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Proteasome inhibitors: Their effects on arachidonic acid release from cells in culture and arachidonic acid metabolism in rat liver cells

机译:蛋白酶体抑制剂:它们对培养细胞中花生四烯酸释放和大鼠肝细胞花生四烯酸代谢的影响

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Background I have postulated that arachidonic acid release from rat liver cells is associated with cancer chemoprevention. Since it has been reported that inhibition of proteasome activities may prevent cancer, the effects of proteasome inhibitors on arachidonic acid release from cells and on prostaglandin I2 production in rat liver cells were studied. Results The proteasome inhibitors, epoxomicin, lactacystin and carbobenzoxy-leucyl-leucyl-leucinal, stimulate the release of arachidonic acid from rat glial, human colon carcinoma, human breast carcinoma and the rat liver cells. They also stimulate basal and induced prostacycin production in the rat liver cells. The stimulated arachidonic acid release and basal prostaglandin I2 production in rat liver cells is inhibited by actinomycin D. Conclusions Stimulation of arachidonic acid release and arachidonic acid metabolism may be associated with some of the biologic effects observed after proteasome inhibition, e.g. prevention of tumor growth, induction of apoptosis, stimulation of bone formation.
机译:背景我推测,大鼠肝细胞中花生四烯酸的释放与化学预防癌症有关。由于已经报道了蛋白酶体活性的抑制可以预防癌症,因此研究了蛋白酶体抑制剂对花生四烯酸从细胞中释放以及对大鼠肝细胞中前列腺素I 2 产生的影响。结果蛋白酶体抑制剂epoxomicin,lactacystin和carbobenzoxy-leucyl-leucyl-leucanal刺激花生四烯酸从大鼠神经胶质,人结肠癌,人乳腺癌和大鼠肝细胞中释放。它们还刺激大鼠肝细胞中基础和诱导型前列腺素的产生。放线菌素D抑制大鼠肝细胞中花生四烯酸的释放和基底前列腺素I 2 的产生。结论花生四烯酸的释放和花生四烯酸代谢的刺激可能与蛋白酶体后观察到的某些生物学效应有关抑制,例如预防肿瘤生长,诱导细胞凋亡,刺激骨形成。

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