A comprehensive pan-cancer analysis of CDH5 in immunological response
Cadherin 5 (CDH5) functions critically in maintaining cell adhesion and integrity of endothelial and vascular cells. The expression of CDH5 is abnormal in tumor cells, which may have great potential to serve as a new immune checkpoint. The current pan-cancer analysis was performed to better understa...
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Published in | Frontiers in immunology Vol. 14; p. 1239875 |
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Abstract | Cadherin 5 (CDH5) functions critically in maintaining cell adhesion and integrity of endothelial and vascular cells. The expression of CDH5 is abnormal in tumor cells, which may have great potential to serve as a new immune checkpoint. The current pan-cancer analysis was performed to better understand the role of CDH5 in tumor.BackgroundCadherin 5 (CDH5) functions critically in maintaining cell adhesion and integrity of endothelial and vascular cells. The expression of CDH5 is abnormal in tumor cells, which may have great potential to serve as a new immune checkpoint. The current pan-cancer analysis was performed to better understand the role of CDH5 in tumor.The clinical significance and immunological function of CDH5 in pan-cancers were comprehensively analyzed based on the correlations between CDH5 and clinicopathologic features, prognosis values, tumor mutation burden (TMB), microsatellite instability (MSI), immune cells infiltration and immune response genes using 33 datasets from The Cancer Genome Atlas (TCGA). We further confirmed the expression of CDH5 in bladder cancer (BCa) tissues and cell lines. The CD8+ T cells were screened from peripheral blood of healthy controls and activated. BCa cell-CD8+ T cell co-culture assay and ELISA assay were carried out to verify the immunological function of CDH5.MethodsThe clinical significance and immunological function of CDH5 in pan-cancers were comprehensively analyzed based on the correlations between CDH5 and clinicopathologic features, prognosis values, tumor mutation burden (TMB), microsatellite instability (MSI), immune cells infiltration and immune response genes using 33 datasets from The Cancer Genome Atlas (TCGA). We further confirmed the expression of CDH5 in bladder cancer (BCa) tissues and cell lines. The CD8+ T cells were screened from peripheral blood of healthy controls and activated. BCa cell-CD8+ T cell co-culture assay and ELISA assay were carried out to verify the immunological function of CDH5.The expression of CDH5 was down-regulated in 8 types of tumors including in BCa but up-regulated in 4 types of tumors. CDH5 was significantly correlated with tumor stage in 6 types of tumors. In addition, CDH5 was positively or negatively correlated with tumor prognosis. Furthermore, CDH5 was closely associated with TMB in 15 types of tumors and with MSI in 9 types of tumors. KEGG-GSEA and Hallmarks-GSEA analyses results indicated that CDH5 was positively related to immune response in most tumor types. In many tumors, CDH5 showed a positive correlation with immune cell infiltration. Enrichment analyses demonstrated that CDH5 was significantly related to the expression of many immunomodulators and chemokines. Further experiments showed that CDH5 was low-expressed in BCa tissues and cell lines in comparison to adjacent normal tissues and normal urothelial cell line, but it was positively associated with a better prognosis of BCa patients. The results of in vitro co-culture assay and ELISA assay demonstrated that CDH5 could promote the function of CD8+ T cells in TME of BCa.ResultsThe expression of CDH5 was down-regulated in 8 types of tumors including in BCa but up-regulated in 4 types of tumors. CDH5 was significantly correlated with tumor stage in 6 types of tumors. In addition, CDH5 was positively or negatively correlated with tumor prognosis. Furthermore, CDH5 was closely associated with TMB in 15 types of tumors and with MSI in 9 types of tumors. KEGG-GSEA and Hallmarks-GSEA analyses results indicated that CDH5 was positively related to immune response in most tumor types. In many tumors, CDH5 showed a positive correlation with immune cell infiltration. Enrichment analyses demonstrated that CDH5 was significantly related to the expression of many immunomodulators and chemokines. Further experiments showed that CDH5 was low-expressed in BCa tissues and cell lines in comparison to adjacent normal tissues and normal urothelial cell line, but it was positively associated with a better prognosis of BCa patients. The results of in vitro co-culture assay and ELISA assay demonstrated that CDH5 could promote the function of CD8+ T cells in TME of BCa.In summary, CDH5 was positively associated with a favorable prognosis and effective immune response in tumors, showing a great potential to serve as a novel tumor biomarker and immune checkpoint.ConclusionIn summary, CDH5 was positively associated with a favorable prognosis and effective immune response in tumors, showing a great potential to serve as a novel tumor biomarker and immune checkpoint. |
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AbstractList | BackgroundCadherin 5 (CDH5) functions critically in maintaining cell adhesion and integrity of endothelial and vascular cells. The expression of CDH5 is abnormal in tumor cells, which may have great potential to serve as a new immune checkpoint. The current pan-cancer analysis was performed to better understand the role of CDH5 in tumor.MethodsThe clinical significance and immunological function of CDH5 in pan-cancers were comprehensively analyzed based on the correlations between CDH5 and clinicopathologic features, prognosis values, tumor mutation burden (TMB), microsatellite instability (MSI), immune cells infiltration and immune response genes using 33 datasets from The Cancer Genome Atlas (TCGA). We further confirmed the expression of CDH5 in bladder cancer (BCa) tissues and cell lines. The CD8+ T cells were screened from peripheral blood of healthy controls and activated. BCa cell-CD8+ T cell co-culture assay and ELISA assay were carried out to verify the immunological function of CDH5.ResultsThe expression of CDH5 was down-regulated in 8 types of tumors including in BCa but up-regulated in 4 types of tumors. CDH5 was significantly correlated with tumor stage in 6 types of tumors. In addition, CDH5 was positively or negatively correlated with tumor prognosis. Furthermore, CDH5 was closely associated with TMB in 15 types of tumors and with MSI in 9 types of tumors. KEGG-GSEA and Hallmarks-GSEA analyses results indicated that CDH5 was positively related to immune response in most tumor types. In many tumors, CDH5 showed a positive correlation with immune cell infiltration. Enrichment analyses demonstrated that CDH5 was significantly related to the expression of many immunomodulators and chemokines. Further experiments showed that CDH5 was low-expressed in BCa tissues and cell lines in comparison to adjacent normal tissues and normal urothelial cell line, but it was positively associated with a better prognosis of BCa patients. The results of in vitro co-culture assay and ELISA assay demonstrated that CDH5 could promote the function of CD8+ T cells in TME of BCa.ConclusionIn summary, CDH5 was positively associated with a favorable prognosis and effective immune response in tumors, showing a great potential to serve as a novel tumor biomarker and immune checkpoint. Cadherin 5 (CDH5) functions critically in maintaining cell adhesion and integrity of endothelial and vascular cells. The expression of CDH5 is abnormal in tumor cells, which may have great potential to serve as a new immune checkpoint. The current pan-cancer analysis was performed to better understand the role of CDH5 in tumor.BackgroundCadherin 5 (CDH5) functions critically in maintaining cell adhesion and integrity of endothelial and vascular cells. The expression of CDH5 is abnormal in tumor cells, which may have great potential to serve as a new immune checkpoint. The current pan-cancer analysis was performed to better understand the role of CDH5 in tumor.The clinical significance and immunological function of CDH5 in pan-cancers were comprehensively analyzed based on the correlations between CDH5 and clinicopathologic features, prognosis values, tumor mutation burden (TMB), microsatellite instability (MSI), immune cells infiltration and immune response genes using 33 datasets from The Cancer Genome Atlas (TCGA). We further confirmed the expression of CDH5 in bladder cancer (BCa) tissues and cell lines. The CD8+ T cells were screened from peripheral blood of healthy controls and activated. BCa cell-CD8+ T cell co-culture assay and ELISA assay were carried out to verify the immunological function of CDH5.MethodsThe clinical significance and immunological function of CDH5 in pan-cancers were comprehensively analyzed based on the correlations between CDH5 and clinicopathologic features, prognosis values, tumor mutation burden (TMB), microsatellite instability (MSI), immune cells infiltration and immune response genes using 33 datasets from The Cancer Genome Atlas (TCGA). We further confirmed the expression of CDH5 in bladder cancer (BCa) tissues and cell lines. The CD8+ T cells were screened from peripheral blood of healthy controls and activated. BCa cell-CD8+ T cell co-culture assay and ELISA assay were carried out to verify the immunological function of CDH5.The expression of CDH5 was down-regulated in 8 types of tumors including in BCa but up-regulated in 4 types of tumors. CDH5 was significantly correlated with tumor stage in 6 types of tumors. In addition, CDH5 was positively or negatively correlated with tumor prognosis. Furthermore, CDH5 was closely associated with TMB in 15 types of tumors and with MSI in 9 types of tumors. KEGG-GSEA and Hallmarks-GSEA analyses results indicated that CDH5 was positively related to immune response in most tumor types. In many tumors, CDH5 showed a positive correlation with immune cell infiltration. Enrichment analyses demonstrated that CDH5 was significantly related to the expression of many immunomodulators and chemokines. Further experiments showed that CDH5 was low-expressed in BCa tissues and cell lines in comparison to adjacent normal tissues and normal urothelial cell line, but it was positively associated with a better prognosis of BCa patients. The results of in vitro co-culture assay and ELISA assay demonstrated that CDH5 could promote the function of CD8+ T cells in TME of BCa.ResultsThe expression of CDH5 was down-regulated in 8 types of tumors including in BCa but up-regulated in 4 types of tumors. CDH5 was significantly correlated with tumor stage in 6 types of tumors. In addition, CDH5 was positively or negatively correlated with tumor prognosis. Furthermore, CDH5 was closely associated with TMB in 15 types of tumors and with MSI in 9 types of tumors. KEGG-GSEA and Hallmarks-GSEA analyses results indicated that CDH5 was positively related to immune response in most tumor types. In many tumors, CDH5 showed a positive correlation with immune cell infiltration. Enrichment analyses demonstrated that CDH5 was significantly related to the expression of many immunomodulators and chemokines. Further experiments showed that CDH5 was low-expressed in BCa tissues and cell lines in comparison to adjacent normal tissues and normal urothelial cell line, but it was positively associated with a better prognosis of BCa patients. The results of in vitro co-culture assay and ELISA assay demonstrated that CDH5 could promote the function of CD8+ T cells in TME of BCa.In summary, CDH5 was positively associated with a favorable prognosis and effective immune response in tumors, showing a great potential to serve as a novel tumor biomarker and immune checkpoint.ConclusionIn summary, CDH5 was positively associated with a favorable prognosis and effective immune response in tumors, showing a great potential to serve as a novel tumor biomarker and immune checkpoint. |
Author | Li, Yuantao Gu, Junwei Lv, Jiancheng Wu, Qikai |
AuthorAffiliation | 1 Department of Gastroenterology, Linyi County People’s Hospital , Dezhou , China 3 Department of Urology, The First People's Hospital of Xiushui County , Jiujiang, Jiangxi , China 2 Laboratory of Urology and Andrology , Jiangsu Clinical Medicine Research Institution, Nanjing , China |
AuthorAffiliation_xml | – name: 3 Department of Urology, The First People's Hospital of Xiushui County , Jiujiang, Jiangxi , China – name: 1 Department of Gastroenterology, Linyi County People’s Hospital , Dezhou , China – name: 2 Laboratory of Urology and Andrology , Jiangsu Clinical Medicine Research Institution, Nanjing , China |
Author_xml | – sequence: 1 givenname: Yuantao surname: Li fullname: Li, Yuantao – sequence: 2 givenname: Qikai surname: Wu fullname: Wu, Qikai – sequence: 3 givenname: Jiancheng surname: Lv fullname: Lv, Jiancheng – sequence: 4 givenname: Junwei surname: Gu fullname: Gu, Junwei |
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Cites_doi | 10.1007/s11912-022-01241-z 10.21873/anticanres.14622 10.1016/j.lfs.2020.118110 10.1186/s13045-022-01325-0 10.1186/bcr3367 10.1016/j.prp.2021.153393 10.1016/j.celrep.2014.09.024 10.1073/pnas.131209798 10.1016/j.cell.2021.02.020 10.3390/ijms232415647 10.1002/advs.202203699 10.1093/neuonc/not029 10.1002/cac2.12416 10.1016/j.canlet.2019.11.009 10.1016/bs.ctdb.2014.11.024 10.1158/0008-5472.CAN-07-2706 10.1186/s13046-023-02614-3 10.1016/S0140-6736(16)32455-2 10.1136/jclinpath-2016-203640 10.1038/s41571-019-0268-3 10.1016/j.yexcr.2005.09.019 10.3390/curroncol29050247 10.1016/j.semcancer.2022.02.007 10.1158/2326-6066.CIR-22-0398 10.1038/s41423-021-00786-6 10.3390/cancers11122002 10.3322/caac.21763 10.1016/j.semcancer.2022.02.005 10.3390/ijms231911943 10.1186/s12943-023-01776-0 10.2478/jtim-2022-0013 10.1016/j.ctrv.2021.102187 10.1016/j.coi.2023.102329 10.3389/fonc.2022.931104 10.1186/s12967-022-03584-4 10.1002/ctm2.1189 10.3390/biology12020218 10.1016/bs.acc.2018.12.005 |
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References | Balar (B28) 2017; 389 Grivas (B27) 2021; 97 Zou (B14) 2023; 10 Dutta (B9) 2023; 12 Goenka (B37) 2023; 43 Sauteur (B32) 2014; 9 Tagliamonte (B17) 2023; 22 Higuchi (B24) 2017; 70 Wang (B33) 2021; 220 Shiravand (B26) 2022; 29 Siegel (B2) 2023; 73 Plazy (B16) 2022; 24 Pan (B30) 2022; 10 KontOmanolis (B3) 2020; 40 Oh (B6) 2020; 17 Hahn (B4) 2021; 184 Liu (B13) 2022; 12 Zheng (B29) 2023; 13 Hendrix (B20) 2001; 98 Rezaei (B22) 2012; 14 Lv (B25) 2023; 42 Silsirivanit (B5) 2019; 89 Mortezaee (B7) 2020; 258 Jia (B36) 2022; 86 Cavallaro (B18) 2006; 312 Mao (B21) 2013; 15 Wang (B15) 2022; 15 Owen (B35) 2019; 11 Chibaya (B10) 2022; 86 Chen (B12) 2022; 23 Lei (B8) 2020; 470 Lutz (B38) 2023; 11 Liu (B1) 2022; 20 Xie (B31) 2022; 23 Labelle (B23) 2008; 68 Sari (B11) 2023; 83 Lagendijk (B19) 2015; 112 Zheng (B34) 2022; 19 |
References_xml | – volume: 24 year: 2022 ident: B16 article-title: Immune checkpoint inhibitor rechallenge and resumption: a systematic review publication-title: Curr Oncol Rep doi: 10.1007/s11912-022-01241-z – volume: 40 year: 2020 ident: B3 article-title: Role of oncogenes and tumor-suppressor genes in carcinogenesis: A review publication-title: Anticancer Res doi: 10.21873/anticanres.14622 – volume: 258 start-page: 118110 year: 2020 ident: B7 article-title: Immune escape: A critical hallmark in solid tumors publication-title: Life Sci doi: 10.1016/j.lfs.2020.118110 – volume: 15 start-page: 111 year: 2022 ident: B15 article-title: Immune checkpoint modulators in cancer immunotherapy: recent advances and emerging concepts publication-title: J Hematol Oncol doi: 10.1186/s13045-022-01325-0 – volume: 14 start-page: R154 year: 2012 ident: B22 article-title: Interplay between neural-cadherin and vascular endothelial-cadherin in breast cancer progression publication-title: Breast Cancer Res BCR doi: 10.1186/bcr3367 – volume: 220 start-page: 153393 year: 2021 ident: B33 article-title: Inverse correlation of miR-27a-3p and CDH5 expression serves as a diagnostic biomarker of proliferation and metastasis of clear cell renal carcinoma publication-title: Pathol Res Practice doi: 10.1016/j.prp.2021.153393 – volume: 9 year: 2014 ident: B32 article-title: Cdh5/VE-cadherin promotes endothelial cell interface elongation via cortical actin polymerization during angiogenic sprouting publication-title: Cell Rep doi: 10.1016/j.celrep.2014.09.024 – volume: 98 year: 2001 ident: B20 article-title: Expression and functional significance of VE-cadherin in aggressive human melanoma cells: role in vasculogenic mimicry publication-title: Proc Natl Acad Sci USA doi: 10.1073/pnas.131209798 – volume: 184 year: 2021 ident: B4 article-title: An expanded universe of cancer targets publication-title: Cell doi: 10.1016/j.cell.2021.02.020 – volume: 23 start-page: 15647 year: 2022 ident: B31 article-title: The pan-cancer multi-omics landscape of FOXO family relevant to clinical outcome and drug resistance publication-title: Int J Mol Sci doi: 10.3390/ijms232415647 – volume: 10 start-page: e2203699 year: 2023 ident: B14 article-title: The single-cell landscape of intratumoral heterogeneity and the immunosuppressive microenvironment in liver and brain metastases of breast cancer publication-title: Adv Sci (Weinheim Baden-Wurttemberg Germany) doi: 10.1002/advs.202203699 – volume: 15 year: 2013 ident: B21 article-title: CDH5 is specifically activated in glioblastoma stemlike cells and contributes to vasculogenic mimicry induced by hypoxia publication-title: Neuro-oncology doi: 10.1093/neuonc/not029 – volume: 43 year: 2023 ident: B37 article-title: Tumor microenvironment signaling and therapeutics in cancer progression publication-title: Cancer Commun (London England) doi: 10.1002/cac2.12416 – volume: 470 year: 2020 ident: B8 article-title: Immune cells within the tumor microenvironment: Biological functions and roles in cancer immunotherapy publication-title: Cancer Lett doi: 10.1016/j.canlet.2019.11.009 – volume: 112 year: 2015 ident: B19 article-title: VE-cadherin in vascular development: a coordinator of cell signaling and tissue morphogenesis publication-title: Curr Topics Dev Biol doi: 10.1016/bs.ctdb.2014.11.024 – volume: 68 year: 2008 ident: B23 article-title: Vascular endothelial cadherin promotes breast cancer progression via transforming growth factor beta signaling publication-title: Cancer Res doi: 10.1158/0008-5472.CAN-07-2706 – volume: 42 start-page: 41 year: 2023 ident: B25 article-title: HNRNPL induced circFAM13B increased bladder cancer immunotherapy sensitivity via inhibiting glycolysis through IGF2BP1/PKM2 pathway publication-title: J Exp Clin Cancer Res CR doi: 10.1186/s13046-023-02614-3 – volume: 389 start-page: 67 year: 2017 ident: B28 article-title: Atezolizumab as first-line treatment in cisplatin-ineligible patients with locally advanced and metastatic urothelial carcinoma: a single-arm, multicentre, phase 2 trial publication-title: Lancet (Lond Engl) doi: 10.1016/S0140-6736(16)32455-2 – volume: 70 year: 2017 ident: B24 article-title: Cadherin 5 expression correlates with poor survival in human gastric cancer publication-title: J Clin Pathol doi: 10.1136/jclinpath-2016-203640 – volume: 17 start-page: 33 year: 2020 ident: B6 article-title: HER2-targeted therapies - a role beyond breast cancer publication-title: Nat Rev Clin Oncol doi: 10.1038/s41571-019-0268-3 – volume: 312 year: 2006 ident: B18 article-title: Endothelial cadherins and tumor angiogenesis publication-title: Exp Cell Res doi: 10.1016/j.yexcr.2005.09.019 – volume: 29 year: 2022 ident: B26 article-title: Immune checkpoint inhibitors in cancer therapy publication-title: Curr Oncol (Toronto Ont) doi: 10.3390/curroncol29050247 – volume: 86 year: 2022 ident: B36 article-title: Chemokines in colon cancer progression publication-title: Semin Cancer Biol doi: 10.1016/j.semcancer.2022.02.007 – volume: 11 year: 2023 ident: B38 article-title: IL18 receptor signaling regulates tumor-reactive CD8+ T-cell exhaustion via activation of the IL2/STAT5/mTOR pathway in a pancreatic cancer model publication-title: Cancer Immunol Res doi: 10.1158/2326-6066.CIR-22-0398 – volume: 19 start-page: 192 year: 2022 ident: B34 article-title: The use of supercytokines, immunocytokines, engager cytokines, and other synthetic cytokines in immunotherapy publication-title: Cell Mol Immunol doi: 10.1038/s41423-021-00786-6 – volume: 11 start-page: 2002 year: 2019 ident: B35 article-title: JAK-STAT signaling: A double-edged sword of immune regulation and cancer progression publication-title: Cancers (Basel) doi: 10.3390/cancers11122002 – volume: 73 start-page: 17 year: 2023 ident: B2 article-title: Cancer statistics, 2023 publication-title: CA Cancer J Clin doi: 10.3322/caac.21763 – volume: 86 year: 2022 ident: B10 article-title: Senescence and the tumor-immune landscape: Implications for cancer immunotherapy publication-title: Semin Cancer Biol doi: 10.1016/j.semcancer.2022.02.005 – volume: 23 start-page: 11943 year: 2022 ident: B12 article-title: Lactate-lactylation hands between metabolic reprogramming and immunosuppression publication-title: Int J Mol Sci doi: 10.3390/ijms231911943 – volume: 22 start-page: 75 year: 2023 ident: B17 article-title: Molecular mimicry and cancer vaccine development publication-title: Mol Cancer doi: 10.1186/s12943-023-01776-0 – volume: 10 year: 2022 ident: B30 article-title: Pan-cancer Landscape of the RUNX Protein Family Reveals their Potential as Carcinogenic Biomarkers and the Mechanisms Underlying their Action publication-title: J Trans Internal Med doi: 10.2478/jtim-2022-0013 – volume: 97 start-page: 102187 year: 2021 ident: B27 article-title: Avelumab first-line maintenance in locally advanced or metastatic urothelial carcinoma: Applying clinical trial findings to clinical practice publication-title: Cancer Treat Rev doi: 10.1016/j.ctrv.2021.102187 – volume: 83 start-page: 102329 year: 2023 ident: B11 article-title: Tumor immune evasion through loss of MHC class-I antigen presentation publication-title: Curr Opin Immunol doi: 10.1016/j.coi.2023.102329 – volume: 12 year: 2022 ident: B13 article-title: A novel strategy to fuel cancer immunotherapy: targeting glucose metabolism to remodel the tumor microenvironment publication-title: Front Oncol doi: 10.3389/fonc.2022.931104 – volume: 20 start-page: 376 year: 2022 ident: B1 article-title: Combined lifestyle, mental health, and mortality in US cancer survivors: a national cohort study publication-title: J Trans Med doi: 10.1186/s12967-022-03584-4 – volume: 13 year: 2023 ident: B29 article-title: Dissecting the role of cancer-associated fibroblast-derived biglycan as a potential therapeutic target in immunotherapy resistance: A tumor bulk and single-cell transcriptomic study publication-title: Clin Trans Med doi: 10.1002/ctm2.1189 – volume: 12 start-page: 218 year: 2023 ident: B9 article-title: Targets of immune escape mechanisms in cancer: basis for development and evolution of cancer immune checkpoint inhibitors publication-title: Biology doi: 10.3390/biology12020218 – volume: 89 start-page: 189 year: 2019 ident: B5 article-title: Glycosylation markers in cancer publication-title: Adv Clin Chem doi: 10.1016/bs.acc.2018.12.005 |
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Snippet | Cadherin 5 (CDH5) functions critically in maintaining cell adhesion and integrity of endothelial and vascular cells. The expression of CDH5 is abnormal in... BackgroundCadherin 5 (CDH5) functions critically in maintaining cell adhesion and integrity of endothelial and vascular cells. The expression of CDH5 is... |
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StartPage | 1239875 |
SubjectTerms | CD8 + T cells cdh5 immune response Immunology pan-cancer prognosis |
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Title | A comprehensive pan-cancer analysis of CDH5 in immunological response |
URI | https://www.proquest.com/docview/2874836320 https://pubmed.ncbi.nlm.nih.gov/PMC10551168 https://doaj.org/article/4eaf5180694840a09c638e48d156f21b |
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