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Growth Promotion and Increased ATP-Binding Cassette Transporters Expression by Liraglutide in Triple Negative Breast Cancer Cell Line MDA-MB-231.

Authors :
Shadboorestan A
Tarighi P
Koosha M
Faghihi H
Ghahremani MH
Montazeri H
Source :
Drug research [Drug Res (Stuttg)] 2021 Jul; Vol. 71 (6), pp. 307-311. Date of Electronic Publication: 2021 Jan 21.
Publication Year :
2021

Abstract

Background: Glucagon-like petide-1 (GLP-1) agonists such as liraglutide are widely employed in type 2 diabetes due to their glucose reducing properties and small risk of hypoglycemia. Recently, it has been shown that GLP-1agonists can inhibit breast cancer cells growth. Nonetheless, concerns are remained about liraglutide tumor promoting effects as stated by population studies.<br />Material and Methods: We evaluated the effects liraglutide on proliferation of MDA-MB-231 cells by MTT assay and then ATP-binding cassette (ABC) transporters expressions assessed by Real time PCR. Statistical comparisons were made using one-way analysis of variance followed by a post hoc Dunnett test.<br />Results: Here, we report that liraglutide can stimulate the growth of highly invasive triple negative cell line MDA-MB-231; which can be attributed to AMPK-dependent epithelial-mesenchymal transition (EMT) happening in MDA-MB-231 context. Toxicity effects were only observed with concentrations far above the serum liraglutide concentration. ATP-binding cassette (ABC) transporters expressions were upregulated, indicating the possible drug resistance and increased EMT.<br />Conclusion: In conclusion, these results suggest that liraglutide should be used with caution in patients who are suffering or have the personal history of triple negative breast cancer. However, more detailed studies are required to deepen understanding of liraglutide consequences in triple negative breast cancer. â–¶Graphical Abstract.<br />Competing Interests: The authors have no conflict of interest to report.<br /> (Thieme. All rights reserved.)

Details

Language :
English
ISSN :
2194-9387
Volume :
71
Issue :
6
Database :
MEDLINE
Journal :
Drug research
Publication Type :
Academic Journal
Accession number :
33477190
Full Text :
https://doi.org/10.1055/a-1345-7890