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bsg, cancer, pubmed, expression, fig, google, scholar, sarscov, tissues, cas, pancancers, cell, patients, cancers, covid, cells, central, protein, methylation, survival, treatment, levels, gene, types, hea, ump, breast, mutation, found, tumor, lung, malignant, analysis, showed, antibody, invasion, disease, including, mutations, expressions, supplementary, full, data, prognostic, susceptibility, significantly, mrna, therapeutic, dna, kirp,

Topics {✒️}

n1-methyladenosine-related risk signature semi-quantitative rt-pcr assays sars-cov-2-related genes predicts recombinant anti-bsg/cd147 antibody semi-quantitative rt-pcr scbt—santa cruz biotechnology hsp70/90/β-actin antibodies anti-cd147/bsg antibody specifically paraffin-embedded tissue sections sars-cov-2 pseudovirus enters cordycepin inhibits drug-resistance gene_list=bsg&cancer_study_list=5c8a7d55e4b046111fee2296 anti-sars-cov-2 drugs t-cell responses basic medical school facilitate tumor-immune escape cd8 + tumor-infiltrating lymphocytes functions including anti-cancer predicted molecular weight cancer=pancancer&gene=bsg affect sars-cov-2 susceptibility pcr product size bsg/cd147 gene expression privacy choices/manage cookies effectively inhibits infection liver hepatocellular carcinoma bar plots show jingliang cheng junjiang fu covid-19-infected cancer patients human respiratory epithelia stem cell engagement anti-viral processes dna methylation profiles anti-fibrillatory effect article fu rt-pcr primers progression-free pan-cancers cancer cell lines sars-cov-2 infection ihc staining-positive patients cd147-spike protein spike protein-cd147 sars-cov-2 receptors coronavirus infections leading bsg remarkably correlated southwest medical university chinese lung cancer activating energy metabolism matched normal tissues

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WebPage:
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         headline:Impact of BSG/CD147 gene expression on diagnostic, prognostic and therapeutic strategies towards malignant cancers and possible susceptibility to SARS-CoV-2
         description:BSG (CD147) is a member of the immunoglobulin superfamily that shows roles for potential prognostics and therapeutics for metastatic cancers and SARS-CoV-2 invasion for COVID-19. The susceptibility of malignant cancers to SARS-CoV-2 as well as the correlations between disease outcome and BSG expression in tumor tissues have not been studied in depth. In this study, we explored the BSG expression profile, survival correlation, DNA methylation, mutation, diagnostics, prognostics, and tumor-infiltrating lymphocytes (TILs) from different types of cancer tissues with corresponding healthy tissues. In vitro studies for cordycepin (CD), N6-(2-hydroxyethyl) adenosine (HEA), N6, N6-dimethyladenosine (m62A) and 5′-uridylic acid (UMP) on BSG expression were also conducted. We revealed that BSG is conserved among different species, and significantly upregulated in seven tumor types, including ACC, ESCA, KICH, LIHC, PAAD, SKCM and THYM, compared with matched normal tissues, highlighting the susceptibility of these cancer patients to SARS-CoV-2 invasion, COVID-19 severity and progression of malignant cancers. High expression in BSG was significantly correlated with a short OS in LGG, LIHC and OV patients, but a long OS in KIRP patients. Methylation statuses in the BSG promoter were significantly higher in BRCA, HNSC, KIRC, KIRP, LUSC, PAAD, and PRAD tumor tissues, but lower in READ. Four CpGs in the BSG genome were identified as potential DNA methylation biomarkers which could be used to predict malignant cancers from normal individuals. Furthermore, a total of 65 mutation types were found, in which SARC showed the highest mutation frequency (7.84%) and THYM the lowest (0.2%). Surprisingly, both for disease-free and progression-free survival in pan-cancers were significantly reduced after BSG mutations. Additionally, a correlation between BSG expression and immune lymphocytes of CD56bright natural killer cell, CD56dim natural killer cell and monocytes, MHC molecules of HLA-A, HLA-B, HLA-C and TAPBP, immunoinhibitor of PVR, PVRL2, and immunostimulators of TNFRSF14, TNFRSF18, TNFRSF25, and TNFSF9, was revealed in most cancer types. Moreover, BSG expression was downregulated by CD, HEA, m62A or UMP in cancer cell lines, suggesting therapeutic potentials for interfering entry of SARS-CoV-2. Altogether, our study highlights the values of targeting BSG for diagnostic, prognostic and therapeutic strategies to fight malignant cancers and COVID-19. Small molecules CD, HEA, m62A and UMP imply therapeutic potentials in interfering with entry of SARS-CoV-2 and progression of malignant cancers.
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            COVID-19
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            N6
            N6-dimethyladenosine (m6 2a)
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            Animal Biochemistry
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      headline:Impact of BSG/CD147 gene expression on diagnostic, prognostic and therapeutic strategies towards malignant cancers and possible susceptibility to SARS-CoV-2
      description:BSG (CD147) is a member of the immunoglobulin superfamily that shows roles for potential prognostics and therapeutics for metastatic cancers and SARS-CoV-2 invasion for COVID-19. The susceptibility of malignant cancers to SARS-CoV-2 as well as the correlations between disease outcome and BSG expression in tumor tissues have not been studied in depth. In this study, we explored the BSG expression profile, survival correlation, DNA methylation, mutation, diagnostics, prognostics, and tumor-infiltrating lymphocytes (TILs) from different types of cancer tissues with corresponding healthy tissues. In vitro studies for cordycepin (CD), N6-(2-hydroxyethyl) adenosine (HEA), N6, N6-dimethyladenosine (m62A) and 5′-uridylic acid (UMP) on BSG expression were also conducted. We revealed that BSG is conserved among different species, and significantly upregulated in seven tumor types, including ACC, ESCA, KICH, LIHC, PAAD, SKCM and THYM, compared with matched normal tissues, highlighting the susceptibility of these cancer patients to SARS-CoV-2 invasion, COVID-19 severity and progression of malignant cancers. High expression in BSG was significantly correlated with a short OS in LGG, LIHC and OV patients, but a long OS in KIRP patients. Methylation statuses in the BSG promoter were significantly higher in BRCA, HNSC, KIRC, KIRP, LUSC, PAAD, and PRAD tumor tissues, but lower in READ. Four CpGs in the BSG genome were identified as potential DNA methylation biomarkers which could be used to predict malignant cancers from normal individuals. Furthermore, a total of 65 mutation types were found, in which SARC showed the highest mutation frequency (7.84%) and THYM the lowest (0.2%). Surprisingly, both for disease-free and progression-free survival in pan-cancers were significantly reduced after BSG mutations. Additionally, a correlation between BSG expression and immune lymphocytes of CD56bright natural killer cell, CD56dim natural killer cell and monocytes, MHC molecules of HLA-A, HLA-B, HLA-C and TAPBP, immunoinhibitor of PVR, PVRL2, and immunostimulators of TNFRSF14, TNFRSF18, TNFRSF25, and TNFSF9, was revealed in most cancer types. Moreover, BSG expression was downregulated by CD, HEA, m62A or UMP in cancer cell lines, suggesting therapeutic potentials for interfering entry of SARS-CoV-2. Altogether, our study highlights the values of targeting BSG for diagnostic, prognostic and therapeutic strategies to fight malignant cancers and COVID-19. Small molecules CD, HEA, m62A and UMP imply therapeutic potentials in interfering with entry of SARS-CoV-2 and progression of malignant cancers.
      datePublished:2022-12-27T00:00:00Z
      dateModified:2022-12-27T00:00:00Z
      pageStart:2269
      pageEnd:2281
      sameAs:https://doi.org/10.1007/s11033-022-08231-1
      keywords:
         The BSG gene
         COVID-19
         Susceptibility
         Malignant cancers
         Cordycepin (CD)
         N6
         N6-dimethyladenosine (m6 2a)
         N6-(2-hydroxyethyl) adenosine (HEA)
         5′-uridylic acid (UMP)
         Animal Biochemistry
         Animal Anatomy / Morphology / Histology
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            address:
               name:Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China
               type:PostalAddress
            type:Organization
      name:Shuguang Liu
      affiliation:
            name:Southwest Medical University
            address:
               name:Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China
               type:PostalAddress
            type:Organization
      name:Jiayue He
      affiliation:
            name:Southwest Medical University
            address:
               name:Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China
               type:PostalAddress
            type:Organization
      name:Ting Xiao
      affiliation:
            name:Southwest Medical University
            address:
               name:Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China
               type:PostalAddress
            type:Organization
            name:Southwest Medical University
            address:
               name:Basic Medical School, Southwest Medical University, Luzhou, China
               type:PostalAddress
            type:Organization
      name:Baixu Zhou
      affiliation:
            name:Southwest Medical University
            address:
               name:Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China
               type:PostalAddress
            type:Organization
            name:Guangdong Women and Children Hospital
            address:
               name:Department of Gynecology and Obstetrics, Guangdong Women and Children Hospital, Guangzhou, China
               type:PostalAddress
            type:Organization
      name:Dabing Li
      affiliation:
            name:Southwest Medical University
            address:
               name:Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China
               type:PostalAddress
            type:Organization
            name:Southwest Medical University
            address:
               name:Basic Medical School, Southwest Medical University, Luzhou, China
               type:PostalAddress
            type:Organization
      name:Xiaoyan Liu
      affiliation:
            name:Southwest Medical University
            address:
               name:Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China
               type:PostalAddress
            type:Organization
      name:Tao He
      affiliation:
            name:Southwest Medical University
            address:
               name:Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China
               type:PostalAddress
            type:Organization
            name:Southwest Medical University
            address:
               name:Institute for Cancer Medicine and Basic Medical School, Southwest Medical University, Luzhou, China
               type:PostalAddress
            type:Organization
      name:Jingliang Cheng
      affiliation:
            name:Southwest Medical University
            address:
               name:Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China
               type:PostalAddress
            type:Organization
      email:[email protected]
      name:Junjiang Fu
      url:http://orcid.org/0000-0002-0708-2200
      affiliation:
            name:Southwest Medical University
            address:
               name:Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China
      name:Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China
      name:Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China
      name:Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China
      name:Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China
      name:Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China
      name:Basic Medical School, Southwest Medical University, Luzhou, China
      name:Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China
      name:Department of Gynecology and Obstetrics, Guangdong Women and Children Hospital, Guangzhou, China
      name:Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China
      name:Basic Medical School, Southwest Medical University, Luzhou, China
      name:Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China
      name:Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China
      name:Institute for Cancer Medicine and Basic Medical School, Southwest Medical University, Luzhou, China
      name:Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China
      name:Key Laboratory of Epigenetics and Oncology, The Research Center for Preclinical Medicine, Southwest Medical University, Luzhou, China

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