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Overexpression of stathmin is resistant to paclitaxel treatment in patients with non-small cell lung cancer
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  • 作者:Ruifang Sun ; Zhigang Liu ; Lumin Wang ; Weidong Lv ; Jia Liu ; Caixia Ding
  • 关键词:STMN1 ; Sensitivity ; Prognosis ; NSCLC ; TAX ; Chemotherapy
  • 刊名:Tumor Biology
  • 出版年:2015
  • 出版时间:September 2015
  • 年:2015
  • 卷:36
  • 期:9
  • 页码:7195-7204
  • 全文大小:671 KB
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  • 作者单位:Ruifang Sun (1)
    Zhigang Liu (2)
    Lumin Wang (3)
    Weidong Lv (2)
    Jia Liu (2)
    Caixia Ding (4)
    Yong Yuan (4)
    Guangyan Lei (2)
    Changfu Xu (1)

    1. Department of Pathology, School of Medicine, Xi’an Jiaotong University, 76 Yanta West Road, Xi’an, 710061, Shaanxi, People’s Republic of China
    2. Department of Thoracic Surgery, Tumor Hospital of Shaanxi Province, 309 Yanta West Road, Xi’an, Shaanxi, People’s Republic of China
    3. Key Laboratory of Environment and Genes Related to Diseases, School of Medicine, Xi’an Jiaotong University, 76 Yanta West Road, Xi’an, Shaanxi, People’s Republic of China
    4. Department of Pathology, Tumor Hospital of Shaanxi Province, 309 Yanta West Road, Xi’an, Shaanxi, People’s Republic of China
  • 刊物主题:Cancer Research;
  • 出版者:Springer Netherlands
  • ISSN:1423-0380
文摘
Paclitaxel can exert therapeutic effects by interacting with microtubules. Stathmin and β-III-tubulin, which have impact on microtubule activity, are believed to be involved in the chemotherapy. The purpose of the present study was to evaluate the associations between stathmin and β-III-tubulin expression and treatment response and survivals in patients with non-small cell lung cancer (NSCLC). Two hundred thirty-eight patients who were treated by platinum-based chemotherapy were enrolled in this study, among them, 111 patients also received paclitaxel treatment. Formalin-fixed and paraffin-embedded tumor tissues were collected for messenger RNA (mRNA) and protein detection. We assessed the associations of the two molecules with treatment response and survival outcome. High level of stathmin exhibited poor response to chemotherapy (for mRNA, P = 0.041; for protein, P = 0.017). Overexpression of stathmin was associated with shorter overall survival (for mRNA, P = 0.012; for protein, P = 0.014) and progression-free survival (for mRNA, P = 0.039; for protein, P = 0.022). Of note, this association was only observed in patients who were treated by both platinum and paclitaxel. Similar effects were not observed for β-III-tubulin. The findings demonstrated that paclitaxel effect may be interfered with stathmin; overexpression of stathmin is a predictive marker for a worse prognosis in patients with NSCLC who were treated by both platinum and paclitaxel chemotherapy.

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