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      MKRN2 inhibits migration and invasion of non-small-cell lung cancer by negatively regulating the PI3K/Akt pathway

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          Abstract

          Background

          Makorin RING zinc finger-2 ( MKRN2) belongs to the makorin RING zinc finger family and is a novel ubiquitin E3 ligase targeting the p65 subunit of NF-κB to negatively regulate inflammatory responses; however, the relationship between MKRN2 and tumorigenesis remains unclear. In this study, we clarified the role of MKRN2 in non-small cell lung cancer (NSCLC).

          Methods

          Tumor specimens collected from 261 NSCLC patients from 2013 to 2017 were retrieved from the Pathology Archive of the First Affiliated Hospital of China Medical University, and we performed assays to evaluate MKRN2 expression and to determine the impact of MKRN2 silencing and overexpression on NSCLC-cell migration and invasion.

          Results

          We demonstrated that MKRN2 expression was associated with lymph node metastasis, p-TNM stage, cancer-cell differentiation, and poor prognosis. By altering the expression of MKRN2 in selected cell lines, we found that MKRN2 inhibited cell migration and invasion through downregulation of the PI3K/Akt pathway.

          Conclusions

          These results suggested that MKRN2 inhibited NSCLC progression by reducing the metastatic potential of cancer cells. Our findings provide critical insight into the association of MKRN2 expression with favorable clinicopathological characteristics in NSCLC patients and suggested that MKRN2 plays a role in inhibiting NSCLC development.

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          Most cited references21

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          Akt signalling in health and disease.

          Akt (also known as protein kinase B or PKB) comprises three closely related isoforms Akt1, Akt2 and Akt3 (or PKBα/β/γ respectively). We have a very good understanding of the mechanisms by which Akt isoforms are activated by growth factors and other extracellular stimuli as well as by oncogenic mutations in key upstream regulatory proteins including Ras, PI3-kinase subunits and PTEN. There are also an ever increasing number of Akt substrates being identified that play a role in the regulation of the diverse array of biological effects of activated Akt; this includes the regulation of cell proliferation, survival and metabolism. Dysregulation of Akt leads to diseases of major unmet medical need such as cancer, diabetes, cardiovascular and neurological diseases. As a result there has been substantial investment in the development of small molecular Akt inhibitors that act competitively with ATP or phospholipid binding, or allosterically. In this review we will briefly discuss our current understanding of how Akt isoforms are regulated, the substrate proteins they phosphorylate and how this integrates with the role of Akt in disease. We will furthermore discuss the types of Akt inhibitors that have been developed and are in clinical trials for human cancer, as well as speculate on potential on-target toxicities, such as disturbances of heart and vascular function, metabolism, memory and mood, which should be monitored very carefully during clinical trial. Copyright © 2011 Elsevier Inc. All rights reserved.
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            Multiple modes of RNA recognition by zinc finger proteins.

            Zinc finger proteins are generally thought of as DNA-binding transcription factors; however, certain classes of zinc finger proteins, including the common C(2)H(2) zinc fingers, function as RNA-binding proteins. Recent structural studies of the C(2)H(2) zinc fingers of transcription factor IIIA (TFIIIA) and the CCCH zinc fingers of Tis11d in complex with their RNA targets have revealed new modes of zinc finger interaction with nucleic acid. The three C(2)H(2) zinc fingers of TFIIIA use two modes of RNA recognition that differ from the classical mode of DNA recognition, whereas the CCCH zinc fingers of Tis11d recognize specific AU-rich sequences through backbone atom interaction with the Watson-Crick edges of the adenine and uracil bases.
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              Pathology of lung cancer.

              This article reviews current concepts in pathologic classification of lung cancer based on 1999 World Health Organization (WHO)/International Association for the Study of Lung Cancer (IASLC) classification. Preinvasive lesions including squamous dysplasia/carcinoma in situ, atypical adenomatous hyperplasia and diffuse idiopathic pulmonary neuroendocrine cell hyperplasia are discussed in addition to current concepts of bronchioloalveolar carcinoma and neuroendocrine tumors.
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                Author and article information

                Contributors
                1634365033@qq.com
                573385698@qq.com
                355970063@qq.com
                809715970@qq.com
                164220719@qq.com
                1191233327@qq.com
                1055381795@qq.com
                JiangXz91@126.com
                jiang116027@163.com
                +86-13386881964 , xsqiu@cmu.edu.cn
                Journal
                J Exp Clin Cancer Res
                J. Exp. Clin. Cancer Res
                Journal of Experimental & Clinical Cancer Research : CR
                BioMed Central (London )
                0392-9078
                1756-9966
                13 August 2018
                13 August 2018
                2018
                : 37
                : 189
                Affiliations
                [1 ]GRID grid.412636.4, Department of Pathology, , First Affiliated Hospital College and of Basic Medical Sciences China Medical University, ; No. 155 Nanjing North Street, Heping District, Shenyang, 110001 Liaoning China
                [2 ]Jilin Zhongzheng Judicial Appraisal Institute, Changchun, China
                [3 ]Department of Pathology, General Hospital of Liaohe Oil Field, Panjin, China
                Author information
                http://orcid.org/0000-0001-9481-8249
                Article
                855
                10.1186/s13046-018-0855-7
                6090690
                30103781
                42cbe193-3d1d-4a46-bf17-428f8d20b9b7
                © The Author(s). 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 19 April 2018
                : 20 July 2018
                Funding
                Funded by: Liaoning Province Colleges and Universities Innovation Team
                Award ID: LC2015029
                Award Recipient :
                Categories
                Research
                Custom metadata
                © The Author(s) 2018

                Oncology & Radiotherapy
                non-small-cell lung cancer,mkrn2,cell migration,cell invasion,pi3k/akt pathway,ubiquitination

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