Anticancer and antimetastatic activity of copper(II)-tropolone complex against human breast cancer cells, breast multicellular spheroids and mammospheres
Journal of Inorganic Biochemistry, ISSN: 0162-0134, Vol: 204, Page: 110975
2020
- 50Citations
- 52Captures
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Metrics Details
- Citations50
- Citation Indexes50
- 50
- CrossRef3
- Captures52
- Readers52
- 52
Article Description
The goal of this work was to display the anticancer and antimetastatic activity of a copper(II) with tropolone (trp), complex [ Cu(trp) 2 ] toward human breast cancer cells in monolayer (2D) and spheroids (3D). Cytotoxicity assays against MCF7 (IC 50(complex) = 5.2 ± 1.8 μM, IC 50(CDDP) = 19.3 ± 2.1 μM) and MDA-MB-231 (IC 50(complex) = 4.0 ± 0.2 μM, IC 50(CDDP) = 27.0 ± 1.9 μM) demonstrate that [ Cu(trp) 2 ] exert greater antitumor potency than cisplatin (CDDP) on 2D and 3D human breast cancer cell models. Besides, [ Cu(trp) 2 ] inhibits cell migration by reducing the metalloproteinases activities and the compound undergoes the breast cancer cells to apoptosis at lower concentrations (2.5–10 μM). Moreover, [ Cu(trp) 2 ] overcame CDDP presenting an IC 50 value 26-fold more lower against breast multicellular spheroids ((IC 50(complex) = 4.9 μM, IC 50(CDDP) = 130 μM)). Also, our results showed that [ Cu(trp) 2 ] inhibited the cell migration and cell invasion of breast multicellular spheroids, showing that [ Cu(trp) 2 ] exhibited antimetastatic properties. On the other hand, [ Cu(trp) 2 ] reduced mammosphere forming capacity affecting the size and number of mammospheres. Taken together, [ Cu(trp) 2 ] exhibited anticancer and antimetastatic properties on monolayer (2D) and spheroids (3D) derived from human breast cancer cells.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0162013419304386; http://dx.doi.org/10.1016/j.jinorgbio.2019.110975; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85077311992&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/31911364; https://linkinghub.elsevier.com/retrieve/pii/S0162013419304386; https://dx.doi.org/10.1016/j.jinorgbio.2019.110975
Elsevier BV
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