Kim Ji-Yoon, Park Han Deuk, Park Eunju, Chon Jeong-Woo, Park Yoo Kyoung
Department of Medical Nutrition, Graduate School of East-West Medical Science, Kyung Hee University, Yongin, Korea.
Ann N Y Acad Sci. 2009 Aug;1171:190-5. doi: 10.1111/j.1749-6632.2009.04897.x.
We tested the anticarcinogenic effect of alpha-linolenic acid (ALA) as a single compound. To test the role of ALA in breast cancer cells (MCF-7), we analyzed the antiproliferative pathway and the proapoptotic pathway. ALA exhibited growth inhibition on MCF-7 cells dose-dependently of ALA in 24, 48, and 72 h, without possible cytotoxicity per se. ALA enhanced the cell growth-inhibitory activity in a dose-dependent manner. Second, the proapoptotic pathway showed a sub-G(1) accumulation with concomitant upregulation of proapoptotic Bax expression, as well as a downregulation of antiapoptotic Bcl-2 expression dose-dependently, causing the Bcl-2/Bax ratio to decrease by about 50%. Subsequent cytochrome c release and proteolytic activation of caspase-3 followed by proteolytic cleavage of poly(ADP-ribose) polymerase all suggest ensuing progression to apoptosis. This finding suggests that ALA alone might also be responsible for growth-inhibitory and proapoptotic effects on estrogen-positive breast cancer cells.
我们测试了单一化合物α-亚麻酸(ALA)的抗癌作用。为了测试ALA在乳腺癌细胞(MCF-7)中的作用,我们分析了其抗增殖途径和促凋亡途径。在24、48和72小时内,ALA对MCF-7细胞表现出剂量依赖性的生长抑制作用,且本身不存在细胞毒性。ALA以剂量依赖性方式增强了细胞生长抑制活性。其次,促凋亡途径显示出现亚G1期积累,同时促凋亡蛋白Bax的表达上调,抗凋亡蛋白Bcl-2的表达剂量依赖性下调,导致Bcl-2/Bax比值降低约50%。随后细胞色素c释放、半胱天冬酶-3的蛋白水解激活以及聚(ADP-核糖)聚合酶的蛋白水解切割均表明随后进入凋亡进程。这一发现表明,单独的ALA也可能对雌激素阳性乳腺癌细胞具有生长抑制和促凋亡作用。