Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 2688-2692 |
| Number of pages | 5 |
| Journal | Bioorganic and Medicinal Chemistry Letters |
| Volume | 28 |
| Issue number | 16 |
| DOIs | |
| State | Published - Sep 1 2018 |
ASJC Scopus Subject Areas
- Biochemistry
- Molecular Medicine
- Molecular Biology
- Pharmaceutical Science
- Drug Discovery
- Clinical Biochemistry
- Organic Chemistry
Keywords
- Protons
- Necrosis/chemically induced
- Pyrroles/pharmacology
- Antibiotics, Antineoplastic/pharmacology
- Humans
- Apoptosis/drug effects
- Glioblastoma
- Cell Survival/drug effects
- Indoles/pharmacology
- Cell Line, Tumor
- Radiation-Sensitizing Agents/pharmacology
- Duocarmycins
- Cell Proliferation/drug effects
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