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选定脂肪酸作为抗癌剂涉及氧自由基的选择性细胞毒性活性的可能中间体。

Selected fatty acids as possible intermediates for selective cytotoxic activity of anticancer agents involving oxygen radicals.

作者信息

Bégin M E, Ells G, Das U N

出版信息

Anticancer Res. 1986 Mar-Apr;6(2):291-5.

PMID:3707065
Abstract

Both polyunsaturated fatty acids (PUFAs) and certain anticancer agents can generate peroxides leading to extensive lipid peroxidation. The link between peroxides, PUFAs and cell killing has been examined by testing the susceptibility of tumor cells to peroxides generated by PUFAs. Our results demonstrate that gammalinolenic, arachidonic and eicosapentaenoic acids are highly effective in killing human breast, lung, and prostate tumor cells while leaving normal cells viable. The availability of PUFAs and the role of lipoperoxidation are discussed with respect to the cytotoxic action of anticancer agents involving oxygen radicals. The results suggest that tumor cell susceptibility to lipid peroxides can be selectively modulated and manipulated by dietary PUFAs, especially those with 3 or more double bonds, and that the suggestion that non-selective toxicities of drugs are mediated by lipid peroxides must be viewed with caution.

摘要

多不饱和脂肪酸(PUFAs)和某些抗癌药物都能产生过氧化物,导致广泛的脂质过氧化。通过测试肿瘤细胞对PUFAs产生的过氧化物的敏感性,研究了过氧化物、PUFAs与细胞杀伤之间的联系。我们的结果表明,γ-亚麻酸、花生四烯酸和二十碳五烯酸在杀死人乳腺癌、肺癌和前列腺肿瘤细胞方面非常有效,同时使正常细胞存活。就涉及氧自由基的抗癌药物的细胞毒性作用,讨论了PUFAs的可用性和脂质过氧化的作用。结果表明,膳食中的PUFAs,尤其是那些具有3个或更多双键的PUFAs,可以选择性地调节和控制肿瘤细胞对脂质过氧化物的敏感性,并且必须谨慎看待药物的非选择性毒性是由脂质过氧化物介导的这一观点。

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