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    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/9571


    Title: JAK2 overexpression is a prognostic indicator for worse outcome in nasopharyngeal carcinoma and is independent of JAK2 exon 12 and JAK2 V617F mutation
    Other Titles: Abstract number
    Authors: Liang, PI;Li, CF
    Contributors: National Institute of Cancer Research
    Abstract: Background: The nasopharyngeal carcinoma (NPC) has distinct incidence in various races and different geographical regions. It is endemic in southern China, Southeast Asia, and the Middle East. The etiology of NPC is likely multifactorial, which include genetic susceptibility, infection by Epstein-Barr virus (EBV), and environmental factors. There are several molecular pathways involved in the pathogenesis of NPC. JAK2 is one of the four members of the Janus kinase (JAK) family, and its mutation is an important oncogenic driver in myeloproliferative neoplasms and certain hematopoietic malignancies. By using public domain datasets and our well-characterized cohort, we intended to analyze the association of JAK2 expression in NPC. Design: Two datasets from GEO (GSE12452 and GSE34573) were used to analyze the significance of JAK2 transcript expression between tumor and non-tumor specimen. JAK2 immunostain was performed on 124 cases of NPC and interpreted using H-score. The result was then correlated with clinicopathological features, disease-specific survival (DSS), distal metastasis-free survival (DMeFS), and local recurrence-free survival (LRFS). Twenty NPC cases with JAK2 overexpression were also submitted for JAK2 exon 12 and JAK2 V617F mutation analyses using PCR followed by direct sequencing. Results: Validation of the datasets in public domain showed that, in contrast with non-tumor specimens, there is an up-regulation of JAK2 transcript in NPC. In the immunohistochemical study, JAK2 overexpression significantly associated with advanced disease stage (stage I-II vs stage III-IV, p = 0.019). Its overexpression also independently predict poor DSS (p =0.005), DMeFS (p =0.036), and LRFS (p =0.012). None of the 20 JAK2 overexpressed NPC cases have JAK2 exon 12 and JAK2 V617F mutation. Conclusions: JAK2 overexpression is associated with advanced disease stage and conferred poor clinical outcome, justifying that JAK2 is a potential prognostic biomarker of NPC. Its overexpression is also independent of JAK2 exon 12 and JAK2 V617F mutation.
    Date: 2016-02
    Relation: Laboratory Investigation. 2016 Feb;96(Suppl. 1):325A.
    Link to: http://dx.doi.org/10.1038/labinvest.2016.12
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=0023-6837&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000369270702032
    Appears in Collections:[其他] 會議論文/會議摘要

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