AI Article Synopsis

  • Breast cancer (BC) is a prevalent cancer and a major cause of death among women globally, with various molecular subtypes complicating targeted treatment options.
  • The inhibition of cell death can lead to cancer progression, making the induction of cell death in cancer cells crucial for new therapeutic approaches.
  • Recent studies focus on lytic forms of cell death, such as pyroptosis and necroptosis, which could enhance the immune response against BC, highlighting the need for further understanding of their signaling pathways for better treatment strategies.

Article Abstract

Breast cancer (BC) is a very common cancer among women and one of the primary causes of death in women worldwide. Because BC has different molecular subtypes, the challenges associated with targeted therapy have increased significantly, and the identification of new therapeutic targets has become increasingly urgent. Blocking apoptosis and inhibiting cell death are important characteristics of malignant tumours, including BC. Under adverse conditions, including exposure to antitumour therapy, inhibition of cell death programmes can promote cancerous transformation and the survival of cancer cells. Therefore, inducing cell death in cancer cells is fundamentally important and provides new opportunities for potential therapeutic interventions. Lytic forms of cell death, primarily pyroptosis, necroptosis and ferroptosis, are different from apoptosis owing to their characteristic lysis, that is, the production of cellular components, to guide beneficial immune responses, and the application of lytic cell death (LCD) in the field of tumour therapy has attracted considerable interest from researchers. The latest clinical research results confirm that lytic death signalling cascades involve the BC cell immune response and resistance to therapies used in clinical practice. In this review, we discuss the current knowledge regarding the various forms of LCD, placing a special emphasis on signalling pathways and their implications in BC, which may facilitate the development of novel and optimal strategies for the clinical treatment of BC.

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Source
http://dx.doi.org/10.1002/cbin.11705DOI Listing

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