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dc.contributor.authorSmith, Jordan L.
dc.contributor.authorLee, Liam C.
dc.contributor.authorRead, Abigail
dc.contributor.authorLi, Qiuning
dc.contributor.authorYu, Bing
dc.contributor.authorLee, Chih-Shia
dc.contributor.authorLuo, Ji
dc.date2022-08-11T08:09:46.000
dc.date.accessioned2022-08-23T16:42:57Z
dc.date.available2022-08-23T16:42:57Z
dc.date.issued2016-11-11
dc.date.submitted2017-04-14
dc.identifier.citationCell Biosci. 2016 Nov 11;6:57. eCollection 2016. <a href="https://doi.org/10.1186/s13578-016-0122-6">Link to article on publisher's site</a>
dc.identifier.issn2045-3701 (Linking)
dc.identifier.doi10.1186/s13578-016-0122-6
dc.identifier.pmid27891214
dc.identifier.urihttp://hdl.handle.net/20.500.14038/40194
dc.description.abstractBACKGROUND: The ability to transform normal human cells into cancer cells with the introduction of defined genetic alterations is a valuable method for understanding the mechanisms of oncogenesis. Easy establishment of immortalized but non-transformed human cells from various tissues would facilitate these genetic analyses. RESULTS: We report here a simple, one-step immortalization method that involves retroviral vector mediated co-expression of the human telomerase protein and a shRNA targeting the CDKN2A gene locus. We demonstrate that this method could successfully immortalize human small airway epithelial cells while maintaining their chromosomal stability. We further showed that these cells retain p53 activity and can be transformed by the KRAS oncogene. CONCLUSIONS: Our method simplifies the immortalization process and is broadly applicable for establishing immortalized epithelial cell lines from primary human tissues for cancer research.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=27891214&dopt=Abstract">Link to Article in PubMed</a>
dc.rights© The Author(s) 2016.
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectCancer Biology
dc.subjectCell Biology
dc.titleOne-step immortalization of primary human airway epithelial cells capable of oncogenic transformation
dc.typeJournal Article
dc.source.journaltitleCell and bioscience
dc.source.volume6
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=3997&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/2992
dc.identifier.contextkey10021731
refterms.dateFOA2022-08-23T16:42:57Z
html.description.abstract<p>BACKGROUND: The ability to transform normal human cells into cancer cells with the introduction of defined genetic alterations is a valuable method for understanding the mechanisms of oncogenesis. Easy establishment of immortalized but non-transformed human cells from various tissues would facilitate these genetic analyses.</p> <p>RESULTS: We report here a simple, one-step immortalization method that involves retroviral vector mediated co-expression of the human telomerase protein and a shRNA targeting the CDKN2A gene locus. We demonstrate that this method could successfully immortalize human small airway epithelial cells while maintaining their chromosomal stability. We further showed that these cells retain p53 activity and can be transformed by the KRAS oncogene.</p> <p>CONCLUSIONS: Our method simplifies the immortalization process and is broadly applicable for establishing immortalized epithelial cell lines from primary human tissues for cancer research.</p>
dc.identifier.submissionpathoapubs/2992
dc.contributor.departmentSchool of Medicine
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.source.pages57


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© The Author(s) 2016.
Except where otherwise noted, this item's license is described as © The Author(s) 2016.