Demand for cholesterol is high in certain cancers making them potentially sensitive to therapeutic strategies targeting cellular cholesterol homoeostasis. A potential approach involves disruption of intracellular cholesterol transport, which occurs in Niemann–Pick disease as a result of acid sphingomyelinase (ASM) deficiency. Hence, a class of lysosomotropic compounds that were identified as functional ASM inhibitors (FIASMAs) might exhibit chemotherapeutic activity by disrupting cancer cell cholesterol homoeostasis.
Here, the chemotherapeutic utility of ASM inhibition was investigated. The effect of FIASMAs on intracellular cholesterol levels, cholesterol homoeostasis, cellular endocytosis and signalling cascades were investigated. The in vivo efficacy of ASM inhibition was demonstrated using melanoma xenografts and a nanoparticle formulation was developed to overcome dose-limiting CNS-associated side effects of certain FIASMAs.
Functional ASM inhibitors inhibited intracellular cholesterol transport leading to disruption of autophagic flux, cellular endocytosis and receptor tyrosine kinase signalling. Consequently, major oncogenic signalling cascades on which cancer cells were reliant for survival were inhibited. Two tested ASM inhibitors, perphenazine and fluphenazine that are also clinically used as antipsychotics, were effective in inhibiting xenografted tumour growth. Nanoliposomal encapsulation of the perphenazine enhanced its chemotherapeutic efficacy while decreasing CNS-associated side effects.
This study suggests that disruption of intracellular cholesterol transport by targeting ASM could be utilised as a potential chemotherapeutic approach for treating cancer.
Cholesterol has an important role in the development of certain malignancies (Montero et al, 2008; Freed-Pastor et al, 2012; Smith and Land, 2012; Sorrentino et al, 2014). Epidemiological studies have shown that elevated serum cholesterol levels can be associated with cancer risk (Platz et al, 2008; Nielsen et al, 2013). Preclinical studies also demonstrate that deregulated intracellular cholesterol homoeostasis can promote cancer development (Montero et al, 2008; Smith and Land, 2012). More recently, an increase in cellular cholesterol demand was reported with EGFR or RAS-mediated oncogenic transformation (Gabitova et al, 2015). Hindering intracellular cholesterol levels by reducing the expression of low-density lipoprotein (LDL) receptors or enhancing expression of cholesterol exporters, impeded the growth of skin tumours (Gabitova et al, 2015). Activation of AKT signalling following loss of tumour suppressor PTEN, a genetic alteration observed in many cancers, triggered cholesteryl ester accumulation in prostate cancer cells (Yue et al, 2014). Importantly, blocking the cholesterol accumulation-reduced cancer cell proliferation and suppressed xenografted tumour growth (Yue et al, 2014). Moreover, in breast cancers, loss of tumour suppressor p53-induced cancer cell proliferation and self-renewal by upregulating of the cholesterol synthesis pathway (Sorrentino et al, 2014). Collectively these studies suggest that therapeutically modulating cholesterol homoeostasis could be useful for inhibiting cancer development.
Targeting intracellular cholesterol transport with leelamine, a naturally derived lysosomotropic compound, has recently been shown to retard melanoma tumour growth (Kuzu et al, 2014). Leelamine-mediated cancer cell death is associated with the shutdown of cholesterol egress from lysosomal/late endosomal cell compartments. Inhibition of lysosomal cholesterol efflux also occurs in a lipid storage disorder called Niemann–Pick disease (Vanier, 2013), loss of function mutations in sphingomyelin phosphodiesterase-1 (SMPD1), which encodes acid sphingomyelinase (ASM), causes types A and B forms of the Niemann–Pick disease (Vanier, 2013). This lysosomal enzyme breaks down sphingomyelin to phosphorylcholine and ceramide. Lack of functional ASM, impairs sphingosine efflux from lysosomes, blocks late endosome-lysosome fusion and causes accumulation of sphingolipid, as well as LDL-derived cholesterol in lysosomes (Lloyd-Evans et al, 2008). However, it is currently unknown whether ASM inhibitors could be used to block intracellular cholesterol transport to treat cancer.
A class of lysosomotropic antidepressant, antipsychotic or antihistamine drugs have been identified as functional ASM inhibitors (FIASMAs) (Kornhuber et al, 2008; Kornhuber et al, 2011). These compounds have also been reported to be effective against cancer in preclinical and large-scale case–control studies (Akiyama et al, 1986; Peer and Margalit, 2006; Kornhuber et al, 2008; Kornhuber et al, 2011; Walker et al, 2011). Despite these observations, the mechanism(s) mediating the anticancer activity of these agents is unknown. To determine whether ASM inhibitors could be effective cancer therapeutics by inhibiting intracellular cholesterol transport, 42 ASM inhibitors were screened. ASM inhibitors were effective at killing cancer cells depending on genetic background. Melanoma cell lines harbouring activating BRAF mutations and loss of functional PTEN, required 2–5-fold lower concentrations of ASM inhibitors than normal skin cells or melanoma cells lacking these genetic alterations.
ASM inhibitor-mediated cell death was triggered by inhibition of cholesterol egress from lysosomes, which consequently deregulated cholesterol homoeostasis and impaired intracellular vesicle transport, cellular endocytosis as well as autophagic flux. The activity of AKT and STAT3 signalling pathways, two important cancer drivers that are downstream of receptor tyrosine kinase/RAS signalling, were suppressed by FIASMAs. Analysis of the data from the LincsCloud database, supported these observations by showing significant similarities between cellular signatures of certain ASM inhibitors and genetic knockdown of RTK/RAS/PI3K pathway genes, KRAS, ERBB3 and AKT3.
Orally administered ASM inhibitors, perphenazine or fluphenazine, led to tumour inhibition but caused CNS-related sedation at concentrations required for anticancer activity. This was overcome by encapsulating the agents into nanoliposomes to modulate drug pharmacokinetics and potentially reduce blood–brain-barrier permeability. Indeed, intravenous delivery of perphenazine nanoliposomes effectively enhanced the antitumour activity while reducing the negative sedative side effects. Since many ASM inhibitors are clinically viable drugs with well-established toxicity profiles, these discoveries could lead to the repurposing of these agents to function as anticancer cholesterol transport inhibitors by reformulating them within nanoparticles.
Materials and methods
Cell lines and plasmids
Metastatic melanoma cell line UACC 903 was provided by Dr Mark Nelson (University of Arizona); MelJuSo cell line was provided by Dr Judith Johnson (University of Munich); human fibroblast cell line (FF2441) and human foreskin keratinocytes (HFK) were provided by Dr Craig Myers (Penn State College of Medicine); FC-0023 epidermal melanocytes were purchased from Lifeline Cell Technologies (Frederick, MD, USA); 451Lu, 451LuR cell lines were provided by Dr Xiaowei Xu (University of Pennsylvania); C8161.Cl9 cell line was provided by Dr Danny Welch (University of Kansas) and all other melanoma cell lines were provided by Dr Herlyn (Wistar Institute). Wild-type and BAX-nockout HCT116 human colon cancer cell lines were provided by Dr Wafik El-Deiry (Penn State College of Medicine). Melanoma cell lines and FF2441 fibroblast cell line were maintained in DMEM (Invitrogen, Carlsbad, CA, USA) supplemented with 1% GlutaMAX (Thermo Fisher, Waltham, MA, USA) and 10% FBS (GE Healthcare, Chicago, IL, USA). HFK and FC0023 cells were grown in Epilife Medium with Human Keratinocyte and Melanocyte Growth Supplement (Thermo Fisher), respectively. Melanoma cell lines were periodically monitored for genotypic characteristics, phenotypic behaviour and tumourigenic potential to confirm cell line identity. GFP-tagged LC3B expressing UACC 903 cell line was generated using the pBABE-puro mCherry-EGFP-LC3B plasmid (Addgene plasmid #22418; Cambridge, MA, USA) (N'Diaye et al, 2009).
Microarray data files (cel files) that contain the expression profile of MCF7 cells treated with different compounds and at least three associated vehicle controls were downloaded from the Connectivity Map project website (www.broadinstitute.org/cmap/; see Supplementary Materials and Methods Section for the C-Map IDs). ArrayStar software (v 12.2, Dnastar, Madison, WI, USA) was used to analyse the data. For the details of microarray analysis please see the Supplementary Materials and Methods Section.
Drug treatment conditions and assessment of IC50
The viability of cells following compound (see Supplementary Materials and Methods Section for compound sources) or liposome treatments was measured using the MTS assay (Promega, Madison, WI, USA) as described previously (Gowda et al, 2014). Briefly, cells were plated in 96-well plates, grown to 70–80% confluency, and treated with either vehicle or varying concentrations of experimental agents. 24 h later, the MTS assay was performed and IC50 estimated for each compound using GraphPad Prism (GraphPad Software, La Jolla, CA, USA). In co-treatment studies, compounds were added simultaneously.
Mitochondrial membrane potential (MMP) and caspase-dependence assays
MMP of cells was measured using the TMRE MMP Assay Kit (Abcam, Cambridge, MA, USA). Caspase-3/7 activity was measured using a fluorogenic substrate Ac-DEVD-AFC using the protocol for the Caspase-3 Inhibitor Screening Assay Kit (Merck, Billerica, MA, USA). Caspase-dependent cell death was assessed by pre-treatment of cells with pan-caspase inhibitor z-VAD-fmk (20 μmol l−1) for 1 h before drug treatments. 24 h after treatments, cell viability was measured by MTS assay.
Cholesterol localisation assay
Localisation of intracellular cholesterol was detected through Filipin-III staining of cells using the Cayman’s Cholesterol Cell-Based Detection Assay Kit (Cayman Chemical, Ann Arbor, MI, USA). Lysosomal/late endosomal localisation of cholesterol was assessed by co-localisation of LAMP1-RFP and Filipin-III signals using iVision software (BioVision Technologies, Chester Springs, PA, USA). An RFP-tagged LAMP1 expressing UACC 903 cell line was created using LAMP1-mRFP-FLAG plasmid (Addgene plasmid #34611) (Zoncu et al, 2011). Images were taken at × 1000 magnification.
Evaluation of cellular endocytosis
The endocytic capacity of cells was measured using Alexa Fluor-488-conjugated transferrin protein (Thermo Fisher) as described previously (Kuzu et al, 2014). Cells were plated into chamber slides (or six-well plates for flow cytometry analysis) and treated with compounds for 3–4 h. Cells were then incubated for 30 min with Alexa Fluor 488-conjugated transferrin protein (5 μg ml−1), washed with phosphate-buffered saline and either fixed with 4% paraformaldehyde for fluorescence microscopy analysis or trypsinised, and collected for flow cytometry analysis.
Western blot analysis
One to two million cells were plated in 100 mm dishes and grown to 75–90% confluency. After drug treatments for various times, cells were harvested in RIPA buffer containing protease and phosphatase inhibitors (Thermo Fisher). BCA Assay (Thermo Fisher) was used for protein quantification and 30 μg of protein was loaded per lane onto NuPage gels (Life Technologies, Carlsbad, CA, USA). Following electrophoresis, proteins were transferred to PVDF membrane and blots probed with antibodies according to supplier’s recommendations (detailed antibody information provided in Supplementary Materials and Methods Section). ECL detection (Thermo Fisher) was used to visualise immunoblots.
All animal experiments were undertaken according to protocols approved by the Institutional Animal Care and Use Committee at The Pennsylvania State University. Effects of the compounds on xenografted tumour growth were measured in athymic-Foxn1−/− (nude) mice (Harlan Laboratories, Indianapolis, IN, USA). Briefly, one million melanoma cells were injected subcutaneously above both the left and right rib cages of 4–6-week-old female mice. Six-days post injection, when the tumour size was ∼100 mm3, animals were randomly separated into groups (four animals/group). For oral administration, perphenazine and nortriptyline were dissolved in glyceryl trioctanoate, while fluphenazine and desipramine were dissolved in water and administered via oral gavage (100 ul per treatment). Nortriptyline and desipramine were administered on alternate days while perphenazine and fluphenazine were administered at 4-day intervals due to the sedation-associated symptoms. Liposomal formulation of perphenazine was administered via intravenous (tail-vein) injection on alternate days. Liposomes were prepared as 5 mg ml−1 drug concentration. Liposomes were diluted with 0.9% saline and injections were performed as 200 ul per injection. Body weight and tumour dimensions were measured on treatment days. At the end of experiments, blood was collected and serum was separated and analysed for blood markers of major organ function and toxicity at The Pennsylvania State University Animal Resource Core. Major organs of the animals were formalin fixed and paraffin embedded to examine changes in cell morphology and tissue organisation following haematoxylin and eosin (H&E) staining.
Statistical analyses were performed using the unpaired Student t-test. A P-value<0.05 was considered statistically significant. *P<0.05; **P<0.01; ***P<0.001. Unless otherwise noted, error bars represent s.e.m.
Genetic knockdown of ASM inhibits intracellular cholesterol transport and decreases cancer cell viability
To determine whether siRNA-mediated inhibition SMPD1 expression would inhibit intracellular cholesterol transport and alter the viability of cancer cell lines, two siRNAs targeting SMPD1 were transfected into melanoma cells. As assessed by qRT-PCR, SMPD1 expression was effectively reduced to 10% of that observed for the mock transfection control (Supplementary Figure 1A). Mimicking the Niemann–Pick Disease, knockdown of the SMPD1 inhibited lysosomal cholesterol export as determined by Fillipin-III staining of the accumulated lysosomal cholesterol (Figure 1A). Furthermore, inhibition of the SMPD1 expression reduced the viability of both UACC 903 and 1205 Lu melanoma cell lines to 35% of that observed for the controls suggesting that ASM could be a potential therapeutic target (Figure 1B).
Identifying ASM inhibitors with anticancer activity
To determine whether ASM inhibitors could promote cancer cell death by inhibiting intracellular cholesterol transport, a library of 42 ASM inhibitors were screened (Kornhuber et al, 2008; Kornhuber et al, 2011). All of these agents have been reported to decrease in ASM activity by 70–90% (Kornhuber et al, 2008; Kornhuber et al, 2011). Leelamine and U18666A, two previously identified cholesterol transport inhibitors, were used as positive controls. Killing efficacy of each ASM inhibitor was tested on UACC 903 and 1205 Lu melanoma cells and compared to normal FF2441 skin fibroblasts. Both melanoma cell lines were killed by ASM inhibitors with significantly lower IC50 values (paired t-test, P<0.001) compared to fibroblasts (Figure 1C and Supplementary Table 1). Average IC50 values for the melanoma cell lines were threefold lower than for the normal fibroblasts. Since the ASM inhibitors killed cancer cells more effectively than normal cells the chemotherapeutic utility of these agents was examined next.
Accumulation of ASM inhibitors in lysosomes was required for killing cancer cells
To identify the mechanism by which ASM inhibitors killed cancer cells, five compounds (desipramine, flupenthixol, fluphenazine, nortriptyline and perphenazine), killing melanoma cells at low IC50 values, were investigated. These lysosomotropic compounds have been reported to inhibit ASM by disrupting the electrostatic attraction between the negatively charged Bis-monoacyl glycerophosphate and the positively charged ASM protein (Kornhuber et al, 2011). Similar to other lysosomotropic compounds, the ASM inhibitors had pKa values of 7–11 and induced cellular vacuolisation following treatment (Supplementary Table 1 and Supplementary Figures 1B-C) (Nadanaciva et al, 2011). UACC 903 cells were 4–6-fold more sensitive to these ASM inhibitors compared to normal fibroblasts (Figure 1D). To assess whether the lysosomotropic accumulation of these ASM inhibitors was required for induction of cancer cell death, cells were co-treated with a vacuolar-ATPase (v-ATPase) inhibitor, Bafilomycin-A1 (BafA1). The v-ATPase functions as a proton pump to ensure the acidity of acidic organelles, which is the driving force underlying lysosomotropic drug accumulation. Therefore, v-ATPase inhibitors, such as BafA1, reduce the uptake of lysosomotropic compounds (Marceau et al, 2012). BafA1 treatment inhibited the lysosomotropic accumulation of the ASM inhibitors as observed by the total loss of cellular vacuolisation induced by these agents (Supplementary Figure 1C). Furthermore, Bafilomycin-A1 co-treatment effectively suppressed cell death induced by these agents suggesting that the lysosomotropic property of the ASM inhibitors was essential for anticancer activity (Figure 1E and Supplementary Table 1).
ASM inhibitors disrupt cholesterol transport from late endosomal/lysosomal cell compartments mediating cancer cell death
Leelamine-mediated cell death involves inhibition of cholesterol egress from lysosomes (Kuzu et al, 2014). To determine whether ASM inhibitors acted in a similar manner, intracellular cholesterol levels were measured by Filipin-III staining. After 6 h, ASM inhibitor treatment promoted intracellular cholesterol accumulation in a manner similar to that occurring with positive controls, leelamine and U18666A (Figure 1F). Cholesterol accumulation inside the late endosomal/lysosomal cell compartments was observed as co-localisation of RFP-tagged LAMP1 (lysosome-associated membrane glycoprotein-1) with accumulating cholesterol (Figure 1F, bottom). At the subcellular level, leelamine-mediated lysosomal cholesterol accumulation-induced the formation of lipofuscin-like lipid-filled lysosomes (Kuzu et al, 2014). Similarly, transmission electron micrographs of UACC 903 cells treated with ASM inhibitors showed lipid-filled lysosomes further confirming the induction of lysosomal cholesterol accumulation by ASM inhibitors (Supplementary Figure 1D). To determine whether cell death initiated by ASM inhibitors could be reversed by restoring cellular cholesterol levels, cells were supplemented with excess amounts of LDL-cholesterol which increased intracellular cholesterol by alternate LDL internalisation processes (Zhao et al, 2006). As predicted, supplementation of LDL-cholesterol overrode the inhibition of lysosomal cholesterol egress and protected UACC 903 cells from cell death induced by the ASM inhibitors (Figure 1G). The protective effect of LDL-cholesterol was dose-dependent and also occurred with 1205 Lu cells (Supplementary Figure 1E). Thus, ASM inhibitors disrupted intracellular cholesterol transport.
ASM inhibitors deregulated cholesterol homoeostasis
Inhibition of intracellular cholesterol transport was predicted to deregulate cholesterol homoeostasis. To identify the signalling cascades altered by ASM inhibitors, genome-wide mRNA sequencing experiments were performed on perphenazine, fluphenazine, nortriptyline or leelamine treated UACC 903 cells. In total, 177 genes were significantly deregulated by ASM inhibitors (Figure 1H and Supplementary Table 2). Ninety-nine of these alterations were common to at least two out of the four treatments (Figure 1H). Enrichment analysis of the altered genes to identify biological processes, pathways and transcription factors affected by the compound showed significant deregulation of cholesterol homoeostasis (Figure 1H, right and Table 1A). The binding site for the transcription factor SREBF, the major regulator of the cholesterol homoeostasis, was significantly enriched among the promoters of the 177 genes (P-Value: 3.1 × 10−10; z-score: −2.05) (Table 1A). Several genes involved in cholesterol biosynthesis were upregulated while cholesterol export genes were downregulated (Figure 1I). As an alternative approach to analyse the RNA-Seq data, cholesterol transport inhibitors were grouped together and compared to the control group using the differential expression analysis tool (DeSeq tool) (Anders and Huber, 2010). Eleven out of the 18 genes in the cholesterol synthesis pathway were among the most significantly altered 300 genes (Figure 1J and Supplementary Table 3) (Anders and Huber, 2010). Cholesterol biosynthetic (P-value: 7.95 × 10−13; z-score: −2.41) and metabolic (P-value: 5.49 × 10−13; z-score: −2.21) processes were significantly altered with the ASM inhibitors (Table 1B).
To confirm that ASM inhibitors deregulate cholesterol homoeostasis in a second cancer type, gene expression profiles of MCF7 breast cancer cells treated independently with 20 different ASM inhibitors and respective vehicle controls were downloaded from the Connectivity Map database (c-Map) and analysed using the ArrayStar software (Lamb et al, 2006). Comparison of each treatment to its respective control showed that 41 genes were significantly deregulated by at least 10 out of the 20 compounds (Supplementary Table 4). Cholesterol biosynthesis (P-value: 1.19 × 10−10; z-score: −2.42) and metabolism (P-value: 1.85 × 10−9; z-score: −2.2) were significantly enriched in this set of ‘commonly deregulated genes’ (Table 1C). INSIG1, a cholesterol sensor in the endoplasmic reticulum (ER), was upregulated by all 20 compounds, and five cholesterol synthesis genes (HMGCR, HMGCS1, SQLE, MVD and SC4MOL) were among the 41 commonly deregulated genes (Supplementary Table 4). As a negative control, several randomly chosen compounds from the c-Map database were selected; however, no deregulation of cholesterol synthesis/metabolism pathways was observed (data not shown).
As a confirmatory approach, all 20 ASM inhibitors were grouped together and compared with the control group, identifying 272 significantly altered probes representing 213 individual genes, at a 99% confidence level with a moderated t-test (Supplementary Table 5). Twenty-six out of the 59 (44%) proteins in the Gene Ontology (GO) category of ‘Cholesterol biosynthetic process’ were significantly deregulated by the ASM inhibitors (P-value: 5.49 × 10−16; z-score: −2.42) (Table 1D). Many cholesterol synthesis (e.g., HMGCS1, SQLE, IDI1) and homoeostasis (e.g., INSIG1) genes were 2–4-fold upregulated by the ASM inhibitors (Figure 1K). Niemann–surya Pick disease, type C1 (NPC1) protein, which exports cholesterol from lysosomes was also upregulated, likely as a response to the inhibition of cholesterol transport from lysosomes (Supplementary Table 5). These results suggested that inhibition of cholesterol egress from lysosomes by ASM inhibitors deregulated intracellular cholesterol homoeostasis. Furthermore, upregulation of the cholesterol biosynthesis genes indicated a cellular response to decreased levels of cholesterol in the ER suggesting that lysosomal cholesterol was invisible to the cholesterol regulatory pathways of the cancer cells. In Niemann–Pick disease, impaired cholesterol trafficking to the ER also upregulated cholesterol synthesis despite cholesterol accumulation in lysosomes (Peake and Vance, 2010), further supporting this possibility.
ASM inhibitors suppress xenografted melanoma tumour growth
To measure the chemotherapeutic potential of ASM inhibition, efficacies of perphenazine, nortriptyline and desipramine were tested on xenografted tumour development. Oral administration of perphenazine-reduced tumour growth by 60% whereas nortriptyline and desipramine led to 50% and 30% tumour inhibition, respectively (Figure 2A). Histological analyses of tumours harvested from perphenazine-treated animals showed cellular vacuolisation with a significant decrease in mitotic figure numbers (Figure 2B and C). Since, perphenazine had the greatest effect on tumour growth, this agent and a related ASM inhibitor, fluphenazine, were subsequently tested for inhibiting UACC 903, 1205 Lu and A2058 tumour development. Oral administration of perphenazine at 50 mg kg−1 or fluphenazine at 25 mg kg−1 at 4-day intervals led to a 40–60% decrease in tumour development (Figure 2D–H). Tumour weights harvested from the drug-treated animals at the end of treatment were 40–60% lower than control groups (Figure 2E and H).
At the end of the perphenazine treatment, blood serum was collected and analysed for blood biomarkers indicative of major organ toxicity. Compared to controls, total bilirubin levels were significantly higher in perphenazine-treated animals, likely due to haemolytic anaemia, a known side effect of phenothiazine antipsychotics, such as perphenazine (Supplementary Table 6) (Ohlow and Moosmann, 2011). Histological analysis of vital organs showed no alteration in cell morphology or tissue architecture (Supplementary Figure 2D). However, both perphenazine and fluphenazine caused CNS-related side effects limiting the maximum drug dosage that could be administered to animals. Thirty to sixty minutes after oral administration, animals became sedated, which persisted for >24 h, limiting feeding and causing a 10% loss of body weight (Figure 2I and Supplementary Figure 2A–C). Thus, administration of certain clinically used ASM inhibitors at doses causing an anticancer effect was limited due to sedative CNS-related effects, necessitating reformulation for use in cancer therapy.
Nanoliposomal encapsulation of perphenazine reduced side effects while enhancing chemotherapeutic efficacy
Liposomal encapsulation of the CNS-active ASM inhibitors was hypothesised to able to decrease CNS-related side effects by reducing blood–brain-barrier permeability. This approach was also predicted to increase efficacy by prolonging the drug circulation lifetime, and through the enhanced permeability and retention (EPR) effect (Greish, 2007). Therefore, perphenazine was encapsulated into nanoliposomes having a neutral charge (in saline) and an average size of 70 nM. Encapsulation efficiency was 66%±3 (s.e.m.) with a drug to lipid ratio of 0.2 (m/m). Nanoliposomal perphenazine was as effective as the free drug at killing cultured cancer cells and was stable at 4 °C for 20 weeks (Supplementary Table 7). Encapsulated perphenazine was released from liposomes at a rate of 2.6% per hour over a 24-h time period (Supplementary Figure 3A). Furthermore, nanoliposomal encapsulation eliminated the haemolytic activity occurring with orally administered perphenazine suggesting that this approach could also lessen haemolytic anaemia associated with high doses of this drug (Supplementary Figure 3B).
To determine whether nanoliposomal encapsulation of perphenazine decreased CNS-related sedative effects, Swiss-Webster mice were examined using video surveillance following treatment. Control mice spent approximately 40% of the day awake and motile, which decreased to 6% when 50 mg kg−1 perphenazine was administered orally (P=5.05 × 10−15) (Figure 3A and B). In contrast, mice treated intravenously with nanoliposomal perphenazine at 15 mg kg−1 were awake and active 30% of the day, which was a significant improvement compared to oral treatment (P=2.8 × 10−10). A dose-matched oral control of 15 mg kg−1 perphenazine had a slightly greater sedative effect compared to liposomal treatment (P=0.037) but caused body weight loss following treatment for 2 days (Figure 3A–C). Nanoliposomal perphenazine treated animals did not lose weight compared to a 10% loss observed following oral treatments (Figure 3C). These results suggest that nanoliposomal encapsulation decreases CNS-associated sedative side effects of perphenazine.
Nanoliposomal perphenazine was as effective as the free drug at killing cultured cancer cells, having an IC50 of 10 uM for UACC 903 melanoma cells (Figure 3D). Intravenous administration of 15 mg kg−1 perphenazine nanoliposomes on alternate days led to 60 and 70% decrease in UACC 903 and 1205 Lu tumour development, respectively (Figure 3E–G). In contrast, the free drug was ineffective at inhibiting UACC 903 tumour development at 12.5 or 25 mg kg−1 concentrations (Supplementary Figure 3C). Weights of the tumours harvested from perphenazine nanoliposome treated xenografts were 2–3-fold lower than the vehicle-treated control group (Figure 3F). No significant weight loss was observed and all serum markers indicative of major organ toxicity were comparable to controls (Figure 3E and G; Supplementary Table 6). Histopathological analysis of major organs showed no differences between experimental and control groups (Figure 3H). Thus, nanoliposomal encapsulation of CNS-active ASM cholesterol transport inhibitors might provide a novel approach for decreasing CNS-related side effects while enhancing the anticancer activity of the compound.
Inhibition of intracellular cholesterol transport blocks autophagic flux
Disruption of intracellular cholesterol transport has been shown to inhibit autophagic flux (Kuzu et al, 2014). Analysis of microarray data from the c-Map database also suggested that ASM inhibitors deregulate autophagic processes (Table 1C). To determine whether ASM inhibitors would deregulate autophagic flux, levels of the autophagosome marker, LC3B, and autophagic flux marker, p62/SQSTM1, were examined by western blotting. Nortriptyline, perphenazine or fluphenazine-treated UACC 903 cells, led to dose-dependent accumulation of LC3B and p62 proteins (Figure 4A). Accumulation of LC3B was also observed through fluorescence microscopy of GFP-tagged LC3B expressing UACC 903 cells (Figure 4B). Thus ASM inhibitors suppressed autophagic flux causing aggregation of autophagosomes in a manner similar to that occurring with the cholesterol transport inhibitor leelamine (Kuzu et al, 2014).
Inhibition of intracellular cholesterol transport by ASM inhibitors suppressed cellular endocytosis
Targeting cholesterol transport using leelamine or disruption of this process in Niemann–Pick disease leads to inhibition of cellular endocytosis (Peake and Vance, 2010; Kuzu et al, 2014). Hence, the effect of ASM inhibitors on cellular endocytosis was examined by measuring uptake of Alexa Fluor-conjugated transferrin. Transferrin is typically internalised into early endosomes through clathrin-mediated endocytosis, which serves as the major pathway for uptake of receptor-ligand complexes (Liu et al, 2010). Uptake of Alexa Fluor-conjugated transferrin protein was measured by fluorescence microscopy and flow cytometry (Kuzu et al, 2014). In contrast to the vehicle-treated control group, cells treated with ASM inhibitors did not take up transferrin, suggesting that these compounds inhibit cellular endocytosis (Figure 4C). Flow cytometric quantitation of transferrin uptake demonstrated a dose-dependent inhibition of endocytosis (Figure 4D). Cellular endocytosis is critical for cancer cell survival as many oncogenic signals are initiated by membrane receptors that are regulated by endocytosis (Polo et al, 2004).
ASM inhibitors deregulated intracellular vesicle trafficking
Transport of LDL-derived cholesterol from the lysosomes to the ER involves the trans-Golgi network (TGN) (Urano et al, 2008). In Niemann–Pick disease, inhibition of cholesterol egress from lysosomes depletes cholesterol levels both in TGN and ER (Garver et al, 2002; Urano et al, 2008; Peake and Vance, 2010). Lower cholesterol levels in these organelles disrupts efficient ER to Golgi vesicle transport (Ridsdale et al, 2006). Enrichment analysis of the RNA-Seq data suggested increased ER stress and disrupted ER to Golgi vesicle-mediated transport following treatment with ASM inhibitors (Table 1). To confirm the cellular consequences of ASM inhibitors on intracellular vesicle trafficking, the perturbation signature similarity data in Lincscloud database was analysed (lincscloud.org). This database contains cellular signatures obtained from various cellular perturbations following chemical treatments, gene knockdown or overexpression studies, enabling comparison of similarities between different perturbations over multiple cell lines. Signature data for 32 ASM inhibitors were available in LincsCloud database. A set of genetic perturbations exhibited significant similarity to the ASM inhibitors (Figure 4E and Supplementary Table 8). Among these, knockdown of the genes involved in cellular endocytosis and vesicle trafficking (ATP6V0B, ATP6V0C, CHMP2A), genes involved in the Golgi to ER retrograde transport (COPA, COPB2, TMED10), and more interestingly RTK/AKT signalling proteins (ERBB3, KRAS, AKT3) exhibited similar signatures to ASM inhibitors (Figure 4E).
Disruption of intracellular vesicle trafficking, cellular endocytosis and the trans-Golgi network may retard maturation and localisation of certain proteins (Gu et al, 2001). Leelamine-mediated inhibition of cholesterol transport altered the localisation of several receptor tyrosine kinases and led to the accumulation of immature forms (Kuzu et al, 2014). Similarly, treatment with ASM inhibitors delocalised the IGF1R receptors to the perinuclear region and caused a dose-dependent accumulation of immature forms of HGFR, IGFIR and cathepsin B proteins while decreasing the levels of mature forms (Figure 4F and G). In agreement with RNA-Seq results, western blotting of ER stress markers, HERPUD1 and EROL1α indicated the induction of ER stress by ASM inhibitors (Figure 4G). Collectively, these results suggested that inhibition of intracellular cholesterol transport by ASM inhibitors disrupted intracellular vesicle trafficking in the ER trans-Golgi network, impaired protein maturation and triggered the ER stress response(Grice et al, 2010).
Inhibition of intracellular cholesterol transport retarded RTK/AKT/STAT3 signalling
Disrupted maturation and localisation of RTKs and inhibition of cellular endocytosis can suppress downstream signalling cascades regulated by these receptors (Sorkin and von Zastrow, 2009). Leelamine-mediated inhibition of intracellular cholesterol transport inhibited downstream PI3K/AKT and STAT3 signalling pathways (Kuzu et al, 2014). Similarly, ASM inhibitors suppressed pAKT, pPRAS40 and pSTAT3 levels (Figure 4G). Interestingly, pERK1/2 levels were upregulated possibly due to strong AKT inhibition, which has been observed following genetic or pharmacological inhibition of AKT signalling (Chen et al, 2012). Thus, inhibition of RTK/PI3K/AKT/STAT3 signalling could partially explain the enhanced sensitivity of cancer cells to ASM inhibitors, as many cancers are addicted to these oncogenic signalling cascades.
Cancer cells with high PI3K/AKT activity exhibited increased sensitivity to ASM inhibitors
PTEN deletion promotes prostate cancer aggressiveness via cholesteryl ester accumulation and consequent PI3K/AKT activation (Yue et al, 2014). Since, ASM inhibitors significantly downregulated AKT signalling, the potential association between loss of PTEN activity and increased sensitivity to cholesterol transport inhibition was investigated in a panel of melanoma and normal skin cell lines. Melanoma cells lacking functional PTEN showed enhanced sensitivity to ASM inhibitors, suggesting that ASM inhibitors might more effectively kill those cancer cells in which AKT signalling is activated (Figure 4H).
Inhibition of intracellular cholesterol transport leads to caspase-independent cell death that involves mitochondrial localisation of BAX
To characterise the mechanism of cell death mediated by ASM inhibitors, alterations in various cell death processes were examined. To identify alive vs early and late apoptotic cells, UACC 903 cells were treated with ASM inhibitors for 24 h and stained with Annexin-V/Propidium iodide (PI). All of the tested agents led to a significant increase in the percentage of early apoptotic cells (Annexin-V+, PI−) (Figure 5A). In the control cells, only 1% underwent apoptosis while that was dose-dependently increased to 4–8% following ASM treatment. Furthermore, a dramatic increase from 0.5% to 10–37% was observed in late apoptotic/necrotic Annexin-V, PI-positive cells. Necrosis was not the cause of cell accumulation in this quadrant as neither of the two necrosis inhibitors, IM-54 and Necrostatin-5, protected UACC 903 cells from ASM inhibitor or leelamine-mediated cell death (Supplementary Figure 4A and B) (Galluzzi et al, 2012).
Next, loss of mitochondrial membrane potential (MMP) was assessed since it has a central role in many apoptotic processes and leelamine treatment decreased MMP (Ly et al, 2003; Kuzu et al, 2014). Following treatment with ASM inhibitors, UACC 903 cells were stained with Tetramethylrhodamine Ethyl Ester (TMRE), a cell-permeant fluorescent dye that accumulates in mitochondria in a membrane potential-dependent manner (Bernas and Dobrucki, 2002). As a positive control, FCCP which is an oxidative phosphorylation uncoupler was used, which effectively reduced the MMP of treated cells. Following 3 h of 10 umol l−1 nortriptyline or perphenazine treatment, 15% of the cells lost MMP (Figure 5B). The decrease in MMP was dose and time-dependent as evidenced by a 19 and 28% decrease after 6 h of 10 or 15 uM perphenazine treatments, respectively.
To determine whether BAX, a proapoptotic member of the Bcl-2 protein family that induces loss of MMP by translocating to the mitochondrial membrane, was involved in cell death, the sensitivity of wild-type and BAX-knockout HCT116 cells to ASM inhibitors was compared (Smaili et al, 2001). BAX-knockout cells were more resistant to increasing concentrations of perphenazine (Figure 5C; left). Moreover, all of the tested ASM inhibitors, more effectively killed wild-type HCT116 cells (Figure 5C; right). Mitochondrial localisation of BAX promotes assembly of the apoptosome and subsequent activation of caspases (Gomez-Crisostomo et al, 2013). Interestingly, the response of cells to NS-3694, an inhibitor of apoptosome formation, was variable, following co-treatment with various ASM inhibitors (Figure 5D). 50 μMol/l NS-3694 partially protected cells from death mediated by perphenazine, fluphenazine or flupenthixol, but not desipramine, nortriptyline or leelamine treatments (Figure 5D). Furthermore, cell death induced by ASM inhibitors was caspase-independent (Figure 5E). Pan-caspase inhibitor z-VAD-fmk, protected cells from apoptosis induced by positive control TRAIL treatment (Figure 5E; left). However, it was ineffective against cell death mediated by ASM inhibitors, suggesting induction of a caspase-independent cell death program (Figure 5E; right).
Cholesterol is an essential lipid for the proper functioning of the cell membrane and membrane-bound organelles (Ikonen, 2008). It has a key role modulating signal transduction from the membrane to cytoplasm and participates in intracellular vesicle trafficking (Ridsdale et al, 2006; Ikonen, 2008). Increased levels of cellular cholesterol and deregulation of its homoeostasis occur in various malignancies (Yue et al, 2014).
Recent studies have dissected the role of cellular cholesterol in cancer progression and suggested targeting it as a potential chemotherapeutic approach (Guo et al, 2011; Freed-Pastor et al, 2012; Sorrentino et al, 2014; Yue et al, 2014; Gabitova et al, 2015). Oncogenic signals initiated from RTK/MAPK, RTK/PI3K/AKT/mTOR or mutant p53 were found to deregulate cholesterol synthesis in cancer cells (Guo et al, 2011; Freed-Pastor et al, 2012; Sorrentino et al, 2014; Gabitova et al, 2015). Mutant KRAS-mediated transformation increased the cellular demand for cholesterol (Gabitova et al, 2015). Activation of AKT pathway induced SREBP-mediated cholesterol synthesis and LDL receptor-mediated cholesterol import while shutting down ABCA1-mediated cholesterol export (Porstmann et al, 2008; Guo et al, 2011). In prostate cancer, intracellular cholesterol levels enhanced by AKT signalling contributed to cancer aggressiveness and bone metastases (Thysell et al, 2010; Yue et al, 2014). In glioblastoma, LDL receptors were induced by over-activated AKT signalling and their pharmacological targeting effectively killed tumour cells (Guo et al, 2011). SREBP-mediated upregulation of cholesterol synthesis was induced by mutant p53, contributing to proliferation and self-renewal of breast cancer cells (Freed-Pastor et al, 2012; Sorrentino et al, 2014). Collectively, these studies suggest that deregulated intracellular cholesterol homoeostasis plays an important role in cancer development.
Recently, inhibition of intracellular cholesterol transport has been shown to induce melanoma cell death (Kuzu et al, 2014). This study expands on these studies by showing that like Niemann–Pick disease, where loss of function mutations in ASM retard intracellular cholesterol transport, certain ASM inhibitors can block cholesterol egress from lysosomes to inhibit cancer cell survival. Upregulation of the genes in the cholesterol synthesis pathway following ASM inhibition suggested decreased cholesterol levels in the ER and potentially also in other membrane-bound organelles. The inhibition of intracellular cholesterol transport mediated by ASM inhibitors also disrupted cellular endocytosis and autophagic flux while causing ER stress and inhibiting AKT as well as STAT3 signalling cascades. Cancer cells with over-activated MAP kinase and PI3K/AKT pathways were threefold more sensitive to ASM inhibitors compared to normal skin cells. This observation could be associated with increased cholesterol demand by these cells due to upregulated MAPK/AKT/SREBP signalling. Moreover, activated AKT/mTOR signalling has been reported to increase proteasomal degradation of NPC1 protein which could also sensitise cancer cells to inhibition of cholesterol egress from lysosomes (Du et al, 2015).
Although lysosomotropic ASM inhibitors have been suggested to inhibit the function of the enzyme by disrupting the electrostatic attraction between intraluminal membranes and ASM, causing degradation of the enzyme by cathepsins, the exact mechanism still needs further study (Schulze et al, 2009; Petersen et al, 2013). Following lysosomotropic accumulation of ASM inhibitors, these agents could interfere with other lysosomal proteins such as NPC1 and NPC2. A recent study suggested U18666A to be a direct inhibitor of NPC1 (Lu et al, 2015).
CNS-active agents, such as tricyclic antidepressants and antipsychotics, also act as ASM inhibitor and have been suggested to prevent cancer in case–control and preclinical studies (Kornhuber et al, 2008; Lieb, 2008; Kornhuber et al, 2011). A case–control study that involved follow-up of a cohort of 6168 chronic schizophrenic patients over 27 years, identified decreased cancer risk for the respiratory system, prostate, bladder and uterine cervix cancers by using high-dose tricyclic antidepressants (Mortensen, 1989). Another case–control study showed an association between previous tricyclic antidepressant usage and cancer incidence (Walker et al, 2011). After stratifying for age, gender, smoking and alcohol usage, a statistically significant inverse association was found between previous tricyclic antidepressant usage and incidence of glioma as well as colorectal cancer, in a dose- and time-dependent manner. No linkage of the anti-ASM activity of these agents was reported, making this study the first to suggest a possible mechanism for these observations.
In preclinical studies, many antidepressants that also act as ASM inhibitors, have been shown to trigger cancer cell death and restore sensitivity of multidrug-resistant (MDR) cancer cell lines (Akiyama et al, 1986; Peer and Margalit, 2006). Perphenazine induced mitochondria-mediated cell death in human neuroblastoma cells and triggered apoptosis in both wild-type and MDR-B16 melanoma cells (Gil-Ad et al, 2006; Perez-Alvarez et al, 2011). Fluphenazine was also effective at killing MDR-B16 cells (Gil-Ad et al, 2006). Flupentixol enhanced the sensitivity of murine fibrosarcoma cells to anticancer drugs (Fan et al, 1994). Another antidepressant, desipramine-triggered apoptotic cell death of colon carcinoma cells (Arimochi and Morita, 2008). Thus, epidemiological and preclinical studies suggest that tricyclic antidepressants may also function as chemotherapeutic agents. Since many ASM inhibitors were shown to enhance sensitivity of drug-resistant cell lines to chemotherapeutic agents, it is possible that these agents could reverse the resistance to V600E-BRAF inhibitors in melanoma, which has been reported to involve activation of AKT and STAT3 signalling (Shao and Aplin, 2010; Liu et al, 2013).
Several compounds that act as an ASM inhibitor are currently being tested in clinical trials for therapeutic efficacy against leukaemia, myeloma, lung, prostate and colorectal cancers (Clinical Trial ID: NCT02096289, NCT00821301, NCT00417274, NCT01719861). The chemotherapeutic potential of quinacrine (mepacrine) on prostate cancer has been assessed in a phase-2 trial (Clinical Trial Id: NCT00417274). The trial was conducted in patients who had not responded to previous chemotherapies. Although only one of the 31 patients showed a partial response to the treatment, ∼50% of the patients showed stabilisation or decrease in the rate of disease progression. More recently, the chemotherapeutic activity of desipramine was examined in a phase-IIa clinical study for small cell lung cancer (Clinical Trial Id: NCT01719861). The plan was to start treating patients at 75 mg day−1 and increase dosing to 450 mg day−1. However, only one patient was able to tolerate a dose above 150 mg day−1 (personal communication). Failure to reach therapeutically effective dosing levels and lack of efficacy led to early study termination suggesting that alternative approaches for administering these drugs may be required for anticancer efficacy.
In this report, the significant anticancer activity of two ASM inhibitors, perphenazine and fluphenazine, was observed. Both agents led to decreased xenografted tumour development, but efficacy was limited by CNS-associated sedative side effects. The dose required for anticancer activity in mice were 4–10 times greater than the standard doses used in the clinic. These levels are impractical in humans and caused sedation of mice. In this study, nanoliposomal encapsulation of perphenazine was identified as a strategy to overcome the side effects of CNS-active agents that are ASM inhibitors. Nanoliposomal encapsulation would alter the pharmacokinetics and tissue distribution of the CNS-active agents by decreasing blood–brain-barrier permeability, protecting the agents from liver metabolism, and assisting in tumour penetration due to the EPR effect (Greish, 2007). Nanoliposomal encapsulation of perphenazine-reduced CNS-associated sedative effects of perphenazine, while enhancing the anticancer activity of the compound. Therefore certain ASM compounds with well-known toxicity profiles might be repurposed for use as anticancer agents by reformulation into nanoparticles.
We are thankful to Dr Arati Sharma for technical assistance with the animal studies. This work was supported by The Foreman Foundation for Melanoma Research, Geltrude Foundation, The Chocolate Tour Cancer Research Fund and NIH grants CA-127892, CA-136667, and CA-138634.
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Supplementary Information accompanies this paper on British Journal of Cancer website (http://www.nature.com/bjc)
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