Exosomes of glioma cells deliver miR-148a to promote proliferation and metastasis of glioblastoma via targeting CADM1

被引:72
|
作者
Cai, Qian [1 ]
Zhu, Anding [2 ]
Gong, Li [3 ]
机构
[1] Cent S Univ, Xiangya Hosp 3, Dept Pediat, Changsha 410013, Hunan, Peoples R China
[2] Cent S Univ, Xiangya Hosp 3, Dept Neurol, Changsha 410013, Hunan, Peoples R China
[3] Cent S Univ, Xiangya Hosp 3, Dept Anesthesiol, Changsha 410013, Hunan, Peoples R China
关键词
Glioma cells; miR-148a; Proliferation; Metastasis; CADM1; TUMOR-SUPPRESSOR; STAT3; ACTIVATION; INHIBITION; CANCER; PROGRESSION; EXPRESSION; MICRORNAS; CARCINOMA; GROWTH;
D O I
10.1016/j.bulcan.2018.05.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:643 / 651
页数:9
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