Microchemical Journal, Journal Year: 2024, Volume and Issue: unknown, P. 112481 - 112481
Published: Dec. 1, 2024
Language: Английский
Microchemical Journal, Journal Year: 2024, Volume and Issue: unknown, P. 112481 - 112481
Published: Dec. 1, 2024
Language: Английский
Molecular Cancer, Journal Year: 2025, Volume and Issue: 24(1)
Published: Jan. 21, 2025
Language: Английский
Citations
3Pharmaceuticals, Journal Year: 2024, Volume and Issue: 17(5), P. 636 - 636
Published: May 15, 2024
Astragalus polysaccharide (APS) derived from A. membranaceus plays a crucial role in traditional Chinese medicine. These polysaccharides have shown antitumor effects and are considered safe. Thus, they become increasingly important cancer immunotherapy. APS can limit the spread of by influencing immune cells, promoting cell death, triggering autophagy, impacting tumor microenvironment. When used combination with other therapies, enhance treatment outcomes reduce toxicity side effects. combined checkpoint inhibitors, relay cellular immunotherapy, vaccines broadened application immunotherapy enhanced effectiveness. By summarizing research on over past two decades, this review elaborates anticancer mechanism its use clinical trials. Considering multiple roles APS, emphasizes importance using as an adjunct to compares APS. This discussion provides insights into specific action reveals molecular targets for developing effective strategies, highlights wide therapy future.
Language: Английский
Citations
10Biomedical Journal, Journal Year: 2024, Volume and Issue: unknown, P. 100741 - 100741
Published: April 1, 2024
The impact and underlying mechanisms of astragalus polysaccharide (APS) on prostate cancer, particularly its role in immunomodulation, remain inadequately elucidated. This study employed the XTT assay for assessing proliferation cancer cells macrophages. T cell was determined using Carboxyfluorescein diacetate succinimidyl ester labeling assay. APS's effect macrophages scrutinized via flow cytometry, Western blot analysis, ELISA, quantitative PCR cytokine membrane arrays. APS interaction between PD-L1 PD-1 investigated by PD-L1/PD-1 homogeneous Additionally, conditioned medium from PC-3 migration explored through assays. It observed that at concentrations 1 5 mg/mL enhanced CD8+ cells. At a concentration mg/mL, activated both CD4+ cells, attenuated expression stimulated with interferon gamma (IFN-γ) or oxaliplatin, moderately decreased population PD-1+ Furthermore, this impeded PD-1, inhibited promotion mediated RAW 264.7 THP-1 initiated apoptosis treated (5 mg/mL)-treated findings indicate potential modulating PD-1/PD-L1 pathway influencing immune response, encompassing Consequently, further vivo research is recommended to assess efficacy APS.
Language: Английский
Citations
4Chinese Medicine, Journal Year: 2024, Volume and Issue: 19(1)
Published: Oct. 29, 2024
Language: Английский
Citations
4Published: Jan. 1, 2025
Language: Английский
Citations
0International Journal of Biological Macromolecules, Journal Year: 2025, Volume and Issue: unknown, P. 140820 - 140820
Published: Feb. 1, 2025
Language: Английский
Citations
0Pharmacognosy Magazine, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 13, 2025
Background Epithelial-mesenchymal transition (EMT) is crucial in liver cancer progression. Developing novel medicines to disrupt the progression of EMT might be a approach managing cancer. Purpose This study investigates protective role Astragalus polysaccharide (APS), bioactive compound derived from membranaceus, modulating HepG2 cells. Methods The effects APS on were evaluated by assessing cell viability, proliferation, invasion, migration, cycle, and apoptosis Furthermore, involvement NOD-like receptor protein 3 (NLRP3) inflammasome this process was explored. Results Results: treatment significantly inhibited migration cells while promoting cycle arrest apoptosis. Notably, reduced expression NLRP3 components, including NLRP3, apoptosis-associated speck-like protein, caspase-1, decreasing levels inflammatory cytokines. In addition, activator Nigericin dampened effect partially rescuing activity NLRP3. Specifically, promoted development exacerbated malignant transformation improved APS. Conclusion Our findings demonstrated function which inhibits activation protect results showed that targeting application appears viable tactic for preventing
Language: Английский
Citations
0Frontiers in Pharmacology, Journal Year: 2025, Volume and Issue: 16
Published: Feb. 18, 2025
Owing to its high mortality rate, lung cancer (LC) remains the most common worldwide, with highest malignancy diagnosis rate. The phosphatidylinositol-3-kinase (PI3K)/protein kinase B (AKT)/mammalian target of rapamycin (mTOR) signaling (PAM) pathway is a critical intracellular involved in various cellular functions and regulates numerous processes, including growth, survival, proliferation, metabolism, apoptosis, invasion, angiogenesis. This review aims highlight preclinical clinical studies focusing on PAM LC underscore potential natural products targeting it. Additionally, this synthesizes existing literature discusses combination therapy future directions for treatment while acknowledging ongoing challenges field. Continuous development novel therapeutic agents, technologies, precision medicine offers an increasingly optimistic outlook LC.
Language: Английский
Citations
0Drug Discovery Today, Journal Year: 2025, Volume and Issue: unknown, P. 104320 - 104320
Published: Feb. 1, 2025
Language: Английский
Citations
0Journal of Ethnopharmacology, Journal Year: 2025, Volume and Issue: unknown, P. 119607 - 119607
Published: March 1, 2025
Language: Английский
Citations
0