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Mechanisms Underlying Tumor Suppressive Properties of Melatonin.

International journal of molecular sciences
January 1, 1970
Stephen C Bondy et al. (2 authors)
Journal ArticleReviewHuman Study
Study Details

Study Goal

The researchers aimed to review evidence on melatonin's potential role in cancer prevention and treatment, including its oncostatic properties and molecular mechanisms.

Results Summary

Melatonin shows promise in slowing tumor progression and complementing standard cancer treatments, with evidence supporting its antioxidant, immunoregulatory, and gene expression-modulating effects. However, complex blends with other agents introduce confounding factors.

Population

Human, animal, and cellular studies (no specific population detailed).

Effective Dosage

Not specified

Duration

Not specified

Interactions

None mentioned

Extracted Claims (10)
InterventionDirectionEndpointPopulationDosageImpactClaim #
melatonin
decrease
cancer
human, animal and cellular studies
-
may be of use in the prevention and treatment
#1
melatonin
decrease
cancer
human, animal and cellular studies
-
has oncostatic properties
#2
melatonin
decrease
cancer
-
-
mitigates pathogenesis
#3
melatonin
decrease
tumorigenic pathway
-
-
preventing the initiation
#4
melatonin
decrease
cancer
-
-
retard the progression
#5
melatonin
decrease
established tumors
-
-
slow down the rate of advancement
#6
melatonin
increase
standard pharmacological and radiation treatment modalities
-
-
constitutes a valuable complement
#7
melatonin
increase
cancer treatment
-
-
beneficial outcomes
#8
melatonin
increase
alterations in gene expression following activation of various transcription factors
-
-
underlie the oncostatic effects
#9
melatonin
increase
antioxidant and immunoregulatory roles
-
-
contribute to its cancer modulatory properties
#10
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.

Medical Subject Headings (MeSH)
AgingAnimalsAnticarcinogenic AgentsAntioxidantsCarcinogenesisDisease Models, AnimalDisease ProgressionGene ExpressionHumansMelatoninNeoplasm MetastasisNeoplasms
Study Links
Quality Scores
SafetyNot Assessed
Efficacy75/10
Quality80/10
Citation Metrics
Total Citations47
Citations/Year6.7
Relative Citation Ratio2.26
NIH Percentile78.1%
Research Impact Scores
APT Score0.50
Weight Score0.93
Normalized Score0.66
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