Abstract

There is considerable evidence that melatonin may be of use in the prevention and treatment of cancer. This manuscript will review some of the human, animal and cellular studies that provide evidence that melatonin has oncostatic properties. Confirmation that melatonin mitigates pathogenesis of cancer will be described from both direct study of its effects on carcinogenesis, and from indirect findings implicating disruption of the circadian cycle. A distinction is made between the role of melatonin in preventing the initiation of the tumorigenic pathway and the ability of melatonin to retard the progression of cancer. Melatonin appears to slow down the rate of advancement of established tumors and there is evidence that it constitutes a valuable complement to standard pharmacological and radiation treatment modalities. There are instances of the beneficial outcomes in cancer treatment which utilize a range of hormones and vitamins, melatonin being among the constituents of the mix. While these complex blends are empirically promising, they are only briefly mentioned here in view of the confounding influence of a multiplicity of agents studied simultaneously. The last section of this review examines the molecular mechanisms that potentially underlie the oncostatic effects of melatonin. Alterations in gene expression following activation of various transcription factors, are likely to be an important mediating event. These changes in gene activity not only relate to cancer but also to the aging process which underlies the onset of most tumors. In addition, epigenetic events such as modulation of histone acetylation and DNA methylation patterns throughout the lifespan of organisms need to be considered. The antioxidant and immunoregulatory roles of melatonin may also contribute to its cancer modulatory properties. Naturally, these mechanisms overlap and interact extensively. Nevertheless, in the interest of clarity and ease of reading, each is discussed as a separate topic section. The report ends with some general conclusions concerning the clinical value of melatonin which has been rather overlooked and understudied.

Highlights

  • Melatonin is a neurohormone derived from serotonin and produced by several areas including the pineal gland, the intestine and within mitochondria [1,2]

  • The maternal hormonal environment is important for proper fetal brain development and besides thyroid hormone and glucocorticoids, melatonin is likely to participate in this regulation [4]

  • First trimester human placental tissue expressed transcripts for melatonin receptors [6] and both human and rat placenta contained much higher levels of the neurohormone compared to serum [7]

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Summary

Introduction

Melatonin is a neurohormone derived from serotonin and produced by several areas including the pineal gland, the intestine and within mitochondria [1,2]. It is best known for its regulation of the circadian rhythm [3]. Many reports indicate that the neurohormone may have various functions depending on the lifecycle stage. The first section of this review focuses on the role of melatonin during different phases of the human lifespan

Role of Melatonin during Human Life Stages
Direct In Vivo Evidence
Direct In Vitro Evidence
Indirect Evidence
Animal Models
Cell-Based Models
Clinical Trials
Melatonin as A Co-Therapeutic Agent
Mechanisms
Epigenetic Changes
Histone Acetylation
Histone and DNA Methylation
Angiogenesis
Role of Various Melatonin Receptors
MT1 and MT2 Receptors
Findings
Conclusions
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