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http://purl.uniprot.org/citations/28404963http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/28404963http://www.w3.org/2000/01/rdf-schema#comment"

Background

Suppressor of cytokine signaling (SOCS) 1 and 3 methylation have been associated with clinical features and outcomes of cancer patients. However, their roles in determining the treatment response to transarterial chemoembolization (TACE) in patients with hepatocellular carcinoma (HCC) remain unknown.

Results

We found that presence of SOCS3 methylation is significantly associated with the major clinical features of HCC patients, including tumor stage, lymph node and vascular invasion. Of note, we observed that the presence of SOCS3 methylation is closely related to TACE response. In prognosis analyses, HCC patients with SOCS3 methylation presence have a poorer prognosis indicated by lower 3-, and 5-year survival rates and shorter mean survival period, than those without. Multivariate COX analysis confirms the prognostic role of the presence of SOCS3 methylation in HCC patients receiving TACE treatment.

Materials and methods

A total of 246 HCC patients receiving TACE were enrolled in this study. Tumor samples was obtained from echo-guided fine needle aspiration and genomic DNA from tumor samples was purified. SOCS1 and SOCS3 methylation status were detected using methylation-specific polymerase chain reaction. The treatment responses to TACE of patients were evaluated after procedure and all patients were followed for prognosis analysis.

Conclusions

This finding suggests that the presence of SOCS3 methylation is a marker to predict treatment response and prognosis in HCC patients receiving TACE therapy."xsd:string
http://purl.uniprot.org/citations/28404963http://purl.org/dc/terms/identifier"doi:10.18632/oncotarget.16157"xsd:string
http://purl.uniprot.org/citations/28404963http://purl.uniprot.org/core/author"Huang J."xsd:string
http://purl.uniprot.org/citations/28404963http://purl.uniprot.org/core/author"Yang Y."xsd:string
http://purl.uniprot.org/citations/28404963http://purl.uniprot.org/core/author"Wang N."xsd:string
http://purl.uniprot.org/citations/28404963http://purl.uniprot.org/core/author"Sun L.L."xsd:string
http://purl.uniprot.org/citations/28404963http://purl.uniprot.org/core/author"Zhou W.P."xsd:string
http://purl.uniprot.org/citations/28404963http://purl.uniprot.org/core/author"Pan Z.Y."xsd:string
http://purl.uniprot.org/citations/28404963http://purl.uniprot.org/core/author"Jiang B.G."xsd:string
http://purl.uniprot.org/citations/28404963http://purl.uniprot.org/core/date"2017"xsd:gYear
http://purl.uniprot.org/citations/28404963http://purl.uniprot.org/core/name"Oncotarget"xsd:string
http://purl.uniprot.org/citations/28404963http://purl.uniprot.org/core/pages"28621-28627"xsd:string
http://purl.uniprot.org/citations/28404963http://purl.uniprot.org/core/title"Tumor SOCS3 methylation status predicts the treatment response to TACE and prognosis in HCC patients."xsd:string
http://purl.uniprot.org/citations/28404963http://purl.uniprot.org/core/volume"8"xsd:string
http://purl.uniprot.org/citations/28404963http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/28404963
http://purl.uniprot.org/citations/28404963http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/28404963
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http://purl.uniprot.org/uniprot/Q6FI39http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/28404963