Down‐expression of miR‐154 suppresses tumourigenesis in CD133+ glioblastoma stem cells |
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Authors: | Liang Yang Zhongjie Yan Yuanyu Wang Wandong Ma Chen Li |
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Affiliation: | Department of Neurosurgery, The Second Hospital of Hebei Medical University, Shijiazhuang, China |
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Abstract: | Glioblastoma multiforme (GBM) is the most common and aggressive form of brain cancer. Evidences have suggested that CD133 is a marker for a subset of glioblastoma cancer stem cells. However, whether miRNA plays a critical role in CD133+ GBM is poorly understood. Here, we identified that miR‐154 was upregulated in CD133+ GBM cell lines. Knockdown of miR‐154 remarkably suppressed proliferation and migration of CD133+ GBM cells. Further study found that PRPS1 was a direct target of miR‐154 in CD133+ GBM cells. Overexpression of PRPS1 exhibited similar effects as miR‐154 knockdown in CD133+ GBMs. Our study identified miR‐154 as a previously unrecognized positive regulator of proliferation and migration in CD133+ GBM cells and a potentially therapeutic target of GBMs. Copyright © 2016 John Wiley & Sons, Ltd. |
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Keywords: | glioblastoma stem cells CD133 miR‐154 PRPS1 cell proliferation |
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