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10.1038/srep40538

http://scihub22266oqcxt.onion/10.1038/srep40538
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C5240092!5240092 !28094304
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suck abstract from ncbi


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pmid28094304
      Sci+Rep 2017 ; 7 (ä): 40538
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  • The different expression of TRPM7 and MagT1 impacts on the proliferation of colon carcinoma cells sensitive or resistant to doxorubicin #MMPMID28094304
  • Cazzaniga A ; Moscheni C ; Trapani V ; Wolf FI ; Farruggia G ; Sargenti A ; Iotti S ; Maier JA ; Castiglioni S
  • Sci Rep 2017[Jan]; 7 (ä): 40538 PMID28094304 show ga
  • The processes leading to anticancer drug resistance are not completely unraveled. To get insights into the underlying mechanisms, we compared colon carcinoma cells sensitive to doxorubicin with their resistant counterpart. We found that resistant cells are growth retarded, and show staminal and ultrastructural features profoundly different from sensitive cells. The resistant phenotype is accompanied by the upregulation of the magnesium transporter MagT1 and the downregulation of the ion channel kinase TRPM7. We demonstrate that the different amounts of TRPM7 and MagT1 account for the different proliferation rate of sensitive and resistant colon carcinoma cells. It remains to be verified whether they are also involved in the control of other "staminal" traits.
  • |Antibiotics, Antineoplastic/*pharmacology [MESH]
  • |Cation Transport Proteins/*genetics [MESH]
  • |Cell Proliferation [MESH]
  • |Colonic Neoplasms/*genetics [MESH]
  • |Doxorubicin/*pharmacology [MESH]
  • |Drug Resistance, Neoplasm/*genetics [MESH]
  • |Gene Expression Regulation, Neoplastic [MESH]
  • |Gene Silencing [MESH]
  • |Humans [MESH]
  • |Protein Serine-Threonine Kinases/*genetics [MESH]


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