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dc.contributor.authorRyu, Hye Guk
dc.contributor.authorJung, Youngseob
dc.contributor.authorLee, Namgyu
dc.contributor.authorSeo, Ji-Young
dc.contributor.authorKim, Sung Wook
dc.contributor.authorLee, Kyung-Ha
dc.contributor.authorKim, Do-Yeon
dc.contributor.authorKim, Kyong-Tai
dc.date2022-08-11T08:10:00.000
dc.date.accessioned2022-08-23T16:51:51Z
dc.date.available2022-08-23T16:51:51Z
dc.date.issued2021-05-23
dc.date.submitted2021-09-21
dc.identifier.citation<p>Ryu HG, Jung Y, Lee N, Seo JY, Kim SW, Lee KH, Kim DY, Kim KT. HNRNP A1 Promotes Lung Cancer Cell Proliferation by Modulating <em>VRK1</em> Translation. Int J Mol Sci. 2021 May 23;22(11):5506. doi: 10.3390/ijms22115506. PMID: 34071140; PMCID: PMC8197126. <a href="https://doi.org/10.3390/ijms22115506">Link to article on publisher's site</a></p>
dc.identifier.issn1422-0067 (Linking)
dc.identifier.doi10.3390/ijms22115506
dc.identifier.pmid34071140
dc.identifier.urihttp://hdl.handle.net/20.500.14038/41936
dc.description.abstractTHeterogeneous nuclear ribonucleoprotein (HNRNP) A1 is the most abundant and ubiquitously expressed member of the HNRNP protein family. In recent years, it has become more evident that HNRNP A1 contributes to the development of neurodegenerative diseases. However, little is known about the underlying role of HNRNP A1 in cancer development. Here, we report that HNRNP A1 expression is significantly increased in lung cancer tissues and is negatively correlated with the overall survival of patients with lung cancer. Additionally, HNRNP A1 positively regulates vaccinia-related kinase 1 (VRK1) translation via binding directly to the 3' untranslated region (UTR) of VRK1 mRNA, thus increasing cyclin D1 (CCND1) expression by VRK1-mediated phosphorylation of the cAMP response element-binding protein (CREB). Furthermore, HNRNP A1 binding to the cis-acting region of the 3'UTR of VRK1 mRNA contributes to increased lung cancer cell proliferation. Thus, our study unveils a novel role of HNRNP A1 in lung carcinogenesis via post-transcriptional regulation of VRK1 expression and suggests its potential as a therapeutic target for patients with lung cancer.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=34071140&dopt=Abstract">Link to Article in PubMed</a></p>
dc.rightsCopyright © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject3′UTR
dc.subjectHNRNP A1
dc.subjectVRK1
dc.subjectlung cancer
dc.subjectpost-transcriptional regulation
dc.subjectAmino Acids, Peptides, and Proteins
dc.subjectCancer Biology
dc.subjectEnzymes and Coenzymes
dc.subjectNeoplasms
dc.subjectNucleic Acids, Nucleotides, and Nucleosides
dc.subjectRespiratory Tract Diseases
dc.titleHNRNP A1 Promotes Lung Cancer Cell Proliferation by Modulating VRK1 Translation
dc.typeJournal Article
dc.source.journaltitleInternational journal of molecular sciences
dc.source.volume22
dc.source.issue11
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=5773&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/4740
dc.identifier.contextkey25048798
refterms.dateFOA2022-08-23T16:51:51Z
html.description.abstract<p>THeterogeneous nuclear ribonucleoprotein (HNRNP) A1 is the most abundant and ubiquitously expressed member of the HNRNP protein family. In recent years, it has become more evident that HNRNP A1 contributes to the development of neurodegenerative diseases. However, little is known about the underlying role of HNRNP A1 in cancer development. Here, we report that HNRNP A1 expression is significantly increased in lung cancer tissues and is negatively correlated with the overall survival of patients with lung cancer. Additionally, HNRNP A1 positively regulates vaccinia-related kinase 1 (VRK1) translation via binding directly to the 3' untranslated region (UTR) of VRK1 mRNA, thus increasing cyclin D1 (CCND1) expression by VRK1-mediated phosphorylation of the cAMP response element-binding protein (CREB). Furthermore, HNRNP A1 binding to the cis-acting region of the 3'UTR of VRK1 mRNA contributes to increased lung cancer cell proliferation. Thus, our study unveils a novel role of HNRNP A1 in lung carcinogenesis via post-transcriptional regulation of VRK1 expression and suggests its potential as a therapeutic target for patients with lung cancer.</p>
dc.identifier.submissionpathoapubs/4740
dc.contributor.departmentDepartment of Molecular, Cell and Cancer Biology
dc.source.pages5506


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Copyright © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's license is described as Copyright © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).