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      Promotion of trophoblast invasion by lncRNA MVIH through inducing Jun‐B

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          Abstract

          Preeclampsia ( PE), a pregnancy‐specific disorder, is associated with impaired uterine spiral artery remodelling, which is related to the dysfunction of trophoblast cells. Lately, mounting evidence has indicated that aberrant expression of long non‐coding RNAs (lnc RNAs) is associated with various human diseases. The lnc RNA MVIH transcript has been shown to decrease the severity of several diseases. However, the biological function of MVIH, which is down‐regulated in placental tissues in PE, has not yet been clarified. Here, we report that MVIH may act as a vital factor in the pathogenesis of PE. In this study, functional analysis revealed that the silencing of MVIH expression via transfection with small interfering RNA (si RNAs) inhibited cell growth, migration, invasion, and angiogenesis in various trophoblast cell lines, and stimulation with MVIH could promote these functions. Mass spectrometry analysis revealed that MVIH could modulate Jun‐B protein expression, which has been reported to potentially regulate cell growth and angiogenesis. Further cotransfection assays were performed, revealing that MVIH and Jun‐B have a synergistic effect on the regulation of angiogenesis and cell proliferation. Taking these findings together, MVIH could be associated with PE and may be a candidate biomarker for its diagnosis and treatment.

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          Transcriptional noise and the fidelity of initiation by RNA polymerase II.

          Eukaryotes transcribe much of their genomes, but little is known about the fidelity of transcriptional initiation by RNA polymerase II in vivo. I suggest that 90% of Pol II initiation events in yeast represent transcriptional noise, and that the specificity of initiation is comparable to that of DNA-binding proteins and other biological processes. This emphasizes the need to develop criteria that distinguish transcriptional noise from transcription with a biological function.
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            Long noncoding RNA associated with microvascular invasion in hepatocellular carcinoma promotes angiogenesis and serves as a predictor for hepatocellular carcinoma patients' poor recurrence-free survival after hepatectomy.

            Survival of patients with hepatocellular carcinoma (HCC) remains poor, which is largely attributed to active angiogenesis. However, the mechanisms underlying angiogenesis in HCC remain to be discovered. In this study, we found that long noncoding RNA associated with microvascular invasion in HCC (lncRNA MVIH) (lncRNA associated with microvascular invasion in HCC) was generally overexpressed in HCC. In a cohort of 215 HCC patients, the overexpression of MVIH was associated with frequent microvascular invasion (P = 0.016) and a higher tumor node metastasis stage (P = 0.009) as well as decreased recurrence-free survival (RFS) (P < 0.001) and overall survival (P = 0.007). Moreover, the up-regulation of MVIH served as an independent risk factor to predict poor RFS. We also found that MVIH could promote tumor growth and intrahepatic metastasis by activating angiogenesis in mouse models. Subsequent investigations indicated that MVIH could activate tumor-inducing angiogenesis by inhibiting the secretion of phosphoglycerate kinase 1 (PGK1). Additionally, in 65 HCC samples, MVIH expression was inversely correlated with the serum level of PGK1 and positively correlated with the microvessel density. Deregulation of lncRNA MVIH is a predictor for poor RFS of HCC patients after hepatectomy and could be utilized as a potential target for new adjuvant therapies against active angiogenesis. Copyright © 2012 American Association for the Study of Liver Diseases.
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              AP-1 in mouse development and tumorigenesis.

              Genetically modified mice have provided important insights into the biological functions of the dimeric transcription factor complex AP-1. Extensive analyses of mice and cells with genetically modified Fos or Jun proteins provide novel insights into the physiological functions of AP-1 proteins. Using knock-out strategies it was found that some components, such as c-Fos, FosB and JunD are dispensable, whereas others, like c-Jun, JunB and Fra-1 are essential in embryonic development and/or in the adult organism. Besides the specific roles of AP-1 proteins in developmental processes, we are beginning to obtain a better molecular understanding of the cell-context dependent function of AP-1 in cell proliferation and apoptosis, in bone biology as well as in multistep tumorigenesis.
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                Author and article information

                Contributors
                sunlizhou101@163.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
                30 October 2017
                February 2018
                : 22
                : 2 ( doiID: 10.1111/jcmm.2018.22.issue-2 )
                : 1214-1223
                Affiliations
                [ 1 ] Department of Obstetrics and Gynecology The Affiliated Yantai Yuhuangding Hospital of Qingdao University Yantai Shandong Province China
                [ 2 ] Department of Obstetrics and Gynecology The First Affiliated Hospital of Nanjing Medical University Nanjing JiangSu Province China
                [ 3 ] Department of General Surgery The Affiliated Yantai Yuhuangding Hospital of Qingdao University Yantai Shandong Province China
                Author notes
                [*] [* ] Correspondence to: Lizhou SUN

                E‐mail: sunlizhou101@ 123456163.com

                [†]

                These authors contributed equally and should be regarded as joint first authors.

                [‡]

                These authors should be regarded as joint corresponding authors.

                Author information
                http://orcid.org/0000-0002-0465-8825
                Article
                JCMM13400
                10.1111/jcmm.13400
                5783851
                29083110
                6d375830-903c-44b3-b584-b1af041cfa98
                © 2017 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 Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 11 April 2017
                : 28 August 2017
                Page count
                Figures: 7, Tables: 1, Pages: 10, Words: 5028
                Funding
                Funded by: National Natural Science Foundation of China
                Award ID: No: 81601307, NO.81771603 and NO. 81401229
                Funded by: Natural Science Foundation of Jiangsu Province
                Award ID: BK20161061
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                jcmm13400
                February 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.3.1 mode:remove_FC converted:24.01.2018

                Molecular medicine
                long non‐coding rnas,mvih,preeclampsia,jun‐b
                Molecular medicine
                long non‐coding rnas, mvih, preeclampsia, jun‐b

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