ;
Libutti, SK ;
Stratakis, CA .
ONCOGENE, 2004, 23 (08) :1575-1585
[9]   Purification and characterization of novel heparin-binding growth factors in uterine secretory fluids - Identification as heparin-regulated M-r 10,000 forms of connective tissue growth factor [J].
Brigstock, DR ;
Steffen, CL ;
Kim, GY ;
Vegunta, RK ;
Diehl, JR ;
Harding, PA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (32) :20275-20282
[10]   The CCN family: a new stimulus package [J].
Brigstock, DR .
JOURNAL OF ENDOCRINOLOGY, 2003, 178 (02) :169-175