Changes in the Sensitivity of MCF-7 and MCF-7/DX Breast Cancer Cells to Cytostatic in the Presence of Metformin

被引:1
作者
Plonka-Czerw, Justyna [1 ]
Zyrek, Luiza [1 ]
Latocha, Malgorzata [1 ]
机构
[1] Med Univ Silesia, Fac Pharmaceut Sci Sosnowiec, Dept Cell Biol, Jednosci 8, PL-41200 Sosnowiec, Poland
关键词
breast cancer cells; multidrug resistance (MDR); metformin; doxorubicin; cytostatics; DRUG-RESISTANCE; THERAPY;
D O I
10.3390/molecules29153531
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Multidrug resistance is a serious problem in modern medicine and the reason for the failure of various therapies. A particularly important problem is the occurrence of multidrug resistance in cancer therapies which affects many cancer patients. Observations on the effect of metformin-a well-known hypoglycemic drug used in the treatment of type 2 diabetes-on cancer cells indicate the possibility of an interaction of this substance with drugs already used and, as a result, an increase in the sensitivity of cancer cells to cytostatics. The aim of this study was to evaluate the effect of metformin on the occurrence of multidrug resistance of breast cancer cells. The MCF-7-sensitive cell line and the MCF-7/DX cytostatic-resistant cell line were used for this study. WST-1 and LDH assays were used to evaluate the effects of metformin and doxorubicin on cell proliferation and viability. The effect of metformin on increasing the sensitivity of MCF-7 and MCF-7/DX cells to doxorubicin was evaluated in an MDR test. The participation of metformin in increasing the sensitivity of resistant cells to the effect of the cytostatic (doxorubicin) has been demonstrated.
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页数:9
相关论文
共 39 条
[1]   In Vivo and In Vitro Enhanced Tumoricidal Effects of Metformin, Active Vitamin D3, and 5-Fluorouracil Triple Therapy against Colon Cancer by Modulating the PI3K/Akt/PTEN/mTOR Network [J].
Almaimani, Riyad Adnan ;
Aslam, Akhmed ;
Ahmad, Jawwad ;
El-Readi, Mahmoud Zaki ;
El-Boshy, Mohamed E. ;
Abdelghany, Abdelghany H. ;
Idris, Shakir ;
Alhadrami, Mai ;
Althubiti, Mohammad ;
Almasmoum, Hussain A. ;
Ghaith, Mazen M. ;
Elzubeir, Mohamed E. ;
Eid, Safaa Yehia ;
Refaat, Bassem .
CANCERS, 2022, 14 (06)
[2]  
[Anonymous], 2011, U.S. Department of Health Human Services: FDA Food and Drug Administration
[3]   Should metformin remain the first-line therapy for treatment of type 2 diabetes? [J].
Baker, Chelsea ;
Retzik-Stahr, Cimmaron ;
Singh, Vatsala ;
Plomondon, Renee ;
Anderson, Victoria ;
Rasouli, Neda .
THERAPEUTIC ADVANCES IN ENDOCRINOLOGY AND METABOLISM, 2021, 12
[4]   Mechanisms of Multidrug Resistance in Cancer Chemotherapy [J].
Bukowski, Karol ;
Kciuk, Mateusz ;
Kontek, Renata .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (09)
[5]   Metformin Potentiates the Anticancer Effect of Everolimus on Cervical Cancer In Vitro and In Vivo [J].
Chen, Ya-Hui ;
Wu, Jyun-Xue ;
Yang, Shun-Fa ;
Chen, Mei-Ling ;
Chen, Tze-Ho ;
Hsiao, Yi-Hsuan .
CANCERS, 2021, 13 (18)
[6]   Molecular and Cellular Mechanisms of Metformin in Cervical Cancer [J].
Chen, Ya-Hui ;
Wang, Po-Hui ;
Chen, Pei-Ni ;
Yang, Shun-Fa ;
Hsiao, Yi-Hsuan .
CANCERS, 2021, 13 (11)
[7]   ABC Transporters in Multidrug Resistance and Pharmacokinetics, and Strategies for Drug Development [J].
Choi, Young Hee ;
Yu, Ai-Ming .
CURRENT PHARMACEUTICAL DESIGN, 2014, 20 (05) :793-807
[8]  
Cwynar-Zajac Lucja, 2021, Pediatr Endocrinol Diabetes Metab, V27, P134, DOI [10.5114/pedm.2021.107166, 10.5114/pedm.2021.107166]
[9]   Metformin inhibits the development, and promotes the resensitization, of treatment-resistant breast cancer [J].
Davies, Gerald ;
Lobanova, Liubov ;
Dawicki, Wojciech ;
Groot, Gary ;
Gordon, John R. ;
Bowen, Matthew ;
Harkness, Troy ;
Arnason, Terra .
PLOS ONE, 2017, 12 (12)
[10]   Crocin and Metformin suppress metastatic breast cancer progression via VEGF and MMP9 downregulations: in vitro and in vivo studies [J].
Farahi, Ali ;
Abedini, Mohammad Reza ;
Javdani, Hossein ;
Arzi, Laleh ;
Chamani, Elham ;
Farhoudi, Ramin ;
Talebloo, Nazanin ;
Hoshyar, Reyhane .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2021, 476 (09) :3341-3351