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dc.contributor.authorNishita, Michiru
dc.contributor.authorPark, Seung-Yeol
dc.contributor.authorNishio, Tadashi
dc.contributor.authorKamizaki, Koki
dc.contributor.authorWang, ZhiChao
dc.contributor.authorTamada, Kota
dc.contributor.authorTakumi, Toru
dc.contributor.authorHashimoto, Ryuju
dc.contributor.authorOtani, Hiroki
dc.contributor.authorPazour, Gregory J.
dc.contributor.authorHsu, Victor W.
dc.contributor.authorMinami, Yasuhiro
dc.date2022-08-11T08:09:46.000
dc.date.accessioned2022-08-23T16:43:12Z
dc.date.available2022-08-23T16:43:12Z
dc.date.issued2017-01-26
dc.date.submitted2017-06-01
dc.identifier.citationSci Rep. 2017 Dec;7(1):1. doi: 10.1038/s41598-016-0028-x. Epub 2017 Jan 26. <a href="https://doi.org/10.1038/s41598-016-0028-x">Link to article on publisher's site</a>
dc.identifier.issn2045-2322 (Linking)
dc.identifier.doi10.1038/s41598-016-0028-x
dc.identifier.pmid28127051
dc.identifier.urihttp://hdl.handle.net/20.500.14038/40245
dc.description.abstractSignaling through the Ror2 receptor tyrosine kinase promotes invadopodia formation for tumor invasion. Here, we identify intraflagellar transport 20 (IFT20) as a new target of this signaling in tumors that lack primary cilia, and find that IFT20 mediates the ability of Ror2 signaling to induce the invasiveness of these tumors. We also find that IFT20 regulates the nucleation of Golgi-derived microtubules by affecting the GM130-AKAP450 complex, which promotes Golgi ribbon formation in achieving polarized secretion for cell migration and invasion. Furthermore, IFT20 promotes the efficiency of transport through the Golgi complex. These findings shed new insights into how Ror2 signaling promotes tumor invasiveness, and also advance the understanding of how Golgi structure and transport can be regulated.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=28127051&dopt=Abstract">Link to Article in PubMed</a>
dc.rightsCopyright © The Author(s) 2017
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectCancer Biology
dc.subjectCell Biology
dc.subjectCellular and Molecular Physiology
dc.titleRor2 signaling regulates Golgi structure and transport through IFT20 for tumor invasiveness
dc.typeJournal Article
dc.source.journaltitleScientific reports
dc.source.volume7
dc.source.issue1
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=4044&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/3039
dc.identifier.contextkey10236364
refterms.dateFOA2022-08-23T16:43:12Z
html.description.abstract<p>Signaling through the Ror2 receptor tyrosine kinase promotes invadopodia formation for tumor invasion. Here, we identify intraflagellar transport 20 (IFT20) as a new target of this signaling in tumors that lack primary cilia, and find that IFT20 mediates the ability of Ror2 signaling to induce the invasiveness of these tumors. We also find that IFT20 regulates the nucleation of Golgi-derived microtubules by affecting the GM130-AKAP450 complex, which promotes Golgi ribbon formation in achieving polarized secretion for cell migration and invasion. Furthermore, IFT20 promotes the efficiency of transport through the Golgi complex. These findings shed new insights into how Ror2 signaling promotes tumor invasiveness, and also advance the understanding of how Golgi structure and transport can be regulated.</p>
dc.identifier.submissionpathoapubs/3039
dc.contributor.departmentProgram in Molecular Medicine
dc.source.pages1


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