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Mysterious link between iron overload and CDKN2A/2B

机译:铁过载和CDKN2A / 2B之间的神秘联系

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摘要

Persistent oxidative stress has been associated with carcinogenesis. Iron overload is considered one such condition that causes oxidative stress. Epidemiological studies support a close link between iron overload and carcinogenesis. Reportedly, regular semiannual phlebotomies reduced cancer risk in an otherwise normal population. More specifically, genetic hemochromatosis, chronic viral hepatitis, ovarian endometriosis and asbestosis induce iron overload, which can lead to hepatocellular carcinoma, ovarian carcinoma or mesothelioma in humans. Through a combination of animal experiments and microarray analyses, homozygous deletion of CDKN2A/2B has been recognized as one of the major target genes involved in iron overload-induced carcinogenesis. CDKN2A/2B are the second most frequently inactivated tumor suppressing genes in human cancers. Currently, when infection is becoming sufficiently controlled worldwide, iron regulation may be the next target for human longevity.
机译:持续的氧化应激与致癌作用有关。铁过载被认为是引起氧化应激的一种情况。流行病学研究支持铁超负荷与致癌作用之间的紧密联系。据报道,定期进行半年静脉切开术可以降低原本正常人群的癌症风险。更具体地说,遗传性血色素沉着病,慢性病毒性肝炎,卵巢子宫内膜异位症和石棉沉醉症会引起铁超负荷,从而导致人类肝细胞癌,卵巢癌或间皮瘤。通过动物实验和微阵列分析的结合,CDKN2A / 2B的纯合缺失已被认为是参与铁超负荷致癌作用的主要靶基因之一。 CDKN2A / 2B是人类癌症中第二个最常见的灭活肿瘤抑制基因。当前,当全球范围内感染受到充分控制时,铁的调节可能成为人类长寿的下一个目标。

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