English  |  正體中文  |  简体中文  |  Items with full text/Total items : 12145/12927 (94%)
Visitors : 855158      Online Users : 994
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    國家衛生研究院 NHRI > 癌症研究所 > 其他 > 期刊論文 >  Item 3990099045/8412
    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/8412


    Title: Overexpression of REG4 confers an independent negative prognosticator in rectal cancers receiving concurrent chemoradiotherapy
    Authors: He, HL;Lee, YE;Shiue, YL;Lee, SW;Lin, LC;Chen, TJ;Wu, TF;Hsing, CH;Huang, HY;Wang, JY;Li, CF
    Contributors: National Institute of Cancer Research
    Abstract: Background and Objectives: Neoadjuvant concurrent chemoradiotherapy (CCRT) followed by surgery is the standard treatment for locally advanced rectal cancer. Through data mining from published transcriptomic database, we identified Regenerating Gene Type IV (REG4) as the most significantly associated gene with resistance to CCRT. This study examined the prognostic impact of REG4 expression in patients with rectal cancer receiving neoadjuvant CCRT. Methods: REG4 immunohistochemistry was retrospectively assessed for pre-treatment biopsy specimens from 172 rectal cancer patients who received neoadjuvant CCRT followed by surgery without initial distant metastasis. The results were correlated with the clinicopathological variables, disease-specific survival (DSS), local recurrence-free survival (LRFS), and distant metastasis-free survival (DMFS), as well as g-H2AX expression in post-treatment tumor samples. Results: High expression of REG4 was associated with advanced pre-treatment nodal status (P.0.026), advanced post-treatment tumor status (P.0.006), advanced post-treatment nodal status (P.0.001), advanced post-treatment tumor stage (P 0.001), and inferior tumor regression grade (P.0.001). Of note, high expression of REG4 emerged as an adverse prognosticator for DSS (P.0.0004), LRFS (P.0.0009), and MeFS (P.0.0254). After multivariate comparisons, it remained independently prognostic for worse DSS (hazard ratio [HR].2.731; P.0.025) and LRFS (HR.2.676; P.0.029). High expression of REG4 was also negatively associated with g-H2AX expression (P 0.0001, r.-0.708). Conclusions: High expression of REG4 is associated with poor therapeutic response, adverse outcome and an aggressive phenotype in rectal cancer patients treated with neoadjuvant CCRT, justifying REG4 is a surrogate marker to predict CCRT resistance.
    Date: 2014-12-15
    Relation: Journal of Surgical Oncology. 2014 Dec 15;110(8):1002-1010.
    Link to: http://dx.doi.org/10.1002/jso.23764
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=0022-4790&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000345174600018
    Cited Times(Scopus): http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84910122125
    Appears in Collections:[其他] 期刊論文

    Files in This Item:

    File Description SizeFormat
    SCP84910122125.pdf1300KbAdobe PDF348View/Open


    All items in NHRI are protected by copyright, with all rights reserved.

    Related Items in TAIR

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback