Stromal CCL5 Promotes Breast Cancer Progression by Interacting with CCR3 in Tumor Cells

Int J Mol Sci. 2021 Feb 15;22(4):1918. doi: 10.3390/ijms22041918.

Abstract

Chemokines secreted from stromal cells have important roles for interactions with carcinoma cells and regulating tumor progression. C-C motif chemokine ligand (CCL) 5 is expressed in various types of stromal cells and associated with tumor progression, interacting with C-C chemokine receptor (CCR) 1, 3 and 5 expressed in tumor cells. However, the expression on CCL5 and its receptors have so far not been well-examined in human breast carcinoma tissues. We therefore immunolocalized CCL5, as well as CCR1, 3 and 5, in 111 human breast carcinoma tissues and correlated them with clinicopathological characteristics. Stromal CCL5 immunoreactivity was significantly correlated with the aggressive phenotype of breast carcinomas. Importantly, this tendency was observed especially in the CCR3-positive group. Furthermore, the risk of recurrence was significantly higher in the patients with breast carcinomas positive for CCL5 and CCR3 but negative for CCR1 and CCR5, as compared with other patients. In summary, the CCL5-CCR3 axis might contribute to a worse prognosis in breast cancer patients, and these findings will contribute to a better understanding of the significance of the CCL5/CCRs axis in breast carcinoma microenvironment.

Keywords: breast carcinoma; chemokine; immunohistochemistry; prognosis; tumor microenvironment.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Breast Neoplasms / metabolism*
  • Breast Neoplasms / pathology
  • Breast Neoplasms / surgery
  • Chemokine CCL5 / metabolism*
  • Disease Progression*
  • Disease-Free Survival
  • Female
  • Follow-Up Studies
  • Humans
  • Immunohistochemistry
  • Middle Aged
  • Neoplasm Recurrence, Local / metabolism
  • Paracrine Communication
  • Prognosis
  • Receptors, CCR1 / metabolism
  • Receptors, CCR3 / metabolism*
  • Receptors, CCR5 / metabolism
  • Signal Transduction*
  • Stromal Cells / metabolism
  • Tumor Microenvironment

Substances

  • CCL5 protein, human
  • CCR1 protein, human
  • CCR3 protein, human
  • CCR5 protein, human
  • Chemokine CCL5
  • Receptors, CCR1
  • Receptors, CCR3
  • Receptors, CCR5