Immunology Microbiology Laboratory, Department of Human Physiology, Tripura University, Agartala, Tripura, India.
Delhi Public School Megacity, Kolkata, West Bengal, India.
Front Immunol. 2023 Jan 19;13:1054186. doi: 10.3389/fimmu.2022.1054186. eCollection 2022.
Current anti-leukemic chemotherapies with multiple targets suffer from side effects. Synthetic drugs with huge off-target effects are detrimental to leukemic patients. Therefore, natural plant-based products are being increasingly tested for new anti-leukemic therapy with fewer or no side effects. Herein, we report the effect of ethanolic olive leaves extract (EOLE) on the K562 cell line and on the bone marrow (BM) of N-ethyl-N-nitrosourea (ENU)-induced leukemic mice.
Using standard methodologies, we assessed viability, chromatin condensation, and induction of apoptosis in EOLE-treated K562 cells . The anti-leukemic activity of EOLE was assayed by measuring ROS, levels of various cytokines, expression of iNOS and COX-2 gene, and changes in the level of important apoptosis regulatory and cell signaling proteins .
K562 cells underwent apoptotic induction after exposure to EOLE. In the BM of leukemic mice, EOLE therapy decreased the number of blast cells, ROS generation, and expression of NF-κB and ERK1/2. IL-6, IL-1β, TNF-α, iNOS, and COX-2 were among the inflammatory molecules that were down-regulated by EOLE therapy. Additionally, it decreased the expression of anti-apoptotic proteins BCL2A1, BCL-xL, and MCL-1 in the BM of leukemic mice.
Chronic inflammation and anomalous apoptotic mechanism both critically contribute to the malignant transformation of cells. Inflammation in the tumor microenvironment promotes the growth, survival, and migration of cancer cells, accelerating the disease. The current investigation showed that EOLE treatment reduces inflammation and alters the expression of apoptosis regulatory protein in the BM of leukemic mice, which may halt the progression of the disease.
目前具有多种靶点的抗白血病化疗药物存在副作用。具有巨大脱靶效应的合成药物对白血病患者有害。因此,越来越多的天然植物产品正在被测试用于新的抗白血病治疗,其副作用更小或没有。在此,我们报告了乙醇橄榄叶提取物(EOLE)对 K562 细胞系和 N-乙基-N-亚硝脲(ENU)诱导的白血病小鼠骨髓的影响。
使用标准方法,我们评估了 EOLE 处理的 K562 细胞的活力、染色质凝聚和细胞凋亡诱导。通过测量 ROS、各种细胞因子的水平、iNOS 和 COX-2 基因的表达以及重要凋亡调节和细胞信号蛋白水平的变化,来检测 EOLE 的抗白血病活性。
K562 细胞在暴露于 EOLE 后发生凋亡诱导。在白血病小鼠的骨髓中,EOLE 治疗减少了原始细胞数量、ROS 生成以及 NF-κB 和 ERK1/2 的表达。IL-6、IL-1β、TNF-α、iNOS 和 COX-2 是 EOLE 治疗下调的炎症分子之一。此外,它还降低了白血病小鼠骨髓中抗凋亡蛋白 BCL2A1、BCL-xL 和 MCL-1 的表达。
慢性炎症和异常的凋亡机制都对细胞的恶性转化有重要贡献。肿瘤微环境中的炎症促进了癌细胞的生长、存活和迁移,加速了疾病的进展。目前的研究表明,EOLE 治疗可减少炎症并改变白血病小鼠骨髓中凋亡调节蛋白的表达,从而可能阻止疾病的进展。