Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13740
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dc.contributor.authorTullavardhana T.
dc.contributor.authorAkranurakkul P.
dc.contributor.authorUngkitphaiboon W.
dc.contributor.authorSongtish D.
dc.date.accessioned2021-04-05T03:26:09Z-
dc.date.available2021-04-05T03:26:09Z-
dc.date.issued2015
dc.identifier.issn22965262
dc.identifier.other2-s2.0-84941046316
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/13740-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84941046316&doi=10.1159%2f000380776&partnerID=40&md5=1dd86bef5a99fa0fb3d43673fa18e22e
dc.description.abstractBACKGROUND: Vascular endothelial growth factor C (VEGF-C) is involved in the development and progression of tumor angio-/lymphangiogenesis. The purpose of this study is to evaluate whether VEGF-C expression is an indicator of aggressiveness and poor prognosis of esophageal squamous cell carcinoma (ESCC).METHOD: A meta-analysis was conducted to investigate the association between VEGF-C expression with clinicopathological characteristics and survival of ESCC patients. The dataset was defined by searching PubMed, Embase, Google Scholar, and the Cochrane database for appropriate articles published until April 2014.RESULT: The final analysis was made from 9 studies, including 656 ESCC patients. Positive VEGF-C expression was defined by immunohistochemistry (IHC) or mRNA expression analysis. The results demonstrated that VEGF-C expression was significantly associated with advanced-stage disease (odds ratio (OR) = 2.29, 95% confidence interval (CI) = 1.37-3.84, P = 0.002), deeper tumor invasion, lymph node metastasis, and lymphatic invasion. The 5-year survival of VEGF-C expression-negative patients was found to be better than that of VEGF-C expression-positive patients (OR = 0.35, 95% CI = 0.21-0.58, P < 0.0001). However, there was no significant association between the VEGF-C expression levels and either poorer tumor differentiation or vascular invasion.CONCLUSION: The results of the meta-analysis strongly indicate that VEGF-C expression could function as a marker for predicting the aggressiveness and prognosis of ESCC. © 2015 S. Karger GmbH, Freiburg.
dc.subjectmessenger RNA
dc.subjecttumor marker
dc.subjectvasculotropin C
dc.subjectVEGFC protein, human
dc.subjectVEGFC protein, human
dc.subjectVEGFC protein, human
dc.subjectCarcinoma, Squamous Cell
dc.subjectEsophageal Neoplasms
dc.subjectgene expression regulation
dc.subjectgenetics
dc.subjecthuman
dc.subjectimmunohistochemistry
dc.subjectlymph node metastasis
dc.subjectmeta analysis
dc.subjectmetabolism
dc.subjectmortality
dc.subjectphysiology
dc.subjectpolymerase chain reaction
dc.subjectprognosis
dc.subjectsurvival rate
dc.subjectBiomarkers, Tumor
dc.subjectBiomarkers, Tumor
dc.subjectBiomarkers, Tumor
dc.subjectCarcinoma, Squamous Cell
dc.subjectCarcinoma, Squamous Cell
dc.subjectCarcinoma, Squamous Cell
dc.subjectEsophageal Neoplasms
dc.subjectEsophageal Neoplasms
dc.subjectEsophageal Neoplasms
dc.subjectGene Expression Regulation, Neoplastic
dc.subjectGene Expression Regulation, Neoplastic
dc.subjectGene Expression Regulation, Neoplastic
dc.subjectHumans
dc.subjectHumans
dc.subjectHumans
dc.subjectImmunohistochemistry
dc.subjectImmunohistochemistry
dc.subjectImmunohistochemistry
dc.subjectLymphatic Metastasis
dc.subjectLymphatic Metastasis
dc.subjectLymphatic Metastasis
dc.subjectPolymerase Chain Reaction
dc.subjectPolymerase Chain Reaction
dc.subjectPolymerase Chain Reaction
dc.subjectPrognosis
dc.subjectPrognosis
dc.subjectPrognosis
dc.subjectRNA, Messenger
dc.subjectRNA, Messenger
dc.subjectRNA, Messenger
dc.subjectSurvival Rate
dc.subjectSurvival Rate
dc.subjectSurvival Rate
dc.subjectVascular Endothelial Growth Factor C
dc.subjectVascular Endothelial Growth Factor C
dc.subjectVascular Endothelial Growth Factor C
dc.titleVascular endothelial growth factor-C expression as a biomarker of poor prognosis in esophageal squamous cell carcinoma: a meta-analysis
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationOncology research and treatment. Vol 38, No.3 (2015), p.110-114
dc.identifier.doi10.1159/000380776
Appears in Collections:Scopus 1983-2021

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