Suppression of miR‐199a maturation by HuR is crucial for hypoxia‐induced glycolytic switch in hepatocellular carcinoma-Reference-Cited by-同舟云学术

Suppression of miR‐199a maturation by HuR is crucial for hypoxia‐induced glycolytic switch in hepatocellular carcinoma

Published:2015-09-07 Issue:21 Volume:34 Page:2671-2685
ISSN:0261-4189
Container-title:The EMBO Journal
language:en
Short-container-title:EMBO J

Author:

Zhang Ling‐Fei¹²,Lou Jia‐Tao³,Lu Ming‐Hua¹²,Gao Chunfang⁴,Zhao Shuang¹²,Li Biao⁵,Liang Sheng⁶,Li Yong⁷,Li Dangsheng⁸,Liu Mo‐Fang¹²

Affiliation:

1. Center for RNA Research State Key Laboratory of Molecular Biology‐University of Chinese Academy of Sciences Institute of Biochemistry and Cell Biology Shanghai Institutes for Biological Sciences Chinese Academy of Sciences Shanghai China

2. Shanghai Key Laboratory of Molecular Andrology Institute of Biochemistry and Cell Biology Shanghai Institutes for Biological Sciences Chinese Academy of Sciences Shanghai China

3. Department of Laboratory Medicine Shanghai Chest Hospital Shanghai Jiao Tong University Shanghai China

4. Department of Laboratory Medicine Eastern Hepatobiliary Surgical Hospital Second Military Medical University Shanghai China

5. Department of Nuclear Medicine and Micro PET Center Rui Jin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine Shanghai China

6. Department of Nuclear Medicine Xin Hua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine Shanghai China

7. Department of Cancer Biology Lerner Research Institute Cleveland Clinic Cleveland OH USA

8. Shanghai Information Center for Life Sciences Shanghai Institutes for Biological Sciences Chinese Academy of Sciences Shanghai China

Publisher

EMBO

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Molecular Biology,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/embj.201591803

Reference50 articles.

1. Hypoxic Regulation of Glucose Transport, Anaerobic Metabolism and Angiogenesis in Cancer: Novel Pathways and Targets for Anticancer Therapeutics

2. Reductive metabolism of the hypoxia marker pimonidazole is regulated by oxygen tension independent of the pyridine nucleotide redox state

3. The Hypoxia-Inducible MicroRNA Cluster miR-199a∼214 Targets Myocardial PPARδ and Impairs Mitochondrial Fatty Acid Oxidation

4. Inhibition of hypoxia-induced miR-155 radiosensitizes hypoxic lung cancer cells

5. MicroRNA-199a targets CD44 to suppress the tumorigenicity and multidrug resistance of ovarian cancer-initiating cells

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