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10.1016/j.stem.2016.10.018

http://scihub22266oqcxt.onion/10.1016/j.stem.2016.10.018
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suck abstract from ncbi


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pmid27889319
      Cell+Stem+Cell 2017 ; 20 (2 ): 191-204.e5
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  • Cell-Type-Specific Chromatin States Differentially Prime Squamous Cell Carcinoma Tumor-Initiating Cells for Epithelial to Mesenchymal Transition #MMPMID27889319
  • Latil M ; Nassar D ; Beck B ; Boumahdi S ; Wang L ; Brisebarre A ; Dubois C ; Nkusi E ; Lenglez S ; Checinska A ; Vercauteren Drubbel A ; Devos M ; Declercq W ; Yi R ; Blanpain C
  • Cell Stem Cell 2017[Feb]; 20 (2 ): 191-204.e5 PMID27889319 show ga
  • Epithelial to mesenchymal transition (EMT) in cancer cells has been associated with metastasis, stemness, and resistance to therapy. Some tumors undergo EMT while others do not, which may reflect intrinsic properties of their cell of origin. However, this possibility is largely unexplored. By targeting the same oncogenic mutations to discrete skin compartments, we show that cell-type-specific chromatin and transcriptional states differentially prime tumors to EMT. Squamous cell carcinomas (SCCs) derived from interfollicular epidermis (IFE) are generally well differentiated, while hair follicle (HF) stem cell-derived SCCs frequently exhibit EMT, efficiently form secondary tumors, and possess increased metastatic potential. Transcriptional and epigenomic profiling revealed that IFE and HF tumor-initiating cells possess distinct chromatin landscapes and gene regulatory networks associated with tumorigenesis and EMT that correlate with accessibility of key epithelial and EMT transcription factor binding sites. These findings highlight the importance of chromatin states and transcriptional priming in dictating tumor phenotypes and EMT.
  • |*Epithelial-Mesenchymal Transition [MESH]
  • |Animals [MESH]
  • |Base Sequence [MESH]
  • |Carcinogenesis/pathology [MESH]
  • |Carcinoma, Squamous Cell/genetics/*pathology [MESH]
  • |Cell Differentiation [MESH]
  • |Cell Lineage/genetics [MESH]
  • |Chromatin/*metabolism [MESH]
  • |Clone Cells [MESH]
  • |Epigenesis, Genetic [MESH]
  • |Epithelial Cells/metabolism/pathology [MESH]
  • |HEK293 Cells [MESH]
  • |Hair Follicle/pathology [MESH]
  • |Humans [MESH]
  • |Mice [MESH]
  • |Neoplasm Metastasis [MESH]
  • |Neoplastic Stem Cells/*pathology [MESH]
  • |Phosphoproteins/metabolism [MESH]
  • |Repressor Proteins/metabolism [MESH]
  • |Skin Neoplasms/genetics/*pathology [MESH]
  • |Trans-Activators/metabolism [MESH]


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