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结直肠癌细胞中外泌体微小RNA的筛选

Screening of exosomal microRNAs from colorectal cancer cells.

作者信息

Clancy Cillian, Khan Sonja, Glynn Claire L, Holian Emma, Dockery Peter, Lalor Pierce, Brown James A L, Joyce Myles R, Kerin Michael J, Dwyer Roisin M

机构信息

Discipline of Surgery, Lambe Institute for Translational Research, National University of Ireland Galway, Galway, Ireland.

School of Mathematics, Statistics and Applied Mathematics, National University of Ireland Galway, Galway, Ireland.

出版信息

Cancer Biomark. 2016;17(4):427-435. doi: 10.3233/CBM-160659.

Abstract

BACKGROUND

Cells release extracellular membrane vesicles including microvesicles known as exosomes. Exosomes contain microRNAs (miRNAs) however the full range within colorectal cancer cell secreted exosomes is unknown.

OBJECTIVE

To identify the full range of exosome encapsulated miRNAs secreted from 2 colorectal cancer cell lines and to investigate engineering of exosomes over-expressing miRNAs.

METHODS

Exosomes were isolated from HCT-116 and HT-29 cell lines. RNA was extracted from exosomes and microRNA array performed. Cells were engineered to express miR-379 (HCT-116-379) or a non-targeting control (HCT-116-NTC) and functional effects were determined. Exosomes secreted by engineered cells were transferred to recipient cells and the impact examined.

RESULTS

Microvesicles 40-100 nm in size secreted by cell lines were visualised and confirmed to express exosomal protein CD63. HT-29 exosomes contained 409 miRNAs, HCT-116 exosomes contained 393, and 338 were common to exosomes from both cell lines. Selected targets were validated. HCT-116-379 cells showed decreased proliferation (12-15% decrease, p < 0.001) and decreased migration (32-86% decrease, p < 0.001) compared to controls. HCT-116-379 exosomes were enriched for miR-379. Confocal microscopy visualised transfer of HCT-116-379 exosomes to recipient cells.

CONCLUSIONS

Colorectal cancer cells secrete a large number of miRNAs within exosomes. miR-379 decreases cell proliferation and migration, and miR-379 enriched exosomes can be engineered.

摘要

背景

细胞释放包括称为外泌体的微泡在内的细胞外膜泡。外泌体含有微小RNA(miRNA),但结直肠癌细胞分泌的外泌体中的全部miRNA种类尚不清楚。

目的

鉴定从2种结直肠癌细胞系分泌的外泌体中封装的全部miRNA种类,并研究过表达miRNA的外泌体的工程改造。

方法

从HCT-116和HT-29细胞系中分离外泌体。从外泌体中提取RNA并进行miRNA芯片分析。对细胞进行工程改造以表达miR-379(HCT-116-379)或非靶向对照(HCT-116-NTC),并确定其功能效应。将工程改造细胞分泌的外泌体转移至受体细胞并检查其影响。

结果

可视化细胞系分泌的大小为40-100nm的微泡,并证实其表达外泌体蛋白CD63。HT-29外泌体含有409种miRNA,HCT-116外泌体含有393种,两种细胞系的外泌体共有338种。对选定的靶标进行了验证。与对照相比,HCT-116-379细胞的增殖降低(降低12-15%,p<0.001),迁移降低(降低32-86%,p<0.001)。HCT-116-379外泌体富含miR-379。共聚焦显微镜观察到HCT-116-379外泌体向受体细胞的转移。

结论

结直肠癌细胞在外泌体中分泌大量miRNA。miR-379可降低细胞增殖和迁移,并且可以对外泌体进行工程改造以富集miR-379。

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