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10.1016/j.meegid.2020.104669

http://scihub22266oqcxt.onion/10.1016/j.meegid.2020.104669
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33301988!7720011!33301988
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suck abstract from ncbi


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pmid33301988      Infect+Genet+Evol 2021 ; 88 (ä): 104669
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  • Covid-19 pathogenesis in prostatic cancer and TMPRSS2-ERG regulatory genetic pathway #MMPMID33301988
  • Afshari A; Janfeshan S; Yaghobi R; Roozbeh J; Azarpira N
  • Infect Genet Evol 2021[Mar]; 88 (ä): 104669 PMID33301988show ga
  • Members of Coronaviridae family have been the source of respiratory illnesses. The outbreak of SARS-CoV-2 that produced a severe lung disease in afflicted patients in China and other countries was the reason for the incredible attention paid toward this viral infection. It is known that SARS-CoV-2 is dependent on TMPRSS2 activity for entrance and subsequent infection of the host cells and TMPRSS2 is a host cell molecule that is important for the spread of viruses such as coronaviruses. Different factors can increase the risk of prostate cancer, including older age, a family history of the disease. Androgen receptor (AR) initiates a transcriptional cascade which plays a serious role in both normal and malignant prostate tissues. TMPRSS2 protein is highly expressed in prostate secretory epithelial cells, and its expression is dependent on androgen signals. One of the molecular signs of prostate cancer is TMPRSS2-ERG gene fusion. In TMPRSS2-ERG-positive prostate cancers different patterns of changed gene expression can be detected. The possible molecular relation between fusion positive prostate cancer patients and the increased risk of lethal respiratory viral infections especially SARS-CoV-2 can candidate TMPRSS2 as an attractive drug target. The studies show that some molecules such as nicotinamide, PARP1, ETS and IL-1R can be studied deeper in order to control SARS-CoV-2 infection especially in prostate cancer patients. This review attempts to investigate the possible relation between the gene expression pattern that is produced through TMPRSS2-ERG fusion positive prostate cancer and the possible influence of these fluctuations on the pathogenesis and development of viral infections such as SARS-CoV-2.
  • |Aged[MESH]
  • |Angiotensin-Converting Enzyme 2/*genetics/metabolism[MESH]
  • |COVID-19/complications/*genetics/pathology/virology[MESH]
  • |Dihydrotestosterone/metabolism[MESH]
  • |Gene Expression Regulation[MESH]
  • |Host-Pathogen Interactions/genetics[MESH]
  • |Humans[MESH]
  • |Male[MESH]
  • |Oncogene Proteins, Fusion/*genetics/metabolism[MESH]
  • |Prostatic Neoplasms/complications/*genetics/pathology/virology[MESH]
  • |Receptors, Androgen/genetics/metabolism[MESH]
  • |SARS-CoV-2/genetics/metabolism/pathogenicity[MESH]
  • |Serine Endopeptidases/*genetics/metabolism[MESH]
  • |Signal Transduction[MESH]
  • |Spike Glycoprotein, Coronavirus/*genetics/metabolism[MESH]
  • |Transcription, Genetic[MESH]


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