AggreWellTM800板培养乳腺癌肿瘤球模型及其用于盐酸青藤碱药敏实验
Breast Cancer Tumor Spheroid Model Established Using the AggreWellTM800 Plate and Its Application in Drug Sensitivity Test of Sinomenine Hydrochloride
DOI: 10.12677/wjcr.2026.162007, PDF,    科研立项经费支持
作者: 王 晗*:杭州医学院公共卫生学院,浙江 杭州;张文元:杭州医学院检验医学院、生物工程学院,浙江 杭州;朱 莲#:杭州医学院基础医学与法医学院,浙江 杭州
关键词: AggreWellTM800板乳腺癌肿瘤球模型盐酸青藤碱药敏试验AggreWellTM800 Plate Breast Cancer Tumor Spheroid Model Sinomenine Hydrochloride Drug Sensitivity Test
摘要: 目的:通过AggreWell板构建乳腺癌肿瘤球模型,并用于盐酸青藤碱对乳腺癌MDA-MB-231细胞的药敏试验。方法:AggreWellTM800板接种MDA-MB-231细胞,构建乳腺癌3D肿瘤球。采用盐酸青藤碱进行药敏试验,CCK-8试剂盒检测。并与2D培养比较。结果:随着加入盐酸青藤碱浓度的升高,MDA-MB-231细胞抑制率逐渐上升,呈剂量依赖性。AggreWell板培养的乳腺癌3D肿瘤球对盐酸青藤碱的药物敏感性显著低于传统2D培养。结论:本实验研究表明,相比于传统2D培养,使用AggreWell板培养的乳腺癌3D肿瘤球对盐酸青藤碱的药敏性显著更低,可能更能反映体内肿瘤的真实情况,在评估抗癌药物方面可能更具优势。
Abstract: Objective: To construct a breast cancer tumor spheroid model using the AggreWell plate and apply it to the drug sensitivity test of sinomenine hydrochloride on breast cancer MDA-MB-231 cells. Methods: MDA-MB-231 cells were seeded in the AggreWellTM800 plate to form 3D breast cancer tumor spheroid. The sinomenine hydrochloride was used for the drug sensitivity test, and the CCK-8 kit was employed for detection. A comparison was made with 2D culture. Results: As the concentration of sinomenine hydrochloride added increased, the inhibition rate of MDA-MB-231 cells gradually rose, showing a dose-dependent manner. The drug sensitivity of the 3D breast cancer tumor spheroid cultured in the AggreWell plate to sinomenine hydrochloride was significantly lower than that of traditional 2D culture. Conclusion: This experimental study indicates that compared with traditional 2D culture, the 3D breast cancer tumor spheroid cultured in the AggreWell plate has significantly lower drug sensitivity to sinomenine hydrochloride, which may better reflect the real situation of the tumor in the body and may have more advantages in evaluating anti-cancer drugs.
文章引用:王晗, 张文元, 朱莲. AggreWellTM800板培养乳腺癌肿瘤球模型及其用于盐酸青藤碱药敏实验[J]. 世界肿瘤研究, 2026, 16(2): 49-55. https://doi.org/10.12677/wjcr.2026.162007

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