4.5 Editorial Material

The RAS-ERK pathway: A route for couples

期刊

SCIENCE SIGNALING
卷 11, 期 554, 页码 -

出版社

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/scisignal.aav0917

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资金

  1. MINECO/FEDER, UE [SAF-2015 63638R]
  2. Red Tematica de Investigacion Cooperativa sobre el Cancer (RTICC) [RD/12/0036/0033]
  3. Asociacion Espanola Contra el Cancer (AECC) [GCB141423113]
  4. ISCIII (MINECO) [FIS PI16/02137, RD12/0036/0001]
  5. JCyL [SA043U16 (UIC 076)]
  6. FEDER funds

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Data accumulated over more than three decades demonstrate that the assembly of macrocomplexes, mainly of dimers, is widespread among the members of the different tiers that constitute the RAS-ERK pathway. In this issue of Science Signaling, Yuan et al. report that MEK1 homodimerization is necessary for signal transduction through the RAF-ERK pathway and that cancer-related MEK1 mutations confer enhanced dimerization and resistance to MEK inhibitors. These findings endorse interference with RAS-ERK pathway-component dimerization as a potential therapeutic strategy in cancer patients.

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