Spatoglossum variabile 和 Gracilaria corticata 甲醇提取物的抗癌活性和生物活性成分的气相色谱-质谱分析

Q2 Pharmacology, Toxicology and Pharmaceutics Current Bioactive Compounds Pub Date : 2024-04-24 DOI:10.2174/0115734072296835240409124751
S. Sruthi, Shahjahan A, Kumaran K, Dannie Macrin, Vijay Murali RM, K.N. Aruljothi
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引用次数: 0

摘要

海藻是生物活性代谢物的宝库,被广泛用于治疗各种疾病。鉴于传统的癌症治疗方法往往会产生令人头疼的副作用,研究人员正越来越多地把目光转向海洋藻类,认为它们是发现新型强效抗癌化合物的大有希望的来源。在这项研究中,我们对来自印度洋的 Spatoglossum variabile 和 Gracilaria corticata 的潜在抗癌活性进行了细致的探索。由于标准癌症治疗方法的不良影响,研究人员已将海洋藻类视为新型和有前景的抗癌化合物。Spatoglossum variabile 的甲醇提取物含有 21 种独特的抗癌化合物,其他生物活性化合物除外。结果表明,藻类提取物浓度的增加会显著降低细胞的活力,对 HCT116 细胞株的 IC50 为 51.49 μg /mL,对 HCT116 细胞株的 IC50 为 37.50 μg /mL。结果显示,结直肠癌细胞集落形成明显减少,细胞增殖逐渐降低。对提取物进行了 GC-MS 分析,并使用 MTT、克隆生成和胰蓝染料排除法分别评估了其在 HCT116 细胞系中的短期和长期细胞毒性及抗增殖能力。我们的研究结果表明,Spatoglossuum variabile 和 Gracilaria corticata 提取物含有多种生物活性化合物,具有长期和短期的细胞毒性和抗增殖作用,这表明它们的组成化合物有可能被进一步提炼成有效的抗结直肠癌药物。结果表明,藻类提取物浓度的增加会显著降低细胞的活力,在 HCT116 细胞系中的 IC50 为 51.49 µg/mL 和 37.50 µg /ml。结果表明,细胞集落形成明显减少,细胞增殖也逐渐减少。
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Anticancer Activity and GC-MS Profiling of Bioactive Constituents in the Methanolic Extracts of Spatoglossum variabile and Gracilaria corticata
Marine algae stand out as repositories of bioactive metabolites, widely harnessed in treating diverse diseases. Given the often-challenging side effects associated with conventional cancer treatments, researchers are increasingly turning their attention to marine algae as a promising source for discovering novel and potent anticancer compounds. In this study, we meticulously explored the potential anticancer activity of Spatoglossum variabile and Gracilaria corticata sourced from the Indian Ocean. Marine algae are rich in bioactive metabolites that are extensively used to treat various diseases. Researchers have considered marine algae for novel and promising anticancer compounds due to the adverse effects of standard cancer treatments The secondary metabolites were extracted using methanol solvent according to the standard protocol. The extract was subjected to GC-MS analysis and evaluated for its short- and long-term cytotoxicity and anti-proliferative ability in the HCT116 cell line using MTT, clonogenic, and trypan blue dye exclusion assays, respectively. The methanolic extract of Spatoglossum variabile contained 21 unique anticancer compounds, except for the other bioactive compounds. The results indicate that increasing the concentration of algal extracts decreased the cell viability significantly, with an IC50 of 51.49 μg/mL and 37.50 μg /mL in the HCT116 cell line. The results showed a significant reduction in colorectal cancer colony formation and a gradual reduction in cell proliferation. These results underscore the potential for targeted, low-toxicity biomedicines due to their selective cytotoxicity against cancer cells. The extract was subjected to GC-MS analysis and evaluated for its short- and long-term cytotoxicity and anti-proliferative ability in HCT116 cell line using MTT, clonogenic, and trypan blue dye exclusion assays, respectively. Our findings show that Spatoglosuum variabile & Gracilaria corticata extracts contain various bioactive compounds, display long-term and short-term cytotoxicity and antiproliferative effects, which indicates that their constituent compounds might be further refined into effective anti-colorectal cancer medications. The methanolic extract of Spatoglossum variabile contained 21 unique anti-cancer compounds, in addition to other bioactive compounds. The results indicate that increasing the concentration of algal extracts decreased the cell viability significantly, with an IC50 of 51.49 µg/mL and 37.50 µg /ml in the HCT116 cell line. The results showed a significant reduction in colony formation and a gradual reduction in cell proliferation
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来源期刊
Current Bioactive Compounds
Current Bioactive Compounds Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.90
自引率
0.00%
发文量
112
期刊介绍: The journal aims to provide comprehensive review articles on new bioactive compounds with proven activities in various biological screenings and pharmacological models with a special emphasis on stereoeselective synthesis. The aim is to provide a valuable information source of bioactive compounds synthesized or isolated, which can be used for further development of pharmaceuticals by industry and academia. The journal should prove to be essential reading for pharmacologists, natural product chemists and medicinal chemists who wish to be kept informed and up-to-date with the most important developments on new bioactive compounds of natural or synthetic origin, including their stereoeselective synthesis.
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