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10.1111/jcmm.16596

http://scihub22266oqcxt.onion/10.1111/jcmm.16596
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33969601!8184717!33969601
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suck abstract from ncbi


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pmid33969601      J+Cell+Mol+Med 2021 ; 25 (12): 5823-5827
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  • Interplay between SARS-CoV-2 and human long non-coding RNAs #MMPMID33969601
  • Moazzam-Jazi M; Lanjanian H; Maleknia S; Hedayati M; Daneshpour MS
  • J Cell Mol Med 2021[Jun]; 25 (12): 5823-5827 PMID33969601show ga
  • The long non-coding RNAs (lncRNAs) play a critical regulatory role in the host response to the viral infection. However, little is understood about the transcriptome architecture, especially lncRNAs pattern during the SARS-CoV-2 infection. In the present study, using publicly available RNA sequencing data of bronchoalveolar lavage fluid (BALF) and peripheral blood mononuclear cells (PBMC) samples from COVID-19 patients and healthy individuals, three interesting findings highlighted: (a) More than half of the interactions between lncRNAs-PCGs of BALF samples established by three trans-acting lncRNAs (HOTAIRM1, PVT1 and AL392172.1), which also exhibited the high affinity for binding to the SARS-CoV-2 genome, suggesting the major regulatory role of these lncRNAs during the SARS-CoV-2 infection. (b) lncRNAs of MALAT1 and NEAT1 are possibly contributed to the inflammation development in the SARS-CoV-2 infected cells. (c) In contrast to the 3' part of the SARS-CoV-2 genome, the 5' part can interact with many human lncRNAs. Therefore, the mRNA-based vaccines will not show any side effects because of the off-label interactions with the human lncRNAs. Overall, the putative functionalities of lncRNAs can be promising to design the non-coding RNA-based drugs and to inspect the efficiency of vaccines to overcome the current pandemic.
  • |*COVID-19/immunology/virology[MESH]
  • |Bronchoalveolar Lavage Fluid/immunology/virology[MESH]
  • |Databases, Nucleic Acid[MESH]
  • |Humans[MESH]
  • |Leukocytes, Mononuclear/cytology/immunology/virology[MESH]
  • |RNA, Long Noncoding/*metabolism[MESH]
  • |RNA, Viral/*metabolism[MESH]


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