Study of the Radiosensitizing Action of Lithium Ascorbate Under Neutron and Photon Irradiation of Tumor Cells

Q3 Pharmacology, Toxicology and Pharmaceutics
M. S. Tretyakova, A. G. Drozd, M. V. Belousov, K. S. Brazovskiy, M. S. Larkina, S. V. Krivoshchekov, A. A. Artamonov, I. A. Miloichikova, A. V. Bezmaga, A. M. Bolshakov, E. S. Sukhikh, E. V. Plotnikov
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引用次数: 1

Abstract

Introduction. Radioresistance of cancer cells is a serious problem in radiation therapy of tumor diseases. Radiosensitizers make malignant cells more sensitive to radiation and increase the effectiveness of radiation therapy; however, their widespread clinical use is limited by significant side effects. The development and study of new radiosensitizers seems to be an urgent task of modern pharmacology. Aim. The purpose of this work was to study the effectiveness of lithium ascorbate as a radiosensitizer under the influence of photon and neutron radiation in wide dose range. Materials and methods. Evaluation of the biological effect was carried out using the tumor line of prostate cancer PC-3. We used a cyclotron to produce neutron radiation and a Cobalt-60 source to produce gamma radiation. Results and discussion. We have proved an increase in the cytotoxic effect with the combined use of different types of ionizing radiation and lithium ascorbate. The resistance of the prostate cancer line to gamma radiation at an absorbed dose of 0.5–3.0 Gy was revealed. It was shown that tumor cells of prostate cancer are more sensitive to the effects of the study drug in minimal concentrations in combination with neutron irradiation compared to gamma radiation in the same absorbed dose. The main mechanism of the radiosensitizing action of lithium ascorbate is the local induction of oxidative stress, which synergistically enhances the action of ionizing radiation. Conclusion. The combination of lithium ascorbate with neutron radiation leads to a more pronounced resulting cytotoxic effect. An increase in the concentration of lithium ascorbate led to the pro-oxidative action with an increase in the damaging effect on cells.
抗坏血酸锂在肿瘤细胞中子和光子照射下的放射增敏作用研究
介绍。肿瘤细胞的放射耐药是肿瘤疾病放射治疗中的一个严重问题。放射增敏剂使恶性细胞对放射更敏感,提高放射治疗的有效性;然而,它们的广泛临床应用受到严重副作用的限制。开发和研究新的放射增敏剂似乎是现代药理学的一项紧迫任务。的目标。研究了抗坏血酸锂在大剂量范围光子和中子辐射作用下作为辐射增敏剂的有效性。材料和方法。采用前列腺癌PC-3细胞系进行生物学效应评价。我们用回旋加速器产生中子辐射,用钴-60源产生伽马辐射。结果和讨论。我们已经证明,结合使用不同类型的电离辐射和抗坏血酸锂会增加细胞毒性作用。结果显示前列腺癌细胞系对吸收剂量0.5 ~ 3.0 Gy的γ射线具有抵抗性。研究表明,与相同吸收剂量的伽马辐射相比,最低浓度的研究药物联合中子照射对前列腺癌肿瘤细胞的影响更为敏感。抗坏血酸锂辐射增敏作用的主要机制是局部诱导氧化应激,协同增强电离辐射的作用。结论。抗坏血酸锂与中子辐射的结合导致更明显的细胞毒性作用。抗坏血酸锂浓度的增加导致促氧化作用,对细胞的破坏作用增加。
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来源期刊
Drug Development and Registration
Drug Development and Registration Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
1.20
自引率
0.00%
发文量
61
审稿时长
8 weeks
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