AI Article Synopsis

  • Breast cancer (BC) and ovarian cancer (OC) are prevalent and lethal cancers in women, often diagnosed at advanced stages despite screening for BC.
  • Recurrences are common in both cancers due to cancer stem cells (CSC), which contribute to therapy resistance and tumor regrowth.
  • The review will explore the unique characteristics of CSC in BC and OC, their interactions with the tumor environment, and potential therapeutic strategies targeting these cells.

Article Abstract

Breast cancer (BC) and ovarian cancer (OC) are among the most common and deadly cancers affecting women worldwide. Both are complex diseases with marked heterogeneity. Despite the induction of screening programs that increase the frequency of earlier diagnosis of BC, at a stage when the cancer is more likely to respond to therapy, which does not exist for OC, more than 50% of both cancers are diagnosed at an advanced stage. Initial therapy can put the cancer into remission. However, recurrences occur frequently in both BC and OC, which are highly cancer-subtype dependent. Therapy resistance is mainly attributed to a rare subpopulation of cells, named cancer stem cells (CSC) or tumor-initiating cells, as they are capable of self-renewal, tumor initiation, and regrowth of tumor bulk. In this review, we will discuss the distinctive markers and signaling pathways that characterize CSC, their interactions with the tumor microenvironment, and the strategies they employ to evade immune surveillance. Our focus will be on identifying the common features of breast cancer stem cells (BCSC) and ovarian cancer stem cells (OCSC) and suggesting potential therapeutic approaches.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10342190PMC
http://dx.doi.org/10.3390/ijms241310683DOI Listing

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