Clinical Laboratory Sciences, College of Applied Medical Sciences, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia.
Department of Natural and Microbial Products Chemistry, National Research Centre, Dokki, Cairo 12622, Egypt.
Curr Pharm Biotechnol. 2022;23(7):988-997. doi: 10.2174/1389201022666210714151419.
Abelmoschus esculentus (AE) (okra), is an edible plant used in many food applications.
This study explored whether sulfated AE (SAE) has promising cancer chemopreventive activities that may recommend it as a functional food supplement instead of (or in addition to) AE for the population at risk of cancer and in the health food industry.
Cytochrome P450-1A (CYP1A) was estimated by fluorescence enzymatic reaction, using β-naphthoflavone-treated cells (CYP1A inducer). Peroxyl and hydroxyl radical scavenging was assayed by oxygen radical absorbance capacity assay. Flow cytometry was used to analyze apoptosis/necrosis in MCF-7 cells, cell cycle phases in MCF-7 cells, and macrophage binding to fluorescein isothiocyanate-lipopolysaccharide (FITC-LPS). Nitric oxide was determined by Griess assay in LPS-stimulated macrophages, and cytotoxicity was determined by MTT assay. Diethylnitrosamine (DEN) was used to induce hepatic tumor initiation in rats. Placental glutathione-S-transferase (GSTP; an initiation marker) was stained in a fluorescence immunohistochemical analysis of liver sections, and histopathological changes were examined.
SAE exhibited strong antitumor initiation and antitumor promotion activities. It suppressed CYP1A, scavenged peroxyl and hydroxyl radicals, induced macrophage proliferation, suppressed macrophage binding to FITC-LPS, inhibited nitric oxide generation, showed specific cytotoxicity to human breast MCF-7 adenocarcinoma cells, and disturbed the cell cycle phases (S and G2/M phases) in association with an increased percentage of apoptotic/necrotic MCF-7 cells. Over a short time period, DEN stimulated liver cancer initiation, but SAE treatment reduced the DEN-induced histopathological alterations and inhibited CYP1A and GSTP.
SAE extract has the potential for use as an alternative to AE in health foods to provide cancer chemoprevention in populations at risk for cancer.
黄蜀葵(AE)(秋葵)是一种可食用植物,用于许多食品应用。
本研究探讨了硫酸化 AE(SAE)是否具有有前景的癌症化学预防活性,使其可作为功能性食品补充剂推荐给癌症风险人群,或应用于保健食品行业。
通过用β-萘黄酮处理的细胞(CYP1A 诱导剂)进行荧光酶促反应来估计细胞色素 P450-1A(CYP1A)。通过氧自由基吸收能力测定法测定过氧自由基和羟自由基的清除率。使用流式细胞术分析 MCF-7 细胞中的细胞凋亡/坏死、MCF-7 细胞的细胞周期阶段以及巨噬细胞与异硫氰酸荧光素脂多糖(FITC-LPS)的结合。用 Griess 测定法测定 LPS 刺激的巨噬细胞中的一氧化氮,并用 MTT 测定法测定细胞毒性。用二乙基亚硝胺(DEN)诱导大鼠肝肿瘤起始。在肝组织切片的荧光免疫组织化学分析中对胎盘谷胱甘肽 S-转移酶(GSTP;起始标志物)进行染色,并检查组织病理学变化。
SAE 表现出很强的抗肿瘤起始和抗肿瘤促进活性。它抑制 CYP1A,清除过氧自由基和羟自由基,诱导巨噬细胞增殖,抑制巨噬细胞与 FITC-LPS 的结合,抑制一氧化氮的产生,对人乳腺癌 MCF-7 腺癌细胞具有特异性细胞毒性,并干扰细胞周期阶段(S 和 G2/M 期),与增加的 MCF-7 细胞凋亡/坏死百分比相关。在短时间内,DEN 刺激肝癌起始,但 SAE 处理减少了 DEN 诱导的组织病理学改变,并抑制了 CYP1A 和 GSTP。
SAE 提取物有可能替代 AE 用于保健食品,为癌症风险人群提供癌症化学预防。