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CCT-3的上调通过miR-223竞争和Wnt/β-连环蛋白信号通路激活诱导乳腺癌细胞增殖。

Upregulation of CCT-3 Induces Breast Cancer Cell Proliferation Through miR-223 Competition and Wnt/β-Catenin Signaling Pathway Activation.

作者信息

Qu Hongbo, Zhu Fang, Dong Huaying, Hu Xiongqiang, Han Mingli

机构信息

Department of Breast and Thyroid Surgery, The First People's Hospital of Chenzhou, Chenzhou, China.

Department of Breast Health Center, The First People's Hospital of Chenzhou (South Hospital), Chenzhou, China.

出版信息

Front Oncol. 2020 Sep 24;10:533176. doi: 10.3389/fonc.2020.533176. eCollection 2020.

Abstract

The clinical significance and the function of chaperonin-containing TCP1 complex 3 (CCT-3) in breast cancer remain unknown. In this study, we found that CCT-3 was markedly overexpressed in breast cancer tissues. Statistical analysis revealed a significant correlation of CCT-3 expression with advanced breast cancer clinical stage and poorer survival. Ablation of CCT-3 knocked down the proliferation and the tumorigenicity of breast cancer cells and . CCT-3 may regulate breast cancer cell proliferation through a ceRNA network between miR-223 and β-catenin, thus affecting Wnt/β-catenin signaling pathway activation. We also validated that CCT-3 and β-catenin are novel direct targets of tumor suppressor miR-223. Our results suggest that both mRNA and the protein levels of CCT-3 are potential diagnosis biomarkers and therapeutic targets for breast cancer.

摘要

含TCP1伴侣蛋白复合体3(CCT-3)在乳腺癌中的临床意义及功能尚不清楚。在本研究中,我们发现CCT-3在乳腺癌组织中显著过表达。统计分析显示,CCT-3表达与晚期乳腺癌临床分期及较差的生存率显著相关。敲除CCT-3可降低乳腺癌细胞的增殖和致瘤性。CCT-3可能通过miR-223与β-连环蛋白之间的ceRNA网络调节乳腺癌细胞增殖,从而影响Wnt/β-连环蛋白信号通路的激活。我们还验证了CCT-3和β-连环蛋白是肿瘤抑制因子miR-223的新型直接靶点。我们的结果表明,CCT-3的mRNA和蛋白水平均是乳腺癌潜在的诊断生物标志物和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ecb/7541898/56317bc16413/fonc-10-533176-g0001.jpg

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