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Study of the cytotoxic/toxic potential of the novel anticancer selenodiazoloquinolone on fibroblast cells and 3D skin model

机译:新型抗癌硒二唑并喹诺酮对成纤维细胞和3D皮肤模型的细胞毒性/毒性潜能研究

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摘要

The new synthetically prepared quinolone derivative 7-ethyl 9-ethyl-6-oxo-6,9-dihydro[1,2,5]selenadiazolo [3,4-h]quinoline-7-carboxylate (E2h) showed in our previous study cytotoxic effects towards tumor cells and immunomodulatory activities on RAW 264.7 cell line murine macrophages. E2h may have a potential use as a novel chemotherapeutic agent with immunomodulatory properties and the ability to induce apoptotic death of cancer cells. The aim of the present study was to examine the antiproliferative/cytotoxic activities of E2h on human non-cancer fibroblast BHNF-1 cells and reconstructed human epidermis EpiDerm™. Further the effects of E2h on tissue structure and morphology were examined. Cytotoxic/toxic studies showed that selenadiazoloquinolone is not toxic on normal human fibroblast cells BHNF-1 and dimensional skin constructs EpiDerm™. Evaluation of morphological changes in EpiDerm™ showed no change in the construction and morphology of skin tissue treated by E2h compared to control.
机译:在我们先前的研究中显示了新的合成制备的喹诺酮衍生物7-乙基9-乙基-6-氧代-6,9-二氢[1,2,5]硒二氮杂[3,4-h]喹啉-7-羧酸酯(E2h) RAW 264.7细胞系鼠巨噬细胞对肿瘤细胞的细胞毒性作用和免疫调节活性。 E2h作为具有免疫调节特性和诱导癌细胞凋亡死亡能力的新型化学治疗剂可能具有潜在用途。本研究的目的是检查E2h对人非癌性成纤维细胞BHNF-1细胞和重建的人表皮EpiDerm™的抗增殖/细胞毒性活性。进一步检查了E2h对组织结构和形态的影响。细胞毒性/毒性研究表明,硒二氮杂喹诺酮对正常人成纤维细胞BHNF-1和立体皮肤构建体EpiDerm™无毒性。与对照相比,EpiDerm™中形态变化的评估显示,用E2h处理的皮肤组织的结构和形态没有变化。

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