Cancer metastasis: Mechanisms of inhibition by melatonin

Melatonin is a naturally occurring molecule secreted by the pineal gland and known as a gatekeeper of circadian clocks. Mounting evidence indicates that melatonin, employing multiple and interrelated mechanisms, exhibits a variety of oncostatic properties in a myriad of tumors during different stage...

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Published inJournal of pineal research Vol. 62; no. 1; pp. np - n/a
Main Authors Su, Shih‐Chi, Hsieh, Ming‐Ju, Yang, Wei‐En, Chung, Wen‐Hung, Reiter, Russel J., Yang, Shun‐Fa
Format Journal Article
LanguageEnglish
Published England 01.01.2017
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Abstract Melatonin is a naturally occurring molecule secreted by the pineal gland and known as a gatekeeper of circadian clocks. Mounting evidence indicates that melatonin, employing multiple and interrelated mechanisms, exhibits a variety of oncostatic properties in a myriad of tumors during different stages of their progression. Tumor metastasis, which commonly occurs at the late stage, is responsible for the majority of cancer deaths; metastases lead to the development of secondary tumors distant from a primary site. In reference to melatonin, the vast majority of investigations have focused on tumor development and progression at the primary site. Recently, however, interest has shifted toward the role of melatonin on tumor metastases. In this review, we highlight current advances in understanding the molecular mechanisms by which melatonin counteracts tumor metastases, including experimental and clinical observations; emphasis is placed on the impact of both cancer and non‐neoplastic cells within the tumor microenvironment. Due to the broad range of melatonin's actions, the mechanisms underlying its ability to interfere with metastases are numerous. These include modulation of cell–cell and cell–matrix interaction, extracellular matrix remodeling by matrix metalloproteinases, cytoskeleton reorganization, epithelial–mesenchymal transition, and angiogenesis. The evidence discussed herein will serve as a solid foundation for urging basic and clinical studies on the use of melatonin to understand and control metastatic diseases.
AbstractList Melatonin is a naturally occurring molecule secreted by the pineal gland and known as a gatekeeper of circadian clocks. Mounting evidence indicates that melatonin, employing multiple and interrelated mechanisms, exhibits a variety of oncostatic properties in a myriad of tumors during different stages of their progression. Tumor metastasis, which commonly occurs at the late stage, is responsible for the majority of cancer deaths; metastases lead to the development of secondary tumors distant from a primary site. In reference to melatonin, the vast majority of investigations have focused on tumor development and progression at the primary site. Recently, however, interest has shifted toward the role of melatonin on tumor metastases. In this review, we highlight current advances in understanding the molecular mechanisms by which melatonin counteracts tumor metastases, including experimental and clinical observations; emphasis is placed on the impact of both cancer and non‐neoplastic cells within the tumor microenvironment. Due to the broad range of melatonin's actions, the mechanisms underlying its ability to interfere with metastases are numerous. These include modulation of cell–cell and cell–matrix interaction, extracellular matrix remodeling by matrix metalloproteinases, cytoskeleton reorganization, epithelial–mesenchymal transition, and angiogenesis. The evidence discussed herein will serve as a solid foundation for urging basic and clinical studies on the use of melatonin to understand and control metastatic diseases.
Author Chung, Wen‐Hung
Su, Shih‐Chi
Yang, Wei‐En
Hsieh, Ming‐Ju
Reiter, Russel J.
Yang, Shun‐Fa
Author_xml – sequence: 1
  givenname: Shih‐Chi
  surname: Su
  fullname: Su, Shih‐Chi
  organization: Chang Gung Memorial Hospital
– sequence: 2
  givenname: Ming‐Ju
  surname: Hsieh
  fullname: Hsieh, Ming‐Ju
  organization: China Medical University
– sequence: 3
  givenname: Wei‐En
  surname: Yang
  fullname: Yang, Wei‐En
  organization: Chung Shan Medical University Hospital
– sequence: 4
  givenname: Wen‐Hung
  surname: Chung
  fullname: Chung, Wen‐Hung
  organization: Chang Gung University
– sequence: 5
  givenname: Russel J.
  surname: Reiter
  fullname: Reiter, Russel J.
  organization: The University of Texas Health Science Center
– sequence: 6
  givenname: Shun‐Fa
  surname: Yang
  fullname: Yang, Shun‐Fa
  email: ysf@csmu.edu.tw
  organization: Chung Shan Medical University Hospital
BackLink https://www.ncbi.nlm.nih.gov/pubmed/27706852$$D View this record in MEDLINE/PubMed
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Issue 1
Keywords matrix metalloproteinase
epithelial-mesenchymal transition
melatonin
metastasis
angiogenesis
Language English
License http://onlinelibrary.wiley.com/termsAndConditions#vor
2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
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PublicationTitle Journal of pineal research
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Snippet Melatonin is a naturally occurring molecule secreted by the pineal gland and known as a gatekeeper of circadian clocks. Mounting evidence indicates that...
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SubjectTerms angiogenesis
Animals
epithelial–mesenchymal transition
Humans
matrix metalloproteinase
melatonin
Melatonin - metabolism
metastasis
Neoplasm Metastasis - pathology
Title Cancer metastasis: Mechanisms of inhibition by melatonin
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fjpi.12370
https://www.ncbi.nlm.nih.gov/pubmed/27706852
https://www.proquest.com/docview/1835363039
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Volume 62
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