Author: Ketenci, Sema; Aynacıoğlu, A. Şükrü
Title: The growth factor/cytokine midkine may participate in cytokine storm and contribute to the pathogenesis of severe acute respiratory syndrome coronavirus 2-infected patients Cord-id: dzmv3cys Document date: 2021_9_25
ID: dzmv3cys
Snippet: BACKGROUND: The current coronavirus disease 2019 (COVID-19) outbreak caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has emerged in Wuhan, China, and has rapidly become a global challenge, creating major challenges to health systems in almost every country in the world it has turned into a pandemic. COVID-19 poses a risky clinical situation that can range from mild illness to severe respiratory failure, requiring admission to intensive care. MAIN BODY: It is known that SAR
Document: BACKGROUND: The current coronavirus disease 2019 (COVID-19) outbreak caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has emerged in Wuhan, China, and has rapidly become a global challenge, creating major challenges to health systems in almost every country in the world it has turned into a pandemic. COVID-19 poses a risky clinical situation that can range from mild illness to severe respiratory failure, requiring admission to intensive care. MAIN BODY: It is known that SARS-CoV-2 infection causes a cytokine storm in some critically ill patients. However, more and more evidence showed that there is a dramatic increase in cytokine levels in patients diagnosed with COVID-19. Midkine (MK) is involved in various physiological and pathological processes, which some of them are desired and beneficial such as controlling tissue repair and antimicrobial effects, but some others are harmful such as promoting inflammation, carcinogenesis, and chemoresistance. Also, MK is expressed in inflammatory cells and released by endothelial cells under hypoxic conditions. CONCLUSIONS: Considering all this information, there are strong data that midkine, an important cytokine known to increase in inflammatory diseases, may be overexpressed in patients who are positive for COVID-19. The overexpression of MK reveals a picture leading to fibrosis and damage in the lung. Therefore, questions arise about how the expression of MK changes in COVID-19 patients and can we use it as an inflammation biomarker or in the treatment protocol in the future.
Search related documents:
Co phrase search for related documents- ace enzyme and acute lung injury: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25
- ace enzyme and acute respiratory distress syndrome: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25
- ace enzyme and low expression: 1, 2, 3, 4, 5, 6
- ace enzyme and lung damage: 1, 2, 3, 4, 5
- ace enzyme and lung edema: 1, 2, 3, 4
- ace enzyme and lung endothelium: 1, 2
- ace enzyme and lung epithelial cell: 1, 2, 3
- ace increase expression and acute lung injury: 1
- ace increase expression and acute respiratory distress syndrome: 1, 2, 3
- ace increase expression and lung endothelium: 1
- activity inhibition and acute lung injury: 1, 2, 3, 4, 5
- activity inhibition and acute respiratory distress syndrome: 1, 2, 3, 4, 5, 6
- activity inhibition and lung damage: 1, 2, 3, 4, 5, 6
- activity inhibition and lung edema: 1, 2
- activity inhibition and lung epithelial cell: 1, 2
- acute lung injury and low expression: 1, 2
- acute lung injury and lung damage: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25
- acute lung injury and lung edema: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25
- acute lung injury and lung endothelium: 1, 2, 3, 4, 5, 6, 7
Co phrase search for related documents, hyperlinks ordered by date