水飞蓟素诱导SPC212人间皮瘤细胞凋亡和生长抑制的机制研究。

IF 1.8 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Cell Biochemistry and Biophysics Pub Date : 2025-01-02 DOI:10.1007/s12013-024-01650-w
Özlem Tomsuk, Sedat Kaçar
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引用次数: 0

摘要

水飞蓟素是一种从水飞蓟中分离得到的类黄酮复合物,具有抗氧化、抗炎、抗糖基化和保护肝脏等多种生物学特性。本实验研究水飞蓟素对人间皮瘤细胞株SPC212的影响。MTT法和中性红法检测水飞蓟素的细胞毒作用。AO/EB、DAPI染色观察细胞凋亡作用,H&E、may - gr nwald染色观察细胞形态学变化。此外,免疫细胞化学检测Bax、Bcl2和PCNA。结果表明,水飞蓟素对SPC212细胞具有剂量依赖性的细胞毒作用,IC50值约为187.5µM。水飞蓟素诱导凋亡的标志,如凋亡小体、细胞收缩和核凝聚。综上所示,水飞蓟素对SPC212人间皮瘤细胞具有细胞毒性和凋亡作用,并能改变细胞形态。水飞蓟素作为抗癌药物的潜力有待进一步深入研究。
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Mechanistic Insights into Silymarin-Induced Apoptosis and Growth Inhibition in SPC212 Human Mesothelioma Cells.

Silymarin, a flavonoid complex isolated from Silybum marianum, possesses various biological properties, including antioxidant, anti-inflammatory, anti-glycation, and hepatoprotective effects. In the present study, we investigated the effects of silymarin on the SPC212 human mesothelioma cell line. MTT and neutral red assays were performed to examine the cytotoxic effects of silymarin. The apoptotic effect was investigated using AO/EB and DAPI staining, and morphological changes were observed using H&E and May-Grünwald staining. Additionally, immunocytochemistry was performed to detect Bax, Bcl2, and PCNA. Our results indicated that silymarin has a dose-dependent cytotoxic effect on SPC212 cells, with an IC50 value of approximately 187.5 µM. Silymarin induces apoptotic hallmarks such as apoptotic bodies, cell shrinkage, and nuclear condensation. In conclusion, silymarin demonstrated cytotoxic and apoptotic effects as well as morphological changes in SPC212 human mesothelioma cells. Further detailed studies are warranted to explore the potential of silymarin as an anti-cancer agent.

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来源期刊
Cell Biochemistry and Biophysics
Cell Biochemistry and Biophysics 生物-生化与分子生物学
CiteScore
4.40
自引率
0.00%
发文量
72
审稿时长
7.5 months
期刊介绍: Cell Biochemistry and Biophysics (CBB) aims to publish papers on the nature of the biochemical and biophysical mechanisms underlying the structure, control and function of cellular systems The reports should be within the framework of modern biochemistry and chemistry, biophysics and cell physiology, physics and engineering, molecular and structural biology. The relationship between molecular structure and function under investigation is emphasized. Examples of subject areas that CBB publishes are: · biochemical and biophysical aspects of cell structure and function; · interactions of cells and their molecular/macromolecular constituents; · innovative developments in genetic and biomolecular engineering; · computer-based analysis of tissues, cells, cell networks, organelles, and molecular/macromolecular assemblies; · photometric, spectroscopic, microscopic, mechanical, and electrical methodologies/techniques in analytical cytology, cytometry and innovative instrument design For articles that focus on computational aspects, authors should be clear about which docking and molecular dynamics algorithms or software packages are being used as well as details on the system parameterization, simulations conditions etc. In addition, docking calculations (virtual screening, QSAR, etc.) should be validated either by experimental studies or one or more reliable theoretical cross-validation methods.
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