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巨噬细胞增强宫颈癌细胞对SN-38的抗性
引用本文:赖丽梨,靳焕,段华英,邹争志.巨噬细胞增强宫颈癌细胞对SN-38的抗性[J].华南师范大学学报(自然科学版),2021,53(1):63-69.
作者姓名:赖丽梨  靳焕  段华英  邹争志
作者单位:广州市增城区人民医院妇产科,广州511300;华南师范大学生物光子学研究院激光生命科学研究所暨激光生命科学教育部重点实验室,广州510631;广州医科大学附属第二医院妇产科,广州510260
基金项目:国家自然科学基金项目81772803国家自然科学基金项目81972479广东省自然科学基金项目2019A1515011100广州市科技计划项目201904010038
摘    要:通过GDSC在线软件,分析了SN-38在数据库中8种宫颈癌细胞系对310多种化疗药的半抑制质量浓度(IC50)Z分数值,并选取HPV-18阳性HeLa细胞、HPV-16阳性SiHa和CaSki细胞以及HPV阴性C-33A细胞,经过SN-38处理24、48 h,通过CCK8试验检测了细胞活力来探究巨噬细胞是否介导宫颈癌细胞对SN-38抵抗. THP1被HeLa和SiHa细胞诱导成肿瘤相关巨噬细胞,通过CCK8试验探讨巨噬细胞在宫颈癌细胞对SN-38敏感性中的作用. 结果显示:CaSki、ME-180、HT-3、C-33A对SN-38极敏感,HeLa和SiHa对SN-38敏感,而CAL-39对SN-38不敏感;CaSki和C-33A的IC50值相对于HeLa和SiHa更低,表明CaSki和C-33A对SN-38更敏感;巨噬细胞显著抑制SN-38对HeLa和SiHa细胞的杀伤. 这些结果表明了肿瘤相关巨噬细胞促进宫颈癌细胞对SN-38抵抗.

关 键 词:巨噬细胞  宫颈癌  SN-38
收稿时间:2020-04-07

Macrophage's Promotion of Cervical Cancer Cell Resistance to SN-38
Institution:1.Department of Obstetrics and Gynecology, Zengcheng District People's Hospital, Guangzhou 511300, China2.MOE Key Laboratory of Laser Life Science and Institute of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, China3.Department of Obstetrics and Gynecology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou 510260, China
Abstract:GDSC (Genomics of Drug Sensitivity in Cancer) online database was analyzed and the IC50 Z Score values of 8 cervical cancer cell lines under more than 310 chemotherapy drugs were obtained. Then HPV-18 positive HeLa cells, HPV-16 positive SiHa and CaSki cells and HPV negative C-33A cells were treated with SN-38 for 24 and 48 hours and the cell viability was detected with CCK8 experiment. Finally, THP1 cells were induced into tumor-associated macrophages (TAM) to explore the role of TAM in the sensitivity of cervical cancer cells to SN-38. The results showed that CaSki, ME-180, HT-3 and C-33A were very sensitive to SN-38, HeLa and SiHa were relatively sensitive to SN-38, and CAL-39 was not sensitive to SN-38. In addition, IC50 values of CaSki and C-33A were lower than those of HeLa and SiHa, indicating that CaSki and C-33A were more sensitive to SN-38. TAM promoted HeLa and SiHa cell resistance to SN-38. In conclusion, the results suggested that TAM promoted the resistance of cervical cancer cells to SN-38.
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