Suppr超能文献

含有微小RNA - 425的人骨髓间充质干细胞衍生外泌体通过下调CPEB1促进迁移、侵袭和肺转移。

Human bone marrow mesenchymal stem cell-derived exosomes containing microRNA-425 promote migration, invasion and lung metastasis by down-regulating CPEB1.

作者信息

Wang Guoqiang, Ji Xiuli, Li Pan, Wang Wei

机构信息

Department of Oncology, Binzhou Central Hospital, Binzhou, Shandong 251700, PR China.

Department of Respiratory, Jinan Municipal Hospital of Traditional Chinese Medicine, Jinan, Shandong 250012, PR China.

出版信息

Regen Ther. 2022 Apr 25;20:107-116. doi: 10.1016/j.reth.2022.03.007. eCollection 2022 Jun.

Abstract

OBJECTIVE

Bone marrow mesenchymal stem cell-derived exosomes (BMSC-Exos) could mediate the malignancy of tumor cells by transmitting targeted cargo. Therein, this study intends to explore the function of BMSC-Exos transmitting microRNA-425 (miR-425)/cytoplasmic polyadenylation binding protein 1 (CPEB1) in lung cancer growth.

METHODS

miR-425 and CPEB1 levels in cancer tissues and cells were measured. BMSCs and their exosomes were collected and identified. After intervention with BMSC-Exos, miR-425 or CPEB1, invasion and migration of A549 and NCI-H1299 cells , and lung metastasis of A549 cells were observed. The relationship between miR-425 and CPEB1 was verified.

RESULTS

miR-425 was highly expressed while CPEB1 was lowly expressed in lung cancer tissues of patients. CPEB1 was the direct target of miR-425. Down-regulating miR-425 or up-regulating CPEB1 decreased cell invasion and migration ability of A549 and NCI-H1299 cells, as well as decreased the number of lung metastasis lesions . After co-culture with BMSC-Exos, A549 and NCI-H1299 cells showed promoted migration and invasion and A549 cells demonstrated increased lung metastasis . Down-regulated miR-425 or up-regulated CPEB1 reversed the promotion of BMSC-Exos on lung cancer cell invasion, migration and lung metastasis.

CONCLUSION

BMSC-Exos could deliver miR-425 to inhibit CPEB1 expression in lung cancer cells, thereby promoting the malignant biological properties of lung cancer cells and their metastasis .

摘要

目的

骨髓间充质干细胞来源的外泌体(BMSC-Exos)可通过传递靶向物质介导肿瘤细胞的恶性行为。本研究旨在探讨BMSC-Exos传递微小RNA-425(miR-425)/细胞质聚腺苷酸化结合蛋白1(CPEB1)在肺癌生长中的作用。

方法

检测癌组织和细胞中miR-425和CPEB1的水平。收集并鉴定BMSCs及其外泌体。用BMSC-Exos、miR-425或CPEB1干预后,观察A549和NCI-H1299细胞的侵袭和迁移能力以及A549细胞的肺转移情况。验证miR-425与CPEB1之间的关系。

结果

患者肺癌组织中miR-425高表达而CPEB1低表达。CPEB1是miR-425的直接靶点。下调miR-425或上调CPEB1可降低A549和NCI-H1299细胞的侵袭和迁移能力,以及减少肺转移灶数量。与BMSC-Exos共培养后,A549和NCI-H1299细胞的迁移和侵袭能力增强,A549细胞的肺转移增加。下调miR-425或上调CPEB1可逆转BMSC-Exos对肺癌细胞侵袭、迁移和肺转移的促进作用。

结论

BMSC-Exos可递送miR-425抑制肺癌细胞中CPEB1的表达,从而促进肺癌细胞的恶性生物学特性及其转移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7ad/9061616/a5710db35ffd/gr1.jpg

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