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MicroRNA-550a-3-5p controls the brain metastasis of lung cancer by directly targeting YAP1

BACKGROUND: This study aimed to explore the potential regulatory mechanisms of brain metastasis and to identify novel underlying targets of lung cancer with brain metastasis. METHODS: Exosomes were isolated from the plasma of lung cancer patients with or without brain metastasis and low or high meta...

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Detalles Bibliográficos
Autores principales: Wei, Liang, Wang, Guangxue, Yang, Cheng, Zhang, Yanfei, Chen, Yiming, Zhong, Chunlong, Li, Qinchuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8444378/
https://www.ncbi.nlm.nih.gov/pubmed/34530822
http://dx.doi.org/10.1186/s12935-021-02197-z
Descripción
Sumario:BACKGROUND: This study aimed to explore the potential regulatory mechanisms of brain metastasis and to identify novel underlying targets of lung cancer with brain metastasis. METHODS: Exosomes were isolated from the plasma of lung cancer patients with or without brain metastasis and low or high metastatic lung cancer cells, and small RNA from plasma-derived exosomes were sequenced. Differentially expressed miRNAs (DE-miRNAs) were identified. Human brain microvascular endothelial cells (HBMECs) were transfected with miR-550a-3-5p mimics or inhibitors and exosomes. Cell viability, migration, and apoptosis/cycle were determined using Cell Counting Kit-8 (CCK-8), Transwell, and flow cytometry, respectively. Western blotting was used to measure the expression of the associated proteins. Finally, a dual-luciferase reporter gene assay was performed to confirm the miR-550a-3-5p target. RESULTS: Transmission electron microscopy, NanoSight, and western blotting showed that exosomes were successfully isolated and cell-derived exosomes could be taken up by HBMECs. Sequencing identified 22 DE-miRNAs which were enriched in the MAPK, chemokine, PPAR, and Wnt signaling pathways. MiR-550a-3-5p was significantly enriched in brain metastatic exosomes. Cellular experiments showed that miR-550a-3-5p and exosome enrichment significantly inhibited cell viability and migration, promoted apoptosis, and regulated the cell cycle of HBMECs compared with the controls (P  <  0.05). Compared with the controls, high levels of both miR-550a-3-5p and exosomes markedly upregulated cleaved-PARP expression, but downregulated the expression of pRB, CDK6, YAP1, CTGF, and CYR61 (P  <  0.05). Finally, YAP1 was confirmed to bind directly to miR-550a-3-5p. CONCLUSION: Our results indicate that miR-550a-3-5p and YAP1 may be novel potential targets for controlling brain metastasis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-021-02197-z.