Literature DB >> 30551403

MDR reversal and pro-apoptotic effects of statins and statins combined with flavonoids in colon cancer cells.

Anna Palko-Łabuz1, Kamila Środa-Pomianek2, Olga Wesołowska2, Edyta Kostrzewa-Susłow3, Anna Uryga2, Krystyna Michalak2.   

Abstract

The resistance of cancer cells to a variety of structurally non-related cytotoxic drugs is known as multidrug resistance phenomenon (MDR). In cellular membranes an activity of MDR transporters such as P-glycoprotein (ABCB1) is affected by their lipid environment. Many various compounds have been examined for their ability to restore drug-sensitivity of resistant cancer cells. Statins, inhibitors of the key enzyme of mevalonate pathway HMG-CoA (3-hydroxy-3-methyl-glutaryl-coenzyme A) reductase are drugs commonly prescribed in order to reduce serum level of cholesterol and to diminish the risk of cardiovascular disease. Statins as drugs that influence lipid composition of cell membrane and in that way they also exert influence on lipid bilayer properties appear to be good candidates as MDR modulators. In this work it was shown that statins - mevastatin and simvastatin exert antiproliferative, pro-apoptotic and reversing drug resistance effect in human colon adenocarcinoma cell line LoVo and its drug-resistant subline LoVo/Dx. A hypothesis was also checked whether flavones, which as it is well known are able to influence the biosynthesis of cholesterol, may change the anticancer activity of statins. Our investigations have revealed that combined use of statins and studied flavonoids results in enhanced cell growth inhibition and apoptosis and lower cancer cell proliferation as compared to the application only statins alone. Moreover, in drug resistant LoVo/Dx cells a stronger decrease of resistance to doxorubicine was observed in the presence of statins in combination with flavones as compared to the effect observed for statins only.
Copyright © 2018 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Apoptosis; Cytotoxicity; Flavonoids; HMG-CoA reductase; Multidrug resistance; P-glycoprotein; Statins

Mesh:

Substances:

Year:  2018        PMID: 30551403     DOI: 10.1016/j.biopha.2018.10.169

Source DB:  PubMed          Journal:  Biomed Pharmacother        ISSN: 0753-3322            Impact factor:   6.529


  10 in total

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6.  Statins as inhibitors of voltage-gated potassium channels Kv1.3 in cancer cells.

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Authors:  Watcharaphong Chaemsawang; Weerapong Prasongchean; Konstantinos I Papadopoulos; Garnpimol Ritthidej; Suchada Sukrong; Phanphen Wattanaarsakit
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  10 in total

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