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脱氢表雄酮对乳腺癌细胞增殖、迁移和死亡的影响。

Effects of dehydroepiandrosterone on proliferation, migration, and death of breast cancer cells.

机构信息

Departamento de Biología Celular, Instituto Nacional de Cardiología Ignacio Chávez, Mexico.

出版信息

Eur J Pharmacol. 2011 Jun 25;660(2-3):268-74. doi: 10.1016/j.ejphar.2011.03.040. Epub 2011 Apr 9.

Abstract

Cancer invasion and metastasis are the leading causes of mortality in patients with breast cancer. Dehydroepiandrosterone (DHEA) has a protective role against cancer, however, the mechanism by which DHEA has this effect remains poorly understood. The present study was aimed at investigating the actions of DHEA on the proliferation, cell cycle, death and migration of breast cancer cell lines. We used MCF-7 cells (estrogen receptors positive) and MDA-MB-231 and Hs578T cells (estrogen receptors negative) for these studies. Cell proliferation was evaluated by crystal violet staining, cell cycle by flow cytometry, and cell death by the carboxyfluorescein FLICA analysis of caspase activation. Migration was evaluated by transwell cell migration and wound assay. We also determined the expression of ECM-1 protein by western blotting and RT-PCR in real time. DHEA inhibited the proliferation of all breast cancer cell lines. This was associated with an arrest in the G1 phase of the cell cycle and death in MCF-7 cells. There was no alteration in any of the cell cycle phases or death in DHEA treated MDA-MB-231 or Hs578T cells. DHEA also suppressed the migration of all breast cancer cell lines, independently of the presence of estrogen receptors and decreased the expression of ECM-1 protein in Hs578T cells. These results suggest that the mechanism of DHEA actions against breast cancer involves the inhibition of cell proliferation and the suppression of migration, indicating that DHEA could be useful in the treatment of breast cancer.

摘要

癌症的侵袭和转移是导致乳腺癌患者死亡的主要原因。脱氢表雄酮(DHEA)对癌症具有保护作用,但 DHEA 发挥这种作用的机制仍知之甚少。本研究旨在探讨 DHEA 对乳腺癌细胞系增殖、细胞周期、死亡和迁移的作用。我们使用 MCF-7 细胞(雌激素受体阳性)和 MDA-MB-231 和 Hs578T 细胞(雌激素受体阴性)进行了这些研究。细胞增殖通过结晶紫染色评估,细胞周期通过流式细胞术评估,细胞死亡通过 caspase 激活的羧基荧光素 FLICA 分析评估。迁移通过 Transwell 细胞迁移和划痕实验评估。我们还通过 Western blot 和实时 RT-PCR 确定了 ECM-1 蛋白的表达。DHEA 抑制了所有乳腺癌细胞系的增殖。这与 MCF-7 细胞中细胞周期的 G1 期阻滞和死亡有关。在 DHEA 处理的 MDA-MB-231 或 Hs578T 细胞中,没有观察到任何细胞周期阶段的改变或死亡。DHEA 还抑制了所有乳腺癌细胞系的迁移,这与雌激素受体的存在无关,并降低了 Hs578T 细胞中 ECM-1 蛋白的表达。这些结果表明,DHEA 对乳腺癌的作用机制涉及抑制细胞增殖和抑制迁移,表明 DHEA 可用于治疗乳腺癌。

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