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Published on: September 28, 2017
Melatonin and breast cancer: cellular mechanisms, clinical studies and future perspectives
Stephen G Grant1, Melissa A Melan, Jean J Latimer
1University of Pittsburgh Cancer Institute, University of Pittsburgh, Pittsburgh, PA 15232, USA.
Abstract:
Recent studies have suggested that the pineal hormone melatonin may protect against breast cancer, and the mechanisms underlying its actions are becoming clearer. Melatonin works through receptors and distinct second messenger pathways to reduce cellular proliferation and to induce cellular differentiation. In addition, independently of receptors melatonin can modulate oestrogen-dependent pathways and reduce free-radical formation, thus preventing mutation and cellular toxicity. The fact that melatonin works through a myriad of signalling cascades that are protective to cells makes this hormone a good candidate for use in the clinic for the prevention and/or treatment of cancer. This review summarises cellular mechanisms governing the action of melatonin and then considers the potential use of melatonin in breast cancer prevention and treatment, with an emphasis on improving clinical outcomes.
Insights
Melatonin, a pineal hormone, shows promise in breast cancer prevention and treatment by reducing cell proliferation and toxicity. Its diverse cellular actions make it a potential clinical candidate for improving cancer outcomes.
Area of Science:
- Endocrinology
- Oncology
- Cellular Biology
Background:
- Emerging research suggests the pineal hormone melatonin possesses protective effects against breast cancer.
- Understanding the mechanisms of melatonin's action is crucial for its clinical application.
Purpose of the Study:
- To review the cellular mechanisms by which melatonin exerts its effects.
- To explore the potential of melatonin in breast cancer prevention and treatment.
- To identify strategies for improving clinical outcomes using melatonin therapy.
Main Methods:
- Literature review of studies on melatonin's cellular mechanisms and breast cancer.
- Analysis of melatonin's receptor-dependent and independent pathways.
- Evaluation of melatonin's role in oestrogen-dependent pathways and free-radical scavenging.
Main Results:
- Melatonin reduces cellular proliferation and induces differentiation via receptor pathways.
- Melatonin modulates oestrogen pathways and reduces free radicals independently of receptors.
- These actions collectively contribute to preventing mutations and cellular toxicity.
Conclusions:
- Melatonin's multifaceted protective signaling cascades position it as a promising agent for cancer prevention and treatment.
- Further clinical investigation is warranted to optimize melatonin's use in breast cancer management.
- Melatonin holds potential for improving patient outcomes in clinical settings.
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