Using gene expression data to direct breast cancer therapy: evidence from a preclinical trial

Shams Reaz1, Deimante Tamkus2, Eran R Andrechek3

  • 1Department of Physiology, Michigan State University, 2194 BPS Building, 567 Wilson Road, East Lansing, MI, 48824, USA.

Journal of Molecular Medicine (Berlin, Germany)
|January 10, 2018
PubMed

Insights

Breast cancer

Area of Science:

  • Oncology
  • Genomics
  • Metabolomics

Background:

  • Breast cancer exhibits significant heterogeneity at genomic and metabolomic levels.
  • This heterogeneity activates numerous signaling networks, leading to treatment resistance.
  • Effective diagnosis and therapy are challenged by intra- and inter-tumor variability.

Purpose of the Study:

  • To review breast cancer classification and therapeutic strategies.
  • To examine model systems for personalized medicine approaches.
  • To assess the efficacy of targeting cell signaling pathways in preclinical models.

Main Methods:

  • Review of breast cancer subtypes: hormone-positive, HER2-positive, and triple-negative.
  • Evaluation of preclinical breast cancer models.
  • Testing a personalized medicine approach based on cell signaling pathway activation.

Main Results:

  • A preclinical trial demonstrated effective and specific blockage of tumor growth.
  • The approach was based solely on cell signaling pathway activation.
  • Personalized medicine targeting signaling pathways shows promise.

Conclusions:

  • Breast cancer heterogeneity necessitates advanced therapeutic strategies.
  • Targeting cell signaling pathways offers a viable personalized medicine approach.
  • Preclinical models are crucial for testing novel breast cancer therapies.

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