AI Article Synopsis

  • Breast cancer is the most common cancer among women, and advances in detection and treatment have improved survival rates, but treatments can lead to cardiovascular issues for survivors.
  • * Cancer treatments like chemotherapy and anti-HER2 antibodies cause cardiovascular toxicity, making cardiovascular disease a significant long-term concern for breast cancer patients.
  • * This review focuses on the effects of different endocrine therapies, particularly tamoxifen, on cardiovascular health and seeks to enhance understanding of CVD risks in breast cancer survivors.*

Article Abstract

Breast cancer is the most common cancer in women. Over the past few decades, advances in cancer detection and treatment have significantly improved survival rate of breast cancer patients. However, due to the cardiovascular toxicity of cancer treatments (chemotherapy, anti-HER2 antibodies and radiotherapy), cardiovascular diseases (CVD) have become an increasingly important cause of long-term morbidity and mortality in breast cancer survivors. Endocrine therapies are prescribed to reduce the risk of recurrence and specific death in estrogen receptor-positive (ER +) early breast cancer patients, but their impact on CVD is a matter of debate. Whereas aromatase inhibitors and luteinizing hormone-releasing hormone (LHRH) analogs inhibit estrogen synthesis, tamoxifen acts as a selective estrogen receptor modulator (SERM), opposing estrogen action in the breast but mimicking their actions in other tissues, including arteries. This review aims to summarize the main clinical and experimental studies reporting the effects of tamoxifen on CVD. In addition, we will discuss how recent findings on the mechanisms of action of these therapies may contribute to a better understanding and anticipation of CVD risk in breast cancer patients.

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Source
http://dx.doi.org/10.1016/j.bcp.2023.115677DOI Listing

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