• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

APTR 在肺腺癌发生发展中的表达及意义。

Expression and Significance of the Long Non-Coding RNA APTR in the Occurrence and Development of Lung Adenocarcinoma.

机构信息

Department of Pulmonary and Critical Care Medicine, Nanjing Drum Tower Hospital Clinical College of Nanjing Medical University, Nanjing, 210008, China.

Nanjing Drum Tower Hospital Clinical College of Nanjing Medical University.

出版信息

J Environ Pathol Toxicol Oncol. 2025;44(1):11-20. doi: 10.1615/JEnvironPatholToxicolOncol.2024053394.

DOI:10.1615/JEnvironPatholToxicolOncol.2024053394
PMID:39462445
Abstract

As one of the three major malignant tumors, lung adenocarcinoma (LUAD), with its rapid progression and high mortality rate, has become the most dangerous factor endangering human health. This study aims to explore new potential molecular targets, explore the regulatory role of lncRNA APTR in LUAD, and provide a more theoretical basis for the selection of LUAD therapeutic targets. The expression of APTR in LUAD was detected by PCR experiments, and the relationship between APTR and patients' clinical conditions and prognosis was analyzed by chi-square test, multifactor Cox regression, and Kaplan-Meier. The interaction between APTR and miR-298 and the regulation of LUAD cellular activities by APTR/miR-298 were explored by the luciferase reporter gene system. APTR expression was found to be upregulated in LUAD tissues and cells, and the expression of APTR was revealed to be substantially linked with lymph node metastases and TNM stage. High expression of LUAD also predicted a poor prognosis for patients. Downregulation of APTR expression significantly inhibited the activities of LUAD cells. In addition, APTR targeted miR-298 and negatively regulated miR-298 expression. The inhibitory effect of APTR knockdown on LUAD cell activity was also reversed after transfection with miR-298 inhibitor. Increasing expression of APTR is associated with patients' poor prognosis, APTR targets miR-298 and promotes LUAD cellular activity through negative regulation of miR-298.

摘要

作为三大恶性肿瘤之一,肺腺癌(LUAD)具有进展迅速、死亡率高的特点,已成为危害人类健康的最危险因素。本研究旨在探索新的潜在分子靶点,探讨 lncRNA APTR 在 LUAD 中的调控作用,为 LUAD 治疗靶点的选择提供更充分的理论依据。通过 PCR 实验检测 APTR 在 LUAD 中的表达,通过卡方检验、多因素 Cox 回归和 Kaplan-Meier 分析 APTR 与患者临床状况和预后的关系。通过荧光素酶报告基因系统探索 APTR 与 miR-298 的相互作用以及 APTR/miR-298 对 LUAD 细胞活性的调节。结果发现,APTR 在 LUAD 组织和细胞中表达上调,APTR 的表达与淋巴结转移和 TNM 分期密切相关。LUAD 高表达也预示着患者预后不良。APTR 表达下调显著抑制 LUAD 细胞的活性。此外,APTR 靶向 miR-298 并负调控 miR-298 的表达。转染 miR-298 抑制剂后,APTR 敲低对 LUAD 细胞活性的抑制作用也得到逆转。APTR 表达的增加与患者预后不良有关,APTR 通过负调控 miR-298 靶向 miR-298 并促进 LUAD 细胞活性。

相似文献

1
Expression and Significance of the Long Non-Coding RNA APTR in the Occurrence and Development of Lung Adenocarcinoma.APTR 在肺腺癌发生发展中的表达及意义。
J Environ Pathol Toxicol Oncol. 2025;44(1):11-20. doi: 10.1615/JEnvironPatholToxicolOncol.2024053394.
2
LncRNA-LINC01089 inhibits lung adenocarcinoma cell proliferation and promotes apoptosis via sponging miR-543.长链非编码 RNA-LINC01089 通过海绵吸附 miR-543 抑制肺腺癌细胞增殖并促进细胞凋亡。
Tissue Cell. 2021 Oct;72:101535. doi: 10.1016/j.tice.2021.101535. Epub 2021 Mar 24.
3
lncRNA AGAP11 Suppresses Lung Adenocarcinoma Progression by miR-494-3p and Predicts Prognosis.lncRNA AGAP11 通过 miR-494-3p 抑制肺腺癌进展并预测预后。
J Environ Pathol Toxicol Oncol. 2024;43(4):1-11. doi: 10.1615/JEnvironPatholToxicolOncol.2024052122.
4
HCP5 is a SMAD3-responsive long non-coding RNA that promotes lung adenocarcinoma metastasis via miR-203/SNAI axis.HCP5 是一个 SMAD3 反应性的长非编码 RNA,通过 miR-203/SNAI 轴促进肺腺癌转移。
Theranostics. 2019 Apr 13;9(9):2460-2474. doi: 10.7150/thno.31097. eCollection 2019.
5
MicroRNA-147b promotes lung adenocarcinoma cell aggressiveness through negatively regulating microfibril-associated glycoprotein 4 (MFAP4) and affects prognosis of lung adenocarcinoma patients.微小 RNA-147b 通过负调控微纤维相关糖蛋白 4(MFAP4)促进肺腺癌细胞侵袭转移,并影响肺腺癌患者的预后。
Gene. 2020 Mar 10;730:144316. doi: 10.1016/j.gene.2019.144316. Epub 2019 Dec 26.
6
The long noncoding RNA LINC00483 promotes lung adenocarcinoma progression by sponging miR-204-3p.长链非编码 RNA LINC00483 通过海绵吸附 miR-204-3p 促进肺腺癌的进展。
Cell Mol Biol Lett. 2019 Dec 16;24:70. doi: 10.1186/s11658-019-0192-7. eCollection 2019.
7
The LncRNA NEAT1 Accelerates Lung Adenocarcinoma Deterioration and Binds to Mir-193a-3p as a Competitive Endogenous RNA.长链非编码RNA NEAT1通过作为竞争性内源RNA与Mir-193a-3p结合来加速肺腺癌恶化。
Cell Physiol Biochem. 2018;48(3):905-918. doi: 10.1159/000491958. Epub 2018 Jul 23.
8
Prognostic value of long noncoding RNA LINC00924 in lung adenocarcinoma and its regulatory effect on tumor progression.长链非编码 RNA LINC00924 在肺腺癌中的预后价值及其对肿瘤进展的调控作用。
Histol Histopathol. 2024 May;39(5):595-602. doi: 10.14670/HH-18-642. Epub 2023 Jun 26.
9
LncRNA TTN-AS1 promotes migration, invasion, and epithelial mesenchymal transition of lung adenocarcinoma via sponging miR-142-5p to regulate CDK5.长链非编码 RNA TTN-AS1 通过海绵吸附 miR-142-5p 调控 CDK5 促进肺腺癌迁移、侵袭和上皮间质转化。
Cell Death Dis. 2019 Jul 30;10(8):573. doi: 10.1038/s41419-019-1811-y.
10
LncRNA LINC00520 aggravates cell proliferation and migration in lung adenocarcinoma via a positive feedback loop.长链非编码 RNA LINC00520 通过正反馈环促进肺腺癌细胞的增殖和迁移。
BMC Pulm Med. 2021 Sep 8;21(1):287. doi: 10.1186/s12890-021-01657-6.

引用本文的文献

1
LncRNA APTR amplification serves as a potential glioma biomarker and promotes glioma progression via miR-6734-5p/ TCF7/LEF1 axis.长链非编码RNA APTR扩增作为一种潜在的神经胶质瘤生物标志物,并通过miR-6734-5p/TCF7/LEF1轴促进神经胶质瘤进展。
Noncoding RNA Res. 2025 Feb 22;12:42-55. doi: 10.1016/j.ncrna.2025.02.007. eCollection 2025 Jun.