Integrative Modeling of Signaling Network Dynamics Identifies Cell Type-Selective Therapeutic Strategies for

Sung-Young Shin1,2, Nicole J Chew1,2, Milad Ghomlaghi1,2

  • 1Cancer Program, Biomedicine Discovery Institute, Monash University, Melbourne, Australia.

Cancer Research
|August 1, 2024
PubMed

Insights

Targeting FGFR4 in cancer can lead to resistance. Computational modeling revealed that combining FGFR4 inhibitors with AKT or ErbB kinase inhibitors can overcome resistance in certain cancers, improving targeted therapy effectiveness.

Area of Science:

  • Oncology
  • Computational Biology
  • Systems Biology

Background:

  • Oncogenic FGFR4 signaling is a therapeutic target in cancers like triple-negative breast cancer and hepatocellular carcinoma.
  • Resistance to single-agent FGFR4 therapy necessitates the development of effective combination treatments.

Purpose of the Study:

  • To develop a computational model of FGFR4 signaling to understand resistance mechanisms.
  • To identify synergistic combination therapies for FGFR4-targeted treatments.

Main Methods:

  • Integrated computational network modeling and experimental validation.
  • Systematic simulation of cotargeting specific network nodes.
  • Incorporation of protein expression data from diverse cancer cell lines.

Main Results:

  • AKT reactivation was observed upon FGFR4 targeting in triple-negative breast cancer cells.
  • Synergy was predicted and validated for cotargeting FGFR4 with AKT or ErbB kinases, but not PI3K.
  • ERK reactivation and synergy with MEK inhibition were observed in specific hepatocellular carcinoma cell lines.

Conclusions:

  • Computational modeling provides insights into drug-induced network remodeling and resistance.
  • Protein expression heterogeneity influences targeted therapy response.
  • This approach enables the design of cell type-selective combination therapies for precision cancer treatment.

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