| Literature DB >> 29921422 |
Qian Cai1, Anding Zhu2, Li Gong3.
Abstract
Exosomes are now considered to be involved in mediating cell-to-cell communication to promote or inhibit tumor progression. However, the role and molecular mechanism of exosomes in promoting glioblastoma (GBM) metastasis remains elusive. Here, we found that circulating exosomal miR-148a levels were significantly higher in serum from GBM patients compared with serum from healthy volunteers. In T98G cells, inhibition of miR-148a suppressed cell proliferation and metastasis. In addition, we identified Cell adhesion molecule 1 (CADM1) as a target gene of miR-148a using luciferase reporter assay. Both protein and mRNA levels of CADM1 were decreased in tissues from GBM patients. There was a strong negative correlation between exosomal miR-148a and CADM1 mRNA levels in samples of patients. Moreover, miR-148a antagonist increased p-STAT3 protein level to activate STAT3 pathway. In conclusion, our findings indicated that miR-148a delivered by exosomes may promote cancer cell proliferation and metastasis via targeting CADM1 to activate STAT3 pathway, suggesting a predictor and therapeutic target role of exosomal miR-148a in GBM patients.Entities:
Keywords: CADM1; Cellules de gliome; Glioma cells; Metastasis; Métastase; Proliferation; Prolifération; miR-148a
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Year: 2018 PMID: 29921422 DOI: 10.1016/j.bulcan.2018.05.003
Source DB: PubMed Journal: Bull Cancer ISSN: 0007-4551 Impact factor: 1.276