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Enhanced RegIV Expression Predicts the Intrinsic 5-Fluorouracil (5-FU) Resistance in Advanced Gastric Cancer
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  • 作者:Li-Sha Ying (1)
    Jiang-Liu Yu (1)
    Xiao-Xiao Lu (1)
    Zhi-Qiang Ling (1)
  • 关键词:Gastric cancer ; Regenerating islet ; derived family ; member 4 (RegIV) ; 5 ; Fluorouracil ; ATP ; tumor chemosensitivity assay ; Real ; time reverse transcriptase ; PCR
  • 刊名:Digestive Diseases and Sciences
  • 出版年:2013
  • 出版时间:February 2013
  • 年:2013
  • 卷:58
  • 期:2
  • 页码:414-422
  • 全文大小:418KB
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  • 作者单位:Li-Sha Ying (1)
    Jiang-Liu Yu (1)
    Xiao-Xiao Lu (1)
    Zhi-Qiang Ling (1)

    1. Zhejiang Cancer Research Institute, Zhejiang Province Cancer Hospital, Zhejiang Cancer Center, No.38 Guangji Rd., Banshanqiao District, Hangzhou, 310022, People’s Republic of China
  • ISSN:1573-2568
文摘
Aim RegIV, a member of the Regenerating (REG) gene family, may be a marker for the prediction of resistance to 5-fluorouracil (5-FU)-based chemotherapy. However, the relationship between the intrinsic drug resistance of gastric cancer (GC) cells to 5-FU used alone (single FU) or in multidrug therapeutic regimens (5-FU combinations) and RegIV expression has not been investigated. Methods The patient cohort comprised 45 patients with primary GC. The chemoresistance of GC cells to therapeutic regimens consisting of single 5-FU or FU combinations was investigated using the ATP-tumor chemosensitivity assay. The level of RegIV mRNA transcripts was determined by real-time reverse transcriptase-PCR. RegIV expression was evaluated as a novel predictive biomarker for the intrinsic drug resistance of primary GC cells to single 5-FU or 5-FU combinations. Results Upregulation of RegIV mRNA transcripts was observed in 36 of the 45 tumor specimens and was positively correlated with the invasive depth of the tumor cells (p?=?0.000), the clinical stages (p?=?0.000) and the in vitro intrinsic drug resistance of primary GC cells to 5-FU (p?=?0.000) or 5-FU combinations. Conclusion RegIV mRNA transcript level was strongly associated with the intrinsic resistance of GC cells to single 5-FU or 5-FU combinations, suggesting that RegIV may play an important role in the intrinsic resistance of GC cells to 5-FU and that targeted therapy against the RegIV gene could be applied to overcome 5-FU resistance in the treatment of GC.

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