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Melatonin as a Pleiotropic Molecule with Therapeutic Potential for Type 2 Diabetes and Cancer.

Current medicinal chemistry
January 1, 1970
Marzena Wojcik et al. (5 authors)
Journal ArticleReviewHuman StudyMolecular Study
Study Details

Study Goal

The researchers aimed to review the molecular mechanisms of melatonin's antidiabetic and anticancer effects and explore its potential as a therapeutic agent for type 2 diabetes and cancer.

Results Summary

Melatonin demonstrated antidiabetic benefits by reducing hyperglycemia, insulin resistance, oxidative stress, and inflammation, and exhibited multi-targeted anticancer effects by modulating cell survival, proliferation, and apoptosis pathways. It also showed synergistic benefits with chemotherapy and radiotherapy without adverse clinical outcomes.

Population

General human health, particularly type 2 diabetes and cancer patients.

Effective Dosage

Not specified

Duration

Not specified

Interactions

None mentioned

Extracted Claims (10)
InterventionDirectionEndpointPopulationDosageImpactClaim #
melatonin (MLT)
decrease
hyperglycemia
in vitro and in vivo studies
-
possesses a number of antidiabetic health benefits
#1
melatonin (MLT)
decrease
insulin resistance
in vitro and in vivo studies
-
possesses a number of antidiabetic health benefits
#2
melatonin (MLT)
decrease
oxidative stress
in vitro and in vivo studies
-
possesses a number of antidiabetic health benefits
#3
melatonin (MLT)
decrease
inflammation
in vitro and in vivo studies
-
possesses a number of antidiabetic health benefits
#4
melatonin (MLT)
decrease
cell survival
numerous human malignancies
-
exhibits multi-targeted anticancer effects
#5
melatonin (MLT)
decrease
cell proliferation
numerous human malignancies
-
exhibits multi-targeted anticancer effects
#6
melatonin (MLT)
increase
apoptosis
numerous human malignancies
-
exhibits multi-targeted anticancer effects
#7
melatonin (MLT)
increase
chemotherapy
-
-
beneficial synergistic action
#8
melatonin (MLT)
increase
radiotherapy
-
-
beneficial synergistic action
#9
melatonin (MLT)
no change
clinical use
-
-
no adverse outcomes
#10
Abstract

BACKGROUND: The incidence of both type 2 diabetes (T2DM) and cancer is increasing worldwide, making these diseases a global health problem along with increasing healthcare expenditures. The current therapeutic approaches for treating these multifactorial diseases are far from satisfactory. As increasing evidence shows beneficial effects of melatonin (MLT) on typical pathological changes occurring during the development of T2DM and cancer, the present review focuses on molecular aspects of antidiabetic and anticancer activities of MLT and, moreover, discusses several future directions of research regarding MLT application as potential therapeutic agent. METHODS: Critical literature analysis in PubMed central combined with personal expertise. RESULTS: Numerous in vitro and in vivo studies have revealed that MLT possesses a number of antidiabetic health benefits by diminishing hyperglycemia, insulin resistance, oxidative stress, and inflammation through modulating various intracellular signaling pathways or other targets involved in the pathophysiology of this disease. Mounting evidence also indicates that MLT exhibits multi-targeted anticancer effects in numerous human malignancies, mainly resulting from its ability to modulate several signal transduction pathways associated with cell survival, proliferation, and apoptosis. Furthermore, beneficial synergistic action of MLT with chemotherapy and radiotherapy has also been observed. Importantly, no adverse outcomes have been found from the clinical use of MLT, which highlights its therapeutic usefulness, either alone or in combination with other conventional therapies, in cancer treatment. CONCLUSION: The findings described in this review suggest that MLT may confer potential benefits to human health, particularly in respect to T2DM and cancer.

Medical Subject Headings (MeSH)
AnimalsAntineoplastic AgentsApoptosisApoptosis Regulatory ProteinsDiabetes Mellitus, Type 2HumansHypoglycemic AgentsIntercellular Signaling Peptides and ProteinsMelatoninNeoplasmsOxidative StressProtein Kinases
Study Links
Quality Scores
Safety90
Efficacy85/10
Quality80/10
Citation Metrics
Total Citations7
Citations/Year0.9
Relative Citation Ratio0.33
NIH Percentile17.7%
Research Impact Scores
APT Score0.25
Weight Score0.81
Normalized Score0.86
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