COMPLEX EFFECT OF LOW-INTENSITY LASER RADIATION AND POTASSIUM CHANNEL PEPTIDE INHIBITOR ON MELANOMA CELL SURVIVAL

E. Pogodina, E. Rastorgueva, E. Yurova, E. Beloborodov, D. Sugak, Y. Saenko
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Abstract

Melanoma is characterized by an aggressive development and a large number of metastases during diagnostics. Photodynamic therapy (PDT) is used to treat this type of cancer. However, the accumulation of photosensitizers is observed not only in malignant tumors, but also in high metabolic rate organs. Shortcomings of melanoma therapy can be eliminated using the complex effect of laser radiation and local administration of inhibitors of cellular processes. The goal. To study the complex effect of low-intensity laser radiation and potassium channel peptide inhibitor on melanoma cell survival. Materials and Methods. A875 melanoma cells were exposed to Kappa-theraphotoxin-Gr1b toxin and laser irradiation. The authors examined the level of apoptosis and necrosis in cells using fluorescence microscopy techniques. The xCELLigence system was used to assess the cytotoxic response of A875 melanoma cells. Results. The maximum number of apoptotic and necrotic cells was observed in the group of patients with A875 tumor cells exposed to a combination of Kappa-TRTX-Gr1b toxin and laser radiation (wavelength=1265 nm). This is due to the inhibition of potassium channels of intracellular cell membranes by Kappa-TRTX-Gr1b peptide, which are associated with the apoptosis. Conclusion. Selective potassium channel inhibition under pathological processes can be regarded as a significant supplement to the superficial malignant neoplasm complex therapy. The combination of toxin and irradiation will make it possible to potentiate their action and avoid the main PDT disadvantages. This approach unites the benefits of the local administration and precise exposure on the malignant tumor.
低强度激光照射与钾通道肽抑制剂对黑色素瘤细胞存活的复杂影响
黑色素瘤的特点是在诊断过程中具有侵袭性发展和大量转移。光动力疗法(PDT)用于治疗这种类型的癌症。然而,光敏剂的积累不仅存在于恶性肿瘤中,也存在于高代谢率器官中。黑色素瘤治疗的缺点可以通过激光辐射的复杂效应和局部施用细胞过程抑制剂来消除。我们的目标。目的:研究低强度激光照射联合钾通道肽抑制剂对黑色素瘤细胞存活的复合影响。材料与方法。将A875黑色素瘤细胞暴露于Kappa-theraphotoxin-Gr1b毒素和激光照射下。作者利用荧光显微镜技术检测了细胞凋亡和坏死的水平。xCELLigence系统用于评估A875黑色素瘤细胞的细胞毒性反应。结果。Kappa-TRTX-Gr1b毒素联合激光照射(波长为1265 nm)的A875肿瘤细胞组凋亡和坏死细胞数量最多。这是由于Kappa-TRTX-Gr1b肽抑制了胞内细胞膜的钾通道,而钾通道与细胞凋亡有关。结论。病理过程中选择性抑制钾通道可作为浅表恶性肿瘤复合治疗的重要补充。毒素和辐照的结合将有可能增强其作用并避免PDT的主要缺点。这种方法结合了当地管理的好处和对恶性肿瘤的精确暴露。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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