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Decreased zinc in the development and progression of malignancy: an important common relationship and potential for prevention and treatment of carcinomas.

Authors :
Costello LC
Franklin RB
Source :
Expert opinion on therapeutic targets [Expert Opin Ther Targets] 2017 Jan; Vol. 21 (1), pp. 51-66. Date of Electronic Publication: 2016 Dec 05.
Publication Year :
2017

Abstract

Introduction: Efficacious chemotherapy does not exist for treatment or prevention of prostate, liver, and pancreatic carcinomas, and some other cancers that exhibit decreased zinc in malignancy. Zinc treatment offers a potential solution; but its support has been deterred by adverse bias. Areas covered: 1. The clinical and experimental evidence for the common ZIP transporter/Zn down regulation in these cancers. 2. The evidence for a zinc approach to prevent and/or treat these carcinomas. 3. The issues that introduce bias against support for the zinc approach. Expert opinion: ZIP/Zn downregulation is a clinically established common event in prostate, hepatocellular and pancreatic cancers. 2. Compelling evidence supports the plausibility that a zinc treatment regimen will prevent development of malignancy and termination of progressing malignancy in these cancers; and likely other carcinomas that exhibit decreased zinc. 3. Scientifically-unfounded issues that oppose this ZIP/Zn relationship have introduced bias against support for research and funding of a zinc treatment approach. 4. The clinically-established and supporting experimental evidence provide the scientific credibility that should dictate the support for research and funding of a zinc approach for the treatment and possible prevention of these cancers. 5. This is in the best interest of the medical community and the public-at-large.<br />Competing Interests: Declaration of interest The authors have no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript.

Details

Language :
English
ISSN :
1744-7631
Volume :
21
Issue :
1
Database :
MEDLINE
Journal :
Expert opinion on therapeutic targets
Publication Type :
Academic Journal
Accession number :
27885880
Full Text :
https://doi.org/10.1080/14728222.2017.1265506