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  • The Effect of Chemoradiotherapy with SRC Tyrosine Kinase Inhibitor, PP2 and Temozolomide on Malignant Glioma Cells in vitro and in vivo.

    The Effect of Chemoradiotherapy with SRC Tyrosine Kinase Inhibitor, PP2 and Temozolomide on Malignant Glioma Cells in vitro and in vivo.

    (서울대: 엄근영, 조봉준, 최은정 ,김인아*)

  • 출처
    Cancer Res Treat
  • 등재일
    2015 Jun 4
  • 저널이슈번호
    [Epub ahead of print]
  • 내용

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    [Abstract]


    Purpose: We investigated the effect of chemoradiotherapy with PP2 and temozolomide (TMZ) on malignant glioma cells using clonogenic assays and in vivo brain tumor model.


    Materials and Methods: The effect of PP2 on radiosensitivity of U251 and T98G cells was investigated using clonogenic assays. The expression of E-cadherin, MMP2, EphA2, and VEGF was measured by Western blotting and an accumulation of γH2AX foci 6 h after radiotherapy was measured after PP2 treatment. The effect of PP2 on migration, invasion, and vasculogenic mimicry formation (VMF) of U251 cells was evaluated. In an orthotopical brain tumor model with U251 cells, PP2 was injected intraperitoneally with or without oral TMZ before, during and after whole brain radiotherapy. Bioluminescence images were taken to visualize in vivo tumors and immunohistochemical staining of VEGF, CD31, EphA2, and HIF1a was performed.

     

    Results: PP2 increased radiosensitivity of U251 and T98G cells without decreasing survival of normal human astrocytes. Chemoradiotherapy with PP2 and TMZ resulted in increased accumulation of γH2AX foci. PP2 induced overexpression of E-cadherin and suppression of MMP2, VEGF, and EphA2. PP2 also compromised invasion, migration, and VMF of U251 cells. In brain tumors, chemoradiotherapy with PP2 and TMZ decreased tumor volume best, but not statistically significantly compared with chemoradiotherapy with TMZ. The expression of VEGF and CD31 was suppressed in PP2-treated tumors.

     

    Conclusion: s PP2 enhances radiosensitivity of malignant glioma cells and suppresses invasion and migration of U251 cells. Chemoradiotherapy with PP2 and TMZ resulted in non-significant tumor volume decrease.

     

    [Author information]

    Eom KY1, Cho BJ1, Choi EJ1, Kim JH2, Chie EK2, Wu HG2, Kim IH2, Paek SH3, Kim JS1, Kim IA1.

    1Department of Radiation Oncology, Seoul National University, Graduate School of Medicine, Seoul, Korea.

    2Department of Radiation Oncology, Seoul National University College of Medicine, Seoul, Korea.

    3Department of Neurosurgery, Seoul National University College of Medicine, Seoul, Korea. 

  • 키워드
    Glioblastoma; PP2; Radiotherapy; Temozolomide; SRC tyrosine kinase inhibitor
  • 연구소개
    악성뇌교종은 최근 Stupp regimen의 도입으로 치료효과가 어느 정도 향상되었지만 여전히 예후가 매우 불량하여 치료효과를 향상시키기 위한 많은 연구들이 진행되고 있습니다. SRC는 악성뇌교종의 invasion & migration에 관여하며 glioblastoma에서 과발현되어 있는 것으로 알려져 있습니다. 이에 방사선치료의 효과를 높이기 위해 현재 표준치료법인 temozolomide 항암-방사선치료에 SRC tyrosine kinase inhibitor를 병합함으로서 세포주 및 동물에서의 치료효과를 더욱 향상시킬 수 있을 것이라는 연구결과를 발표하였습니다.
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