Clinical Laboratory Sciences Department, College of Applied Medical Sciences, Taif University, At Taif, Saudi Arabia.
Cancer Biology and Genetics Laboratory, Centre of Excellence for Advanced Sciences, National Research Centre, Dokki, Egypt.
Nutr Cancer. 2021;73(5):856-868. doi: 10.1080/01635581.2020.1773512. Epub 2020 Jun 2.
(EC) is an edible plant and a gum source for food industries. Its sulfated polysaccharide extract (SEC) was examined for cancer chemopreventive properties to estimate its anti-tumor activity. The modulation of carcinogen metabolism and the antioxidant activity revealed that SEC is a potent tumor anti-initiator since it inhibited cytochrome P450-1A (CYP1A) and induced carcinogen detoxification enzyme glutathione-S-transferase. SEC is also a weak scavenger for hydroxyl and peroxyl radicals. SEC was found to modulate macrophage functions into an anti-inflammatory pattern, where it enhanced macrophage proliferation and phagocytosis of fluorescein isothiocyanate-lipopolysaccharide (FITC-LPS). In addition, SEC strongly inhibited the nitric oxide (NO) generation in LPS-stimulated macrophages and induced the binding affinity of FITC-LPS to macrophages. SEC exhibited specific cytotoxicity against human hepatocellular Hep G2 carcinoma cells. SEC disturbed the cell cycle phase, as indicated by the concomitant arrest in S- and G2/M-phases that was associated with necrosis induction. A short-term initiation model for liver cancer was prepared using diethylnitrosamine (DEN) in rats. SEC inhibited the DEN-histopathological findings and reduced both CYP1A and the tumor initiation marker placental glutathione S-transferase (GSTP). Taken together, SEC could be used as an alternative gum in health food industries to provide cancer prevention in high-risk populations.
(EC) 是一种食用植物,也是食品工业用胶的来源。人们研究了其硫酸多糖提取物 (SEC) 的抗癌特性,以评估其抗肿瘤活性。研究表明,SEC 可调节致癌物质代谢并具有抗氧化活性,是一种有效的肿瘤起始抑制剂,因为它可抑制细胞色素 P450-1A (CYP1A) 并诱导致癌物质解毒酶谷胱甘肽-S-转移酶。SEC 也是羟基和过氧自由基的弱清除剂。SEC 可调节巨噬细胞功能向抗炎模式转变,增强巨噬细胞增殖和对异硫氰酸荧光素脂多糖 (FITC-LPS) 的吞噬作用。此外,SEC 可强烈抑制脂多糖刺激的巨噬细胞中一氧化氮 (NO) 的生成,并诱导 FITC-LPS 与巨噬细胞的结合亲和力。SEC 对人肝癌 Hep G2 癌细胞具有特异性细胞毒性。SEC 扰乱细胞周期阶段,S 期和 G2/M 期同时停滞与诱导坏死有关。使用二乙基亚硝胺 (DEN) 在大鼠中制备肝癌短期起始模型。SEC 抑制 DEN 的组织病理学发现,并降低 CYP1A 和肿瘤起始标志物胎盘谷胱甘肽 S-转移酶 (GSTP)。总之,SEC 可用作保健食品工业中的替代胶,为高危人群提供癌症预防。