Frequency-Modulated Pulses of ERK Activity Transmit Quantitative Proliferation Signals

John Albeck, Gordon B. Mills, Joan S. Brugge

Research output: Contribution to journalArticle

206 Citations (Scopus)

Abstract

The EGF-stimulated ERK/MAPK pathway is a key conduit for cellular proliferation signals and a therapeutic target in many cancers. Here, we characterize two central quantitative aspects of this pathway: the mechanism by which signal strength is encoded and the response curve relating signal output to proliferation. Under steady-state conditions, we find that ERK is activated in discrete, asynchronous pulses with frequency and duration determined by extracellular concentrations of EGF spanning the physiological range. In genetically identical sister cells, cell-to-cell variability in pulse dynamics influences the decision to enter S phase. While targeted inhibition of EGFR reduces the frequency of ERK activity pulses, inhibition of MEK reduces their amplitude. Continuous response curves measured in multiple cell lines reveal that proliferation is effectively silenced only when ERK pathway output falls below a threshold of ∼10%, indicating that high-dose targeting of the pathway is necessary to achieve therapeutic efficacy.

Original languageEnglish (US)
Pages (from-to)249-261
Number of pages13
JournalMolecular Cell
Volume49
Issue number2
DOIs
StatePublished - Jan 24 2013
Externally publishedYes

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MAP Kinase Signaling System
Epidermal Growth Factor
Mitogen-Activated Protein Kinase Kinases
S Phase
Cell Proliferation
Cell Line
Therapeutics
Neoplasms

ASJC Scopus subject areas

  • Molecular Biology
  • Cell Biology

Cite this

Frequency-Modulated Pulses of ERK Activity Transmit Quantitative Proliferation Signals. / Albeck, John; Mills, Gordon B.; Brugge, Joan S.

In: Molecular Cell, Vol. 49, No. 2, 24.01.2013, p. 249-261.

Research output: Contribution to journalArticle

Albeck, John ; Mills, Gordon B. ; Brugge, Joan S. / Frequency-Modulated Pulses of ERK Activity Transmit Quantitative Proliferation Signals. In: Molecular Cell. 2013 ; Vol. 49, No. 2. pp. 249-261.
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