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CORONAVIRUS SARS-COV-2 MODIFIES ANTITUMOR REDOX STATUS OF BLOOD AND INTERCELLULAR MATRIX IN METASTATIC COLORECTAL
A P Burlaka1, D L Liubenko2, A A Burlaka3
1R.E. Kavetsky Institute of Experimental Pathology, Oncology and Radiobiology, NAS of Ukraine, Kyiv, Ukraine.
Experimental Oncology
|February 8, 2024
Summary
COVID-19 infection in metastatic colorectal cancer (mCRC) patients increases oxidative stress and inflammation. This redox imbalance heightens the risk of disease exacerbation and poorer outcomes in mCRC patients.
Area of Science:
- Oncology
- Infectious Diseases
- Biochemistry
Background:
- SARS-CoV-2 infection elevates mortality risk and complications in cancer patients.
- COVID-19 induces oxidative stress, a key factor in cancer progression and inflammation.
Purpose of the Study:
- To investigate the impact of SARS-CoV-2-induced hypoxia on blood redox status in metastatic colorectal cancer (mCRC) patients.
Main Methods:
- Analyzed blood biochemistry (C-reactive protein, ferritin, transferrin, free iron) in mCRC patients with and without prior SARS-CoV-2 infection.
- Measured superoxide radical (ROS) levels using electron paramagnetic resonance (EPR).
- Assessed metalloproteinase activity via polyacrylamide gel zymography.
Main Results:
- mCRC patients with prior SARS-CoV-2 infection showed a 1.26-fold increase in ROS generation by neutrophils.
- Elevated levels of C-reactive protein (2-fold), transferrin (6-fold), and free iron (1.4-fold) were observed in these patients.
- Increased gelatinase activity in platelets (1.4-fold) and neutrophils (1.2-fold) was noted.
Conclusions:
- Prior COVID-19 infection in mCRC patients is associated with heightened inflammatory responses.
- SARS-CoV-2 infection disrupts redox balance, potentially worsening mCRC prognosis.
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