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一种用于控制播散性癌症的完全营养性“多焦点血管生成抑制疗法”。

A wholly nutritional 'multifocal angiostatic therapy' for control of disseminated cancer.

作者信息

McCarty M F

机构信息

Pantox Laboratories, San Diego, California 92129, USA.

出版信息

Med Hypotheses. 2003 Jul;61(1):1-15. doi: 10.1016/s0306-9877(02)00227-x.

Abstract

A great deal of effort is now being devoted to the development of new drugs that hopefully will control the spread of inoperable cancer by safely inhibiting tumor-evoked angiogenesis. However, there is growing evidence that certain practical nutritional measures have the potential to slow tumor angiogenesis, and it is reasonable to anticipate that, by combining several measures that work in distinct but complementary ways to impede the angiogenic process, a clinically useful 'multifocal angiostatic therapy' (MAT) might be devised. Several measures which might reasonably be included in such a protocol are discussed below, and include: a low-fat, low-glycemic index vegan diet, which may down-regulate the systemic IGF-I activity that supports angiogenesis; supplemental omega-3-rich fish oil, which has been shown to inhibit endothelial expression of Flk-1, a functionally crucial receptor for VEGF, and also can suppress tumor production of pro-angiogenic eicosanoids; high-dose selenium, which has recently been shown to inhibit tumor production of VEGF; green tea polyphenols, which can suppress endothelial responsiveness to both VEGF and fibroblast growth factor; and high-dose glycine, whose recently reported angiostatic activity may reflect inhibition of endothelial cell mitosis, possibly mediated by activation of glycine-gated chloride channels. In light of evidence that tumor-evoked angiogenesis has a high requirement for copper, copper depletion may have exceptional potential as an angiostatic measure, and is most efficiently achieved with the copper-chelating drug tetrathiomolybdate. If logistical difficulties make it difficult to acquire this experimental drug, high-dose zinc supplementation can achieve a slower depletion of the body's copper pool, and in any case can be used as maintenance therapy to maintain an adequate level of copper depletion. A provisional protocol is offered for a nutritionally based MAT entailing a vegan diet and supplemental intakes of fish oil, selenium, green tea polyphenols, glycine, and zinc. Inasmuch as cox-2 is overexpressed in many cancers, and cAMP can boost tumor production of various angiogenic factors as well as autogenous growth factors, adjunctive use of cox-2-specific NSAIDS may be warranted in some cases.

摘要

目前正在投入大量精力研发新药,有望通过安全抑制肿瘤诱发的血管生成来控制无法手术切除的癌症的扩散。然而,越来越多的证据表明,某些实用的营养措施有可能减缓肿瘤血管生成,并且可以合理预期,通过结合几种以不同但互补方式作用来阻碍血管生成过程的措施,可能会设计出一种临床上有用的“多靶点血管生成抑制疗法”(MAT)。下面讨论了一些可能合理纳入该方案的措施,包括:低脂肪、低血糖指数的纯素饮食,这可能会下调支持血管生成的全身胰岛素样生长因子 - I(IGF - I)活性;富含ω - 3的鱼油补充剂,已证明其可抑制血管内皮生长因子(VEGF)功能关键受体Flk - 1的内皮表达,还可抑制肿瘤产生促血管生成的类花生酸;高剂量硒,最近已证明其可抑制肿瘤产生VEGF;绿茶多酚,其可抑制内皮细胞对VEGF和成纤维细胞生长因子的反应性;以及高剂量甘氨酸,其最近报道的血管生成抑制活性可能反映了对内皮细胞有丝分裂的抑制,可能是由甘氨酸门控氯离子通道的激活介导的。鉴于有证据表明肿瘤诱发的血管生成对铜有高度需求,铜耗竭作为一种血管生成抑制措施可能具有特殊潜力,使用铜螯合剂四硫代钼酸盐可最有效地实现这一点。如果后勤困难使得难以获得这种实验性药物,高剂量补锌可较慢地消耗体内铜储备,并且无论如何都可作为维持疗法以维持足够的铜耗竭水平。提供了一个基于营养的MAT临时方案,包括纯素饮食以及鱼油、硒、绿茶多酚、甘氨酸和锌的补充摄入。鉴于环氧化酶 - 2(cox - 2)在许多癌症中过度表达,并且环磷酸腺苷(cAMP)可促进肿瘤产生各种血管生成因子以及自身生长因子,在某些情况下可能有必要辅助使用cox - 2特异性非甾体抗炎药(NSAIDS)。

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