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酸性肿瘤微环境通过miR-451a/MEF2D轴促进胰腺癌。

Acidic Tumor Microenvironment Promotes Pancreatic Cancer through miR-451a/MEF2D Axis.

作者信息

Xu Jingyong, Li Yao, Li Zhe, Shao Weiwei, Song Jinghai, Wei Junmin

机构信息

Department of General Surgery & Hepato-Bilio-Pancreatic Surgery, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing 100730, China.

出版信息

J Oncol. 2022 Jan 12;2022:3966386. doi: 10.1155/2022/3966386. eCollection 2022.

Abstract

Pancreatic cancer (PC), as a highly malignant and aggressive solid tumor, is common in the digestive system. The acidic microenvironment is one of the critical markers of cancer. Nonetheless, there are few studies on how the acidic microenvironment affects the development of PC. This study focused on investigating the specific molecular mechanisms of the acidic microenvironment in PC. In our study, qRT-PCR was conducted for examining microRNA (miR)-451a and myocyte enhancer factor 2D (MEF2D) expressions in PANC-1 cells. Then, detailed functional effects of an acidic environment on miR-451a and MEF2D in PANC-1 cells were detected by CCK-8, colony formation, flow cytometry, wound healing, transwell, mitochondrial functionality measurement, JC-1 staining, DCFH-DA staining, and sphere formation assays. The relationship between miR-451a and MEF2D was confirmed by luciferase reporter analysis. Under acidic conditions, the increase of proliferation, migration, and invasion of PANC-1 cells was observed. Moreover, the mitochondrial oxidative respiration-related gene miR-451a was reduced in acidic conditions. In addition, we found that, in PANC-1 cells under an acidic environment, miR-451a overexpression enhanced oxygen consumption, mitochondrial membrane potential (MMP) loss, and ROS generation and inhibited proliferation, migration, invasion, and stemness via sponging MEF2D. In a word, our results revealed that the acidic microenvironment regulated PC progression by affecting the miR-451a/MEF2D axis, indicating a novel avenue for the future treatment of PC.

摘要

胰腺癌(PC)作为一种高度恶性且侵袭性强的实体瘤,在消化系统中较为常见。酸性微环境是癌症的关键标志物之一。然而,关于酸性微环境如何影响胰腺癌发展的研究较少。本研究聚焦于探究酸性微环境在胰腺癌中的具体分子机制。在我们的研究中,通过qRT-PCR检测PANC-1细胞中微小RNA(miR)-451a和肌细胞增强因子2D(MEF2D)的表达。然后,通过CCK-8、集落形成、流式细胞术、伤口愈合、transwell、线粒体功能测定、JC-1染色、DCFH-DA染色和球体形成实验,检测酸性环境对PANC-1细胞中miR-451a和MEF2D的详细功能影响。通过荧光素酶报告基因分析证实了miR-451a与MEF2D之间的关系。在酸性条件下,观察到PANC-1细胞的增殖、迁移和侵袭增加。此外,酸性条件下线粒体氧化呼吸相关基因miR-451a减少。另外,我们发现,在酸性环境下的PANC-1细胞中,miR-451a过表达通过海绵化MEF2D增强了氧消耗、线粒体膜电位(MMP)丧失和ROS生成,并抑制了增殖、迁移、侵袭和干性。总之,我们的结果表明酸性微环境通过影响miR-451a/MEF2D轴调节胰腺癌进展,为未来胰腺癌的治疗指明了一条新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/debf/8769849/625f6014bb72/JO2022-3966386.001.jpg

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