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作 者:隋文君[1] 李红智[1] 郑易[1] 谢丽微[2] 林鹏[1]
机构地区:[1]温州医学院生命科学学院,浙江温州325035 [2]温州医学院第二附属医院病理科,浙江温州325035
出 处:《温州医学院学报》2008年第3期200-202,共3页Journal of Wenzhou Medical College
基 金:浙江省教育厅科研基金资助项目(20020469);温州市科技局科研基金资助项目(S2002A122)
摘 要:目的:研究Herceptin下调乳腺癌细胞HER2表达对PI3K/Akt通路相关蛋白表达的影响,探讨该通路在Herceptin抗肿瘤效应中的作用。方法:Herceptin处理HER2过表达的乳腺癌细胞株SKBR-3,免疫细胞化学检测HER2、p21Cip1和p27Kip1的表达,Westernblot检测p-Akt和Bad的表达。结果:Herceptin处理组细胞HER2阳性表达率(37.4%)显著低于对照组(78.3%)(P<0.01)。Herceptin处理组与对照组比较,p-Akt蛋白含量降低53.5%(P<0.01),Bad蛋白含量升高0.83倍(P<0.01)。Herceptin处理组细胞p21Cip1和p27Kip1阳性表达率(分别为67%和56.1%)显著高于对照组(分别为19%和21.4%)(P<0.01)。结论:Herceptin下调HER2表达后,通过下调p-Akt表达而上调其下游Bad、p21Cip1和p27Kip1的表达,从而抑制肿瘤细胞增殖,促进肿瘤细胞凋亡。Objective: To evaluate the influence of downregulated HER2 expression by Herceptin of breast cancer cells on the related protein expression via PI3K/Akt pathway, and to investigate the action of this pathway in the anti-tumor effect of Herceptin. Methods: The HER2 overexpressed breast cancer cell line SKBR-3 was treated with Herceptin, the expressions of HER2, p21^Cipl and p27^Kipl were detected by immunocytochemistry, and the expressions of p-Akt and Bad were detected by Western blot. Results: The rate of HER2 positive cells of Herceptin treated group(37.4%) compared to the untreated group(78.3%) decreased significantly (P〈0.01). Compared to the untreated group, the amount of p-kt protein of Herceptin treated group decreased significantly to 53.5% (P〈0.01), the amount of Bad protein of Herceptin treated group increased significantly by 0.83 fold(P〈0.01). The rates of p21^Cipl and p27^Kipl positive cells of Herceptin treated group (67% and 56.1% respectively) compared to the untreated group (19% and 21.4% respectively) increased significantly (P〈0.01). Conclusion: Herceptin can downregulate HER2 expression, to downregulate p-Akt expression and then to upregulate the expression of its downstream protein Bad, p21^Cipl and p27^Kipl, thus to inhibit the proliferation and promote the apoptosis of tumor cells.
关 键 词:HERCEPTIN HER2 P13K/AKT通路 乳腺癌
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