Breast Cancer and Microcalcifications: An Osteoimmunological Disorder?

Int J Mol Sci. 2020 Nov 15;21(22):8613. doi: 10.3390/ijms21228613.

Abstract

The presence of microcalcifications in the breast microenvironment, combined with the growing evidences of the possible presence of osteoblast-like or osteoclast-like cells in the breast, suggest the existence of active processes of calcification in the breast tissue during a woman's life. Furthermore, much evidence that osteoimmunological disorders, such as osteoarthritis, rheumatoid arthritis, or periodontitis influence the risk of developing breast cancer in women exists and vice versa. Antiresorptive drugs benefits on breast cancer incidence and progression have been reported in the past decades. More recently, biological agents targeting pro-inflammatory cytokines used against rheumatoid arthritis also demonstrated benefits against breast cancer cell lines proliferation, viability, and migratory abilities, both in vitro and in vivo in xenografted mice. Hence, it is tempting to hypothesize that breast carcinogenesis should be considered as a potential osteoimmunological disorder. In this review, we compare microenvironments and molecular characteristics in the most frequent osteoimmunological disorders with major events occurring in a woman's breast during her lifetime. We also highlight what the use of bone anabolic drugs, antiresorptive, and biological agents targeting pro-inflammatory cytokines against breast cancer can teach us.

Keywords: T-cells; breast cancer; hydroxyapatite; inflammation; lobular involution; microcalcifications; osteoblast-like cells; osteoclast-like; osteoimmunological disorders; osteoimmunology.

Publication types

  • Review

MeSH terms

  • Anabolic Agents / therapeutic use*
  • Animals
  • Anti-Inflammatory Agents / therapeutic use*
  • Antineoplastic Agents / therapeutic use*
  • Arthritis, Rheumatoid / drug therapy
  • Arthritis, Rheumatoid / immunology
  • Arthritis, Rheumatoid / pathology
  • Breast Neoplasms* / drug therapy
  • Breast Neoplasms* / immunology
  • Breast Neoplasms* / pathology
  • Calcinosis* / drug therapy
  • Calcinosis* / immunology
  • Calcinosis* / pathology
  • Female
  • Humans
  • Mice
  • Tumor Microenvironment* / drug effects
  • Tumor Microenvironment* / immunology
  • Xenograft Model Antitumor Assays

Substances

  • Anabolic Agents
  • Anti-Inflammatory Agents
  • Antineoplastic Agents