Comparative aspects of canine and human inflammatory breast cancer

Semin Oncol. 2017 Aug;44(4):288-300. doi: 10.1053/j.seminoncol.2017.10.012. Epub 2018 Jan 19.

Abstract

Inflammatory breast cancer (IBC) in humans is the most aggressive form of mammary gland cancer and shares clinical, pathologic, and molecular patterns of disease with canine inflammatory mammary carcinoma (CIMC). Despite the use of multimodal therapeutic approaches, including targeted therapies, the prognosis for IBC/CIMC remains poor. The aim of this review is to critically analyze IBC and CIMC in terms of biology and clinical features. While rodent cancer models have formed the basis of our understanding of cancer biology, the translation of this knowledge into improved outcomes has been limited. However, it is possible that a comparative "one health" approach to research, using a natural canine model of the disease, may help advance our knowledge on the biology of the disease. This will translate into better clinical outcomes for both species. We propose that CIMC has the potential to be a useful model for developing and testing novel therapies for IBC. Further, this strategy could significantly improve and accelerate the design and establishment of new clinical trials to identify novel and improved therapies for this devastating disease in a more predictable way.

Keywords: CIMC; Canine inflammatory mammary carcinoma; Comparative oncology; Dog; IBC; Immunotherapy; Inflammatory breast cancer; Preclinical models.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Dog Diseases / etiology
  • Dog Diseases / therapy*
  • Dogs
  • EGF Family of Proteins / genetics
  • EGF Family of Proteins / metabolism
  • Female
  • Humans
  • Inflammatory Breast Neoplasms / etiology*
  • Inflammatory Breast Neoplasms / pathology
  • Inflammatory Breast Neoplasms / therapy
  • Inflammatory Breast Neoplasms / veterinary*
  • Prognosis
  • Receptor, ErbB-2 / genetics
  • Receptor, ErbB-2 / metabolism
  • Receptors, Chemokine / genetics
  • Receptors, Chemokine / metabolism

Substances

  • EGF Family of Proteins
  • Receptors, Chemokine
  • ERBB2 protein, human
  • Receptor, ErbB-2