Department of Systems Biology, School of Medicine and Health Sciences, University of Alcala, Alcalá de Henares, Madrid, Spain.
University Institute of Biomedical and Health Research (IUIBS), Department of Biochemistry and Molecular Biology, Physiology, Genetics and Immunology, University of Las Palmas de Gran Canaria, Las Palmas, Spain.
PLoS One. 2019 Jan 29;14(1):e0211420. doi: 10.1371/journal.pone.0211420. eCollection 2019.
Capsaicin is a natural compound present in chili and red peppers and the responsible of their spicy flavor. It has recently provoked interest because of its antitumoral effects in many cell types although its action mechanism is not clearly understood. As metabolic dysregulation is one of the hallmarks of cancer cells and the key metabolic sensor in the AMP-activated kinase (AMPK), in this study we explored the ability of capsaicin to modulate AMPK activity. We found that capsaicin activated AMPK in HepG2 cells by increasing AMPK phosphorylation and its downstream target ACC. Mechanistically, we determined that capsaicin activated AMPK through the calcium/calmodulin-dependent protein kinase kinase β, CaMKKβ as either the CaMKK inhibitor STO-609 or CaMKK knock down with siRNA abrogated the activation of AMPK. Moreover, capsaicin decreased cell viability, inhibited Akt/mTOR pathway and increased reactive oxygen species (ROS) in HepG2 cells. AMPK activation was involved in the underpinning mechanism of capsaicin-induced cell death.
辣椒素是辣椒和红辣椒中存在的一种天然化合物,也是它们辣味的来源。由于其在许多细胞类型中的抗肿瘤作用,辣椒素最近引起了人们的兴趣,尽管其作用机制尚不清楚。由于代谢失调是癌细胞的一个标志,而关键的代谢传感器是 AMP 激活的蛋白激酶(AMPK),在这项研究中,我们探讨了辣椒素调节 AMPK 活性的能力。我们发现,辣椒素通过增加 AMPK 磷酸化及其下游靶标 ACC 来激活 HepG2 细胞中的 AMPK。从机制上讲,我们确定辣椒素通过钙/钙调蛋白依赖性蛋白激酶激酶β(CaMKKβ)激活 AMPK,因为 CaMKK 抑制剂 STO-609 或用 siRNA 敲低 CaMKKβ 均可消除 AMPK 的激活。此外,辣椒素降低了 HepG2 细胞的活力,抑制了 Akt/mTOR 通路,并增加了活性氧物种(ROS)。AMPK 的激活参与了辣椒素诱导细胞死亡的潜在机制。