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Cancer drugs inhibit morphogenesis in the human fungal pathogen, Candida albicans

Madhushree M Routh Nitin M Chauhan S Mohan Karuppayil About the authors

Abstract

Candida infections are very common in cancer patients and it is a common practice to prescribe antifungal antibiotics along with anticancer drugs. Yeast to hyphal form switching is considered to be important in invasive candidiasis. Targeting morphogenetic switching may be useful against invasive candidiasis. In this study, we report the antimorphogenetic properties of thirty cancer drugs.

Candida albicans; morphogenetic switching; cancer drugs; antifungal antibiotics


MEDICAL MICROBIOLOGY

SHORT COMMUNICATION

Cancer drugs inhibit morphogenesis in the human fungal pathogen, Candida albicans

Madhushree M Routh; Nitin M Chauhan; S Mohan Karuppayil

DST-FIST and UGC-SAP Sponsored School of Life Sciences, SRTM University, MS, India

Correspondence

ABSTRACT

Candida infections are very common in cancer patients and it is a common practice to prescribe antifungal antibiotics along with anticancer drugs. Yeast to hyphal form switching is considered to be important in invasive candidiasis. Targeting morphogenetic switching may be useful against invasive candidiasis. In this study, we report the antimorphogenetic properties of thirty cancer drugs.

Key words:Candida albicans, morphogenetic switching, cancer drugs, antifungal antibiotics.

Candida albicans is an important opportunistic fungal pathogen of the humans. Systemic candidiasis is a serious situation in patients undergoing treatment for cancer (Safdar and Armstrong, 2002). Candida species now rank among the ten most prominent pathogens in leukemia patients, accounting for 75% of fungal infections in general and these infections result in 25-60% mortality (Winston et al., 2000). In the last two decades, use of azole antifungals has rapidly led to the development of drug resistance in patients with advance cancers, AIDS, organ transplantations, and surgeries etc. C. albicans cells exist in different morphological forms, including yeast, pseudohyphal and true hyphal forms (Pauw, 2004). Yeast to hyphal form morphogenesis in C. albicans is believed to be related to its virulence, since mutants defective in hyphal growth are less virulent in mouse models than their wild-type (Lo et al., 1997). There are various reports on drugs inhibiting yeast to hyphal form switching. For example, 6-Amino-2n-pentyl-thiobenzothiazole an antifungal agent is reported to inhibit hyphal growth (Fabry et al., 1999). Antimetabolite class of anticancer agents are also tested for their hyphal inhibitory activity along with mRNA, DNA synthesis and protein synthesis inhibitors. Among all these, cyclohexamide showed most potential activity against hyphal induction (Imanishi et al., 2004). The known actin inhibiting drugs, latrunculin-A and jasplakinolide inhibited yeast to hyphal form transition in a dose dependent and reversible manner (Toenje et al., 2005). Undecylenic acid inhibits the switch from yeast form to hyphae, in sublethal concentrations (McLain et al., 2000). Earlier we have reported the potential morphogenetic role for ethyl alcohol and its first oxidation product acetaldehyde in C. albicans. Both of them, inhibited yeast to hyphal form morphogenesis induced by four standard inducers in a concentration dependent manner (Chauhan et al., 2010, 2011). Most of the commonly used anticancer drugs inhibit fundamental steps involved in eukaryotic metabolism or cell cycle like inhibition of DNA, RNA and protein synthesis (Liscovitch and Lavie., 2002). Some of the anticancer drugs targeting tubulin function, DNA synthesis, induction of apoptosis, DNA replication, protein synthesis, estrogen receptors etc, are known to have in-vitro anti-Candida activity (Davies et al., 2000; Kesavan et al., 2005). Amino acid induced yeast to hypha formation was inhibited by treatment with Actinomycin-D, Bleomycin, 5-Flourouracil and Hydroxyurea at varying concentration in the range of 100-1000 µg/mL in C. albicans 5685 strain (Land et al., 1980). However no direct roles for antimorphogenetic properties for anticancer drugs are reported in C. albicans. Considering the eukaryotic nature of C. albicans, it can be expected that anticancer drugs may exert anti-Candida activity also. Recently, we reported antifungal activity of thirty commonly prescribed anti-cancer drugs. Most of the drugs are tested for the first time. These drugs exhibited growth inhibitory effects on fluconazole sensitive as well as fluconazole resistant strains (Routh et al., 2011). Here in this comprehensive study we report the inhibitory effect of thirty anticancer agents on yeast to hyphal form transition of C. albicans.

C. albicans, ATCC 90028 was used throughout the study. Methodology for growth and storage of C. albicans were same as per described previously (Chauhan et al., 2010, 2011). 10% Horse serum was used for germ tube induction. Thirty anticancer drugs from different classes were used for this work. All the drugs were purchased from the local market. To study the effect of anticancer drugs on germ tube formation, Candida filamentation assay was done using microtiter plate assay in 96 well microtiter plates (Chauhan et al., 2010, 2011). Cells from a stock solution were inoculated in 10% serum to get1x 106 cells/mL. Various concentrations of anticancer drug (ranging from 0.781 µg/mL to 50 µg/mL) were added to the wells. Wells without drugs were kept as control. Final volume in each well was kept 200 µL. The plates were incubated at 37 °C at 200 rpm on an orbital shaker for two hours. After incubation cells were observed microscopically. Every time 100 cells were counted and numbers of yeast and germ tube forms are noted. Percentage of germ tube inhibition was calculated by comparing with control (without drug). As shown in Table 1 and Figure 1, anticancer drugs effectively prevent yeast to hyphal form transition induced by 10% serum. Among the four antimicrotubule anticancer agents, Docetaxel significantly inhibited (around 80%) morphogenesis at 25 µg/mL, while 50 µg/mL showed complete inhibition of filamentation (Figure 1 B). Vinblastine did not alter morphogenesis upto 50 flg/mL. Whereas Paclitaxel caused inhibition of yeast to hyphal form morphogenesis at 50 µg/mL, while Vincristine at same concentration caused 80% inhibition of filamentation (Table 1). Platinum analogs showed efficient activity. Cisplatin, Oxaliplatin and Carboplatin (Figure 1J) completely blocked germ tubes at 50 µg/mL (Table 1). Cyclophosphamide inhibited filamentation at 50 µg/mL. At 6.25 µg/mL it inhibited almost 50% morphogenesis. Busulfan and Ifosfamide also blocked 60-80% switching at 12.5 µg/mL and complete inhibition at 50 µg/mL. Melphalan (Figure 1D) and Carmustine exherted inhibition of germ tubes at 50 µg/mL (Table 1).









Among the three antimetabolites tested, Methotrexate completely restricted morphogenesis at 25 µg/mL, followed by Gemcitabine which inhibited complete morphogenesis at 50 µg/mL (Figure 1E). Hydroxyurea was not effective upto 50 µg/mL, where 100% germ tubes were seen (Table 1).

Among various antitumor antibiotic drugs, Doxorubicin and 5-flurouracil were most efficient agents which inhibited morphogenesis around 80% at 12.5 µg/mL, while 25 µg/mL of Doxorubicin (Figure 1 C) and Daunorubicin completely inhibited filamentation. 5-flurouracil, Bleomycin, Mitoxantrone, Epirubicin and Mitomycin-C were found to exhibit morphogenetic switching inhibitory potential at 50 µg/mL (Table 1). Etoposide which is an epipodophyllotoxins exhibited inhibition of morphogenesis at 25 µg/mL (Figure 1G). Non classic alkalyting agent Dacarbazine completely halted filamentation at 50 µg/mL (Figure 1I). Leuprolide (Figure 1H), Tamoxifen (Figure 1L), Irinotecan (Figure 1K) and Formestane (Figure 1F) completely inhibited serum induced morphogenesis of C. albicans at drug concentration 50 µg/mL. Leucovorin (Figure 1A) did not have inhibitory effect on serum induced yeast to hyphal form morphogenesis (Table 1).

To demonstrate the effect of anticancer drugs on viability of C. albicans cell, viability plate count was done (Chauhan et al. 2010 and 2011). Briefly, various concentrations of drugs ranging from 25 µg/mL to 16,000 µg/mL were added to 10% Serum in 96-well microtiter plates. Each well was inoculated with a cell density of 1 x 106 cells/mL. The plates were incubated at 37 °C on a shaker for various time intervals (2 and 4 h, respectively). Cells from the respective wells were diluted to get countable colonies and an aliquot of sample was spread on YPD agar plates. Plates were incubated at 30 °C for 48 h and colony count was done. The germ tube inhibitory concentrations of various anticancer drugs did not alter the viability of C. albicans cells at various time points studied (Table 1). However higher concentrations of some antifungal drugs affects the viability. For example as shown in Table 1, Docetaxel showed significant reduction in viability at 1600 µg/mL, while Paclitaxel, Vinblastine, Vincristine, Bleomycin, Mitoxantrone, Cyclophosphamide, Melphalan, Leuprolide, Dacarbazine, Carboplatin, Cisplatin, Oxaliplatin and Irinotecan required 600-800 µg/mL of concentration to produce the similar effect at various time points. While, Vincristine, Doxorubicin and Busulfan caused significant reduction (around 50%) in viability at 200-400 µg/mL of concentration. Whereas, other drugs such as Tamoxifen, daunorubicin, 5-flurouracil, Mitomycin-C, Epirubicin, Carmustine, Ifosamide, Gemcitabine, Methotrexate, Hydroxyurea, Formestane, Etoposide and Leucovorine fails to affect the viability of Candida cells even at a concentration of 1600 µg/mL (Table 1).

C. albicans can exist in various morphological forms, among these hyphae are very important because cells that do not readily form hyphae often show reduced virulence. (Lo et al., 1997). Currently available antifungal chemotherapy such as amphotericin, azoles and echinocandins, etc. are limited to drugs that directly inhibit growth of C. albicans cells but not any virulence factor. Exploration of unknown properties of existing drugs has provided a new focus to the field of antifungal chemotherapy. For example non steroidal anti-inflamatory drugs which are cycloxygenase inhibitors have been found to inhibit dimorphism and biofilm formation in C. albicans. Some protein synthesis inhibitors are also screened for their antimorphogenetic activity suggesting that de novo mRNA or protein synthesis is essential for germ tube formation (Imanishi et al., 2004; Toenje et al., 2005).

Our results suggest that all the anticancer drugs used in this study may be having similar targets in C. albicans as in mammals, because of their common ancestral heritage. Mitomycin-C was the most efficient inhibitor of morphogenesis which inhibited yeast to hyphal form transition at 1/16th of its MIC. This was followed by Daunorubicin which was effective at 1/8th of its MIC value .These two anticancer agents belong to the same class of antitumor antibiotics. Mitomycin –C inhibits transcription by targeting DNA dependent RNA polymerase. It acts as an alkalyting agent to cross link DNA resulting in inhibition of DNA synthesis and function. Whereas Daunorubicin inhibits topoisomerase II by forming a cleavable complex with DNA and topoisomerase II to create uncompensated DNA helix which creates a torsional tension leading to eventual DNA breaks (Toenje et al., 2005). Epirubicin, Melphalan, Gemcitabine, Methotrexate, Etoposide and Leuprolide were inhibiting 100% germtubes at 1/4th of their MIC which suggest their good antimorphogenetic potentials without affecting growth. Some drugs like Docetaxel, Paclitaxel, Tamoxifen, 5-Flurouracil, Dactinomycin, Carmustine, Ifosfamide, Formestane, and Dacarbazine inhibited 100% germ tubes at half of their MIC values. Rest few drugs were completely inhibiting at MIC (Table 1). The two anti-microtubule i.e Docetaxel and Paclitaxel may affect microtubule formation resulting in inhibition of morphogenesis. 5-Flurouracil, the antitumor antibiotic is reported to inhibit protein synthesis in C. albicans which can block the proteins which are essential for filamentation (Chen et al., 2011). An anti-metabolite agent, Methorexate is reported to produce higher amount of catalase, a marker for oxitatative stress which may cause inhibition of filamentation (Linaris et al., 2006).

Candida infections are very common in cancer patients. As such it is a common practice to prescribe antifungal antibiotics along with anticancer drugs (Pauw, 2004). Recently we have reported the anti C. albicans properties of a variety of popularly used anticancer drugs (Routh et al., 2011). Our study suggests rethinking on the logic of prescribing antifungal antibiotics against C. albicans infections in cancer patients undergoing chemotherapy. C. albicans is usually found in various morphological types in vivo. Among these, yeast to hyphal form switching is considered to be important in invasive candidiasis. Targeting yeast to hyphal form morphogenetic switching may be useful against invasive candidiasis. However such antibiotics are not in practice currently. Most of the drugs inhibited yeast to hyphal form morphogenesis at concentrations lower than their MIC and MFC. The different class of anticancer drugs may exert similar effects depending on its concentrations. At lower concentrations it may inhibit morphogenetic switching and support yeast phase growth. While high concentrations of drugs may slow down the growth rate suggesting good antifungal properties. This is the first report on the antimorphogenetic properties of thirty anticancer drugs. Our study indicates the possibility of repositioning cancer drugs as anti-morphogenetic agents in C. albicans.

Acknowledgments

MMR is thankful to UGC, New Delhi, for providing UGC Meritorious fellowship Ref. no. F. 4-1/2006 (BSR)/11-21/2008(BSR). We are thankful to Prof. S.B. Nimse, Honorable Vice Chancellor, SRTM University and Dr. Anand Bhagat, Oncologist, Yashoda Hospital, Nanded, Maharashtra State, India for their kind support.

  • Correspondence
    S.M. Karuppayil
    School of Life Sciences, SRTM University
    431 606 Nanded, MS, India
    E-mail:
  • Submitted: January 21, 2012;

    Approved: September 10, 2012.

    All the content of the journal, except where otherwise noted, is licensed under a Creative Commons License CC BY-NC.

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    Correspondence S.M. Karuppayil School of Life Sciences, SRTM University 431 606 Nanded, MS, India E-mail: prof.karuppayil@gmail.com

    Publication Dates

    • Publication in this collection
      03 Feb 2014
    • Date of issue
      Sept 2013

    History

    • Received
      21 Jan 2012
    • Accepted
      10 Sept 2012
    Sociedade Brasileira de Microbiologia USP - ICB III - Dep. de Microbiologia, Sociedade Brasileira de Microbiologia, Av. Prof. Lineu Prestes, 2415, Cidade Universitária, 05508-900 São Paulo, SP - Brasil, Ramal USP 7979, Tel. / Fax: (55 11) 3813-9647 ou 3037-7095 - São Paulo - SP - Brazil
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