Public neoantigens in breast cancer immunotherapy (Review).

Int J Mol Med

Department of Immunology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.

Published: July 2024

AI Article Synopsis

  • Breast cancer is the most common cancer among women and a leading cause of cancer-related deaths, with less than 15% of cases linked to family history, indicating many are caused by sporadic genetic mutations.
  • The field of cancer genomics is evolving, and neoantigen-based immunotherapy is becoming a significant approach, exploring unique proteins from mutations for personalized and general cancer treatments.
  • The review focuses on shared neoantigens as potential therapeutic targets for breast cancer, discussing common genetic mutations and the clinical application of these therapies to benefit a broader range of patients.

Article Abstract

Among women globally, breast cancer is the most prevalent cancer and the leading cause of cancer‑related death. Interestingly, though genetic mutations contribute to the disease, <15% of women diagnosed with breast cancer have a family history of the disease, suggesting a prevalence of sporadic genetic mutations in breast cancer development. In the rapidly rising field of cancer genomics, neoantigen‑based immunotherapy has come to the fore. The investigation of novel proteins arising from unique somatic mutations or neoantigens have opened a new pathway for both individualized and public cancer treatments. Because they are shared among individuals with similar genetic changes, public neoantigens provide an opportunity for 'off‑the‑shelf' anticancer therapies, potentially extending the benefits to a wider patient group. The present review aimed to highlight the role of shared or public neoantigens as therapeutic targets for patients with breast cancer, emphasizing common hotspot mutations of certain genes identified in breast cancer. The clinical utilization of public neoantigen‑based therapies for breast cancer treatment were also discussed.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11188978PMC
http://dx.doi.org/10.3892/ijmm.2024.5388DOI Listing

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