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[漆树酸(一种热休克蛋白90抑制剂)对乳腺癌MDA-MB-231细胞增殖、侵袭和迁移的影响]

[Effect of anacardic acid, a Hsp90 inhibitor, on proliferation, invasion and migration of breast cancer MDA-MB-231 cells].

作者信息

Li Hongmei, Nie Lijuan, Huo Qiang, Zhao Surong, Ma Tao, Wu Chengzhu, Liu Hao

机构信息

Faculty of Pharmacy, Bengbu Medical College, Bengbu 233030, China.E-mail: athongmei@ foxmail.com.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2015 Mar;35(3):355-9.

Abstract

OBJECTIVE

To explore the effect of the Hsp90 inhibitor anacardic acid on cell proliferation, invasion and migration of breast cancer MDA-MB-231 cells.

METHODS

The inhibitory effect of anacardic acid on Hsp90 was assessed with in vitro ATPase inhibition assay and ATP-sepharose binding assay. MTT assay was used to detect the growth inhibition induced by anacardic acid in MDA-MB-231 cells. Transwell assays were used to evaluate MDA-MB-231 cell invasion and migration. Western blotting was performed to assess the effect of anacardic acid in triggering the degradation of MMP-9, TIMP-1, Hsp90, and Hsp70.

RESULTS

Anacardic acid exhibited a modest activity of ATPase inhibition with an IC50 value of 82.5 µmol/L. Anacardic acid significantly suppressed the proliferation of MDA-MB-231 cells in a dose-dependent manner (IC50 value of 29.3 µmol/L). Treatment with 12.5, 25, and 50 µmol/L anacardic acid for 36 h caused inhibition of cell invasion by 23.6%, 56.6%, and 67.0% in MDA-MB-231 cells, respectively (P<0.05), and anacardic acid treatment for 24 h inhibited the cell migration by 30.0%, 45.5%, and 77.5%, respectively (P<0.05). Anacardic acid dose-dependently induced MMP-9 degradation, but did not obviously affect Hsp90 or Hsp70 expressions.

CONCLUSION

Anacardic acid can significantly inhibit the proliferation, invasion, and migration of MDA-MB-231 cells, the mechanism of which may involve the inhibition of Hsp90 ATPse activity and down-regulation of MMP-9 expression.

摘要

目的

探讨热休克蛋白90(Hsp90)抑制剂漆树酸对乳腺癌MDA-MB-231细胞增殖、侵袭和迁移的影响。

方法

采用体外ATP酶抑制试验和ATP-琼脂糖结合试验评估漆树酸对Hsp90的抑制作用。采用MTT法检测漆树酸对MDA-MB-231细胞生长的抑制作用。采用Transwell试验评估MDA-MB-231细胞的侵袭和迁移能力。采用蛋白质免疫印迹法检测漆树酸对基质金属蛋白酶-9(MMP-9)、金属蛋白酶组织抑制因子-1(TIMP-1)、Hsp90和热休克蛋白70(Hsp70)降解的影响。

结果

漆树酸表现出适度的ATP酶抑制活性,IC50值为82.5 μmol/L。漆树酸以剂量依赖性方式显著抑制MDA-MB-231细胞的增殖(IC50值为29.3 μmol/L)。用12.5、25和50 μmol/L漆树酸处理36小时,MDA-MB-231细胞的侵袭分别受到23.6%、56.6%和67.0%的抑制(P<0.05),用漆树酸处理24小时,细胞迁移分别受到30.0%、45.5%和77.5%的抑制(P<0.05)。漆树酸剂量依赖性地诱导MMP-9降解,但对Hsp90或Hsp70的表达没有明显影响。

结论

漆树酸可显著抑制MDA-MB-231细胞的增殖、侵袭和迁移,其机制可能与抑制Hsp90 ATP酶活性和下调MMP-9表达有关。

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