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GSK-3β及β-catenin的表达定位与肺腺癌顺铂耐药作用机制研究[J]. 肿瘤防治研究, 2015, 42(10): 960-964. DOI: 10.3971/j.issn.1000-8578.2015.10.002
引用本文: GSK-3β及β-catenin的表达定位与肺腺癌顺铂耐药作用机制研究[J]. 肿瘤防治研究, 2015, 42(10): 960-964. DOI: 10.3971/j.issn.1000-8578.2015.10.002
Mechanism of GSK-3β and β-catenin Expression Localization Mediating Cisplatinresistance of Lung Adenocarcinoma[J]. Cancer Research on Prevention and Treatment, 2015, 42(10): 960-964. DOI: 10.3971/j.issn.1000-8578.2015.10.002
Citation: Mechanism of GSK-3β and β-catenin Expression Localization Mediating Cisplatinresistance of Lung Adenocarcinoma[J]. Cancer Research on Prevention and Treatment, 2015, 42(10): 960-964. DOI: 10.3971/j.issn.1000-8578.2015.10.002

GSK-3β及β-catenin的表达定位与肺腺癌顺铂耐药作用机制研究

Mechanism of GSK-3β and β-catenin Expression Localization Mediating Cisplatinresistance of Lung Adenocarcinoma

  • 摘要: 目的 研究人肺腺癌细胞系A549和其顺铂耐药细胞系A549/DDP中GSK-3β及β-catenin的表达定位差异,以探讨其与肺腺癌顺铂耐药的作用机制。方法 MTT法检测A549和A549/DDP细胞对顺铂的IC50 ;免疫细胞荧光法检测顺铂处理前后两种细胞GSK-3β及β-catenin的定位表达。结果 顺铂对A549/DDP细胞的IC50值为(28.984±1.404)μmol/L高于A549细胞的(5.888±0.338)μmol/L(t=27.696,P<0.001);A549/DDP细胞中的GSK-3β表达主要在胞质,顺铂处理后GSK-3β定位在胞质和胞核;β-catenin表达主要在胞膜、胞质,顺铂处理后定位转移至胞核。而A549细胞中GSK-3β及β-catenin表达定位无变化。结论 肺腺癌顺铂耐药的机制可能与GSK-3β胞质和胞核共同定位、β-catenin核转移定位相关。

     

    Abstract: Objective To explore the mechanism of cisplatin-resistance of lung adenocarcinoma by evaluating the differences of GSK-3β and β-catenin expression localization in lung adenocarcinoma cell line A549 and its cisplatin resistance cell line A549/DDP. Methods MTT assay was used to determine IC50 values of cisplatin in A549 and A549/DDP cells. Immunofluorescence method was used to detect GSK-3β and β-catenin expression localization. Results IC50 value of cisplatin in A549/DDP cells was (28.984±1.404) μmol/L, higher than (5.888±0.338)μmol/L in A549 cells(t=27.696, P<0.001). GSK-3β expression localization in A549/DDP cell was mainly in the cytoplasm, while cisplatin changed its location to cytoplasm and nucleus. β-Catenin expression localization in A549/DDP cell was mainly in the membrance and cytoplasm, while cisplatin changed its location from cytoplasm to nuclear. However, GSK-3β and β-catenin expression localization in A549 cells had no change. Conclusion The mechanism of cisplatin-resistance of lung adenocarcinoma may be related to co-location of GSK-3β in cytoplasm and nucleus, and β-catenin location from cytoplasm to nuclear.

     

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