LncRNA AATBC regulates Pinin to promote metastasis in nasopharyngeal carcinoma

Ting Tang(Central South University), Liting Yang(Central South University), Yujian Cao(Central South University), Maonan Wang(Central South University), Shanshan Zhang(Central South University), Zhaojian Gong(Central South University), Fang Xiong(Central South University), Yi He(Central South University), Yujuan Zhou(Central South University), Qianjin Liao(Central South University), Bo Xiang(Central South University), Ming Zhou(Central South University), Can Guo(Central South University), Xiaoling Li(Central South University), Yong Li(Baylor College of Medicine), Wei Xiong(Central South University), Guiyuan Li(Central South University), Zhaoyang Zeng(Central South University)
Molecular Oncology
May 4, 2020
Cited by 97Open Access
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Abstract

Long noncoding RNA (lncRNA) have emerged as crucial regulators for a myriad of biological processes, and perturbations in their cellular expression levels have often been associated with cancer pathogenesis. In this study, we identified AATBC (apoptosis-associated transcript in bladder cancer, LOC284837) as a novel lncRNA. AATBC was found to be highly expressed in nasopharyngeal carcinoma (NPC), and increased AATBC expression was associated with poor survival in patients with NPC. Furthermore, AATBC promoted migration and invasion of NPC cells in vitro, as well as metastasis in vivo. AATBC upregulated the expression of the desmosome-associated protein pinin (PNN) through miR-1237-3p sponging. In turn, PNN interacted with the epithelial-mesenchymal transition (EMT) activator ZEB1 and upregulated ZEB1 expression to promote EMT in NPC cells. Collectively, our results indicate that AATBC promotes NPC progression through the miR-1237-3p-PNN-ZEB1 axis. Our findings indicate AATBC as a potential prognostic biomarker or therapeutic target in NPC.


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