Abstract

BackgroundAlthough demonstrated as a selective anticancer drug, the clinical use of clotrimazole (CTZ) is limited due to its low solubility in hydrophilic fluids. Thus, we prepared a water-soluble nanomicellar formulation of CTZ (nCTZ) and tested on the human breast cancer cell line MCF-7 biology.Methodology/Principal FindingsCTZ was nanoencapsulated in tween 80 micelles, which generated nanomicelles of, approximately, 17 nm of diameter. MCF-7 cells were treated with nCTZ and unencapsulated DMSO-solubilized drug (sCTZ) was used for comparison. After treatment, the cells were evaluated in terms of metabolism, proliferation, survival and structure. We found that nCTZ was more efficient than sCTZ at inhibiting glycolytic and other cytosolic and mitochondrial enzymes. Moreover, this increased activity was also observed for lactate production, intracellular ATP content, ROS production and antioxidant potential. As a consequence, nCTZ-treated MCF-7 cells displayed alterations to the plasma membrane, mitochondria and the nucleus. Finally, nCTZ induced both apoptosis and necrosis in MCF-7 cells.Conclusions/SignificanceMCF-7 cells are more sensible to nCTZ than to sCTZ. This was especially evident on regard to antioxidant potential, which is an important cell defense against drugs that affect cell metabolism. Moreover, this water-soluble formulation of CTZ strengths its potential use as an anticancer medicine.

Highlights

  • Cancer chemotherapy continues to suffer from the same problem: undesirable and toxic side effects [1,2,3]

  • We found that nanomicellar formulation of CTZ (nCTZ) was more efficient than soluble CTZ (sCTZ) at inhibiting glycolytic and other cytosolic and mitochondrial enzymes

  • Cell viability was tested with the MTT assay (Fig 1C) and by the leakage of lactate dehydrogenase (LDH) into the culture medium (Fig 1D)

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Summary

Introduction

Cancer chemotherapy continues to suffer from the same problem: undesirable and toxic side effects [1,2,3]. Mitochondria are constantly metabolizing metabolites other than pyruvate—especially glutamine—that are largely used as carbon sources for the biosynthesis of lipids and amino acids primarily for the construction of membranes and proteins, respectively [5,12,14,15,16]. This aerobic glycolytic preference of cancer cells is named the Warburg effect for its first description by Otto Warburg in 1956 [17]. We prepared a water-soluble nanomicellar formulation of CTZ (nCTZ) and tested on the human breast cancer cell line MCF-7 biology.

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