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10.18632/aging.104147

http://scihub22266oqcxt.onion/10.18632/aging.104147
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33231569!7746364!33231569
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suck abstract from ncbi


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pmid33231569      Aging+(Albany+NY) 2020 ; 12 (22): 22370-22389
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  • Genomic, epigenomic, and immune subtype analysis of CTSL/B and SARS-CoV-2 receptor ACE2 in pan-cancer #MMPMID33231569
  • Li H; Xie L; Chen L; Zhang L; Han Y; Yan Z; Guo X
  • Aging (Albany NY) 2020[Nov]; 12 (22): 22370-22389 PMID33231569show ga
  • SARS-coronavirus 2 (SARS-CoV-2) has been spreading widely and posing an international challenge for both healthcare and society. At present, cancer has been identified as an individual risk factor for COVID-19. Angiotensin converting enzyme 2 (ACE2) and Cathepsin L/Cathepsin B (CTSL/B), which act as the receptor and entry-associated proteases of SARS-CoV-2 respectively, are pivotal for SARS-CoV-2 infection. To investigate the possible SARS-CoV-2 infection risk of pan-cancer, we analyzed the genetic alterations, RNA expression, DNA methylation, and the association with immune subtypes of ACE2 and CTSL/B with the prognosis in pan-cancer. Results showed the upregulation of CTSL/B and ACE2 in Pancreatic adenocarcinoma (PAAD) and Stomach adenocarcinoma (STAD) and demonstrated a positive correlation between copy number alteration (CNA) and gene expression for CTSB in PAAD and STAD. Hypomethylation and a negative correlation of gene expression and methylation for CTSB were detected in PAAD. In addition, ACE2 and CTSL/B are overexpressed in the IFN-gamma immune subtype of ovarian serous Cystadenocarcinoma (OV), Cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), and Bladder urothelial carcinoma (BLCA). Our study presents a bioinformatics assessment for the potential risk of SARS-CoV-2 infection in pan-cancer.
  • |Angiotensin-Converting Enzyme 2/*genetics/immunology/metabolism[MESH]
  • |COVID-19/*epidemiology/immunology/virology[MESH]
  • |Cathepsin B/*genetics/immunology[MESH]
  • |Cathepsin L/*genetics/immunology[MESH]
  • |Computational Biology[MESH]
  • |DNA Methylation[MESH]
  • |Epigenesis, Genetic[MESH]
  • |Epigenomics[MESH]
  • |Female[MESH]
  • |Gene Expression Regulation, Neoplastic/immunology[MESH]
  • |Genetic Variation[MESH]
  • |Humans[MESH]
  • |Mutation[MESH]
  • |Neoplasms/complications/*genetics/immunology[MESH]
  • |Pandemics[MESH]
  • |Risk Assessment[MESH]
  • |Risk Factors[MESH]
  • |SARS-CoV-2/*immunology/pathogenicity[MESH]
  • |Transcriptome[MESH]


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