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Mechanisms of Cytotoxicity of Chemical Agents to Giant Cell Tumors: An In Vitro Study.
Stem Cells International ( IF 4.3 ) Pub Date : 2020-09-01 , DOI: 10.1155/2020/8827192
Achmad Fauzi Kamal 1, 2 , Akbar Rizki Beni Asdi 1 , Ahmad Jabir Rahyussalim 1, 3 , Rio Wikanjaya 1 , Resda Akhra Syahrani 3 , Tri Kurniawati 2, 3 , Septelia Inawati Wanandi 3, 4
Affiliation  

Background. Various chemical agents have been used as an adjuvant treatment for giant cell tumor (GCT). However, the comparative effect of these chemicals remains unclear. Methods. Multinucleated and spindle cells from cultured GCT patients, characterized by Nanog and Oct4 expression with RT-PCR, were directly administered, in vitro, with concentrations of 1%, 3%, and 5% of H2O2 and 75%, 85%, and 95% of ethanol for 10 minutes and concentrations of 0.003%, 0.005%, 0.01%, 0.03%, 0.1%, and 0.3% of H2O2 for 5 minutes and were incubated for 24 hours. Cell morphology, cell viability, and flow cytometry after various concentrations of H2O2 and ethanol exposure were assessed. Results. H2O2 in all concentrations caused loss of cell viability. The number of viable cells after H2O2 exposure was related to the concentration-dependent effect. The initial viable spindle-shaped cell, multinucleated giant cell, and round-epithelioid cell had morphological changes into fragmented nonviable cells after exposure to H2O2. Flow cytometry using Annexin V showed cell death due to necrosis, with the highest concentration amounting to 0.3%. Conclusion. Administering local chemical adjuvants of H2O2 in vitro caused loss of viable GCT cells. The number of viable cells after H2O2 exposure was related to the concentration-dependent effect, whereas reducing concentration of H2O2 may cause loss of viability and morphology of cultured GCT cells with the apoptotic mechanism.

中文翻译:

化学试剂对巨细胞肿瘤的细胞毒性机制:一项体外研究。

背景。各种化学试剂已被用作巨细胞瘤 (GCT) 的辅助治疗。然而,这些化学物质的比较效果仍不清楚。方法。来自培养的 GCT 患者的多核细胞和梭形细胞,其特征是通过 RT-PCR 表达 Nanog 和 Oct4,在体外直接施用浓度为 1%、3% 和 5% 的 H 2 O 2和 75%、85% , 和 95% 的乙醇 10 分钟和 0.003%、0.005%、0.01%、0.03%、0.1% 和 0.3% 的 H 2 O 2浓度5 分钟并孵育 24 小时。不同浓度 H 2 O 2后的细胞形态、细胞活力和流式细胞术和乙醇暴露进行了评估。结果。所有浓度的H 2 O 2都会导致细胞活力丧失。H 2 O 2暴露后的活细胞数量与浓度依赖性效应有关。最初的有活力的梭形细胞、多核巨细胞和圆形上皮样细胞在暴露于H 2 O 2后形态发生变化,变成破碎的无活力细胞。使用 Annexin V 的流式细胞术显示细胞因坏死而死亡,最高浓度为 0.3%。结论施用 H 2 O 2的局部化学助剂在体外导致活的 GCT 细胞丢失。H 2 O 2暴露后的活细胞数量与浓度依赖性效应有关,而降低H 2 O 2浓度可能导致具有凋亡机制的培养的GCT细胞的活力和形态丧失。
更新日期:2020-09-01
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