Use of Melatonin in Cancer Treatment: Where Are We?

被引:61
作者
Wang, Leilei [1 ]
Wang, Chuan [2 ]
Choi, Wing Shan [1 ]
机构
[1] Univ Hong Kong, Fac Dent, Div Oral & Maxillofacial Surg, Hong Kong, Peoples R China
[2] Univ Hong Kong, Fac Dent, Div Periodontol & Implant Dent, Hong Kong, Peoples R China
关键词
anticancer; melatonin; molecular mechanisms; reactive oxygen species (ROS); combination therapy; PLUS MELATONIN; PINEAL-GLAND; IN-VIVO; TUMOR MICROENVIRONMENT; HORMONE MELATONIN; PHASE-II; CELLS; RECEPTORS; SLEEP; MIGRATION;
D O I
10.3390/ijms23073779
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
Cancer represents a large group of diseases accounting for nearly 10 million deaths each year. Various treatment strategies, including surgical resection combined with chemotherapy, radiotherapy, and immunotherapy, have been applied for cancer treatment. However, the outcomes remain largely unsatisfying. Melatonin, as an endogenous hormone, is associated with the circadian rhythm moderation. Many physiological functions of melatonin besides sleep-wake cycle control have been identified, such as antioxidant, immunomodulation, and anti-inflammation. In recent years, an increasing number of studies have described the anticancer effects of melatonin. This has drawn our attention to the potential usage of melatonin for cancer treatment in the clinical setting, although huge obstacles still exist before its wide clinical administration is accepted. The exact mechanisms behind its anticancer effects remain unclear, and the specific characters impede its in vivo investigation. In this review, we will summarize the latest advances in melatonin studies, including its chemical properties, the possible mechanisms for its anticancer effects, and the ongoing clinical trials. Importantly, challenges for the clinical application of melatonin will be discussed, accompanied with our perspectives on its future development. Finally, obstacles and perspectives of using melatonin for cancer treatment will be proposed. The present article will provide a comprehensive foundation for applying melatonin as a preventive and therapeutic agent for cancer treatment.
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页数:18
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共 134 条
[1]   Metabolic reprogramming in the tumour microenvironment: a hallmark shared by cancer cells and T lymphocytes [J].
Allison, Katrina E. ;
Coomber, Brenda L. ;
Bridle, Byram W. .
IMMUNOLOGY, 2017, 152 (02) :175-184
[2]   Melatonin as a Radio-Sensitizer in Cancer [J].
Alonso-Gonzalez, Carolina ;
Gonzalez, Alicia ;
Menendez-Menendez, Javier ;
Martinez-Campa, Carlos ;
Cos, Samuel .
BIOMEDICINES, 2020, 8 (08)
[3]   Melatonin-Induced Cytoskeleton Reorganization Leads to Inhibition of Melanoma Cancer Cell Proliferation [J].
Alvarez-Artime, Alejandro ;
Cernuda-Cernuda, Rafael ;
Francisco-Artime-Naveda ;
Cepas, Vanesa ;
Gonzalez-Menendez, Pedro ;
Fernadez-Vega, Sheila ;
Quiros-Gonzalez, Isabel ;
Sainz, Rosa M. ;
Mayo, Juan C. .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (02)
[4]  
BARNI S, 1995, ONCOLOGY, V52, P243
[5]  
BECKERANDRE M, 1994, J BIOL CHEM, V269, P28531
[6]   Randomized phase II trial of high-dose melatonin and radiation therapy for RPA class 2 patients with brain metastases (RTOG 0119) [J].
Berk, Lawrence ;
Berkey, Brian ;
Rich, Tyvin ;
Hrushesky, William ;
Blask, David ;
Gallagher, Michael ;
Kudrimoti, Mahesh ;
McGarry, Ronald C. ;
Suh, John ;
Mehta, Minesh .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2007, 68 (03) :852-857
[7]   Long Noncoding RNA and Cancer: A New Paradigm [J].
Bhan, Arunoday ;
Soleimani, Milad ;
Mandal, Subhrangsu S. .
CANCER RESEARCH, 2017, 77 (15) :3965-3981
[8]   Melatonin and its ubiquitous anticancer effects [J].
Bhattacharya, Sankha ;
Patel, Krishna Kumar ;
Dehari, Deepa ;
Agrawal, Ashish Kumar ;
Singh, Sanjay .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2019, 462 (1-2) :133-155
[9]   Molecular mechanisms of the pro-apoptotic actions of melatonin in cancer: a review [J].
Bizzarri, Mariano ;
Proietti, Sara ;
Cucina, Alessandra ;
Reiter, Russel J. .
EXPERT OPINION ON THERAPEUTIC TARGETS, 2013, 17 (12) :1483-1496
[10]   Is There Sufficient Evidence that the Melatonin Binding Site MT3 Is Quinone Reductase 2? [J].
Boutin, Jean A. ;
Ferry, Gilles .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2019, 368 (01) :59-65