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                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Keyes, William M., 1973-</mods:namePart>
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               <mods:name>
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                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Pecoraro, Matteo, 1984-</mods:namePart>
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                  <mods:namePart>Aranda, Victoria</mods:namePart>
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                  <mods:namePart>Vernersson Lindahl, Emma</mods:namePart>
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                  <mods:namePart>Li, Wangzhi</mods:namePart>
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                  <mods:namePart>Vogel, Hannes</mods:namePart>
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                  <mods:namePart>Guo, Xuecui</mods:namePart>
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                  <mods:namePart>Garcia, Elvin L.</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Michurina, Tatyana V.</mods:namePart>
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                  <mods:namePart>Enikolopov, Grigori</mods:namePart>
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                  <mods:namePart>Muthuswamy, Senthil K.</mods:namePart>
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                  <mods:namePart>Mills, Alea A.</mods:namePart>
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                  <mods:dateIssued encoding="iso8601">2020-12-01T08:02:50Z2020-12-01T08:02:50Z2011</mods:dateIssued>
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               <mods:abstract>The p53 homolog p63 is essential for development, yet its role in cancer is not clear. We discovered that p63 deficiency evokes the tumor-suppressive mechanism of cellular senescence, causing a striking absence of stratified epithelia such as the skin. Here we identify the predominant p63 isoform, ΔNp63α, as a protein that bypasses oncogene-induced senescence to drive tumorigenesis in vivo. Interestingly, bypass of senescence promotes stem-like proliferation and maintains survival of the keratin 15-positive stem cell population. Furthermore, we identify the chromatin-remodeling protein Lsh as a new target of ΔNp63α that is an essential mediator of senescence bypass. These findings indicate that ΔNp63α is an oncogene that cooperates with Ras to promote tumor-initiating stem-like proliferation and suggest that Lsh-mediated chromatin-remodeling events are critical to this process.We thank Johannes Zuber, Michael Hemann, and Scott Lowe for assistance and advice; Yuri Lazebnik and Dominik Duelli for DMBA-treated tissues; Chris Johns and Sohail Khan for microarray analysis; and Leif Ellisen and James W. Rocco for HNSCC cell lines. W.M.K. was funded by the Spanish Ministry of Science and Innovation (Plan Nacional –SAF2010-18829). A.A.M. was funded by an ACS Research Scholar Award (RSG-06-190-01-MGO).</mods:abstract>
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               <mods:accessCondition type="useAndReproduction">© Elsevier This is the published version of an article http://dx.doi.org/10.1016/j.stem.2010.12.009 that appeared in the journal Cell stem cell. It is published in an Open Archive under an Elsevier user license. Details of this licence are available here: https://www.elsevier.com/about/our-business/policies/open-access-licenses/elsevier-user-license http://www.elsevier.com/open-access/userlicense/1.0/ info:eu-repo/semantics/openAccess</mods:accessCondition>
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                  <mods:title>ΔNp63α is an oncogene that targets chromatin remodeler Lsh to drive skin stem cell proliferation and tumorigenesis</mods:title>
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