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Arachidonic and docosahexaenoic acids reduce the growth of A549 human lung-tumor cells increasing lipid peroxidation and PPARs.

机译:花生四烯酸和二十二碳六烯酸会减少A549人肺肿瘤细胞的生长,从而增加脂质过氧化作用和PPAR。

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摘要

Polyunsaturated fatty acids (PUFAs) play an important role in both induction and prevention of carcinogenic process. It is well known that several types of neoplastic cells show decreased total PUFA content, contributing to their resistance to chemotherapy and lipid peroxidation. In the light of this, human lung cancer A549 cells, with low PUFA content, were exposed to arachidonic or docosahexaenoic acid to investigate the effect of n-6 and n-3 PUFAs on growth and elucidate underlying mechanisms. The bulk of the results showed that both n-6 PUFAs and n-3 PUFAs decrease human lung-tumor cell growth in a concentration-dependent manner, inducing cell death mainly evident at 100microM concentration. The mechanism underlying the antiproliferative effect of n-6 and n-3 PUFAs appeared to be the same, involving changes in fatty acid composition of biomembranes, production of cytostatic aldehydes derived from lipid peroxidation and able to affect DNA-binding activity of AP-1, and induction of PPAR. From these results it may be hypothesized that n-6 PUFAs, like n-3 PUFAs, are able to inhibit tumor growth.
机译:多不饱和脂肪酸(PUFA)在诱导和预防致癌过程中都起着重要作用。众所周知,几种类型的肿瘤细胞的总PUFA含量降低,有助于其对化学疗法和脂质过氧化的抵抗力。有鉴于此,将低PUFA含量的人肺癌A549细胞暴露于花生四烯酸或二十二碳六烯酸中,以研究n-6和n-3 PUFA对生长的影响并阐明其潜在机制。大量结果表明,n-6 PUFA和n-3 PUFA均以浓度依赖的方式降低人肺肿瘤细胞的生长,主要在100microM浓度下诱导细胞死亡。 n-6和n-3 PUFA的抗增殖作用的机制似乎是相同的,涉及生物膜脂肪酸组成的变化,脂质过氧化作用产生的细胞抑制性醛的产生并能够影响AP-1的DNA结合活性。 ,并诱导PPAR。根据这些结果,可以假设n-6 PUFA与n-3 PUFA一样能够抑制肿瘤的生长。

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