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从人结直肠腺瘤和癌衍生的类器官中进行 microRNA 谱的综合分析。

Comprehensive Analysis of microRNA Profiles in Organoids Derived from Human Colorectal Adenoma and Cancer.

机构信息

Division of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.

Division of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan,

出版信息

Digestion. 2021;102(6):860-869. doi: 10.1159/000513882. Epub 2021 Mar 1.

Abstract

INTRODUCTION

Exosomes are membrane-enclosed nanovesicles, which are increasingly being recognized as important cell communication components for their role in transmitting microRNAs (miRNAs). No previous study has addressed the exosomal miRNA profile in colorectal adenomas (CRAs) because the long-term culture of CRA is challenging. This study aimed to identify the miRNA signature in organoid exosomes derived from human CRA and colorectal cancer (CRC) samples.

METHODS

Organoid cultures were developed from resected colorectal tissues of patients with CRA or CRC undergoing surgery or endoscopic mucosal resection. Exosomes were prepared from the conditioned medium of the organoids. miRNAs were prepared from the exosomes and their source organoids. The miRNA expression profiles were compared using microarray analysis. The impact of alteration of miRNA expression on cell proliferation was examined using miRNA mimics or inhibitors in HT-29 human CRC cells.

RESULTS

We established 6 organoid lines from CRC and 8 organoid lines from CRA. Exosomal miRNA signatures were different between the organoids derived from CRA and CRC. Both exosomal and cellular miR-1246 expressions were upregulated in CRC-derived organoids compared to their expression in CRA-derived organoids. Alteration of miR-1246 expression by the miR-1246 mimic or inhibitor increased or decreased cell proliferation in HT-29 cells, respectively.

CONCLUSIONS

We report for the first time the miRNA profiles of exosomes in CRA- and CRC-derived organoids. The upregulation of miR-1246 might play a role in increased cell proliferation in the process of CRA-carcinoma transition.

摘要

简介

外泌体是一种膜封闭的纳米囊泡,由于其在传递 microRNAs(miRNAs)方面的作用,它们越来越被认为是重要的细胞通讯成分。以前没有研究报道过结直肠腺瘤(CRAs)中外泌体的 miRNA 谱,因为长期培养 CRA 具有挑战性。本研究旨在鉴定源自人 CRA 和结直肠癌(CRC)样本的类器官外泌体中的 miRNA 特征。

方法

从接受手术或内镜黏膜切除术的 CRA 或 CRC 患者的切除结直肠组织中开发类器官培养物。从类器官的条件培养基中制备外泌体。从外泌体及其来源类器官中制备 miRNA。使用微阵列分析比较 miRNA 表达谱。使用 HT-29 人 CRC 细胞中的 miRNA 模拟物或抑制剂检查 miRNA 表达改变对细胞增殖的影响。

结果

我们从 CRC 建立了 6 个类器官系,从 CRA 建立了 8 个类器官系。源自 CRA 和 CRC 的类器官中外泌体 miRNA 特征不同。与 CRA 衍生的类器官相比,CRC 衍生的类器官中外泌体和细胞 miR-1246 的表达均上调。miR-1246 模拟物或抑制剂改变 miR-1246 的表达分别增加或减少 HT-29 细胞的增殖。

结论

我们首次报道了 CRA 和 CRC 衍生的类器官中外泌体的 miRNA 谱。miR-1246 的上调可能在 CRA-癌转变过程中增加细胞增殖中起作用。

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