MMP-9 Activation via ROS/NF-κB Signaling in Colorectal Cancer Progression: Molecular Insights and Prognostic-Therapeutic Perspectives

  • 0Faculty of Medicine, University of Nis, 18000 Nis, Serbia.

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Summary

This summary is machine-generated.

Colorectal cancer progression involves oxidative stress and inflammation, linked by the ROS-NF-κB-MMP-9 pathway. MMP-9 shows high predictive value for CRC, suggesting it as a key diagnostic marker.

Area Of Science

  • Oncology
  • Biochemistry
  • Molecular Biology

Background

  • Colorectal cancer (CRC) involves complex interactions between inflammation, oxidative stress, and extracellular matrix remodeling.
  • The reactive oxygen species (ROS)-nuclear factor kappa B (NF-κB)-matrix metalloproteinase-9 (MMP-9) axis is significant in CRC invasion and metastasis.
  • Understanding this axis is crucial for developing targeted therapies.

Purpose Of The Study

  • To analyze advanced oxidation protein products (AOPPs), NF-κB expression, and MMP-9 activity in CRC tissues.
  • To investigate the correlation between oxidative stress markers and MMP-9 activity.
  • To evaluate MMP-9 as a potential diagnostic and theranostic marker for CRC.

Main Methods

  • Analysis of AOPPs, NF-κB, and MMP-9 in tumor, adjacent, and healthy colon tissues from 50 CRC patients.
  • Utilized ELISA, spectrophotometry, and indirect immunofluorescence for biochemical analyses.
  • Correlated marker levels with clinical data and disease progression.

Main Results

  • Significantly elevated AOPPs, NF-κB, and MMP-9 in tumor tissues compared to controls.
  • Adjacent tissues showed increased NF-κB and MMP-9 compared to healthy tissues.
  • AOPP levels strongly correlated with MMP-9 activity; MMP-9 had the highest predictive value for CRC.

Conclusions

  • The ROS-NF-κB-MMP-9 axis is integral to colorectal cancer progression, particularly in T2-T3 stages.
  • MMP-9 emerges as a promising diagnostic and theranostic marker for CRC.
  • Targeting this pathway offers potential therapeutic strategies for CRC invasion and recurrence.

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