Matches in SemOpenAlex for { <https://semopenalex.org/work/W2301478824> ?p ?o ?g. }
- W2301478824 endingPage "11486" @default.
- W2301478824 startingPage "11478" @default.
- W2301478824 abstract "// Jana Jezkova 1, * , Jason S. Williams 1, * , Filipe Pinto 2, 3 , Stephen J. Sammut 1 , Geraint T. Williams 4 , Simon Gollins 5 , Ramsay J. McFarlane 1, 6 , Rui Manuel Reis 2, 3, 7 , Jane A. Wakeman 1 1 North West Cancer Research Institute, School of Medical Sciences, Bangor University, Bangor, UK 2 Life and Health Sciences Research Institute (ICVS), School Health Sciences, University Minho, Braga, Portugal 3 ICVS/3B’s - PT Government Associate Laboratory, Braga/Guimarães, Portugal 4 Institute of Cancer and Genetics, Cardiff University Medical School, Cardiff, UK 5 North Wales Cancer Treatment Centre, Betsi Cadwaladr University Health Board, Bodelwyddan, UK 6 NISCHR Cancer Genetics Biomedical Research Unit, Cardiff, UK 7 Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos, SP, Brazil * These authors contributed equally to this work Correspondence to: Jane A. Wakeman, e-mail: j.a.wakeman@bangor.ac.uk Keywords: Brachyury, enteroendocrine cells, small intestine/colon, crypts, colorectal cancer Received: September 16, 2015 Accepted: January 23, 2016 Published: February 05, 2016 ABSTRACT Normal homeostasis of adult intestinal epithelium and repair following tissue damage is maintained by a balance of stem and differentiated cells, many of which are still only poorly characterised. Enteroendocrine cells of the gut are a small population of differentiated, secretory cells that are critical for integrating nutrient sensing with metabolic responses, dispersed amongst other epithelial cells. Recent evidence suggests that sub-sets of secretory enteroendocrine cells can act as reserve stem cells. Given the link between cells with stem-like properties and cancer, it is important that we identify factors that might provide a bridge between the two. Here, we identify a sub-set of chromogranin A-positive enteroendocrine cells that are positive for the developmental and cancer-associated transcription factor Brachyury in normal human small intestinal and colonic crypts. Whilst chromogranin A-positive enteroendocrine cells are also Brachyury-positive in colorectal tumours, expression of Brachyury becomes more diffuse in these samples, suggesting a more widespread function in cancer. The finding of the developmental transcription factor Brachyury in normal adult human intestinal crypts may extend the functional complexity of enteroendocrine cells and serves as a platform for assessment of the molecular processes of intestinal homeostasis that underpins our understanding of human health, cancer and aging." @default.
- W2301478824 created "2016-06-24" @default.
- W2301478824 creator A5000649001 @default.
- W2301478824 creator A5007814076 @default.
- W2301478824 creator A5028820548 @default.
- W2301478824 creator A5029890517 @default.
- W2301478824 creator A5033841355 @default.
- W2301478824 creator A5035432368 @default.
- W2301478824 creator A5043688244 @default.
- W2301478824 creator A5061698750 @default.
- W2301478824 creator A5072353812 @default.
- W2301478824 date "2016-02-05" @default.
- W2301478824 modified "2023-10-13" @default.
- W2301478824 title "Brachyury identifies a class of enteroendocrine cells in normal human intestinal crypts and colorectal cancer" @default.
- W2301478824 cites W1964118189 @default.
- W2301478824 cites W1970355875 @default.
- W2301478824 cites W1979433345 @default.
- W2301478824 cites W1980262797 @default.
- W2301478824 cites W1981656841 @default.
- W2301478824 cites W1988758354 @default.
- W2301478824 cites W1992583931 @default.
- W2301478824 cites W1995222383 @default.
- W2301478824 cites W1997085654 @default.
- W2301478824 cites W2002363917 @default.
- W2301478824 cites W2003299661 @default.
- W2301478824 cites W2004878973 @default.
- W2301478824 cites W2021013870 @default.
- W2301478824 cites W2043979562 @default.
- W2301478824 cites W2053352622 @default.
- W2301478824 cites W2082068596 @default.
- W2301478824 cites W2090562908 @default.
- W2301478824 cites W2114881954 @default.
- W2301478824 cites W2130217982 @default.
- W2301478824 cites W2133580699 @default.
- W2301478824 cites W2146328311 @default.
- W2301478824 cites W2157910818 @default.
- W2301478824 cites W2157987659 @default.
- W2301478824 cites W2158409531 @default.
- W2301478824 cites W2167479335 @default.
- W2301478824 cites W2171560127 @default.
- W2301478824 cites W2171759387 @default.
- W2301478824 cites W2172044251 @default.
- W2301478824 cites W2317164051 @default.
- W2301478824 cites W263786452 @default.
- W2301478824 doi "https://doi.org/10.18632/oncotarget.7202" @default.
- W2301478824 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4905487" @default.
- W2301478824 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26862851" @default.
- W2301478824 hasPublicationYear "2016" @default.
- W2301478824 type Work @default.
- W2301478824 sameAs 2301478824 @default.
- W2301478824 citedByCount "46" @default.
- W2301478824 countsByYear W23014788242016 @default.
- W2301478824 countsByYear W23014788242017 @default.
- W2301478824 countsByYear W23014788242018 @default.
- W2301478824 countsByYear W23014788242020 @default.
- W2301478824 countsByYear W23014788242021 @default.
- W2301478824 countsByYear W23014788242022 @default.
- W2301478824 countsByYear W23014788242023 @default.
- W2301478824 crossrefType "journal-article" @default.
- W2301478824 hasAuthorship W2301478824A5000649001 @default.
- W2301478824 hasAuthorship W2301478824A5007814076 @default.
- W2301478824 hasAuthorship W2301478824A5028820548 @default.
- W2301478824 hasAuthorship W2301478824A5029890517 @default.
- W2301478824 hasAuthorship W2301478824A5033841355 @default.
- W2301478824 hasAuthorship W2301478824A5035432368 @default.
- W2301478824 hasAuthorship W2301478824A5043688244 @default.
- W2301478824 hasAuthorship W2301478824A5061698750 @default.
- W2301478824 hasAuthorship W2301478824A5072353812 @default.
- W2301478824 hasBestOaLocation W23014788241 @default.
- W2301478824 hasConcept C103395026 @default.
- W2301478824 hasConcept C121608353 @default.
- W2301478824 hasConcept C126322002 @default.
- W2301478824 hasConcept C2908647359 @default.
- W2301478824 hasConcept C46699223 @default.
- W2301478824 hasConcept C502942594 @default.
- W2301478824 hasConcept C71315377 @default.
- W2301478824 hasConcept C71924100 @default.
- W2301478824 hasConcept C99454951 @default.
- W2301478824 hasConceptScore W2301478824C103395026 @default.
- W2301478824 hasConceptScore W2301478824C121608353 @default.
- W2301478824 hasConceptScore W2301478824C126322002 @default.
- W2301478824 hasConceptScore W2301478824C2908647359 @default.
- W2301478824 hasConceptScore W2301478824C46699223 @default.
- W2301478824 hasConceptScore W2301478824C502942594 @default.
- W2301478824 hasConceptScore W2301478824C71315377 @default.
- W2301478824 hasConceptScore W2301478824C71924100 @default.
- W2301478824 hasConceptScore W2301478824C99454951 @default.
- W2301478824 hasIssue "10" @default.
- W2301478824 hasLocation W23014788241 @default.
- W2301478824 hasLocation W23014788242 @default.
- W2301478824 hasLocation W23014788243 @default.
- W2301478824 hasLocation W23014788244 @default.
- W2301478824 hasLocation W23014788245 @default.
- W2301478824 hasLocation W23014788246 @default.
- W2301478824 hasLocation W23014788247 @default.
- W2301478824 hasOpenAccess W2301478824 @default.
- W2301478824 hasPrimaryLocation W23014788241 @default.
- W2301478824 hasRelatedWork W1506200166 @default.