| Autor: |
Meirelles LEF; Department of Clinical Analysis and Biomedicine, State University of Maringá, Maringá 87020-900, PR, Brazil., Souza MVF; Department of Clinical Analysis and Biomedicine, State University of Maringá, Maringá 87020-900, PR, Brazil., Carobeli LR; Department of Clinical Analysis and Biomedicine, State University of Maringá, Maringá 87020-900, PR, Brazil., Morelli F; Department of Clinical Analysis and Biomedicine, State University of Maringá, Maringá 87020-900, PR, Brazil., Mari NL; Department of Clinical Analysis and Biomedicine, State University of Maringá, Maringá 87020-900, PR, Brazil., Damke E; Department of Clinical Analysis and Biomedicine, State University of Maringá, Maringá 87020-900, PR, Brazil., Shinobu Mesquita CS; Department of Clinical Analysis and Biomedicine, State University of Maringá, Maringá 87020-900, PR, Brazil., Teixeira JJV; Department of Clinical Analysis and Biomedicine, State University of Maringá, Maringá 87020-900, PR, Brazil., Consolaro MEL; Department of Clinical Analysis and Biomedicine, State University of Maringá, Maringá 87020-900, PR, Brazil., Silva VRSD; Department of Clinical Analysis and Biomedicine, State University of Maringá, Maringá 87020-900, PR, Brazil. |
| Abstrakt: |
Despite the options available for breast cancer (BC) therapy, several adverse effects and resistance limit the success of the treatment. Furthermore, the use of a single drug is associated with a high failure rate. We investigated through a systematic review the in vitro effects of the combination between conventional drugs and bioactive compounds derived from cinnamic acid in BC treatment. The information was acquired from the following databases: PubMed, Web of Science, Embase, Scopus, Lilacs and Cochrane library. We focused on "Cinnamates", "Drug Combinations" and "Breast neoplasms" for publications dating between January 2012 and December 2022, based on the PRISMA statement. The references of the articles were carefully reviewed. Finally, nine eligible studies were included. The majority of these studies were performed using MCF-7, MDA-MB-231, MDA-MB-468 and BT-20 cell lines and the combination between cisplatin, paclitaxel, doxorubicin, tamoxifen, dactolisib and veliparib, with caffeic acid phenethyl ester, eugenol, 3-caffeoylquinic acid, salvianolic acid A, ferulic acid, caffeic acid, rosmarinic acid and ursolic acid. The combination improved overall conventional drug effects, with increased cytotoxicity, antimigratory effect and reversing resistance. Combining conventional drugs with bioactive compounds derived from cinnamic acid could emerge as a privileged scaffold for establishing new treatment options for different BC types. |
