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Apoptosis Markers in Breast Cancer Therapy. | LitMetric

AI Article Synopsis

  • Cancer is associated with reduced apoptosis, which plays a key role in tumor growth and response to chemotherapy.
  • Chemotherapy effectiveness is linked to its ability to trigger apoptosis, highlighting the need for new cancer therapies targeting this process and the potential for unique biomarker identification.
  • Current apoptosis biomarkers in breast cancer, like soluble FasL and granzyme B, show promise in monitoring therapy response, but more extensive research is needed to validate these findings.

Article Abstract

Cancer is a disease characterized by a very little apoptosis, ie, genetically programmed cell death. Aberrations in apoptotic pathways are central to tumorigenesis, tumor progression, and overall tumor growth and regression in response to chemotherapy. It is now increasingly accepted that chemotherapeutic drug efficacy is partially related to its ability to induce apoptosis. Apoptosis, therefore, represents not only a vital target in cancer therapy but also a unique biomarker opportunity that has thus far been largely unexploited. In response to therapy, tumor cells undergo apoptosis and release their cellular components in the circulation. As such, these materials may serve as biomarkers to assess response. Apoptosis markers in breast cancer include circulating soluble FasL, granzyme B, and cytochrome c that increase following chemotherapy. Unfortunately, there is a paucity of information in the literature with respect to this approach. As such, large-scale prospective studies are clearly needed to validate this approach and more fully elucidate clinical usefulness.

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Source
http://dx.doi.org/10.1016/bs.acc.2015.12.003DOI Listing

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