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长非编码 RNA LINC00930 靶向 miR-6792-3p/ZBTB16 调控胰腺癌的增殖和 EMT。

Long non-coding RNA LINC00930 targeting miR-6792-3p/ZBTB16 regulates the proliferation and EMT of pancreatic cancer.

机构信息

Research Center of Clinical Medical, Department of General Surgery, Affiliated Hospital of Nantong University, Medical School of Nantong University, Nantong, 226001, P. R. China.

The Sixth People's Hospital of Nantong, Nantong, 226001, P. R. China.

出版信息

BMC Cancer. 2024 May 24;24(1):638. doi: 10.1186/s12885-024-12365-9.

DOI:10.1186/s12885-024-12365-9
PMID:38789960
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11127394/
Abstract

Emerging evidence suggests the dysregulation of long non-coding RNAs (lncRNAs) involved in pancreatic cancer (PC). However, the function of LINC00930 in PC has not been elaborated. In this study, we found that LINC00930 was significantly down-regulated in PC cell lines and tissues, and associated with tumor size, lymphatic metastasis, TNM stage and poor prognosis. According to the bioinformatics database, the downregulation of LINC00930 was a common event in PC associated with prognosis and EMT. Overexpression of LINC00930 inhibited the aggressive cancer phenotypes including proliferation, metastasis and epithelial-mesenchymal transition (EMT) of PC in vitro and in vivo. Bioinformatics and dual-luciferase reporter assay indicated that miR-6792-3p could directly bind to LINC00930. Additionally, the Zinc finger and BTB domain containing 16 (ZBTB16) was significantly declined in PC, which was predicted to be the downstream gene of miR-6792-3p. MiR-6792-3p mimic rescued the decreased proliferation, metastasis and EMT caused by ZBTB16 in PC cells. The LINC00930/miR-6792-3p/ZBTB16 axis was associated with the malignant progression and process of PC. The relative expression of LINC00930 was negatively correlated with the expression of miR-6792-3p and was closely linked with ZBTB16 levels in PC. LINC00930 might serve as a potential prognostic biomarker and therapeutic target for PC.

摘要

越来越多的证据表明,长链非编码 RNA(lncRNA)在胰腺癌(PC)中的失调。然而,LINC00930 在 PC 中的功能尚未阐述。在本研究中,我们发现 LINC00930 在 PC 细胞系和组织中显著下调,并与肿瘤大小、淋巴转移、TNM 分期和预后不良相关。根据生物信息学数据库,LINC00930 的下调是 PC 中与预后和 EMT 相关的常见事件。LINC00930 的过表达抑制了 PC 体外和体内侵袭性癌症表型,包括增殖、转移和上皮-间充质转化(EMT)。生物信息学和双荧光素酶报告基因实验表明,miR-6792-3p 可以直接结合 LINC00930。此外,锌指和 BTB 结构域包含 16 (ZBTB16)在 PC 中显著下降,预测是 miR-6792-3p 的下游基因。miR-6792-3p 模拟物挽救了 ZBTB16 引起的 PC 细胞增殖、转移和 EMT 的减少。LINC00930/miR-6792-3p/ZBTB16 轴与 PC 的恶性进展和过程有关。LINC00930 的相对表达与 miR-6792-3p 的表达呈负相关,并且与 PC 中 ZBTB16 水平密切相关。LINC00930 可能作为 PC 的潜在预后生物标志物和治疗靶点。

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