In this issue of , Xia and colleagues show that MYC-induced metabolic reprograming results in dependency on the serine-glycine-one-carbon (SGOC) metabolic pathway in neuroblastoma. This occurs through MYCN and ATF4 activation of the SGOC biosynthetic pathway in -amplified cells. Furthermore, inhibition of serine synthesis generates metabolic stress in -amplified neuroblastoma cells, causing cell-cycle arrest and autophagy. Together, these data suggest that the SGOC pathway is an attractive therapy target in neuroblastoma..
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http://dx.doi.org/10.1158/0008-5472.CAN-19-1816 | DOI Listing |
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