| Literature DB >> 22592534 |
Chao Zou1, Qing Xu, Feng Mao, Dan Li, Chuanxiu Bian, Ling-Zhi Liu, Yue Jiang, Xiaona Chen, Yanting Qi, Xiaolong Zhang, Xuejing Wang, Qiang Sun, Hsiang-Fu Kung, Marie C Lin, Andreas Dress, Fiona Wardle, Bing-Hua Jiang, Lihui Lai.
Abstract
MiR-145 is known as a tumor suppressor in numerous human cancers. However, its role in tumor angiogenesis remains poorly defined. In this study, we found that miR-145 was significantly downregulated in breast cancer tissues by using 106 cases of normal and cancer tissues as well as in breast cancer cells. MiR-145 exhibited inhibitory role in tumor angiogenesis, cell growth and invasion and tumor growth through the post-transcriptional regulation of the novel targets N-RAS and VEGF-A. In addition, we provide evidence that the expression levels of miR-145 correlate inversely with malignancy stages of breast tumors, although there is no association between miR-145 levels and hormone receptor levels in breast cancer. Taken together, these results demonstrate that miR-145 plays important inhibitory role in breast cancer malignancy by targeting N-RAS and VEGF-A, which may be potential therapeutic and diagnostic targets.Entities:
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Year: 2012 PMID: 22592534 PMCID: PMC3368865 DOI: 10.4161/cc.20598
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534