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cells, pubmed, crc, cell, article, lsttn, cancer, httn, google, scholar, cocultured, antigen, mscs, tumor, oglycans, stem, cas, spmscs, tsynthase, core, sphpmscs, fig, sphucmscs, derived, mesenchymal, cosmc, migration, apoptosis, activity, central, expression, human, proliferation, huvecs, hpmscs, cgnt, hucmscs, oglycosylation, protein, colorectal, data, tissue, china, colon, inhibit, results, differentiation, tissues, usa, wang,

Topics {✒️}

complex structure galβ1-3galnac-1-o-ser/thr ser/thr formed galnac-1-o-ser/thr mtor/hif-1alpha/vegf signaling axis dkk-1/wnt/beta-catenin signaling pathway complex disease–mucin-type o-glycans cellular o-glycome reporter/amplification gal β1-3 galnac-ser/thr apc-labeled anti-ssea-3 antibody supplementary figures real-time impedance-based assays springer nature multilineage-differentiating stress enduring induce epithelial–mesenchymal transition glcnac-galnac-ser/thr anti-mouse igm microbeads aberrant o-glycosylation contributes msc-derived extracellular vesicles promote ligand-stimulated clustering nf-kappab signaling pathway galnt14-mediated dr5 glycosylation tumor-bearing nude mice proapoptotic ligand apo2l/trail healthy-term pregnant women core 1-derived o-lycans modify o-glycosylation status core 2-derived o-glycan core 3-derived o-glycan core 1-derived o-glycan modify abnormal o-glycosylation core 1-derived o-glycans core 3-derived o-glycans core 2-derived o-glycans bone marrow-derived mscs centrifugation bn-o-glycans apc-labeled anti-tn correct abnormal o-glycosylation compound bn-α-galnac anti-tumour immune response o-linked glycan branching t-synthase promote ls174t-tn− real-time cell analysis additional information publisher' bmc cancer rabbit anti-t-synthase truncated o-glycans expressed secondary antibody conjugated human colorectal cancer 10% sds-page aberrant o-glycosylation data materials

Questions {❓}

• Are mesenchymal cells indeed pluripotent stem cells or just stromal cells?
• Mesenchymal stromal cells (MSCs) and colorectal cancer: a troublesome twosome for the anti-tumour immune response?

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WebPage:
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         headline:Side population cells derived from hUCMSCs and hPMSCs could inhibit the malignant behaviors of Tn+ colorectal cancer cells from modifying their O-glycosylation status
         description:Cosmc (C1GalT1C1) mutation could cause aberrant O-glycosylation and result in expression of Tn antigen on the surface of tumor cells (Tn+ cells), which is associated with the metastasis and prognosis of cancer progression. Mesenchymal stem cells (MSCs) could participate in immunoregulation, tissue damage repair, and tumor inhibition and be seen as an ideal candidate for tumor therapy due to their inherent capacity to migrate to tumor sites. However, their therapeutic effectiveness in different tumors is inconsistent and still controversial. Of note, emerging data reveal that side population (SP) cells have a stronger multilineage developmental potential than main population cells and can function as stem/progenitor cells. The effect of SP cells derived from MSCs on the biological behaviors and the O-glycosylation status of tumor cells remains unclear. SP cells were isolated from human umbilical cord MSCs (hUCMSCs) and human placenta MSCs (hPMSCs). Tn+ cells (LS174T-Tn+ and HT-29-Tn+ cells) and matching Tn− cells (LS174T-Tn− and HT-29-Tn− cells) were isolated from human colorectal cancer cell (CRC) lines LS174T and HT-29 by immune magnetic beads. The proliferation, migration, apoptosis, Tn antigen expression, and O-glycome in Tn+ and Tn− CRC cells before and after co-cultured with SP-MSCs were detected using real-time cell Analysis (RTCA), flow cytometry (FCM), and cellular O-glycome reporter/amplification (CORA), respectively. Cosmc protein and O-glycosyltransferase (T-synthase and C3GnT) activity in CRC cells were, respectively, assessed using western blotting and fluorescence method. Both SP cells derived from hUCMSCs and hPMSCs could inhibit proliferation and migration, promote apoptosis of CRC cells, significantly reduce Tn antigen expression on Tn+ CRC cells, generate new core 1-, 2-, and 3-derived O-glycans, increase T-synthase and C3GnT activity, and elevate the levels of Cosmc and T-synthase protein. SP-hUCMSCs and SP-hPMSCs could inhibit proliferation and migration and promote apoptosis of Tn+ CRC cells via increasing O-glycosyltransferase activity to modify O-glycosylation status, which further adds a new dimension to the treatment of CRC.
         datePublished:2023-05-26T00:00:00Z
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            Colorectal cancer cells
            SP-hUCMSCs
            SP-hPMSCs
             O-glycosylation
            Cosmc
            Stem Cells
            Cell Biology
            Regenerative Medicine/Tissue Engineering
            Biomedical Engineering and Bioengineering
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      headline:Side population cells derived from hUCMSCs and hPMSCs could inhibit the malignant behaviors of Tn+ colorectal cancer cells from modifying their O-glycosylation status
      description:Cosmc (C1GalT1C1) mutation could cause aberrant O-glycosylation and result in expression of Tn antigen on the surface of tumor cells (Tn+ cells), which is associated with the metastasis and prognosis of cancer progression. Mesenchymal stem cells (MSCs) could participate in immunoregulation, tissue damage repair, and tumor inhibition and be seen as an ideal candidate for tumor therapy due to their inherent capacity to migrate to tumor sites. However, their therapeutic effectiveness in different tumors is inconsistent and still controversial. Of note, emerging data reveal that side population (SP) cells have a stronger multilineage developmental potential than main population cells and can function as stem/progenitor cells. The effect of SP cells derived from MSCs on the biological behaviors and the O-glycosylation status of tumor cells remains unclear. SP cells were isolated from human umbilical cord MSCs (hUCMSCs) and human placenta MSCs (hPMSCs). Tn+ cells (LS174T-Tn+ and HT-29-Tn+ cells) and matching Tn− cells (LS174T-Tn− and HT-29-Tn− cells) were isolated from human colorectal cancer cell (CRC) lines LS174T and HT-29 by immune magnetic beads. The proliferation, migration, apoptosis, Tn antigen expression, and O-glycome in Tn+ and Tn− CRC cells before and after co-cultured with SP-MSCs were detected using real-time cell Analysis (RTCA), flow cytometry (FCM), and cellular O-glycome reporter/amplification (CORA), respectively. Cosmc protein and O-glycosyltransferase (T-synthase and C3GnT) activity in CRC cells were, respectively, assessed using western blotting and fluorescence method. Both SP cells derived from hUCMSCs and hPMSCs could inhibit proliferation and migration, promote apoptosis of CRC cells, significantly reduce Tn antigen expression on Tn+ CRC cells, generate new core 1-, 2-, and 3-derived O-glycans, increase T-synthase and C3GnT activity, and elevate the levels of Cosmc and T-synthase protein. SP-hUCMSCs and SP-hPMSCs could inhibit proliferation and migration and promote apoptosis of Tn+ CRC cells via increasing O-glycosyltransferase activity to modify O-glycosylation status, which further adds a new dimension to the treatment of CRC.
      datePublished:2023-05-26T00:00:00Z
      dateModified:2023-05-26T00:00:00Z
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         Colorectal cancer cells
         SP-hUCMSCs
         SP-hPMSCs
          O-glycosylation
         Cosmc
         Stem Cells
         Cell Biology
         Regenerative Medicine/Tissue Engineering
         Biomedical Engineering and Bioengineering
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      name:Department of Immunology, Binzhou Medical University, Yantai, People’s Republic of China
      name:Department of Immunology, Binzhou Medical University, Yantai, People’s Republic of China
      name:Qingdao University, Qingdao, People’s Republic of China
      name:Department of Immunology, Binzhou Medical University, Yantai, People’s Republic of China

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