Bielecka Izabela, Natorska-Chomicka Dorota, Dołomisiewicz Wioleta, Rodrigues Fortes Arlindo, Dos Santos Szewczyk Katarzyna
Department of Pharmaceutical Botany, Medical University of Lublin, 20-093 Lublin, Poland.
Chair and Department of Toxicology, Faculty of Pharmacy, Medical University of Lublin, 20-090 Lublin, Poland.
Molecules. 2025 Jun 25;30(13):2739. doi: 10.3390/molecules30132739.
L. (alfavaca-de-cobra) was investigated as a potential source of anticancer compounds. Leaf extracts obtained using solvents of different polarities were evaluated for their phytochemical profiles and cytotoxic activities against a panel of human cancer cell lines (glioblastoma LN-229, lung NCI-H1563, breast MDA-MB-231, liver HepG2, renal 769-P, cervical HeLa, and melanoma A-375) and a noncancerous HEK-293 cell line. LC-ESI-MS/MS analysis confirmed that the extracts are rich in polyphenols, including phenolic acids and flavonoids. Cytotoxicity was assessed via MTT and SRB assays, demonstrating dose-dependent antiproliferative effects. Among the extracts, the ethanolic fraction (PJ-E) exhibited the strongest cytotoxicity, with an IC of 11.82 µg/mL against HeLa cells, while displaying a significantly higher IC (139.42 µg/mL) against HEK-293, indicating tumor selectivity. The water extract (PJ-W) showed selective activity against lung cancer cells (IC = 87.69 µg/mL), with minimal toxicity toward normal cells. The methanol/acetone extract (PJ-M) displayed intermediate activity, whereas the hexane extract (PJ-H) was the least effective. These findings highlight , particularly its ethanolic extract, as a promising source of natural anticancer agents. Further research focusing on the isolation of active constituents, formulation development, and in vivo validation is warranted to support its therapeutic potential.
对L.(眼镜蛇艾草)作为抗癌化合物潜在来源进行了研究。使用不同极性溶剂获得的叶提取物针对一组人类癌细胞系(胶质母细胞瘤LN - 229、肺癌NCI - H1563、乳腺癌MDA - MB - 231、肝癌HepG2、肾癌769 - P、宫颈癌HeLa和黑色素瘤A - 375)以及非癌性HEK - 293细胞系评估了其植物化学特征和细胞毒性活性。液相色谱 - 电喷雾串联质谱(LC - ESI - MS/MS)分析证实提取物富含多酚,包括酚酸和黄酮类化合物。通过MTT和SRB试验评估细胞毒性,显示出剂量依赖性的抗增殖作用。在提取物中,乙醇提取物(PJ - E)表现出最强的细胞毒性,对HeLa细胞的IC₅₀为11.82 μg/mL,而对HEK - 293的IC₅₀显著更高(139.42 μg/mL),表明具有肿瘤选择性。水提取物(PJ - W)对肺癌细胞表现出选择性活性(IC₅₀ = 87.69 μg/mL),对正常细胞毒性最小。甲醇/丙酮提取物(PJ - M)表现出中等活性,而己烷提取物(PJ - H)效果最差。这些发现突出了L.,特别是其乙醇提取物,作为天然抗癌剂的有前景来源。有必要进一步开展研究,聚焦于活性成分的分离、制剂开发和体内验证,以支持其治疗潜力。