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               <dc:title>Zonation of Ribosomal DNA Transcription Defines a Stem Cell Hierarchy in Colorectal Cancer</dc:title>
               <dc:creator>Morral, Clara</dc:creator>
               <dc:creator>Stanisavljevic, Jelena</dc:creator>
               <dc:creator>Hernando Momblona, Xavier</dc:creator>
               <dc:creator>Mereu, Elisabetta</dc:creator>
               <dc:creator>Álvarez Varela, Adrián</dc:creator>
               <dc:creator>Cortina, Carme</dc:creator>
               <dc:creator>Stork, Diana</dc:creator>
               <dc:creator>Slebe, Felipe</dc:creator>
               <dc:creator>Turon, Gemma</dc:creator>
               <dc:creator>Whissell, Gavin</dc:creator>
               <dc:creator>Sevillano, Marta</dc:creator>
               <dc:creator>Merlos Suárez, Anna</dc:creator>
               <dc:creator>Casanova Martí, Angela</dc:creator>
               <dc:creator>Moutinho, Cátia</dc:creator>
               <dc:creator>Lowe, Scott W.</dc:creator>
               <dc:creator>Dow, Lukas E.</dc:creator>
               <dc:creator>Villanueva Garatachea, Alberto</dc:creator>
               <dc:creator>Sancho, Elena</dc:creator>
               <dc:creator>Heyn, Holger</dc:creator>
               <dc:creator>Batlle, Eduard</dc:creator>
               <dc:subject>Càncer colorectal</dc:subject>
               <dc:subject>Cèl·lules mare</dc:subject>
               <dc:subject>Transcripció genètica</dc:subject>
               <dc:subject>Colorectal cancer</dc:subject>
               <dc:subject>Stem cells</dc:subject>
               <dc:subject>Genetic transcription</dc:subject>
               <dc:description>Colorectal cancers (CRCs) are composed of an amalgam of cells with distinct genotypes and phenotypes. Here, we reveal a previously unappreciated heterogeneity in the biosynthetic capacities of CRC cells. We discover that the majority of ribosomal DNA transcription and protein synthesis in CRCs occurs in a limited subset of tumor cells that localize in defined niches. The rest of the tumor cells undergo an irreversible loss of their biosynthetic capacities as a consequence of differentiation. Cancer cells within the biosynthetic domains are characterized by elevated levels of the RNA polymerase I subunit A (POLR1A). Genetic ablation of POLR1A-high cell population imposes an irreversible growth arrest on CRCs. We show that elevated biosynthesis defines stemness in both LGR5+ and LGR5− tumor cells. Therefore, a common architecture in CRCs is a simple cell hierarchy based on the differential capacity to transcribe ribosomal DNA and synthesize proteins.</dc:description>
               <dc:date>2020-05-15T11:54:19Z</dc:date>
               <dc:date>2021-05-11T05:10:17Z</dc:date>
               <dc:date>2020-05-11</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
               <dc:relation>Versió postprint del document publicat a: https://doi.org/10.1016/j.stem.2020.04.012</dc:relation>
               <dc:relation>Cell Stem Cell, 26, June, 2020</dc:relation>
               <dc:relation>https://doi.org/10.1016/j.stem.2020.04.012</dc:relation>
               <dc:rights>cc-by-nc-nd (c) Elsevier, 2020</dc:rights>
               <dc:rights>http://creativecommons.org/licenses/by-nc-nd/3.0/es/</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>Elsevier</dc:publisher>
               <dc:source>Articles publicats en revistes (Institut de Recerca Biomèdica (IRB Barcelona))</dc:source>
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