4.4 Article

A triple combination gemcitabine plus romidepsin plus cisplatin to effectively control triple-negative breast cancer tumor development, recurrence, and metastasis

期刊

CANCER CHEMOTHERAPY AND PHARMACOLOGY
卷 88, 期 3, 页码 415-425

出版社

SPRINGER
DOI: 10.1007/s00280-021-04298-y

关键词

Triple-negative breast cancer; Reactive oxygen species; Metastasis; Recurrence; Combination regimens

资金

  1. National Institutes of Health [CA177834]
  2. University of Tennessee, Center of Excellence in Livestock Diseases and Human Health

向作者/读者索取更多资源

The study demonstrated the efficacy of gemcitabine plus romidepsin + cisplatin regimen in controlling TNBC tumor development, recurrence, and metastasis in animal models, showing significant inhibition effects in reducing tumor growth and metastatic nodules.
Purpose Triple-negative breast cancer (TNBC) is an aggressive, lethal, heterogeneous type of breast cancer (BC). TNBC tends to have a lower response rate to chemotherapy and a lower 5-year survival rate than other types of BC due to recurrence and metastasis. Our previous study revealed that a combination of gemcitabine, romidepsin, and cisplatin was efficacious in controlling TNBC tumor development. In this study, we extended our investigation of gemcitabine + romidepsin + cisplatin in controlling TNBC tumor recurrence and metastasis. Methods We investigated the ability of gemcitabine + romidepsin + cisplatin to control cell survival and invasiveness using cell viability, soft agar colony formation, and transwell invasion assays. We determined the efficacy of gemcitabine + romidepsin + cisplatin in controlling tumor recurrence and metastasis using cell-derived xenograft animal models. We used immunoblotting to study signaling modulators regulated by gemcitabine + romidepsin + cisplatin in TNBC cells and tumor tissues. Results Treatment with gemcitabine + romidepsin + cisplatin reduced the TNBC MDA-MB231 and MDA-MB468 cell survival to similar to 50% and similar to 15%, as well as invasiveness to similar to 31% and similar to 13%, respectively. Gemcitabine + romidepsin + cisplatin suppressed modulators involved in epithelial-mesenchymal transition in an ROS-dependent manner. Controlling tumor recurrence, the Gem plus Rom + Cis regimen (similar to 112%) was more efficacious than the Gem plus Cis regimen (similar to 21%) in tumor growth inhibition. The Gem plus Rom + Cis regimen efficaciously reduced the development of metastatic nodules to 20% in animals. Conclusion The gemcitabine plus romidepsin + cisplatin regimen was highly efficacious in controlling TNBC tumor development, recurrence, and metastasis in animals. The combination regimen should be poised for efficient translation into clinical trials for controlling the recurrence and metastasis, ultimately contributing to reducing mortality and improving TNBC patients' quality of life.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据