4.8 Article

Cisplatin prevents breast cancer metastasis through blocking early EMT and retards cancer growth together with paclitaxel

期刊

THERANOSTICS
卷 11, 期 5, 页码 2442-2459

出版社

IVYSPRING INT PUBL
DOI: 10.7150/thno.46460

关键词

cisplatin; paclitaxel; neoadjuvant therapy; TGF beta; metastasis

资金

  1. Chair Professor Grant [CPG 2017-00016-FHS, MYRG2016-00132-FHS, MYRG2017-00113-FHS]
  2. University of Macau, Macau SAR, China
  3. Macao Science and Technology Development Fund (FDCT) grant [0034/2019/AGJ, 0011/2019/AKP]
  4. FDCT, Macau SAR, China

向作者/读者索取更多资源

Cisplatin at different doses has varying effects on breast cancer growth and metastasis, with higher doses inhibiting both growth and metastasis but causing severe side effects, and lower doses only blocking metastasis. Cisplatin prevents breast cancer metastasis by blocking early EMT steps.
Cancer growth is usually accompanied by metastasis which kills most cancer patients. Here we aim to study the effect of cisplatin at different doses on breast cancer growth and metastasis. Methods: We used cisplatin to treat breast cancer cells, then detected the migration of cells and the changes of epithelial-mesenchymal transition (EMT) markers by migration assay, Western blot, and immunofluorescent staining. Next, we analyzed the changes of RNA expression of genes by RNA-seq and confirmed the binding of activating transcription factor 3 (ATF3) to cytoskeleton related genes by ChIP-seq. Thereafter, we combined cisplatin and paclitaxel in a neoadjuvant setting to treat xenograft mouse models. Furthermore, we analyzed the association of disease prognosis with cytoskeletal genes and ATF3 by clinical data analysis. Results: When administered at a higher dose (6 mg/kg), cisplatin inhibits both cancer growth and metastasis, yet with strong side effects, whereas a lower dose (2 mg/kg) cisplatin blocks cancer metastasis without obvious killing effects. Cisplatin inhibits cancer metastasis through blocking early steps of EMT. It antagonizes transforming growth factor beta (TGF beta) signaling through suppressing transcription of many genes involved in cytoskeleton reorganization and filopodia formation which occur early in EMT and are responsible for cancer metastasis. Mechanistically, TGF beta and fibronectin-1 (FN1) constitute a positive reciprocal regulation loop that is critical for activating TGF beta/SMAD3 signaling, which is repressed by cisplatin induced expression of ATF3. Furthermore, neoadjuvant administration of cisplatin at 2 mg/kg in conjunction with paclitaxel inhibits cancer growth and blocks metastasis without causing obvious side effects by inhibiting colonization of cancer cells in the target organs. Conclusion: Thus, cisplatin prevents breast cancer metastasis through blocking early EMT, and the combination of cisplatin and paclitaxel represents a promising therapy for killing breast cancer and blocking tumor metastasis.

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