Rouhimoghadam2018 - GPR30/PI3K/MAPK/STAT signaling pathway in normal and cancer cells

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Short description

In the current study, we aimed to simulate the GPR30/PI3K/MAPK/STAT signaling pathway in normal and cancer cells by the use of ordinary differential equation modeling. In addition, we planned to show that MAPK activation pattern is different between normal and cancer models.

Format
SBML (L2V4)
Related Publication
  • Tamoxifen-induced apoptosis of MCF-7 cells via GPR30/PI3K/MAPKs interactions: Verification by ODE modeling and RNA sequencing
  • Milad Rouhimoghadam, Shahrokh Safarian, Jason S. Carroll, Nader Sheibani, Gholamreza Bidkhori
  • Frontiers in Physiology , 7/ 2018 , Volume 9 , Issue 907
  • Science for Life Laboratory, KTH - Royal Institute of Technology, SE-171 21, Stockholm, Sweden
  • Tamoxifen (Nolvadex) is one of the most widely used and effective therapeutic agent for breast cancer. It benefits nearly 75% of patients with ER-positive breast cancer that receive this drug. Its effectiveness is mainly attributed to its capacity to function as an estrogen receptor (ER) antagonist, blocking estrogen binding sites on the receptor, and inhibiting the proliferative action of the receptor-hormone complex. Although, tamoxifen can induce apoptosis in breast cancer cells via upregulation of pro-apoptotic factors, it can also promote uterine hyperplasia in some women. Thus, tamoxifen as a multi-functional drug could have different effects on cells based on the utilization of effective concentrations or availability of specific co-factors. Evidence that tamoxifen functions as a GPR30 (G-Protein Coupled Receptor 30) agonist activating adenylyl cyclase and EGFR (Epidermal Growth Factor Receptor) intracellular signaling networks, provides yet another means of explaining the multi-functionality of tamoxifen. Here ordinary differential equation (ODE) modeling, RNA sequencing and real time qPCR analysis were utilized to establish the necessary data for gene network mapping of tamoxifen-stimulated MCF-7 cells, which express the endogenous ER and GPR30. The gene set enrichment analysis and pathway analysis approaches were used to categorize transcriptionally upregulated genes in biological processes. Of the 2,713 genes that were significantly upregulated following a 48 h incubation with 250 μM tamoxifen, most were categorized as either growth-related or pro-apoptotic intermediates that fit into the Tp53 and/or MAPK signaling pathways. Collectively, our results display that the effects of tamoxifen on the breast cancer MCF-7 cell line are mediated by the activation of important signaling pathways including Tp53 and MAPKs to induce apoptosis.
Contributors
Milad Rouhimoghadam, Rahuman Sheriff

Metadata information

Curation status
Non-curated
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Model file

Rouhi 2018-GPR30 Axis - Normal Model.xml SBML L2V4 representation of Rouhimoghadam2018 - GPR30/PI3K/MAPK/STAT signaling pathway in normal and cancer cells 182.47 KB Preview | Download

Additional files

Rouhi 2018 - TMX-treated GPR30 axis.xml Rouhimoghadam 2018 - Tamoxifen-treated GPR30 axis - MCF-7 183.33 KB Preview | Download

  • Model originally submitted by : Milad Rouhimoghadam
  • Submitted: 12-Jul-2018 15:55:39
  • Last Modified: 12-Jul-2018 15:55:39
Revisions
  • Version: 6 public model Download this version
    • Submitted on: 12-Jul-2018 15:55:39
    • Submitted by: Rahuman Sheriff
    • With comment: Edited model metadata online.