医学分子生物学杂志 ›› 2022, Vol. 19 ›› Issue (4): 295-299.doi: 10.3870/j.issn.1672-8009.2022.04.005

• 论著 • 上一篇    下一篇

异氟醚对膀胱癌 5637 细胞恶性生物学行为及化疗敏感性的影响

  

  1. 秦皇岛市第一医院麻醉科 河北省秦皇岛市, 066099
  • 出版日期:2022-07-31 发布日期:2022-08-15

Effect of Isoflurane on Malignant Phenotype and Chemotherapeutic Sensitivity of Bladder Cancer Cell Line 5637

  1. Department of Anesthesiology, Qinhuangdao First Hospital, Qinhuangdao, Hebei, 066099, China
  • Online:2022-07-31 Published:2022-08-15

摘要: 目的 探究异氟醚对膀胱癌 5637 细胞恶性生物学行为及化疗敏感性的影响。 方法 单独或联合 给予异氟醚及顺铂处理膀胱癌 5637 细胞, 将细胞随机分为 4 组: 对照组、 异氟醚组、 顺铂组和异氟醚 + 顺 铂联合处理组。 BrdU 染色检测 BrdU 阳性细胞数; 流式细胞仪检测细胞凋亡率和细胞周期分布; Transwell 检测侵袭细胞数; 划痕愈合实验检测划痕愈合率; Western 印迹检测 Ki67、 PCNA、 Bax、 Bcl-2、 cleaved caspase-3 和 caspase-3 蛋白表达; 结果 与顺铂组相比较, 异氟醚 + 顺铂联合处理组 BrdU 阳性细胞数和 Ki67、 PCNA 蛋白表达降低, G0 / G1期比率和 S 期细胞数降低, G2 / M 期比率升高, 细胞凋亡率和 Bax / Bcl-2、 cleaved caspase-3 / caspase-3 比值升高, 侵袭细胞数、 划痕愈合率降低, 均有显著性差异 (P< 0. 05)。 结论 异氟醚可通过抑制细胞增殖、 侵袭、 迁移, 诱导细胞凋亡, 提高 5637 细胞对顺铂的敏感性。

关键词: 膀胱癌, 异氟醚, 顺铂, 化疗敏感性 

Abstract: Objective To investigate the effect of isoflurane on malignant phenotype and chemotherapy sensitivity of bladder cancer cell line 5637. Methods The 5637 bladder cancer cells were divided into groups as follows: control group, isoflurane group, cisplatin group and isoflurane + cisplatin group. The number of BrdU positive cells was determined by BrdU staining. The cell apoptosis and cell cycle were measured by flow cytometry. The number of invasive cells were measured by transwell assay. The scratch healing rate was measured by wound healing experiment. The expression levels of Ki67, PCNA, Bax, Bcl-2, cleaved caspase-3 and caspase-3 proteins were detected by Western blotting. Results The number of BrdU positive cells, the expression levels of Ki67 and PCNA proteins, the G0 / G1 phase ratio, the number of S phase cells were decreased significantly in the isoflurane + cisplatin group compared to the cisplatin group, while the G2 / M phase ratio was increased significantly (P< 0. 05). The number of invasive cells and the scratch healing rate were decreased significantly in the isoflurane + cisplatin group when compared to the cisplatin group (P < 0. 05). The apoptosis rate, the Bax / Bcl-2 ratio, and the cleaved caspase-3 / caspase-3 ratio were increased significantly in the isoflurane + cisplatin group compared to the cisplatin group (P< 0. 05). Conclusion Isoflurane can induce apoptosis by inhibiting cell proliferation, invasion and migration, and enhance the sensitivity of 5637 cells to cisplatin. 

Key words: bladder cancer, isoflurane, cisplatin, chemotherapeutic sensitivity

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