Multi-Drug Resistance and Breast Cancer Progression via Toll-Like Receptors (TLRs) Signaling

Cell Biochem Biophys. 2024 Dec;82(4):3015-3030. doi: 10.1007/s12013-024-01418-2. Epub 2024 Aug 7.

Abstract

Toll-like receptors (TLRs) are essential receptors involved in inflammation and innate immunity. Various types of cancer cells, as well as innate immune cells, express TLRs. There is mounting proof that TLRs are critical to the development and spread of cancer as well as metabolism. In breast cancer, up-regulated levels of TLRs have been linked to the aggressiveness of the diseases, worse treatment outcomes, and the emergence of therapeutic resistance. Patients with advanced non-resectable, recurring, and metastatic breast cancer currently have few available treatment choices. An intriguing new strategy is an innate immunity-mediated anticancer immunotherapy, either used alone or in conjunction with existing treatments. In fact, several TLR agonists and antagonists have been used in clinical studies for anti-cancer immunotherapy. Consequently, TLRs serve as critical targets for controlling the course of breast cancer and treatment resistance in addition to being implicated in immune responses against pathogen infection and cancer immunology. In this review, we deliver an overview of the most current findings on TLR involvement in the development of breast cancer and treatment resistance.

Keywords: Breast cancer; Drug resistance; Pathogenesis; Progression; Toll-like receptors (TLRs).

Publication types

  • Review

MeSH terms

  • Breast Neoplasms* / drug therapy
  • Breast Neoplasms* / immunology
  • Breast Neoplasms* / metabolism
  • Breast Neoplasms* / pathology
  • Disease Progression
  • Drug Resistance, Multiple
  • Drug Resistance, Neoplasm*
  • Female
  • Humans
  • Immunity, Innate / drug effects
  • Signal Transduction* / drug effects
  • Toll-Like Receptors* / metabolism

Substances

  • Toll-Like Receptors