Downregulation of circulating miR 802-5p and miR 194-5p and upregulation of brain MEF2C along breast cancer brain metastasization

Breast cancer brain metastases (BCBM) have been under-investigated despite their high incidence and poor outcome. Micro RNAs (miRNAs), and particularly circulating miRNAs, regulate multiple cellular functions and their deregulation has been reported in different types of cancer and metastasis. Howev...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Sereno Marta
Haskó János
Molnár Kinga
Medina Sarah J
Reisz Zita
Malhó Rui
Videira Mafalda
Tiszlavicz László
Booth Stephanie A.
Wilhelm Imola Mária
Krizbai István Adorján
Brito Maria Alexandra
Dokumentumtípus: Cikk
Megjelent: 2020
Sorozat:MOLECULAR ONCOLOGY 14 No. 3
doi:10.1002/1878-0261.12632

mtmt:31133268
Online Access:http://publicatio.bibl.u-szeged.hu/20541
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520 3 |a Breast cancer brain metastases (BCBM) have been under-investigated despite their high incidence and poor outcome. Micro RNAs (miRNAs), and particularly circulating miRNAs, regulate multiple cellular functions and their deregulation has been reported in different types of cancer and metastasis. However, their signature in plasma along brain metastasis development and their relevant targets remain undetermined. Here, we used a mouse model of BCBM and Next-Generation Sequencing (NGS) to establish the alterations in circulating miRNAs during brain metastasis formation and development. We further performed bioinformatics analysis to identify their targets with relevance in the metastatic process. We additionally analyzed human resected brain metastasis samples of breast cancer patients for target expression validation. Breast cancer cells were injected in the carotid artery of mice to preferentially induce metastasis in the brain, and samples were collected at different time points (5 h, 3, 7 and 10 days) to follow metastasis development. Metastases were detected from 7 days onwards, mainly in the brain. NGS revealed a deregulation of circulating miRNA profile during BCBM progression, raising from 18% at 3 days to 30% at 10 days following malignant cells' injection. Work was focused on those altered prior to metastasis detection, among which were miR-802-5p and miR-194-5p, whose downregulation was validated by qPCR. Using TargetScan and DIANA Tools the transcription factor myocyte enhancer factor 2C (MEF2C) was identified as a target for both miRNAs, and its expression was increasingly observed in malignant cells along brain metastasis development. Its upregulation was also observed in peritumoral astrocytes pointing to a role of MEF2C in the crosstalk between tumor cells and astrocytes. MEF2C expression was also observed in human BCBM, validating the observation in mouse. Collectively, downregulation of circulating miR-802-5p and miR-194-5p appears as a precocious event in BCBM and MEF2C emerges as a new player in brain metastasis development. 
700 0 1 |a Haskó János  |e aut 
700 0 1 |a Molnár Kinga  |e aut 
700 0 1 |a Medina Sarah J  |e aut 
700 0 1 |a Reisz Zita  |e aut 
700 0 1 |a Malhó Rui  |e aut 
700 0 1 |a Videira Mafalda  |e aut 
700 0 1 |a Tiszlavicz László  |e aut 
700 0 1 |a Booth Stephanie A.  |e aut 
700 0 1 |a Wilhelm Imola Mária  |e aut 
700 0 1 |a Krizbai István Adorján  |e aut 
700 0 1 |a Brito Maria Alexandra  |e aut 
856 4 0 |u http://publicatio.bibl.u-szeged.hu/20541/1/SerenoMolOncol.pdf  |z Dokumentum-elérés