Evidence that Human Prostate Cancer is a ZIP1-Deficient Malignancy that could be Effectively Treated with a Zinc

Leslie C Costello1, Renty B Franklin1, Jing Zou2

  • 1Department of Oncology and Diagnostic Sciences; Dental School; and The Greenebaum Cancer Center; University of Maryland; Baltimore, USA.

Chemotherapy
|August 15, 2015
PubMed

Insights

Prostate cancer malignancy is linked to decreased zinc levels. Clioquinol, a zinc ionophore, shows promise in increasing malignant zinc and suppressing prostate cancer, warranting further clinical trials.

Area of Science:

  • Oncology
  • Biochemistry
  • Mineral Metabolism

Background:

  • Prostate cancer lacks effective chemotherapy options.
  • Malignant prostate tissue exhibits significantly reduced zinc levels compared to normal tissue.
  • Downregulation of the ZIP1 zinc transporter contributes to decreased intracellular zinc in prostate cancer.

Purpose of the Study:

  • To investigate the potential of targeting zinc levels for prostate cancer treatment.
  • To evaluate Clioquinol, a zinc ionophore, as a therapeutic agent for prostate cancer.
  • To address skepticism and present evidence supporting zinc-based therapies.

Main Methods:

  • Review of existing clinical and experimental data on prostate cancer and zinc.
  • Presentation of new experimental data on Clioquinol's effect on prostate malignancy.
  • Evaluation of counterarguments and challenges to zinc-based treatments.

Main Results:

  • Experimental data demonstrates Clioquinol's suppression of prostate malignancy.
  • Increased malignant zinc levels via ionophore treatment show therapeutic potential.
  • Evidence supports the hypothesis that prostate cancer is a "ZIP1-deficient" malignancy.

Conclusions:

  • Compelling evidence supports pursuing a zinc-treatment approach for prostate cancer.
  • Further research and clinical trials are warranted to validate zinc ionophore therapy.
  • Targeting zinc transport offers a plausible new avenue for prostate cancer treatment.