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The Correlation Between Immune Invasion and SARS-COV-2 Entry Protein ADAM17 in Cancer Patients by Bioinformatic
Kai Wang1, Haoyue Deng1, Binghui Song1
1Key Laboratory of Epigenetics and Oncology, Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China.
Abstract:
SARS-Cov-2 caused the COVID-19 pandemic worldwide. ADAM17 functions as a disintegrin and transmembrane metalloproteinase domain protein involved in the regulation of SARS-CoV-2 receptor ACE2. However, its impact on cancer patients infected with COVID-19 and its correlation with immune cell infiltration is unclear. This study compared ADAM17 expression between normal and tumor tissues based on GEPIA. The correlations between ADAM17 expression and immune cell infiltration and immunomodulators were investigated. Besides, treated drugs for targeting ADAM17 were searched in the TISDB database. We found that ADAM17 was highly conserved in many species and was mainly expressed in lung, brain, female tissues, bone marrow and lymphoid tissues. It was also highly expressed in respiratory epithelial cells of rhinitis and bronchus. ADAM17 expression in tumors was higher than that in several paired normal tissues and was negatively correlated with the prognosis of patients with malignant tumors. Interestingly, ADAM17 expression significantly correlated with immunomodulators and immune cell infiltration in normal and tumor tissues. Moreover, eight small molecules targeting ADAM17 only demonstrate therapeutic significance. These findings imply important implications for ADAM17 in cancer patients infected with COVID-19 and provide new clues for development strategy of anti-COVID-19.
Insights
ADAM17, a protein regulating SARS-CoV-2 entry, is highly expressed in tumors and linked to poor prognosis. Its correlation with immune cells suggests therapeutic potential for COVID-19 cancer patients.
Area of Science:
- Oncology
- Virology
- Immunology
Background:
- Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) caused the COVID-19 pandemic.
- ADAM17 (a disintegrin and transmembrane metalloproteinase domain protein) regulates the SARS-CoV-2 receptor ACE2.
- The role of ADAM17 in COVID-19 infected cancer patients and its immune cell infiltration correlation remain unclear.
Purpose of the Study:
- To investigate ADAM17 expression in normal versus tumor tissues.
- To analyze the correlation between ADAM17 expression, immune cell infiltration, and immunomodulators.
- To identify potential drugs targeting ADAM17.
Main Methods:
- Gene Expression Profiling Interactive Analysis (GEPIA) for tissue expression comparison.
- Correlation analysis for ADAM17 with immune infiltration and immunomodulators.
- Therapeutic drug screening using the TISDB database.
Main Results:
- ADAM17 is highly conserved and expressed in lung, brain, lymphoid tissues, and respiratory cells.
- Tumor ADAM17 expression is elevated compared to normal tissues, correlating with negative patient prognosis.
- ADAM17 expression significantly correlates with immunomodulators and immune cell infiltration in both normal and tumor tissues.
- Eight small molecules targeting ADAM17 showed therapeutic significance.
Conclusions:
- ADAM17 has significant implications for cancer patients with COVID-19.
- ADAM17's role in immune modulation and infiltration offers new therapeutic strategies for COVID-19.
- Targeting ADAM17 may provide a novel approach for treating COVID-19 in cancer patients.
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