Melatonin, a Full Service Anti-Cancer Agent: Inhibition of Initiation, Progression and Metastasis

被引:354
作者
Reiter, Russel J. [1 ]
Rosales-Corral, Sergio A. [2 ]
Tan, Dun-Xian [1 ]
Acuna-Castroviejo, Dario [3 ]
Qin, Lilan [1 ]
Yang, Shun-Fa [4 ]
Xu, Kexin [5 ]
机构
[1] UT Hlth, Dept Cell Syst & Anat, San Antonio, TX 78229 USA
[2] Del Inst Mexicano Seguro Social, Ctr Invest Biomed Occidente, Guadalajara 44340, Jalisco, Mexico
[3] Univ Granada, Ctr Invest Biomed, Granada 18916, Spain
[4] Med Univ, Inst Med, Taichung 40201, Taiwan
[5] UT Hlth, Dept Mol Med, San Antonio, TX 78229 USA
关键词
ionizing radiation; antioxidant; free radicals; apoptosis; angiogenesis; molecular mechanisms; invasion; breast; prostate; melatonin receptors; chemotherapy; BREAST-CANCER CELLS; DNA-DAMAGE RESPONSE; EPITHELIAL-MESENCHYMAL TRANSITIONS; IN-VIVO MODEL; NF-KAPPA-B; RECEPTOR-MEDIATED INHIBITION; CISPLATIN-INDUCED APOPTOSIS; LINOLEIC-ACID METABOLISM; PINEAL HORMONE MELATONIN; RAT HEPATOMA 7288CTC;
D O I
10.3390/ijms18040843
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There is highly credible evidence that melatonin mitigates cancer at the initiation, progression and metastasis phases. In many cases, the molecular mechanisms underpinning these inhibitory actions have been proposed. What is rather perplexing, however, is the large number of processes by which melatonin reportedly restrains cancer development and growth. These diverse actions suggest that what is being observed are merely epiphenomena of an underlying more fundamental action of melatonin that remains to be disclosed. Some of the arresting actions of melatonin on cancer are clearly membrane receptor-mediated while others are membrane receptor-independent and involve direct intracellular actions of this ubiquitously-distributed molecule. While the emphasis of melatonin/cancer research has been on the role of the indoleamine in restraining breast cancer, this is changing quickly with many cancer types having been shown to be susceptible to inhibition by melatonin. There are several facets of this research which could have immediate applications at the clinical level. Many studies have shown that melatonin's co-administration improves the sensitivity of cancers to inhibition by conventional drugs. Even more important are the findings that melatonin renders cancers previously totally resistant to treatment sensitive to these same therapies. Melatonin also inhibits molecular processes associated with metastasis by limiting the entrance of cancer cells into the vascular system and preventing them from establishing secondary growths at distant sites. This is of particular importance since cancer metastasis often significantly contributes to death of the patient. Another area that deserves additional consideration is related to the capacity of melatonin in reducing the toxic consequences of anti-cancer drugs while increasing their efficacy. Although this information has been available for more than a decade, it has not been adequately exploited at the clinical level. Even if the only beneficial actions of melatonin in cancer patients are its ability to attenuate acute and long-term drug toxicity, melatonin should be used to improve the physical wellbeing of the patients. The experimental findings, however, suggest that the advantages of using melatonin as a co-treatment with conventional cancer therapies would far exceed improvements in the wellbeing of the patients.
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页数:47
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共 380 条
[1]   Effect of Melatonin on Telocytes in the Seminal Vesicle of the Soay Ram: An Immunohistochemical, Ultrastructural and Morphometrical Study [J].
Abd-Elhafeez, Hanan H. ;
Mokhtar, Doaa M. ;
Hassan, Ahmed H. S. .
CELLS TISSUES ORGANS, 2017, 203 (01) :29-54
[2]   Epithelial-mesenchymal transitions: the importance of changing cell state in development and disease [J].
Acloque, Herve ;
Adams, Meghan S. ;
Fishwick, Katherine ;
Bronner-Fraser, Marianne ;
Angela Nieto, M. .
JOURNAL OF CLINICAL INVESTIGATION, 2009, 119 (06) :1438-1449
[3]   Extrapineal melatonin: sources, regulation, and potential functions [J].
Acuna-Castroviejo, Dario ;
Escames, Germaine ;
Venegas, Carmen ;
Diaz-Casado, Maria E. ;
Lima-Cabello, Elena ;
Lopez, Luis C. ;
Rosales-Corral, Sergio ;
Tan, Dun-Xian ;
Reiter, Russel J. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2014, 71 (16) :2997-3025
[4]   Polymorphism in Endothelin-1 Gene: An Overview [J].
Ahmed, Musa ;
Rghigh, Abir .
CURRENT CLINICAL PHARMACOLOGY, 2016, 11 (03) :191-210
[5]   The chemistry of melatonin's interaction with reactive species [J].
Allegra, M ;
Reiter, RJ ;
Tan, DX ;
Gentile, C ;
Tesoriere, L ;
Livrea, MA .
JOURNAL OF PINEAL RESEARCH, 2003, 34 (01) :1-10
[6]   Melatonin enhancement of the radiosensitivity of human breast cancer cells is associated with the modulation of proteins involved in estrogen biosynthesis [J].
Alonso-Gonzalez, Carolina ;
Gonzalez, Alicia ;
Martinez-Campa, Carlos ;
Menendez-Menendez, Javier ;
Gomez-Arozamena, Jose ;
Garcia-Vidal, Angela ;
Cos, Samuel .
CANCER LETTERS, 2016, 370 (01) :145-152
[7]   Melatonin sensitizes human breast cancer cells to ionizing radiation by downregulating proteins involved in double-strand DNA break repair [J].
Alonso-Gonzalez, Carolina ;
Gonzalez, Alicia ;
Martinez-Campa, Carlos ;
Gomez-Arozamena, Jose ;
Cos, Samuel .
JOURNAL OF PINEAL RESEARCH, 2015, 58 (02) :189-197
[8]   Melatonin improves bone mineral density at the femoral neck in postmenopausal women with osteopenia: a randomized controlled trial [J].
Amstrup, Anne Kristine ;
Sikjaer, Tanja ;
Heickendorff, Lene ;
Mosekilde, Leif ;
Rejnmark, Lars .
JOURNAL OF PINEAL RESEARCH, 2015, 59 (02) :221-229
[9]   The Safety of Melatonin in Humans [J].
Andersen, Lars Peter Holst ;
Gogenur, Ismail ;
Rosenberg, Jacob ;
Reiter, Russel J. .
CLINICAL DRUG INVESTIGATION, 2016, 36 (03) :169-175
[10]   Epithelial Plasticity: A Common Theme in Embryonic and Cancer Cells [J].
Angela Nieto, M. .
SCIENCE, 2013, 342 (6159) :708-+