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NPTX2 通过激活 FZD6 促进经典 Wnt/β-catenin 通路进而促进结直肠癌生长和肝转移。

NPTX2 promotes colorectal cancer growth and liver metastasis by the activation of the canonical Wnt/β-catenin pathway via FZD6.

机构信息

Department of Gastrointestinal Surgery, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, 160 Pujian Road, Shanghai, 200127, P.R. China.

State Key Laboratory of Oncogenes and Related Genes, Shanghai Cancer Institute, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, P.R. China.

出版信息

Cell Death Dis. 2019 Mar 4;10(3):217. doi: 10.1038/s41419-019-1467-7.

Abstract

Accumulating evidence from clinical and epidemiological studies has highlighted the close correlation between the individual risk of cancer and nervous system diseases. The expression of neuronal pentraxin 2 (NPTX2) is absent in Alzheimer's disease, anxiety, and depression. Herein, we found that NPTX2 mRNA and protein expression was significantly upregulated in colorectal carcinoma (CRC). NPTX2 expression level gradually increased with CRC progression and was closely associated with poor prognosis. In vitro and in vivo studies demonstrated that NPTX2 promoted CRC proliferation and metastasis through the activation of the Wnt/β-catenin signaling pathway. As NPTX2 receptors are absent on CRC cells, NPTX2 was shown to physically interact with frizzled class receptor 6 (FZD6) to promote β-catenin translocation into the cell nucleus, resulting in an increase in the expression of MYC, cyclin D1, snail, and N-cadherin along with a decrease in the expression of E-cadherin. Knockdown of FZD6 expression with a small-interfering RNA almost completely reversed the proliferative effects of NPTX2 on CRC development. In conclusion, NPTX2, a molecule related to nervous system diseases, promotes CRC cell proliferation and metastasis through the activation of the Wnt/β-catenin pathway via direct interaction with FZD6.

摘要

越来越多的临床和流行病学研究证据强调了个体患癌症和神经系统疾病的风险之间的密切相关性。神经元五联素 2(NPTX2)在阿尔茨海默病、焦虑症和抑郁症中的表达缺失。在此,我们发现 NPTX2mRNA 和蛋白表达在结直肠癌(CRC)中显著上调。NPTX2 的表达水平随着 CRC 的进展逐渐升高,并与预后不良密切相关。体外和体内研究表明,NPTX2 通过激活 Wnt/β-catenin 信号通路促进 CRC 的增殖和转移。由于 CRC 细胞上不存在 NPTX2 受体,NPTX2 被证明与卷曲蛋白受体 6(FZD6)发生物理相互作用,促进 β-catenin 向细胞核内易位,从而导致 MYC、cyclin D1、snail 和 N-cadherin 的表达增加,E-cadherin 的表达减少。用小干扰 RNA 敲低 FZD6 表达几乎完全逆转了 NPTX2 对 CRC 发展的增殖作用。总之,与神经系统疾病相关的分子 NPTX2 通过与 FZD6 的直接相互作用,通过激活 Wnt/β-catenin 通路促进 CRC 细胞的增殖和转移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b245/6399240/4ac2ca954d8a/41419_2019_1467_Fig1_HTML.jpg

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