Molecular and Cellular Mechanisms of Melatonin in Osteosarcoma

Abstract

Osteosarcoma, the most common primary bone malignancy, occurs most frequently in adolescents with a peak of incidence at 11-15 years. Melatonin, an indole amine hormone, shows a wide range of anticancer activities. The decrease in melatonin levels simultaneously concurs with the increase in bone growth and the peak age distribution of osteosarcoma during puberty, so melatonin has been utilized as an adjunct to chemotherapy to improve the quality of life and clinical outcomes. While a large amount of research has been conducted to understand the complex pleiotropic functions and the molecular and cellular actions elicited by melatonin in various types of cancers, a few review reports have focused on osteosarcoma. Herein, we summarized the anti-osteosarcoma effects of melatonin and its underlying molecular mechanisms to illustrate the known significance of melatonin in osteosarcoma and to address cellular signaling pathways of melatonin in vitro and in animal models. Even in the same kind of osteosarcoma, melatonin has been sparingly investigated to counteract tumor growth, apoptosis, and metastasis through different mechanisms, depending on different cell lines. We highlighted the underlying mechanism of anti-osteosarcoma properties evoked by melatonin, including antioxidant activity, anti-proliferation, induction of apoptosis, and the inhibition of invasion and metastasis. Moreover, we discussed the drug synergy effects of the role of melatonin involved and the method to fortify the anti-cancer effects on osteosarcoma. As a potential therapeutic agent, melatonin is safe for children and adolescents and is a promising candidate for an adjuvant by reinforcing the therapeutic effects and abolishing the unwanted consequences of chemotherapies.

Keywords: apoptosis; melatonin; metastasis; osteosarcoma; pathway.

Figure 1

The process of the melatonin’s biosynthesis.

Figure 2

Multiple functions of melatonin relating to the bone.

Figure 3

A summary of various signaling pathways involved in melatonin on human osteosarcoma. MT1: melatonin receptor 1; ERK: extracellular signal-regulated protein kinase; JNK: c-Jun N-terminal kinase; ROS: reactive oxygen species; GSH: glutathione; Bcl-2: B-cell lymphoma/leukemia 2; BAX: Bcl-2-associated X protein; SIRT1: sirtuin 1; EMT: epithelial–mesenchymal transition; CCL24: C-C motif chemokine ligand 24; and MG-63, 143B, HOS, U2OS, and SOSP-9607: human osteosarcoma cell lines; Stem: osteosarcoma stem cells.