Fang Fang, Zhao Wen-Yi, Li Rong-Kun, Yang Xiao-Mei, Li Jun, Ao Jun-Ping, Jiang Shu-Heng, Kong Fan-Zhi, Tu Lin, Zhuang Chun, Qin Wen-Xin, He Ping, Zhang Wen-Ming, Cao Hui, Zhang Zhi-Gang
State Key Laboratory of Oncogenes and Related Genes, Shanghai Cancer Institute, Renji Hospital, Shanghai Jiao Tong University School of Medicine Shanghai 200240, P.R. China.
Department of General Surgery, Renji Hospital, Shanghai Jiao Tong University School of Medicine Shanghai, China.
Int J Clin Exp Pathol. 2014 Sep 15;7(10):6447-61. eCollection 2014.
CCN6/Wnt1-inducible signaling protein-3 (CCN6/WISP3) is a cysteine-rich protein that belongs to the CCN (Cyr61, CTGF, Nov) family of matricellular proteins, which are often dysregulated in cancers. However, the functional role and clinical significance of WISP3 in gastric cancer remain unclear. In this study, we found that silencing of WISP3 suppressed gastric cancer cell proliferation, migration and invasion. Cell adhesion to collagens (collagen I and IV), but not to fibronectin, were significantly inhibited by silencing of WISP3. Furthermore, silencing of WISP3 prevented β-catenin transferring from cell cytoplasm to nuclear, and suppressed canonical Wnt/β-catenin signaling and its downstream target genes, cyclin D1 and TCF-4. By immunohistochemical analysis of 379 patients, we found that the expression of WISP3 is closely associated with gastric cancer size and tumor invasion, and indicates a poor prognosis in both test cohort (253 patients) and validation cohort (126 patients). Moreover, the expression of WISP3 was positively correlated with the expression of cyclin D1 and TCF-4 in gastric cancer tissues. Taken together, our data suggests that WISP3 might be a promising prognostic factor and WISP3-Wnt/β-catenin axis may be a new therapeutic target for the intervention of gastric cancer growth and metastasis.
CCN6/ Wnt1诱导信号蛋白3(CCN6/ WISP3)是一种富含半胱氨酸的蛋白质,属于基质细胞蛋白的CCN(Cyr61、CTGF、Nov)家族,该家族蛋白在癌症中常发生失调。然而,WISP3在胃癌中的功能作用和临床意义仍不清楚。在本研究中,我们发现WISP3沉默可抑制胃癌细胞的增殖、迁移和侵袭。WISP3沉默显著抑制细胞与胶原蛋白(I型和IV型胶原蛋白)的黏附,但不影响其与纤连蛋白的黏附。此外,WISP3沉默可阻止β-连环蛋白从细胞质转移至细胞核,抑制经典Wnt/β-连环蛋白信号通路及其下游靶基因细胞周期蛋白D1和TCF-4。通过对379例患者进行免疫组化分析,我们发现WISP3的表达与胃癌大小和肿瘤侵袭密切相关,并且在测试队列(253例患者)和验证队列(126例患者)中均提示预后不良。此外,WISP3的表达与胃癌组织中细胞周期蛋白D1和TCF-4的表达呈正相关。综上所述,我们的数据表明WISP3可能是一个有前景的预后因素,WISP3-Wnt/β-连环蛋白轴可能是干预胃癌生长和转移的新治疗靶点。