ung2008_Fig2

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Model Manuscripts

Simulation of the regulation of EGFR endocytosis and EGFR-ERK signaling by endophilin-mediated RhoA-EGFR crosstalk.

  • Choong Yong Ung
  • Hu Li
  • Xiao Hua Ma
  • Jia Jia
  • Bao Wen Li
  • Boon Chuan Low
  • Yu Zong Chen
FEBS Lett. 2008; 582 (15): 2283-2290
Abstract
Deregulations of EGFR endocytosis in EGFR-ERK signaling are known to cause cancers and developmental disorders. Mutations that impaired c-Cbl-EGFR association delay EGFR endocytosis and produce higher mitogenic signals in lung cancer. ROCK, an effector of small GTPase RhoA was shown to negatively regulate EGFR endocytosis via endophilin A1. A mathematical model was developed to study how RhoA and ROCK regulate EGFR endocytosis. Our study suggested that over-expressing RhoA as well as ROCK prolonged ERK activation partly by reducing EGFR endocytosis. Overall, our study hypothesized an alternative role of RhoA in tumorigenesis in addition to its regulation of cytoskeleton and cell motility.
Id Name JWS model
model0_Ung2008_EGFR_Endocytosis Ung2008_EGFR_Endocytosis ung1
Id Name Source Number of Data Sources
Id Name Model Simulation Simulation Simulation
task0_model0_Ung2008_EGFR_Endocytosis Ung2008_EGFR_Endocytosis 0.0 4000.0 1000

2D Plots

Id Name Number of Curves
Figure_2_Active_ERK_Control Figure 2 Active ERK (Control) 1
Figure_2_Internalised_endophilin_associated_EGFR_Control Figure 2 Internalised endophilin associated EGFR (Control) 1

CSV Reports

Id Name Number of Columns