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10.1186/s12943-015-0330-4

http://scihub22266oqcxt.onion/10.1186/s12943-015-0330-4
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suck abstract from ncbi


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pmid25879211
      Mol+Cancer 2015 ; 14 (ä): 61
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  • The calcium-sensing receptor suppresses epithelial-to-mesenchymal transition and stem cell- like phenotype in the colon #MMPMID25879211
  • Aggarwal A ; Prinz-Wohlgenannt M ; Gröschel C ; Tennakoon S ; Meshcheryakova A ; Chang W ; Brown EM ; Mechtcheriakova D ; Kállay E
  • Mol Cancer 2015[Mar]; 14 (ä): 61 PMID25879211 show ga
  • BACKGROUND: The calcium sensing receptor (CaSR), a calcium-binding G protein-coupled receptor is expressed also in tissues not directly involved in calcium homeostasis like the colon. We have previously reported that CaSR expression is down-regulated in colorectal cancer (CRC) and that loss of CaSR provides growth advantage to transformed cells. However, detailed mechanisms underlying these processes are largely unknown. METHODS AND RESULTS: In a cohort of 111 CRC patients, we found significant inverse correlation between CaSR expression and markers of epithelial-to-mesenchymal transition (EMT), a process involved in tumor development in CRC. The colon of CaSR/PTH double-knockout, as well as the intestine-specific CaSR knockout mice showed significantly increased expression of markers involved in the EMT process. In vitro, stable expression of the CaSR (HT29(CaSR)) gave a more epithelial-like morphology to HT29 colon cancer cells with increased levels of E-Cadherin compared with control cells (HT29(EMP)). The HT29(CaSR) cells had reduced invasive potential, which was attributed to the inhibition of the Wnt/?-catenin pathway as measured by a decrease in nuclear translocation of ?-catenin and transcriptional regulation of genes like GSK-3? and Cyclin D1. Expression of a spectrum of different mesenchymal markers was significantly down-regulated in HT29(CaSR) cells. The CaSR was able to block upregulation of mesenchymal markers even in an EMT-inducing environment. Moreover, overexpression of the CaSR led to down-regulation of stem cell-like phenotype. CONCLUSIONS: The results from this study demonstrate that the CaSR inhibits epithelial-to-mesenchymal transition and the acquisition of a stem cell-like phenotype in the colon of mice lacking the CaSR as well as colorectal cancer cells, identifying the CaSR as a key molecule in preventing tumor progression. Our results support the rationale to develop new strategies either preventing CaSR loss or reversing its silencing.
  • |Animals [MESH]
  • |Cadherins/genetics [MESH]
  • |Cell Line, Tumor [MESH]
  • |Colon/*metabolism [MESH]
  • |Colonic Neoplasms/genetics [MESH]
  • |Cyclin D1/genetics [MESH]
  • |Down-Regulation/genetics [MESH]
  • |Epithelial-Mesenchymal Transition/*genetics/physiology [MESH]
  • |Gene Expression Regulation, Neoplastic/genetics [MESH]
  • |Glycogen Synthase Kinase 3 beta [MESH]
  • |Glycogen Synthase Kinase 3/genetics [MESH]
  • |HT29 Cells [MESH]
  • |Humans [MESH]
  • |Mice [MESH]
  • |Mice, Knockout [MESH]
  • |Phenotype [MESH]
  • |Receptors, Calcium-Sensing/*genetics [MESH]
  • |Stem Cells/*metabolism [MESH]
  • |Transcription, Genetic/genetics [MESH]
  • |Up-Regulation/genetics [MESH]
  • |Wnt Signaling Pathway/genetics [MESH]


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