AI Article Synopsis

  • Esophageal-squamous Cell Carcinoma (ESCC) is typically diagnosed in later stages, prompting the need for better treatment methods, such as enhancing the anti-tumor effects of matrine (MA) using nanotechnology.
  • Researchers created MA-loaded Nano-Liposomes (MNLs) that showed favorable characteristics like small size, stability, and high encapsulation efficiency, which helped improve the anti-cancer effects on KYSE-150 cells.
  • Findings revealed that MNLs significantly reduced cell viability, increased pro-apoptotic proteins, and are suggested as a more effective therapeutic option for treating ESCC compared to MA alone.

Article Abstract

Introduction: Esophageal-squamous Cell Carcinoma (ESCC) is often diagnosed at the middle or late stage, thus requiring more effective therapeutic strategies. Pharmacologically, the anti-tumor activity of the principal active constituent of , matrine (MA), has been explored widely. Notwithstanding, it is significant to nanotechnologically enhance the anti-tumor activity of MA in view of its potential to distribute non-tumor cells.

Methods: Herein, MA-loaded Nano-Liposomes (MNLs) were prepared to enhance the effect of anti-ESCC. The MNL showed a smaller sized particle (25.95 ± 1.02 nm) with a low polydispersed index (PDI = 0.130 ± 0.054), uniform spherical morphology, good solution stability, and encapsulated efficiency (65.55% ± 2.47). Furthermore, we determined the characteristics of KYSE-150 cells by cell viability assay, IC, Mitochondrial Membrane Potential (MMP), Western blot, and apoptotic analysis, which indicated that MNLs down-regulated the cell viability and IC in a concentration-dependent manner and induced a significant change in JC-1 fluorescence from red to green.

Results: The above observations resulted in increased Bax and Caspase-3 levels, coupled with a substantial decrease in Bcl-2 and apoptotic promotion at the advanced stage compared with MA.

Conclusion: Based on these results, MNLs may serve as a more effective and promising therapeutic option for ESCC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11475104PMC
http://dx.doi.org/10.2174/0113816128306477240625101849DOI Listing

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