Oncotarget

Research Papers:

Circadian clock components RORα and Bmal1 mediate the anti-proliferative effect of MLN4924 in osteosarcoma cells

Shuju Zhang, Jiaming Zhang, Zhiyuan Deng, Huadie Liu, Wei Mao, Fang Jiang, Zanxian Xia and Jia-Da Li _

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Oncotarget. 2016; 7:66087-66099. https://doi.org/10.18632/oncotarget.11807

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Abstract

Shuju Zhang1, Jiaming Zhang1, Zhiyuan Deng2, Huadie Liu1, Wei Mao1, Fang Jiang1, Zanxian Xia1, Jia-Da Li1

1The State Key Laboratory of Medical Genetics and School of Life Sciences, Central South University, Changsha, Hunan 410078, China

2Xiangya Stomatological Hospital, Central South University, Changsha, Hunan 410078, China

Correspondence to:

Jia-Da Li, email: lijiada@sklmg.edu.cn

Keywords: MLN4924, osteosarcoma, RORα, Bmal1, neddylation

Received: May 03, 2016    Accepted: August 24, 2016    Published: September 01, 2016

ABSTRACT

The anticancer small molecule MLN4924, a Nedd8-activating enzyme (NAE) inhibitor, triggers cell-cycle arrest, apoptosis, and senescence in cancer cells. In this study, we demonstrate that MLN4924 suppresses osteosarcoma cell proliferation by inducing G2/M cell cycle arrest and apoptosis. Our results indicate that MLN4924 stabilizes the retinoid orphan nuclear receptor alpha (RORα) by decreasing its ubiquitination. RNA interference of RORα attenuates the anti-proliferative effect of MLN4924 in U2OS osteosarcoma cells. MLN4924 up-regulates the expression of p21 and Bmal1, two transcriptional targets of RORα. However, p21 plays a minimal role in the anti-proliferative effect of MLN4924 in U2OS osteosarcoma cells. In contrast, Bmal1 suppression by siRNA attenuates the anti-proliferative effect of MLN4924 in U2OS osteosarcoma cells, indicating that the MLN4924-mediated cell growth inhibition is mediated by Bmal1. These results show MLN4924 to be a promising therapeutic agent for the treatment of osteosarcoma and suggest that MLN4924-induced tumor growth inhibition is mediated by the circadian clock components RORα and Bmal1.


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