Molecular Targets of Triple-Negative Breast Cancer: Where Do We Stand?

Cancers (Basel)

Department of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, LA 70112, USA.

Published: January 2022

AI Article Synopsis

  • Triple-negative breast cancer (TNBC) is an aggressive subtype of breast cancer that lacks hormone receptors, making it more likely to spread and resist treatment compared to other types.
  • Treatment traditionally focuses on chemotherapy and breast conserving surgery, but many patients experience chemotherapy resistance and local tumor recurrence.
  • Emerging immunotherapies targeting specific immune pathways are showing promise in improving survival rates, with ongoing research likely to transform TNBC treatment options in the future.

Article Abstract

Triple-negative breast cancer (TNBC) is a highly aggressive form of breast cancer. Due to its heterogeneity and lack of hormone receptor expression, this subtype is more likely to metastasize and resist treatment attempts than are other forms of breast cancer. Due to the absence of targetable receptors, chemotherapy and breast conserving surgery have been the predominant treatment options for patients. However, resistance to chemotherapy and local recurrence of the tumors is frequent. Emerging immunotherapies have begun to change treatment plans for patients diagnosed with TNBC. In this review, we discuss the various immune pathways identified in TNBC and the role they play as targets for new potential treatment choices. Various therapeutic options that inhibit key pathways in cellular growth cycles, DNA repair mechanisms, epithelial mesenchymal transition, and immunosuppression have been shown to improve survival in patients with this disease. With promising results thus far, continued studies of immunotherapy and neoadjuvant therapy options for TNBC are likely to alter the treatment course for these diagnoses in the future.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8833442PMC
http://dx.doi.org/10.3390/cancers14030482DOI Listing

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