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从. 中提取多糖的优化及抗肿瘤活性研究

Extraction Optimization and Anti-Tumor Activity of Polysaccharides from .

机构信息

Guangxi Key Laboratory for Polysaccharide Materials and Modifications, School of Marine and Biotechnology, Guangxi University for Nationalities, Nanning 530006, China.

出版信息

Mar Drugs. 2024 Aug 2;22(8):356. doi: 10.3390/md22080356.


DOI:10.3390/md22080356
PMID:39195472
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11355090/
Abstract

polysaccharides (CRPs) are bioactive compounds derived from , yet their potential in cancer therapy remains largely unexplored. This study optimized the ultrasound-assisted extraction conditions using response surface methodology and proceeded with the isolation and purification of these polysaccharides. The optimal extraction conditions were identified as a sodium hydroxide concentration of 1.5%, ultrasonic power of 200 W, a solid-to-liquid ratio of 1:25 g/mL, an ultrasonic treatment time of 10 min, and a water bath duration of 2.5 h, yielding an actual extraction rate of 5.71 ± 0.001%, which closely aligns with the predicted value of 5.639%. Infrared analysis revealed that CRP-1 and CRP-2 are α-pyranose structures containing furoic acid, while CRP-3 and CRP-4 are β-pyranose structures containing furoic acid. Experimental results demonstrated that all four purified polysaccharides inhibited the proliferation of cervical (HeLa) hepatoma (HepG-2) and colon (HCT-116) cancer cells, with CRP-4 showing the most significant inhibitory effect on colon cancer and cervical cancer, achieving inhibition rates of 60.58 ± 0.88% and 40.44 ± 1.44%, respectively, and significantly reducing the migration of HeLa cells. DAPI staining confirmed that the four purified polysaccharides inhibit cell proliferation and migration by inducing apoptosis in HeLa cells. CRP-1 has the most significant inhibitory effect on the proliferation of liver cancer cells. This study not only elucidates the potential application of polysaccharides in cancer therapy but also provides a scientific basis for their further development and utilization.

摘要

多糖(CRPs)是从 中提取的生物活性化合物,但它们在癌症治疗中的潜力在很大程度上尚未得到探索。本研究采用响应面法优化了超声辅助提取条件,并进行了这些多糖的分离和纯化。确定的最佳提取条件为氢氧化钠浓度 1.5%、超声功率 200 W、固液比 1:25 g/mL、超声处理时间 10 min 和水浴时间 2.5 h,实际提取率为 5.71±0.001%,与预测值 5.639%非常接近。红外分析表明,CRP-1 和 CRP-2 是含有呋喃酸的α-吡喃糖结构,而 CRP-3 和 CRP-4 是含有呋喃酸的β-吡喃糖结构。实验结果表明,四种纯化的多糖均能抑制宫颈(HeLa)肝癌(HepG-2)和结肠(HCT-116)癌细胞的增殖,其中 CRP-4 对结肠癌和宫颈癌的抑制作用最为显著,对结肠癌和宫颈癌的抑制率分别达到 60.58±0.88%和 40.44±1.44%,并显著降低了 HeLa 细胞的迁移。DAPI 染色证实,四种纯化的多糖通过诱导 HeLa 细胞凋亡抑制细胞增殖和迁移。CRP-1 对肝癌细胞增殖的抑制作用最为显著。本研究不仅阐明了多糖在癌症治疗中的潜在应用,还为其进一步开发利用提供了科学依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/5fb721b1897c/marinedrugs-22-00356-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/d90ecb354c61/marinedrugs-22-00356-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/68fe8c67c910/marinedrugs-22-00356-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/eff81d13e578/marinedrugs-22-00356-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/58a48e32b261/marinedrugs-22-00356-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/492c37ba5fac/marinedrugs-22-00356-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/9475bd2f329e/marinedrugs-22-00356-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/35e32ae369c4/marinedrugs-22-00356-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/9669417b54c5/marinedrugs-22-00356-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/8cdfa50ba224/marinedrugs-22-00356-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/614c1ac5cdfc/marinedrugs-22-00356-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/5fb721b1897c/marinedrugs-22-00356-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/d90ecb354c61/marinedrugs-22-00356-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/68fe8c67c910/marinedrugs-22-00356-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/eff81d13e578/marinedrugs-22-00356-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/58a48e32b261/marinedrugs-22-00356-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/492c37ba5fac/marinedrugs-22-00356-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/9475bd2f329e/marinedrugs-22-00356-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/35e32ae369c4/marinedrugs-22-00356-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/9669417b54c5/marinedrugs-22-00356-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/8cdfa50ba224/marinedrugs-22-00356-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/614c1ac5cdfc/marinedrugs-22-00356-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa2b/11355090/5fb721b1897c/marinedrugs-22-00356-g011.jpg

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[5]
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[7]
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