24
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      DCLK1 marks a morphologically distinct subpopulation of cells with stem cell properties in preinvasive pancreatic cancer.

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          As in other tumor types, progression of pancreatic cancer may require a functionally unique population of cancer stem cells. Although such cells have been identified in many invasive cancers, it is not clear whether they emerge during early or late stages of tumorigenesis. Using mouse models and human pancreatic cancer cell lines, we investigated whether preinvasive pancreatic neoplasia contains a subpopulation of cells with distinct morphologies and cancer stem cell-like properties.

          Related collections

          Author and article information

          Journal
          Gastroenterology
          Gastroenterology
          Elsevier BV
          1528-0012
          0016-5085
          Jan 2014
          : 146
          : 1
          Affiliations
          [1 ] Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland; The McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
          [2 ] Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland.
          [3 ] Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
          [4 ] Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
          [5 ] Department of Medicine, Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts; Department of Internal Medicine, Medical University Hospital, Tuebingen, Germany.
          [6 ] Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
          [7 ] Department of Medicine, Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, Massachusetts.
          [8 ] Department of Pathology, The Sol Goldman Pancreatic Cancer Research Center, Johns Hopkins University School of Medicine, Baltimore, Maryland.
          [9 ] Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland; The McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland. Electronic address: stleach@jhmi.edu.
          Article
          S0016-5085(13)01411-X NIHMS544570
          10.1053/j.gastro.2013.09.050
          3910427
          24096005
          365f8185-9c7d-446e-aefc-924daa82e49c
          History

          ADM,AcTub,Acetylated Tubulin,Dclk1,FACS,GFP,Kras,Notch,PDAC,PanIN,TEM,acetylated α-tubulin,acinar-to-ductal metaplasia,doublecortin and Ca(2+)/calmodulin-dependent kinase-like 1,fluorescence-activated cell sorting,green fluorescent protein,mPanIN,murine pancreatic intraepithelial neoplasia,pancreatic ductal adenocarcinoma,pancreatic intraepithelial neoplasia,transmission electron microscopy

          Comments

          Comment on this article