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6-碘内酯,碘抗肿瘤特性的关键介质。

6-iodolactone, key mediator of antitumoral properties of iodine.

作者信息

Nava-Villalba Mario, Aceves Carmen

机构信息

Instituto de Neurobiología, Universidad Nacional Autónoma de México, Campus Juriquilla, Querétaro, Mexico.

出版信息

Prostaglandins Other Lipid Mediat. 2014 Aug;112:27-33. doi: 10.1016/j.prostaglandins.2014.07.001. Epub 2014 Jul 10.

Abstract

An iodinated derivative of arachidonic acid, 5-hydroxy-6-iodo-8,11,14-eicosatrienoic acid, δ-lactone (6-IL) has been implicated as a possible intermediate in the autoregulation of the thyroid gland by iodine. In addition to antiproliferative and apoptotic effects observed in thyrocytes, this iodolipid could also exert similar actions in cells derived from extrathyroidal tissues like mammary gland, prostate, colon, or the nervous system. In mammary cancer (solid tumors or tumor cell lines), 6-IL has been detected after molecular iodine (I2) supplement, and is a potent activator of peroxisome proliferator-activated receptor type gamma (PPARγ). These observations led us to propose I2 supplement as a novel coadjutant therapy which, by inducing differentiation mechanisms, decreases tumor progression and prevents chemoresistance. Some kinds of tumoral cells, in contrast to normal cells, contain high concentrations of arachidonic acid, making the I2 supplement a potential "magic bullet" that enables local, specific production of 6-IL, which then exerts antineoplastic actions with minimal deleterious effects on normal tissues.

摘要

花生四烯酸的一种碘化衍生物,5-羟基-6-碘-8,11,14-二十碳三烯酸δ-内酯(6-IL)被认为可能是碘对甲状腺进行自身调节的一种中间产物。除了在甲状腺细胞中观察到的抗增殖和凋亡作用外,这种碘脂质在源自甲状腺外组织(如乳腺、前列腺、结肠或神经系统)的细胞中也可能发挥类似作用。在乳腺癌(实体瘤或肿瘤细胞系)中,补充分子碘(I2)后可检测到6-IL,它是过氧化物酶体增殖物激活受体γ(PPARγ)的强效激活剂。这些观察结果促使我们提出补充I2作为一种新型辅助治疗方法,通过诱导分化机制,减少肿瘤进展并预防化疗耐药性。与正常细胞相比,某些肿瘤细胞含有高浓度的花生四烯酸,这使得补充I2成为一种潜在的“神奇子弹”,能够局部、特异性地产生6-IL,然后以对正常组织最小的有害影响发挥抗肿瘤作用。

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