4.6 Article

HMGCR positively regulated the growth and migration of glioblastoma cells

Journal

GENE
Volume 576, Issue 1, Pages 22-27

Publisher

ELSEVIER
DOI: 10.1016/j.gene.2015.09.067

Keywords

HMGCR; Glioblastoma; Cell growth and migration; Hippo pathway

Funding

  1. National Natural Science Foundation of China [81402963]
  2. China Postdoctoral Science Foundation [2013T60791]
  3. Science & Technology Project of Shenzhen Longgang District [YLWS20140609111127924]
  4. Healthy and Family Planning Commission of Hunan Province [B2015-120]

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The metabolic program of cancer cells is significant different from the normal cells, which makes it possible to develop novel strategies targeting cancer cells. Mevalonate pathway and its rate-limiting enzyme HMG-CoA reductase (HMGCR) have shown important roles in the progression of several cancer types. However, their roles in glioblastoma cells remain unknown. In this study, up-regulation of HMGCR in the clinical glioblastoma samples was observed. Forced expression of HMGCR promoted the growth and migration of U251 and U373 cells, while knocking down the expression of HMGCR inhibited the growth, migration and metastasis of glioblastoma cells. Molecular mechanism studies revealed that HMGCR positively regulated the expression of TAZ, an important mediator of Hippo pathway, and the downstream target gene connective tissue growth factor (CTGF), suggesting HMGCR might activate Hippo pathway in glioblastoma cells. Taken together, our study demonstrated the oncogenic roles of HMGCR in glioblastoma cells and HMGCR might be a promising therapeutic target. (C) 2015 Elsevier B.V. All rights reserved.

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