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10.1038/bjc.2017.118

http://scihub22266oqcxt.onion/10.1038/bjc.2017.118
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suck abstract from ncbi

pmid28472819
      Br+J+Cancer 2017 ; 116 (12 ): 1499-1504
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  • One-carbon metabolism in cancer #MMPMID28472819
  • Newman AC ; Maddocks ODK
  • Br J Cancer 2017[Jun]; 116 (12 ): 1499-1504 PMID28472819 show ga
  • Cells require one-carbon units for nucleotide synthesis, methylation and reductive metabolism, and these pathways support the high proliferative rate of cancer cells. As such, anti-folates, drugs that target one-carbon metabolism, have long been used in the treatment of cancer. Amino acids, such as serine are a major one-carbon source, and cancer cells are particularly susceptible to deprivation of one-carbon units by serine restriction or inhibition of de novo serine synthesis. Recent work has also begun to decipher the specific pathways and sub-cellular compartments that are important for one-carbon metabolism in cancer cells. In this review we summarise the historical understanding of one-carbon metabolism in cancer, describe the recent findings regarding the generation and usage of one-carbon units and explore possible future therapeutics that could exploit the dependency of cancer cells on one-carbon metabolism.
  • |*Metabolic Networks and Pathways [MESH]
  • |Amino Acids/*metabolism [MESH]
  • |Carbon/*metabolism [MESH]
  • |Humans [MESH]
  • |Methylation [MESH]
  • |NAD/biosynthesis [MESH]
  • |NADP/biosynthesis [MESH]
  • |Neoplasms/*drug therapy/*metabolism [MESH]


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