Caloric restriction coupled with radiation decreases metastatic burden in triple negative breast cancer

Cell Cycle. 2016 Sep;15(17):2265-74. doi: 10.1080/15384101.2016.1160982. Epub 2016 Mar 30.

Abstract

Purpose: Metastatic breast cancer is devastating and triple negative breast cancers (TNBC) have a higher propensity for metastasis. Improved local control upfront in this aggressive cancer could potentially decrease its propensity toward metastasis. We sought to determine if using caloric restriction (CR) as a systemic therapy, combined with radiation therapy (IR) to the primary tumor, may impact metastatic disease.

Methods: An orthotopic mouse model using a highly metastatic, luciferase-tagged TNBC cell line (4T1), was used to generate palpable tumors. Mice were then treated with CR, IR, and a combination of the two. In vivo imaging was performed for metastatic evaluation. Molecular evaluation of the tumors was performed, generating a mechanistic hypothesis for CR, which was then tested with pertinent pathway inhibition in the model.

Results: CR significantly increased the time to developing metastases, decreased the overall number and volume of lung metastases, and increased survival. CR decreased proliferation, increased apoptosis and globally downregulated the IGF-1R signaling pathway. Adding an IGF-1R/INSR inhibitor to local IR in vivo accomplished a decrease in metastases similar to CR plus IR, demonstrating the importance of the IGF-1R signaling pathway, and underscoring it as a possible mechanism for CR.

Conclusions: CR decreased metastatic burden and therefore may complement cytotoxic therapies being used in the clinical setting for metastatic disease. Downregulation of the IGF-1R pathway, is in part responsible for this response and modulating IGF-1R directly resulted in similar improved progression-free survival. The novel use of CR has the potential to enhance clinical outcomes for patients with metastatic breast cancer.

Keywords: Caloric restriction; breast cancer; metastases.

MeSH terms

  • Animals
  • Apoptosis
  • Caloric Restriction*
  • Cell Proliferation
  • Combined Modality Therapy
  • Female
  • Humans
  • Insulin-Like Growth Factor I / metabolism
  • Luminescent Measurements
  • Lung / pathology
  • Lung Neoplasms / pathology
  • Lung Neoplasms / secondary*
  • Mammary Neoplasms, Experimental / pathology*
  • Mammary Neoplasms, Experimental / radiotherapy
  • Mammary Neoplasms, Experimental / therapy*
  • Mice, Inbred BALB C
  • Proto-Oncogene Proteins c-akt / metabolism
  • Radiation, Ionizing
  • Receptor, IGF Type 1 / metabolism
  • Signal Transduction
  • Survival Analysis
  • Tissue Extracts
  • Triple Negative Breast Neoplasms / pathology*
  • Triple Negative Breast Neoplasms / radiotherapy
  • Triple Negative Breast Neoplasms / therapy*

Substances

  • Tissue Extracts
  • Insulin-Like Growth Factor I
  • Receptor, IGF Type 1
  • Proto-Oncogene Proteins c-akt