Costello Leslie C, Franklin Renty B
Department of Oncology and the Greenebaum Comprehensive Cancer Center, The University of Maryland School of Dentistry, Baltimore, Maryland, USA.
Acta Sci Cancer Biol. 2020 May;4(5):33-39. doi: 10.31080/ascb.2020.04.0223. Epub 2020 Apr 27.
Evidence is evolving that support the relationship that all carcinomas exhibit the following important relationships: The malignant cells exhibit a significant decreased zinc compared to the normal cells. The higher zinc levels that exist in the normal cells are cytotoxic in the malignant cells. The decrease in zinc is due to the down regulation of the ZIP-family zinc uptake transporter. These cells are as "ZIP-deficient/decreased zinc" malignancies. This provides a target for a chemotherapy that can restore the high zinc levels that will manifest cytotoxic effects in the malignant cells. In order to achieve this, a vehicle that facilitates the uptake and accumulation of zinc in the ZIP-deficient cells is required. The zinc ionophore, clioquinol, exhibits the properties that will provide these requirements. This is demonstrated by the treatment of a patient with 3% Clioquinol Cream, which successfully suppressed the progression of androgen-dependent prostate cancer. This treatment should also be efficacious for pancreatic cancer, liver cancer, breast cancer, thyroid cancer, kidney cancer, stomach cancer, gall bladder cancer, and lung cancer; which are carcinomas that exhibit decreased zinc. Thus, it is appropriate to describe that "Zinc is the wonder drug for the treatment of carcinomas".
与正常细胞相比,恶性细胞中的锌含量显著降低。正常细胞中较高的锌水平对恶性细胞具有细胞毒性。锌含量的降低是由于ZIP家族锌摄取转运体的下调。这些细胞属于“ZIP缺陷/锌减少”的恶性肿瘤。这为一种化疗提供了靶点,这种化疗可以恢复高锌水平,从而在恶性细胞中表现出细胞毒性作用。为了实现这一点,需要一种能够促进锌在ZIP缺陷细胞中摄取和积累的载体。锌离子载体氯碘羟喹具有满足这些要求的特性。用3%氯碘羟喹乳膏治疗一名患者成功抑制了雄激素依赖性前列腺癌的进展,这证明了这一点。这种治疗对胰腺癌、肝癌、乳腺癌、甲状腺癌、肾癌、胃癌、胆囊癌和肺癌也应该有效;这些都是锌含量降低的癌症。因此,“锌是治疗癌症的神奇药物”这一描述是恰当的。