Quinalizarin as a potential antifungal drug for the treatment of Candida albicans fungal infection in cancer patients

被引:2
作者
Janeczko, Monika [1 ]
Kochanowicz, Elzbieta [1 ]
Gorka, Kamila [1 ]
Skrzypek, Tomasz [2 ]
机构
[1] John Paul II Catholic Univ Lublin, Fac Med, Dept Mol Biol, Lublin, Poland
[2] John Paul II Catholic Univ Lublin, Fac Med, Dept Biomed & Environm Res, Lublin, Poland
关键词
antifungal activity; anthraquinones; biofilm; Candida albicans; Candida auris; cancer; fungal infection; hyphae; SEM; ROS; quinalizarin; PROTEIN-KINASE CK2; OXYGEN SPECIES ROS; IN-VITRO; APOPTOSIS; INHIBITOR; PATHWAYS; ANTIBACTERIAL; FILAMENTATION; EPIDEMIOLOGY; MITOCHONDRIA;
D O I
10.1128/spectrum.03652-23
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
This study aims to analyze the antifungal properties of quinalizarin, a plant-derived compound with proven anticancer effects. Quinalizarin exhibited antifungal activity against opportunistic pathogenic Candida species and Geotrichum capitatum. The treatment with this anthraquinone reduced hyphal growth, inhibited biofilm formation, and damaged mature Candida albicans biofilms. Real-time RT-PCR revealed that quinalizarin downregulated the expression of hyphae-related and biofilm-specific genes. The flow cytometry method used in the study showed that both apoptosis and necrosis were the physiological mechanisms of quinalizarin-induced C. albicans cell death, depending on the dose of the antifungal agent. A further study revealed an increase in the levels of intracellular reactive oxygen species and alterations in mitochondrial membrane potential after treatment with quinalizarin. Finally, quinalizarin was found to have low toxicity in a hemolytic test using human erythrocytes. In conclusion, we have identified quinalizarin as a potential antifungal compound.
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页数:18
相关论文
共 73 条
[1]   Adapting to survive: How Candida overcomes host-imposed constraints during human colonization [J].
Alves, Rosana ;
Barata-Antunes, Claudia ;
Casal, Margarida ;
Brown, Alistair J. P. ;
Van Dijck, Patrick ;
Paiva, Sandra .
PLOS PATHOGENS, 2020, 16 (05)
[2]   Environmental sensing and signal transduction pathways regulating morphopathogenic determinants of Candida albicans [J].
Biswas, Subhrajit ;
Van Dijck, Patrick ;
Datta, Asis .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2007, 71 (02) :348-+
[3]  
Braun BR, 2000, GENETICS, V155, P57
[4]   cDNA microarray analysis of differential gene expression in Candida albicans biofilm exposed to farnesol [J].
Cao, YY ;
Cao, YB ;
Xu, Z ;
Ying, K ;
Li, Y ;
Xie, Y ;
Zhu, ZY ;
Chen, WS ;
Jiang, YY .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (02) :584-589
[5]   Apoptosis in yeast: triggers, pathways, subroutines [J].
Carmona-Gutierrez, D. ;
Eisenberg, T. ;
Buettner, S. ;
Meisinger, C. ;
Kroemer, G. ;
Madeo, F. .
CELL DEATH AND DIFFERENTIATION, 2010, 17 (05) :763-773
[6]   Utilizing coordination chemistry through formation of a CuII-quinalizarin complex to manipulate cell biology: An in vitro, in silico approach [J].
Chatterjee, Sayantani ;
Jain, Chetan Kumar ;
Saha, Tanmoy ;
Roychoudhury, Susanta ;
Majumder, Hemanta Kumar ;
Das, Saurabh .
JOURNAL OF INORGANIC BIOCHEMISTRY, 2023, 249
[7]   Differential secretion of Sap4-6 proteins in Candida albicans during hyphae formation [J].
Chen, YC ;
Wu, CC ;
Chung, WL ;
Lee, FJS .
MICROBIOLOGY-SGM, 2002, 148 :3743-3754
[8]   The Selectivity of CK2 Inhibitor Quinalizarin: A Reevaluation [J].
Cozza, Giorgio ;
Venerando, Andrea ;
Sarno, Stefania ;
Pinna, Lorenzo A. .
BIOMED RESEARCH INTERNATIONAL, 2015, 2015
[9]   Quinalizarin as a potent, selective and cell-permeable inhibitor of protein kinase CK2 [J].
Cozza, Giorgio ;
Mazzorana, Marco ;
Papinutto, Elena ;
Bain, Jenny ;
Elliott, Matthew ;
Di Maira, Giovanni ;
Gianoncelli, Alessandra ;
Pagano, Mario A. ;
Sarno, Stefania ;
Ruzzene, Maria ;
Battistutta, Roberto ;
Meggio, Flavio ;
Moro, Stefano ;
Zagotto, Giuseppe ;
Pinna, Lorenzo A. .
BIOCHEMICAL JOURNAL, 2009, 421 :387-395
[10]  
Cumbo Thomas A, 2004, J Natl Compr Canc Netw, V2, P455