Collaborative Drug Discovery Research (CDDR) Group, Faculty of Pharmacy, University Teknologi MARA (UiTM) Cawangan Selangor, Kampus Puncak Alam, 42300 Bandar Puncak Alam, Selangor Darul Ehsan, Malaysia.
Department of Pharmaceutical and Toxicological Chemistry Named after Arzamastsev of the Institute of Pharmacy, I.M. Sechenov First Moscow State Medical University (Sechenov University), Bolshaya Pirogovskaya 2, p 4, 119991, Moscow, Russia; School of Pharmacy and Applied Science, La Trobe Institute of Molecular Sciences, La Trobe University, Edwards Rd, Bendigo, VIC, 3550, Australia.
J Pharm Biomed Anal. 2021 Jan 30;193:113702. doi: 10.1016/j.jpba.2020.113702. Epub 2020 Oct 18.
Bioactive compounds from endophytic fungi exhibit diverse biological activities which include anticancer effect. Capitalising on the abundance of unexplored endophytes that reside within marine plants, this study assessed the anticancer potential of ethyl acetate endophytic fungal extracts (i.e. MBFT Tip 2.1, MBL 1.2, MBS 3.2, MKS 3 and MKS 3.1) derived from leaves, stem and fruits of marine plants that grow along Morib Beach, Malaysia. For identification of endophytic fungi, EF 4/ EF 3 and ITS 1/ ITS 4 PCR primer pairs were used to amplify the fungal 18S rDNA sequence and ITS region sequence, respectively. The resultant sequences were subjected to similarity search via the NCBI GenBank database. High-performance thin layer chromatography (HPTLC) hyphenated with bioassays was used to characterise the extracts in terms of their phytochemical profiles and bioactivity. Microchemical derivatisation was used to assess polyphenolic and phytosterol/ terpenoid content whereas biochemical derivatisation was used to establish antioxidant activities and α-amylase enzyme inhibition. The sulforhodamine B (SRB) assay was used to assess the anticancer effect of the extracts against HCT116 (a human colorectal cancer cell line). The present results indicated MBS 3.2 (Penicillium decumbens) as the most potent extract against HCT116 (IC = 0.16 μg/mL), approximately 3-times more potent than 5-flurouracil (IC = 0.46 μg/mL). Stepwise multiple regression method suggests that the anticancer effect of MBS 3.2 could be associated with high polyphenolic content and antioxidant potential. Nonlinear regression analysis confirmed that low to moderate α-amylase inhibition exhibits maximum anticancer activity. Current findings warrant further in-depth mechanistic studies.
从内生真菌中提取的生物活性化合物具有多种生物活性,包括抗癌作用。本研究利用马来西亚莫立海滨生长的海洋植物中丰富的未被开发的内生真菌,评估了从海洋植物的叶、茎和果实中提取的乙酸乙酯内生真菌提取物(即 MBFT Tip 2.1、MBL 1.2、MBS 3.2、MKS 3 和 MKS 3.1)的抗癌潜力。为了鉴定内生真菌,使用 EF 4/EF 3 和 ITS 1/ITS 4 PCR 引物对分别扩增真菌 18S rDNA 序列和 ITS 区序列。所得序列通过 NCBI GenBank 数据库进行相似性搜索。采用高效薄层层析(HPTLC)与生物测定相结合的方法,根据提取物的植物化学成分谱和生物活性对其进行表征。微化学衍生化用于评估多酚和植物甾醇/萜烯含量,而生化衍生化用于建立抗氧化活性和α-淀粉酶酶抑制作用。采用磺基罗丹明 B(SRB)测定法评估提取物对 HCT116(人结直肠癌细胞系)的抗癌作用。目前的结果表明,MBS 3.2(Penicillium decumbens)是对 HCT116 最有效的提取物(IC = 0.16 μg/mL),大约比 5-氟尿嘧啶(IC = 0.46 μg/mL)强 3 倍。逐步多元回归方法表明,MBS 3.2 的抗癌作用可能与高多酚含量和抗氧化潜力有关。非线性回归分析证实,低至中度的α-淀粉酶抑制作用表现出最大的抗癌活性。目前的研究结果需要进一步深入的机制研究。