Development of LC-MS method for analysis of paclitaxel-inhibited growth and enhanced therapeutic response in human glioblastoma cells

Cai-Hou Lin Xue-Xia Lin Ling Lin Jun-Ming Wang Zhi-Xiong Lin Jin-Ming Lin

Citation:  Cai-Hou Lin, Xue-Xia Lin, Ling Lin, Jun-Ming Wang, Zhi-Xiong Lin, Jin-Ming Lin. Development of LC-MS method for analysis of paclitaxel-inhibited growth and enhanced therapeutic response in human glioblastoma cells[J]. Chinese Chemical Letters, 2015, 26(10): 1225-1230. doi: 10.1016/j.cclet.2015.03.007 shu

Development of LC-MS method for analysis of paclitaxel-inhibited growth and enhanced therapeutic response in human glioblastoma cells

    通讯作者: Zhi-Xiong Lin,
    Jin-Ming Lin,
  • 基金项目:

    We thank Dr. Yan-Li Guo, Qian Yang (The Frontier Science Department of Shiseido China Co., Ltd.) (The Frontier Science Department of Shiseido China Co., Ltd.)

    Qiushui Chen (Department of Chemistry, Tsinghua University) for assistance with MS analysis. We also thank Jun Dong, Xinliang DAI of the neurosurgery department of The Second Affiliated Hospital of Soochow University for assistance with cell culture. The work was supported by National Nature Science Foundation of China (Nos. 214350002, 81373373)  (Department of Chemistry, Tsinghua University)

    Education Resources System (No. CERS-1-75). (No. CERS-1-75)

摘要: Glioma stem cells are considered responsible for drug resistance and glioma relapse resulting in poor prognosis in glioblastomamultiforme. SU3 glioma cell is a highly invasive glioma stemcell line from the patients with glioblastoma multifrome. It is of great significance to study the efficacy and molecular mechanism for anticancer drug effects on SU3 glioma cells. In this work, we develop a liquid chromatography-mass spectrometry (LC-MS) method for direct analysis of the role of drugs (paclitaxel) on SU3 glioma cells at themolecular level. Weuse the specific fluorescence dyes to evaluate cell viability, the levels of ROS and GSH when the cells were treated with drugs. In addition, the LC-MS platform was successfully employed to detect the amount of 6-O-methylguanine, demonstrating that it is effective to induce cell apoptosis and enhance the cytotoxic response of SU3 glioma cells. The analytical linear equals are Y=9.49×105X+2.42×104 for 6-O-methylguanine (R2=0.9998) and Y=4.72×104X+2.21×103(R2=0.9996) for 7-methylguanine. Thus, the combination of cell-specific fluorescence dyes and LC-MS method enables us to reveal the molecular mechanism of paclitaxel-inhibited growth and enhanced therapeutic response in the chemotherapy for glioma multiforme.

English

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  • 发布日期:  2015-03-10
  • 收稿日期:  2015-02-07
  • 网络出版日期:  2015-03-03
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