MicroRNA-378 is associated with non-small cell lung cancer brain metastasis by promoting cell migration, invasion and tumor angiogenesis

被引:208
作者
Chen, Lan-tao [1 ]
Xu, Shi-dong [2 ]
Xu, Hai [2 ]
Zhang, Jin-feng [2 ]
Ning, Jin-feng [2 ]
Wang, Sheng-fa [1 ]
机构
[1] Harbin Med Univ, Affiliated Hosp 1, Dept Thorac Surg, Harbin 150001, Heilongjiang Pr, Peoples R China
[2] Harbin Med Univ, Affiliated Hosp 3, Dept Thorac Surg, Harbin 150001, Heilongjiang Pr, Peoples R China
关键词
NSCLC; MicroRNAs; Angiogenesis; VASCULOGENIC MIMICRY; EXPRESSION; SURVIVAL; PRECURSORS; MECHANISM; GROWTH; VEGF;
D O I
10.1007/s12032-011-0083-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Lung cancer is the leading cause of cancer deaths in the world. Brain metastasis (BM) can affect about 25% of non-small cell lung cancer (NSCLC) patients during their lifetime. Efforts to characterize patients that will develop BM have been disappointing. MicroRNAs (miRNAs) play a role in regulating a variety of targets and, consequently, multiple pathways, which make them a powerful tool for early detection of disease, risk assessment and prognosis. In this study, using RT-PCR and further northern blot validation, we confirmed that miR-378 was significantly differentially expressed in the matched NSCLC from 8 patients with BM and 21 without BM. Our study showed evidences that miR-378 is associated with non-small cell lung cancer brain metastasis by promoting cell migration, invasion and tumor angiogenesis. MiR-378 may be a potential biomarker for characterizing non-small cell lung cancer brain metastasis and assisting clinicians in stratifying the high-risk patients on a clinical trial for either prophylactic cranial irradiation or a new intervention that may mitigate BM development, ultimately leading to a new standard of care for NSCLC patients.
引用
收藏
页码:1673 / 1680
页数:8
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