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      Gene expression changes in subcutaneous adipose tissue due to Cushing's disease

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          Abstract

          Glucocorticoids have major effects on adipose tissue metabolism. To study tissue mRNA expression changes induced by chronic elevated endogenous glucocorticoids, we performed RNA sequencing on the subcutaneous adipose tissue from patients with Cushing's disease ( n=5) compared to patients with nonfunctioning pituitary adenomas ( n=11). We found a higher expression of transcripts involved in several metabolic pathways, including lipogenesis, proteolysis and glucose oxidation as well as a decreased expression of transcripts involved in inflammation and protein synthesis. To further study this in a model system, we subjected mice to dexamethasone treatment for 12 weeks and analyzed their inguinal (subcutaneous) fat pads, which led to similar findings. Additionally, mice treated with dexamethasone showed drastic decreases in lean body mass as well as increased fat mass, further supporting the human transcriptomic data. These data provide insight to transcriptional changes that may be responsible for the comorbidities associated with chronic elevations of glucocorticoids.

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          Most cited references42

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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              Mechanisms of glucocorticoid-induced insulin resistance: focus on adipose tissue function and lipid metabolism.

              Glucocorticoids (GCs) are critical in the regulation of the stress response, inflammation and energy homeostasis. Excessive GC exposure results in whole-body insulin resistance, obesity, cardiovascular disease, and ultimately decreased survival, despite their potent anti-inflammatory effects. This apparent paradox may be explained by the complex actions of GCs on adipose tissue functionality. The wide prevalence of oral GC therapy makes their adverse systemic effects an important yet incompletely understood clinical problem. This article reviews the mechanisms by which supraphysiologic GC exposure promotes insulin resistance, focusing in particular on the effects on adipose tissue function and lipid metabolism. Copyright © 2014 Elsevier Inc. All rights reserved.
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                Author and article information

                Journal
                J Mol Endocrinol
                J. Mol. Endocrinol
                JME
                Journal of Molecular Endocrinology
                Bioscientifica Ltd (Bristol )
                0952-5041
                1479-6813
                October 2015
                6 July 2015
                : 55
                : 2
                : 81-94
                Affiliations
                [1 ]Institute of Endocrinology, Diabetes and Metabolism, Rambam Health Care Campus , Haifa, Israel
                [2 ]Life Science Institute, University of Michigan , Ann Arbor, MI, USA
                [3 ]Physiology, UTHSC , Memphis, TN, USA
                [4 ]Preventive Medicine, UTHSC , Memphis, TN, USA
                [5 ]Internal Medicine, University of Michigan , Ann Arbor, TN, USA
                [6 ]Neurosurgery, University of Michigan , Ann Arbor, MI, USA
                [7 ]Pediatrics, UTHSC , Memphis, TN, USA
                Author notes
                Correspondence should be addressed to I Hochberg or D Bridges Emails: i_hochberg@ 123456rambam.health.gov.il or dbridge9@ 123456uthsc.edu
                Article
                JME150119
                10.1530/JME-15-0119
                4543687
                26150553
                8917eb83-a82d-4d0a-b461-545c052fec5f
                © 2015 The authors

                This work is licensed under a Creative Commons Attribution 3.0 Unported License

                History
                : 26 June 2015
                : 6 July 2015
                Categories
                Research

                Endocrinology & Diabetes
                cushing's syndrome,lipolysis,insulin resistance,glucocorticoid,lipogenesis,rna sequencing,transcriptome

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