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      N6‐methyladenosine demethylase FTO suppresses clear cell renal cell carcinoma through a novel FTO‐PGC‐1α signalling axis

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          Abstract

          The abundant and reversible N6‐methyladenosine (m6A) R NA modification and its modulators have important roles in regulating various gene expression and biological processes. Here, we demonstrate that fat mass and obesity associated ( FTO), as an m6A demethylase, plays a critical anti‐tumorigenic role in clear cell renal cell carcinoma (cc RCC). FTO is suppressed in cc RCC tissue. The low expression of FTO in human cc RCC correlates with increased tumour severity and poor patient survival. The Von Hippel‐Lindau‐deficient cells expressing FTO restores mitochondrial activity, induces oxidative stress and ROS production and shows impaired tumour growth, through increasing expression of PGC‐1α by reducing m6A levels in its mRNA transcripts. Our work demonstrates the functional importance of the m6A methylation and its modulator, and uncovers a critical FTOPGC‐1α axis for developing effective therapeutic strategies in the treatment of cc RCC.

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          Most cited references21

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          Mutations of the VHL tumour suppressor gene in renal carcinoma.

          Multiple, bilateral renal carcinomas are a frequent occurrence in von Hippel-Lindau (VHL) disease. To elucidate the aetiological role of the VHL gene in human kidney tumorigenesis, localized and advanced tumours from 110 patients with sporadic renal carcinoma were analysed for VHL mutations and loss of heterozygosity (LOH). VHL mutations were identified in 57% of clear cell renal carcinomas analysed and LOH was observed in 98% of those samples. Moreover, VHL was mutated and lost in a renal tumour from a patient with familial renal carcinoma carrying the constitutional translocation, t(3;8)(p14;q24). The identification of VHL mutations in a majority of localized and advanced sporadic renal carcinomas and in a second form of hereditary renal carcinoma indicates that the VHL gene plays a critical part in the origin of this malignancy.
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            The genetic basis of kidney cancer: a metabolic disease.

            Kidney cancer is not a single disease but comprises a number of different types of cancer that occur in the kidney, each caused by a different gene with a different histology and clinical course that responds differently to therapy. Each of the seven known kidney cancer genes, VHL, MET, FLCN, TSC1, TSC2, FH and SDH, is involved in pathways that respond to metabolic stress or nutrient stimulation. The VHL protein is a component of the oxygen and iron sensing pathway that regulates hypoxia-inducible factor (HIF) levels in the cell. HGF-MET signaling affects the LKB1-AMPK energy sensing cascade. The FLCN-FNIP1-FNIP2 complex binds AMPK and, therefore, might interact with the cellular energy and nutrient sensing pathways AMPK-TSC1/2-mTOR and PI3K-Akt-mTOR. TSC1-TSC2 is downstream of AMPK and negatively regulates mTOR in response to cellular energy deficit. FH and SDH have a central role in the mitochondrial tricarboxylic acid cycle, which is coupled to energy production through oxidative phosphorylation. Mutations in each of these kidney cancer genes result in dysregulation of metabolic pathways involved in oxygen, iron, energy or nutrient sensing, suggesting that kidney cancer is a disease of cell metabolism. Targeting the fundamental metabolic abnormalities in kidney cancer provides a unique opportunity for the development of more-effective forms of therapy for this disease.
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              ALKBH5-dependent m6A demethylation controls splicing and stability of long 3'-UTR mRNAs in male germ cells.

              N6-methyladenosine (m6A) represents one of the most common RNA modifications in eukaryotes. Specific m6A writer, eraser, and reader proteins have been identified. As an m6A eraser, ALKBH5 specifically removes m6A from target mRNAs and inactivation ofAlkbh5leads to male infertility in mice. However, the underlying molecular mechanism remains unknown. Here, we report that ALKBH5-mediated m6A erasure in the nuclei of spermatocytes and round spermatids is essential for correct splicing and the production of longer 3'-UTR mRNAs, and failure to do so leads to aberrant splicing and production of shorter transcripts with elevated levels of m6A that are rapidly degraded. Our study identified reversible m6A modification as a critical mechanism of posttranscriptional control of mRNA fate in late meiotic and haploid spermatogenic cells.
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                Author and article information

                Contributors
                fangtingzhang@126.com
                guiyaoting2007@aliyun.com
                Journal
                J Cell Mol Med
                J. Cell. Mol. Med
                10.1111/(ISSN)1582-4934
                JCMM
                Journal of Cellular and Molecular Medicine
                John Wiley and Sons Inc. (Hoboken )
                1582-1838
                1582-4934
                16 January 2019
                March 2019
                : 23
                : 3 ( doiID: 10.1111/jcmm.2019.23.issue-3 )
                : 2163-2173
                Affiliations
                [ 1 ] The Guangdong and Shenzhen Key Laboratory of Male Reproductive Medicine and Genetics Peking University Shenzhen Hospital, Institute of Urology of Shenzhen PKU‐HKUST Medical Center Shenzhen P.R. China
                [ 2 ] Assisted Reproduction Unit, Department of Obstetrics and Gynecology Sir Run Run Shaw Hospital, Zhejiang University School of Medicine Hangzhou P.R. China
                Author notes
                [*] [* ] Correspondence

                Yaoting Gui and Fangting Zhang, Guangdong and Shenzhen Key Laboratory of Male Reproductive Medicine and Genetics, Institute of Urology, Peking University Shenzhen Hospital, Shenzhen‐Peking University‐the Hong Kong University of Science and Technology Medical Center, Shenzhen, P.R. China.

                Emails: guiyaoting2007@ 123456aliyun.com and fangtingzhang@ 123456126.com

                Author information
                https://orcid.org/0000-0001-9989-1840
                Article
                JCMM14128
                10.1111/jcmm.14128
                6378205
                30648791
                07fd3172-c0e6-4212-aa15-1b2c4a3e1f15
                © 2019 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 28 August 2018
                : 26 November 2018
                : 09 December 2018
                Page count
                Figures: 7, Tables: 0, Pages: 11, Words: 5889
                Funding
                Funded by: Guangdong Key Laboratory of Male Reproductive Medicine and Genetics
                Award ID: 2017B030314074
                Funded by: Shenzhen Project of Science and Technology
                Award ID: JCYJ20170413100245260
                Funded by: “San‐ming” Project of Medicine in Shenzhen
                Award ID: SZSM201612066
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                jcmm14128
                March 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.5.9 mode:remove_FC converted:17.02.2019

                Molecular medicine
                ccrcc,fto,m6a,mitochondria,oxidative stress,pgc‐1α
                Molecular medicine
                ccrcc, fto, m6a, mitochondria, oxidative stress, pgc‐1α

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