Systematic analysis of prognostic and immunologic characteristics associated with coronavirus disease 2019 regulators

Mingjie Shi1,2, Lidan Chen3, Yue Wei4

  • 1Key Laboratory of Research in Maternal and Child Medicine and Birth Defects, Guangdong Medical University, Foshan, China.

Frontiers in Genetics
|September 23, 2022
PubMed

Insights

This study identified 76 COVID-19-related genes (C-DEGs) in acute myeloid leukemia (AML) patients, revealing shared pathways and a prognostic model. This helps understand how COVID-19 complicates AML treatment and predicts patient survival.

Area of Science:

  • * Oncology
  • * Virology
  • * Bioinformatics

Background:

  • * The COVID-19 pandemic complicates cancer treatment, particularly for acute myeloid leukemia (AML).
  • * There is a lack of understanding regarding the interactions between COVID-19 and AML, hindering evidence-based treatment guidelines.
  • * Publicly available RNA-seq data from AML patients is crucial for investigating these interactions.

Purpose of the Study:

  • * To identify COVID-19-related differentially expressed genes (C-DEGs) in AML patients.
  • * To explore the enrichment pathways and candidate drugs associated with these C-DEGs.
  • * To construct a prognostic model for AML patients with COVID-19 infection.

Main Methods:

  • * Analysis of RNA-seq data from public databases to identify C-DEGs in AML patients.
  • * Functional enrichment analysis to explore shared pathways between COVID-19 and AML.
  • * Application of bioinformatics algorithms to recognize protein-protein interactions (PPIs) and protein-drug interactions.
  • * Construction of a COVID-19 gene-associated prognostic model (C-GPM) using risk scores.

Main Results:

  • * Identified 76 C-DEGs associated with both AML progression and COVID-19 infection.
  • * Functional analysis revealed shared biological links between COVID-19 and AML.
  • * Developed a C-GPM that accurately predicts survival outcomes in AML patients.
  • * High-risk patients exhibited immune-activated phenotypes, including increased monocyte/neutrophil infiltration and higher expression of immunosuppressants.

Conclusions:

  • * The identified C-DEGs and their associated pathways offer insights into the complex interactions between COVID-19 and AML.
  • * The C-GPM can predict survival in AML patients, potentially aiding in treatment optimization.
  • * Findings suggest immune dysregulation as a common factor complicating COVID-19 and AML treatment.
  • * Further clinical validation is needed, but the study provides a valuable framework for understanding and managing AML patients with COVID-19 infections.