Cancer Center, Wan Fang Hospital, Taipei Medical University, Taipei 11696, Taiwan.
Division of Hematology and Medical Oncology, Department of Internal Medicine, Wan Fang Hospital, Taipei Medical University, Taipei 11696, Taiwan.
Nutrients. 2018 Oct 8;10(10):1458. doi: 10.3390/nu10101458.
Selenium has been intensively studied for the use of cancer prevention and treatment. However, the clinical effects are still plausible. To enhance its efficacy, a combinational study of selenium yeast (SY) and fish oil (FO) was performed in A549, CL1-0, H1299, HCC827 lung adenocarcinoma (LADC) cells to investigate the enhancement in apoptosis induction and underlying mechanism. By sulforhodamine B staining, Western blot and flow cytometric assays, we found a synergism between SY and FO in growth inhibition and apoptosis induction of LADC cells. In contrast, the fetal lung fibroblast cells (MRC-5) were unsusceptible to this combination effect. FO synergized SY-induced apoptosis of A549 cells, accompanied with synergistic activation of AMP-activated protein kinase (AMPK) and reduction of Cyclooxygenase (COX)-2 and β-catenin. Particularly, combining with FO not only enhanced the SY-elevated proapoptotic endoplasmic reticulum (ER) stress marker CCAAT/enhancer-binding protein homologous protein (CHOP), but also reduced the cytoprotective glucose regulated protein of molecular weight 78 kDa (GRP78). Consequently, the CHOP downstream targets such as phospho-JNK and death receptor 5 were also elevated, along with the cleavage of caspase-8, -3, and the ER stress-related caspase-4. Accordingly, inhibition of AMPK by compound C diminished the synergistic apoptosis induction, and elevated CHOP/GRP78 ratio by SY combined with FO. The AMPK-dependent synergism suggests the combination of SY and FO for chemoprevention and integrative treatment of LADC.
硒已被广泛研究用于癌症的预防和治疗。然而,其临床效果仍有待探讨。为了增强其疗效,本研究将富硒酵母(SY)和鱼油(FO)联合应用于 A549、CL1-0、H1299、HCC827 肺腺癌细胞,以研究其在诱导细胞凋亡方面的增效作用及其潜在机制。通过磺酰罗丹明 B 染色、Western blot 和流式细胞术检测,我们发现 SY 和 FO 联合应用可协同抑制肺腺癌细胞的生长并诱导其凋亡,而胎肺成纤维细胞(MRC-5)对此联合作用不敏感。FO 增强了 SY 诱导的 A549 细胞凋亡,同时协同激活 AMP 激活的蛋白激酶(AMPK),并降低环氧化酶(COX)-2 和 β-连环蛋白的表达。此外,与 FO 联合应用不仅增强了 SY 上调的促凋亡内质网应激标志物 CCAAT/增强子结合蛋白同源蛋白(CHOP),还降低了葡萄糖调节蛋白 78 kDa(GRP78)的细胞保护作用。因此,CHOP 下游靶点如磷酸化 JNK 和死亡受体 5 的表达也随之升高,同时伴随着胱天蛋白酶-8、-3 的剪切以及与内质网应激相关的胱天蛋白酶-4 的剪切。因此,AMPK 的抑制剂 Compound C 可减弱协同诱导的细胞凋亡,而 SY 与 FO 联合应用可增加 CHOP/GRP78 比值。该 AMPK 依赖性协同作用提示 SY 和 FO 的联合应用可用于肺腺癌的化学预防和综合治疗。