胎盘螺壳的生物和分子效率体外研究:通过 Nrf2/HMOX-1/ 和 HIF-1α /VEGF 信号通路对 T47D 乳腺癌细胞株的抗氧化和血管生成作用。

IF 2.5 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Abeer A. Khamis, Mai M. Elkeiy, Mona M. El-Gamal, Khalil M. Saad-Allah, Maha M. Salem
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引用次数: 0

摘要

海胆(Paracentrotus lividus)壳的研究揭示了丰富的生物活性化合物。采用UPLCMS/MS分析方法对活性成分进行观察。以NO、MDA、CAT、SOD水平为指标评价鹅毛螺壳提取物的抗糖尿病、抗氧化、抗菌和抗炎性能。同时,对结肠癌(Caco-2)和乳腺癌(T47D)癌细胞的细胞毒性和抗血管生成影响进行了评估,并量化了Nrf2/HMOX-1和HIF-1α/VEGF通路的表达。结果表明,该提取物具有显著的抗氧化活性,IC50分别为(0.1056±0.083)和(30.42±1.52)μg/mL;抗糖尿病IC50(1.572±0.13 μg/mL),抗炎IC50(2.090±0.49 μg/mL)。特别是对人乳腺癌(T47D)和结肠癌(Caco-2)癌细胞具有较强的抗肿瘤作用,分别为(30.55±1.19µg/mL和31.34±1.22µg/mL)。通过提高NO和MDA水平,降低SOD和CAT活性,该提取物可诱导氧化应激和细胞凋亡。此外,Nrf2/HMOX-1和HIF-1α/VEGF通路表达的下调表明其抗癌特性的复杂分子机制,可能涉及氧化应激和血管生成的调节。这些发现强调了海胆(P. lividus)外壳作为一种有效的生物活性成分储存库,在药物研究中具有广阔的应用前景,并为药物发现提供了新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biological and Molecular Efficiency of Paracentrotus lividus Shell in vitro Study: Antioxidant and Angiogenesis Effects Against T47D Breast Cancer Cell Line Via Nrf2/HMOX-1/ and HIF-1α /VEGF Signaling Pathways

The sea urchin (Paracentrotus lividus) shell investigation reveals a wealth of bioactive compounds. The bioactive ingredients were observed using UPLCMS/MS profiling. The anti-diabetic, antioxidant, antimicrobial, and anti-inflammatory qualities of P. lividus shell extract were assessed concerning NO, MDA, CAT, and SOD levels. Also, cytotoxic, and anti-angiogenic impact on colon (Caco-2) and breast (T47D) carcinoma cells and quantificated of Nrf2/HMOX-1 and HIF-1α/VEGF pathway expression were evaluated. Our findings indicate that the extract possesses remarkable antioxidant activity with IC50 equal to (0.1056 ± 0.083 and 30.42 ± 1.52 μg/mL; for DPPH and ABTS+ respectively), antidiabetic with IC50 (1.572 ± 0.13 μg/mL) and anti-inflammatory with IC50 (2.090 ± 0.49 μg/mL). Notably, it exhibits potent anticancer effects against human breast (T47D) and colon (Caco-2) cancer cell lines, (30.55 ± 1.19 and 31.34 ± 1.22 µg/mL respectively). The extract induces oxidative stress and apoptosis, as evidenced by elevated NO and MDA levels, alongside reduced SOD and CAT activities. Moreover, the downregulation of Nrf2/HMOX-1 and HIF-1α/VEGF pathways expression suggests intricate molecular mechanisms underlying its anticancer properties, potentially involving the modulation of oxidative stress and angiogenesis. These findings underscore the sea urchin (P. lividus) shell as a potent reservoir of bioactive constituents with promising applications in pharmaceutical research and offering new avenues for drug discovery.

Graphical Abstract

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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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