Prognostic significance of BRCA1-associated protein 1 in colorectal cancer
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  • 作者:Jianjun Tang (1)
    Shaoyan Xi (2)
    Gang Wang (1)
    Boqing Wang (1) (4)
    Shumei Yan (2)
    Yuanzhong Wu (1)
    Yi Sang (1)
    Wenjing Wu (1) (3)
    Ruhua Zhang (1)
    Tiebang Kang (1)
  • 关键词:BRCA1 ; associated protein 1 ; BAP1 ; Colorectal cancer ; Prognosis
  • 刊名:Medical Oncology
  • 出版年:2013
  • 出版时间:June 2013
  • 年:2013
  • 卷:30
  • 期:2
  • 全文大小:759KB
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  • 作者单位:Jianjun Tang (1)
    Shaoyan Xi (2)
    Gang Wang (1)
    Boqing Wang (1) (4)
    Shumei Yan (2)
    Yuanzhong Wu (1)
    Yi Sang (1)
    Wenjing Wu (1) (3)
    Ruhua Zhang (1)
    Tiebang Kang (1)

    1. State Key Laboratory of Oncology in South China, Sun Yat-Sen University Cancer Center, No 651, Dongfeng Road East, Guangzhou, 510060, China
    2. Department of Pathology, Sun Yat-Sen University Cancer Center, Guangzhou, 510060, China
    4. Department of Hepatobiliarypancreatic Surgery, Affiliated Tumor Hospital, Xinjiang Medical University, Urumqi, 830000, China
    3. Department of Medical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, 510060, China
文摘
Mutations of BRCA1-associated protein 1 (BAP1), a nuclear-localized deubiquitinating enzyme, had been documented in multiple human cancers. However, its role and clinical relevance in colorectal cancer is unknown. The purpose of this study was to reveal the prognostic significance of BAP1 in colorectal cancer. We performed quantitative PCR and Western blotting analyses to examine BAP1 expression in 8 cases of CRC tissues and matched adjacent non-cancerous tissues. And immunohistochemistry was used to evaluate BAP1 expression in archived 252 paraffin-embedded CRC specimens. We found that the mRNA and protein levels of BAP1 were down-regulated in 6 out of 8 cases of CRC tissues compared with their adjacent non-cancerous tissues. The BAP1 expression was closely correlated with age (p?=?0.037), clinical stage (p?=?0.001), T classification (p?<?0.001), N classification (p?<?0.001), and pathologic differentiation (p?=?0.008) and histological type (p?=?0.047) in CRC. The CRC patients with lower BAP1 expression survived shorter than those with higher BAP1 expression. Importantly, multivariate analysis demonstrated that BAP1 expression was an independent prognostic factor for CRC (p?=?0.037). Collectively, we provide the first evidence that reduced BAP1 expression is associated with poor prognosis of CRC and BAP1 may serve as a novel prognostic biomarker for CRC.

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