Yachnin S
Oncodev Biol Med. 1982;3(2-3):111-23.
Mevalonic acid (5 x 10(-4)-1 x 10(-2) M) stimulates DNA synthesis, morphologic transformation and cell cycling in peripheral blood human lymphocytes. Other organic acid anions which serve as cholesterol and mevalonate precursors are devoid of such effects. Both ML-236B and 25-hydroxycholesterol, inhibitors of 3-hydroxy-3-methylglutaryl-coenzyme A reductase, inhibit concanavalin A-induced lymphocyte transformation, but only the inhibition by ML-236B can be overcome by exogenous mevalonate. In contrast, only 25-hydroxycholesterol inhibits mevalonate-induced lymphocyte DNA synthesis. The effects of mevalonic acid on lymphocytes cannot be reproduced by isopentenyl adenine or isopentenyl adenosine. Unregulated endogenous cellular synthesis of mevalonic acid may contribute to uncontrolled growth in certain malignant cell lines.
甲羟戊酸(5×10⁻⁴ - 1×10⁻² M)可刺激人外周血淋巴细胞中的DNA合成、形态转化和细胞周期。作为胆固醇和甲羟戊酸前体的其他有机酸酸根则没有此类作用。3-羟基-3-甲基戊二酰辅酶A还原酶的抑制剂ML-236B和25-羟基胆固醇均能抑制伴刀豆球蛋白A诱导的淋巴细胞转化,但只有ML-236B的抑制作用可被外源性甲羟戊酸克服。相比之下,只有25-羟基胆固醇能抑制甲羟戊酸诱导的淋巴细胞DNA合成。异戊烯基腺嘌呤或异戊烯基腺苷无法重现甲羟戊酸对淋巴细胞的作用。甲羟戊酸不受调控的内源性细胞合成可能导致某些恶性细胞系的生长失控。