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Duocarmycin SA a potent antitumor antibiotic sensitizes glioblastoma cells to proton radiation

机译:一种有效的抗肿瘤抗生素Duocarmycin SA使胶质母细胞瘤细胞对质子辐射敏感

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摘要

New treatment modalities for glioblastoma multiforme (GBM) are urgently needed. Proton therapy is considered one of the most effective forms of radiation therapy for GBM. DNA alkylating agents such as temozolomide (TMZ) are known to increase the radiosensitivity of GBM to photon radiation. TMZ is a fairly impotent agent, while duocarmycin SA (DSA) is an extremely potent cytotoxic agent capable of inducing a sequence-selective alkylation of duplex DNA. Here, the effects of sub-nM concentrations of DSA on the radiosensitivity of a human GBM cell line (U-138) to proton irradiation were examined. Radiation sensitivity was determined by viability, apoptosis, necrosis and clonogenic assays. DSA concentrations as low as 0.001 nM significantly sensitized U-138 cells to proton irradiation. DSA demonstrates synergistic cytotoxicity against GBM cells treated with proton radiation in vitro, which may represent a novel therapeutic alternative for the treatment of GBM.
机译:迫切需要新的胶质母细胞瘤(GBM)治疗方法。质子治疗被认为是GBM放射治疗最有效的形式之一。已知DNA烷基化剂(例如替莫唑胺(TMZ))可提高GBM对光子辐射的放射敏感性。 TMZ是一种相当无力的药物,而杜卡霉素SA(DSA)是一种极强的细胞毒性剂,能够诱导双链DNA的序列选择性烷基化。在此,研究了nMA浓度以下的DSA对人GBM细胞系(U-138)对质子辐射的放射敏感性的影响。放射敏感性通过生存力,凋亡,坏死和克隆形成测定来确定。低至0.001 nM的DSA浓度可使U-138细胞对质子辐射敏感。 DSA证明了体外对质子辐射治疗的GBM细胞具有协同细胞毒性,这可能是治疗GBM的一种新的治疗选择。

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