Matches in SemOpenAlex for { <https://semopenalex.org/work/W3111037181> ?p ?o ?g. }
- W3111037181 abstract "Abstract Background This study explored the prognostic significance of Glypican (GPC) family genes in patients with pancreatic ductal adenocarcinoma (PDAC) after pancreaticoduodenectomy using data from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO). Methods A total of 112 PDAC patients from TCGA and 48 patients from GEO were included in the analysis. The relationship between overall survival and the expression of GPC family genes as well as basic clinical characteristics was analyzed using the Kaplan-Meier method with the log-rank test. Joint effects survival analysis was performed to further examine the relationship between GPC genes and prognosis. A prognosis nomogram was established based on clinical characteristics and prognosis-related genes. Prognosis-related genes were investigated by genome-wide co-expression analysis and gene set enrichment analysis (GSEA) was carried out to identify potential mechanisms of these genes affecting prognosis. Results In TCGA database, high expression of GPC2 , GPC3 , and GPC5 was significantly associated with favorable survival (log-rank P = 0.031, 0.021, and 0.028, respectively; adjusted P value = 0.005, 0.022, and 0.020, respectively), and joint effects analysis of these genes was effective for prognosis prediction. The prognosis nomogram was applied to predict the survival probability using the total scores calculated. Genome-wide co-expression and GSEA analysis suggested that the GPC2 may affect prognosis through sequence-specific DNA binding, protein transport, cell differentiation and oncogenic signatures (KRAS, RAF, STK33, and VEGFA). GPC3 may be related to cell adhesion, angiogenesis, inflammatory response, signaling pathways like Ras, Rap1, PI3K-Akt, chemokine, GPCR, and signatures like cyclin D1, p53, PTEN. GPC5 may be involved in transcription factor complex, TFRC1, oncogenic signatures (HOXA9 and BMI1), gene methylation, phospholipid metabolic process, glycerophospholipid metabolism, cell cycle, and EGFR pathway. Conclusion GPC2 , GPC3 , and GPC5 expression may serve as prognostic indicators in PDAC, and combination of these genes showed a higher efficiency for prognosis prediction." @default.
- W3111037181 created "2020-12-21" @default.
- W3111037181 creator A5000436077 @default.
- W3111037181 creator A5008919007 @default.
- W3111037181 creator A5014716924 @default.
- W3111037181 creator A5021705042 @default.
- W3111037181 creator A5022434547 @default.
- W3111037181 creator A5023103876 @default.
- W3111037181 creator A5029609881 @default.
- W3111037181 creator A5031208933 @default.
- W3111037181 creator A5032874546 @default.
- W3111037181 creator A5040403951 @default.
- W3111037181 creator A5048708798 @default.
- W3111037181 creator A5058218812 @default.
- W3111037181 creator A5072664727 @default.
- W3111037181 creator A5074233771 @default.
- W3111037181 creator A5086083806 @default.
- W3111037181 creator A5087548272 @default.
- W3111037181 date "2020-12-01" @default.
- W3111037181 modified "2023-10-14" @default.
- W3111037181 title "Prognostic value of Glypican family genes in early-stage pancreatic ductal adenocarcinoma after pancreaticoduodenectomy and possible mechanisms" @default.
- W3111037181 cites W1533942137 @default.
- W3111037181 cites W1767882197 @default.
- W3111037181 cites W1926642623 @default.
- W3111037181 cites W1942602300 @default.
- W3111037181 cites W1968812902 @default.
- W3111037181 cites W2002641593 @default.
- W3111037181 cites W2011062674 @default.
- W3111037181 cites W2018838463 @default.
- W3111037181 cites W2021880506 @default.
- W3111037181 cites W2053643795 @default.
- W3111037181 cites W2069626330 @default.
- W3111037181 cites W2088484876 @default.
- W3111037181 cites W2090364967 @default.
- W3111037181 cites W2105253426 @default.
- W3111037181 cites W2122683221 @default.
- W3111037181 cites W2129756622 @default.
- W3111037181 cites W2133271589 @default.
- W3111037181 cites W2139658078 @default.
- W3111037181 cites W2153084473 @default.
- W3111037181 cites W2155637224 @default.
- W3111037181 cites W2171030481 @default.
- W3111037181 cites W2184502627 @default.
- W3111037181 cites W2441351280 @default.
- W3111037181 cites W2561946116 @default.
- W3111037181 cites W2591074784 @default.
- W3111037181 cites W2598922954 @default.
- W3111037181 cites W2604869661 @default.
- W3111037181 cites W2607129810 @default.
- W3111037181 cites W2618026677 @default.
- W3111037181 cites W2734434358 @default.
- W3111037181 cites W2739323872 @default.
- W3111037181 cites W2739435673 @default.
- W3111037181 cites W2751875288 @default.
- W3111037181 cites W2753814296 @default.
- W3111037181 cites W2754294524 @default.
- W3111037181 cites W2755839585 @default.
- W3111037181 cites W2756336276 @default.
- W3111037181 cites W2763174443 @default.
- W3111037181 cites W2796292443 @default.
- W3111037181 cites W2803441813 @default.
- W3111037181 cites W2888367509 @default.
- W3111037181 cites W2889931773 @default.
- W3111037181 cites W2892617983 @default.
- W3111037181 cites W2893622300 @default.
- W3111037181 cites W2895552871 @default.
- W3111037181 cites W2895684352 @default.
- W3111037181 cites W2902613833 @default.
- W3111037181 cites W2911188335 @default.
- W3111037181 cites W2914157137 @default.
- W3111037181 cites W2914873020 @default.
- W3111037181 cites W2941196604 @default.
- W3111037181 cites W2954910819 @default.
- W3111037181 cites W2967470918 @default.
- W3111037181 cites W2972277405 @default.
- W3111037181 cites W2980219769 @default.
- W3111037181 cites W2981746321 @default.
- W3111037181 cites W2984992104 @default.
- W3111037181 cites W2985645328 @default.
- W3111037181 cites W2985771661 @default.
- W3111037181 cites W2987941021 @default.
- W3111037181 cites W2991036720 @default.
- W3111037181 cites W3003996315 @default.
- W3111037181 cites W3006466102 @default.
- W3111037181 cites W4210976084 @default.
- W3111037181 cites W4211208840 @default.
- W3111037181 cites W4241399562 @default.
- W3111037181 doi "https://doi.org/10.1186/s12876-020-01560-0" @default.
- W3111037181 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7731467" @default.
- W3111037181 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/33302876" @default.
- W3111037181 hasPublicationYear "2020" @default.
- W3111037181 type Work @default.
- W3111037181 sameAs 3111037181 @default.
- W3111037181 citedByCount "8" @default.
- W3111037181 countsByYear W31110371812021 @default.
- W3111037181 countsByYear W31110371812022 @default.
- W3111037181 countsByYear W31110371812023 @default.
- W3111037181 crossrefType "journal-article" @default.
- W3111037181 hasAuthorship W3111037181A5000436077 @default.
- W3111037181 hasAuthorship W3111037181A5008919007 @default.