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LRIG1 Improves Chemosensitivity Through Inhibition of BCL-2 and MnSOD in Glioblastoma
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  • 作者:Jianjun Ding (1) (3)
    Baohui Liu (2)
    Yi He (3)
    Xianhou Yuan (1)
    Daofeng Tian (2)
    Baowei Ji (2)
    Long Wang (2)
    Liquan Wu (2)
    Huimin Dong (2)
    Junmin Wang (2)
    Xiaonan Zhu (2)
    Qiang Cai (2)
    Shenqi Zhang (2)
    Qianxue Chen (2)

    1. Zhongnan Hospital
    ; Wuhan University ; 125 Donghu Street ; Wuhan ; 430071 ; Hubei ; China
    3. The Second Renmin Hospital of Shenzhen
    ; 3002 Yigangxi Street ; Shenzhen ; 518039 ; Guangdong ; China
    2. Renmin Hospital
    ; Wuhan University ; 238 Jiefang Street ; Wuhan ; 430060 ; Hubei ; China
  • 关键词:Leucine ; rich repeats and immunoglobulin ; like domains 1 (LRIG1) ; Chemosensitivity ; B cell lymphoma 2 (BCL ; 2) ; Manganese superoxide dismutase (MnSOD)
  • 刊名:Cell Biochemistry and Biophysics
  • 出版年:2015
  • 出版时间:January 2015
  • 年:2015
  • 卷:71
  • 期:1
  • 页码:27-33
  • 全文大小:353 KB
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  • 刊物主题:Biochemistry, general; Pharmacology/Toxicology; Biotechnology; Cell Biology; Biophysics and Biological Physics;
  • 出版者:Springer US
  • ISSN:1559-0283
文摘
We have reported that Leucine-rich repeats and immunoglobulin-like domains 1 (LRIG1) can improve the chemosensitivity in U251 cells. However, the underlying mechanisms how LRIG1 improves the chemosensitivity remain unknown. In this study, we reported that LRIG1 can improve the chemosensitivity through the inhibition of B cell lymphoma 2 (BCL-2) and manganese superoxide dismutase (MnSOD). In addition, we showed that the expression level of LRIG1 was significantly negatively correlated with BCL-2 and MnSOD expression in glioma. Our research demonstrated that overexpression of LRIG1 can enhance the chemosensitivity. BCL-2 and MnSOD were inhibited in LRIG1 overexpressing cells. On the other hand, when BCL-2 and MnSOD were knocked down, the chemosensitivity of U251 cells decreased, and the effect of LRIG1 in regulating chemosensitivity was compromised. For the first time, our results showed that LRIG1 can enhance chemosensitivity in glioblastoma by inhibition of BCL-2 and MnSOD.

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