Zinc ion dyshomeostasis increases resistance of prostate cancer cells to oxidative stress via upregulation of HIF1α
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David Wetherell1,2, Graham S. Baldwin1, Arthur Shulkes1, Damien Bolton1,2, Joseph Ischia1,2 and Oneel Patel1
1Department of Surgery, University of Melbourne, Austin Health, Heidelberg, Victoria, 3084, Australia
2Department of Urology, Austin Health, Heidelberg, Victoria, 3084, Australia
Oneel Patel, email: firstname.lastname@example.org
Keywords: castrate resistant; hypoxia inducible factor 1 alpha; prostate cancer; zinc; iron
Received: September 07, 2017 Accepted: November 14, 2017 Published: January 03, 2018
Zinc ions (Zn2+) are known to influence cell survival and proliferation. However the homeostatic regulation of Zn2+ and their role in prostate cancer (PC) progression is poorly understood. Therefore the subcellular distribution and uptake of Zn2+ in PC cells were investigated. Inductively coupled plasma mass spectroscopy and fluorescent microscopy with the Zn2+-specific fluorescent probe FluoZin-3 were used to quantify total and free Zn2+, respectively, in the normal prostate epithelial cell line (PNT1A) and three human PC cell lines (PC3, DU145 and LNCaP). The effects of Zn2+ treatment on proliferation and survival were measured in vitro using MTT assays and in vivo using mouse xenografts. The ability of Zn2+ to protect against oxidative stress via a HIF1α-dependent mechanism was investigated using a HIF1α knock-down PC3 model. Our results demonstrate that the total Zn2+ concentration in normal PNT1A and PC cells is similar, but PC3 cells contain significantly higher free Zn2+ than PNT1A cells (p < 0.01). PNT1A cells can survive better in the presence of high concentrations of Zn2+ than PC3 cells. Exposure to 10 μM Zn2+ over 72 hours significantly reduces PC3 cell proliferation in vitro but not in vivo. Zn2+ increases PC3 cell survival up to 2.3-fold under oxidative stress, and this protective effect is not seen in PNT1A cells or in a HIF1α-KD PC3 cell model. A state of Zn2+ dyshomeostasis exists in PC. HIF1α is an integral component of a Zn2+-dependent protective mechanism present in PC3 cells. This pathway may be clinically significant through its contribution to castrate-resistant PC survival.
The essential trace metal zinc, as the divalent Zn2+ ion, is a critical structural component of many proteins including transcription factors, and a component and/or co-factor for > 300 enzymes . The prostate gland contains a very high concentration of zinc ions particularly in the peripheral zone, where most prostate tumours occur. In a normal prostate epithelial cell, zinc ions inhibit the mitochondrial enzyme aconitase (mAC), and consequently citrate accumulates and is secreted at high concentrations into seminal fluid .
Compared to the normal prostate, the Zn2+ concentration in prostate cancer (PC) is reduced by 80% . Excessive Zn2+ is toxic to cells, and therefore regulated homeostasis is critical, but the homeostatic mechanism in PC is poorly understood. Human serum Zn2+ concentrations range from 10 to 25μM, most of which is bound to proteins, and the interstitial Zn2+ concentration is normally 2 to 5 μM . The majority of Zn2+ is tightly bound and considered inactive, and the amount of free Zn2+, which is considered biologically active, is in the pM to nM range . Unlike most cells in which Zn2+ is sequestered into vesicles and organelles, in normal prostate cells 35% of free Zn2+ in located in the cytoplasm and 30% is sequestered in the mitochondria . The recent development of fluorescent probes specific for the Zn2+ ion has made quantifying free Zn2+ achievable via fluorescent microscopy/spectroscopy, but their application in PC has been limited and little is known about the intracellular free Zn2+ concentration, Zn2+ uptake, or the subcellular distribution of Zn2+ in PC cells .
Zn2+ treatment has been shown to reverse the effects of oxidative stress in vivo and to increase resistance to chemo- or radiation-induced apoptosis. Therefore, Zn2+ has been implicated in PC survival mechanisms . Hypoxia-inducible factor 1α (HIF1α) forms part of a transcriptional complex which stimulates the expression of > 200 survival genes in response to hypoxia. We have previously demonstrated that overexpression of HIF1α in PC is an independent indicator for PC recurrence, metastatic spread and progression to castration-resistant prostate cancer (CRPC) .
The aims of the present study were to measure baseline free and total Zn2+ concentrations in PC cells and determine the role of Zn2+ in the proliferation of prostate cancer cells in vitro and in vivo. Finally, the ability of Zn2+ to protect against oxidative stress, and in particular the role of Zn2+ in a HIF1α-dependent mechanism, were investigated.
Intracellular distribution of Zn2+ is altered in CRPC-like cells
Zn2+ is abundant in prostate tissue, but cellular Zn2+ homeostasis is complex and poorly understood in PC. To address this issue total Zn2+ in normal and PC cell lines was measured by Inductively Coupled Plasma Mass Spectroscopy (ICP-MS), which accurately detects Zn2+ concentrations as low as 0.5 ppb. Zn2+ concentrations (ppb) were 52 ± 8, 79 ± 19, 80 ± 17 and 57 ± 5 for PNT1A, LNCaP, DU145 and PC3 cells, respectively, and there was no significant difference in baseline total Zn2+ concentration between normal and PC cells (Figure 1A).
Figure 1: CRPC-like cells contain significantly higher basal free Zn2+ ions but equal total zinc compared to normal controls. (A) Total zinc concentration (ppb) measured by Inductively Coupled Plasma Mass Spectroscopy (ICP-MS) in untreated PNT1A, LNCaP, DU145 and PC3 cells. (B) Baseline intracellular free zinc (Zn2+) concentration (nM) was measured using a FluoZin-3 fluorescent probe in the same 4 prostate cell lines. Zn (nM) = Kd x (F-Fmin)/(Fmax-F) was used to calculate zinc concentration. Intracellular Zn2+ uptake following exposure to 10 μM (C) or 50 μM (D) ZnCl2 for 4 or 24 hours was measured in PNT1A and PC3 cells. ***p < 0.001 PNT1A vs. PC3 ##p < 0.05 and ##p < 0.01. Values are expressed as the mean ± SEM of at least three separate experiments.
Nearly all intracellular Zn2+ ions are tightly bound to proteins and are considered inactive with regard to dynamic biological processes. The very small fraction of free Zn2+ ions is biologically active and critical to the physiological functions of the cell. A transformation in the pool of free Zn2+ caused by carcinogenesis could dramatically alter enzymatic reactions and nuclear transcription, thus altering normal cellular functions, including increased survival. Therefore, the concentration (nM) of free Zn2+ ions was quantified using a fluorescent indicator specific for Zn2+ (FluoZin-3) in all four prostate cell lines (Figure 1B). Basal free Zn2+ concentration (nM) was 4.5 ± 0.2, 2.8 ± 0.3, 6.4 ± 0.3 and 6.8 ± 0.5 in PNT1A, LNCaP, DU145 and PC3 cells, respectively. The CRPC-like PC3 and DU145 cells contained significantly higher, and the androgen-sensitive LNCaP cells significantly lower, free Zn2+ compared to PNT1A cells (p < 0.01).
To rule out the possibility that a difference in Zn2+ uptake between PC3 and PNT1A cells could account for the higher free Zn2+ in PC3 cells, intracellular free Zn2+ was measured using FluoZin-3 following treatment of both cell types with 10 μM Zn2+. Surprisingly free Zn2+ was actually higher in PNT1A cells than in PC3 cells (Figure 1C). At a higher Zn2+ concentration of 50μM, the fold increase in intracellular free Zn2+ was similar in both cell lines (p > 0.05) (Figure 1D). Thus the increased free Zn2+ in PC3 cells is not due to more rapid Zn2+ uptake.
To investigate further the disparity in Zn2+ homeostasis between PC3 and PNT1A cells, the distribution of Zn2+ was evaluated using MitoTracker Red FM (a far red-fluorescent mitochondrial dye) and Hoechst 33342 (a blue nuclear DNA stain) in combination with FluoZin-3 (a green Zn2+ indicator). Untreated PC3 cells (Figure 2A) appeared to have larger, distinct intracellular Zn2+ pools, which were located more peripherally than in PNT1A cells (Figure 2B). Following exposure to 10μM ZnCl2, Zn2+ was rapidly (30 min) co-localised to the mitochondria in both cell lines as assessed by coalescence of green and red fluorescence to form yellow. This phenomenon persisted for up to 120 min in PNT1A cells, and beyond 240 min in PC3 cells, before distinct Zn2+ pools reappeared similar to the appearance of untreated control cells. The scatter plots in Figure 2A and Figure 2B illustrate the prolonged co-localisation of Zn2+ to the mitochondria. The Pearson correlation coefficient (PCC) has been recommended as the gold-standard assessment tool to quantify the degree of co-localisation between two fluorophores . Zn2+ was localised to the mitochondria in both the cell lines at 120 min post Zn2+ treatment, however at 240 min a clear divergence in behaviour of each cell line was visible with PNT1A cells rapidly returning to the pre-treatment distribution but PC3 cells continuing to localise Zn2+ to the mitochondria (p < 0.001) (Figure 2C). Thus baseline free Zn2+, Zn2+ uptake and subsequent subcellular distribution of Zn2+ in CRPC-like PC cells was strikingly different to normal prostate epithelial cells.
Figure 2: Co-localisation of Zn2+ to mitochondria in prostate cells. (A) PC3 cells and (B) PNT1A cells were exposed to 10 μM ZnCl2 for 30, 120 and 240 minutes and stained with Hoechst (DAPI), FluoZin-3 (FITC) and MitoTracker (TRITC) fluorescent dyes. Immunofluorescent microscopy images were acquired at 60× (oil immersion) magnification using a Nikon DS-Qi 1Mc Camera with 250 ms, 120 ms and 35 ms exposure times for DAPI, FITC and TRITC channels respectively. Composite images were created by merging blue (DAPI), green (FITC) and red (TRITC) channels. FITC and TRITC colour intensity for each pixel in the corresponding composite image is plotted on scatter plots. (C) Co-localisation of Zn2+ to mitochondria for PNT1A and PC3 cells was estimated using Pearson correlation coefficient between FITC (FluoZin-3) and TRITC (MitoTracker) colours. Values are expressed as fold change compared to time 0 hours. Statistical significance for the PNT1A vs. PC3 comparison was determined using the Bonferroni-Sidak method with α = 0.05. ***p < 0.001. Values are expressed as the mean ± SEM of at least three separate experiments.
Exogenous Zn2+ is cytotoxic to prostate cells at high doses
The effect of zinc ions on prostate cell lines was investigated in vitro in order to ascertain the sensitivity to Zn2+ of normal prostate cells compared to cancer cells. The dose-response of normal prostate (PNT1A), androgen-sensitive (LNCaP) and CRPC-like prostate cancer cells (PC3) to Zn2+ (ZnCl2) was measured using an MTT cell survival/proliferation assay. All cell lines tolerated exposure to low ZnCl2 concentrations (12.5 μM) for 24 hours with 93%, 91% and 113%, of PC3, LNCaP and PNT1A cells surviving, respectively (Figure 3A). However, at 25 μM Zn2+ cell survival was 19% in PC3 and 28% in LNCaP compared to 104% in PNT1A cells. Furthermore at a higher concentration (50 μM) Zn2+ was cytotoxic to all three cell lines. This observation suggests that normal prostate epithelial cells can survive better in the presence of higher concentrations of Zn2+ than prostate cancer cells.
Figure 3: Zinc chloride treatment inhibits in vitro cell proliferation in CRPC-like PC3 cells. (A) Cell viability in PNT1A, LNCaP and PC3 cells after 48 hours of exposure to various concentration of ZnCl2 was analysed by MTT assay. Proliferation of cells exposed to serum-free medium only (Ctrl) or to ZnCl2 was assessed by MTT assay at 0, 24, 48 and 72 hours respectively in (B) PC3, (C) PNT1A and (D) LNCaP cells. Statistical analysis using one-way ANOVA (Ctrl vs. Zinc) was performed *p < 0.05, **p < 0.01 and ***p < 0.001. Values are expressed as the mean ± SEM of at least three separate experiments. (E) PC3 xenograft tumour volume in SCID mice in three treatment arms: control (n = 7), ZnCl2 3mg/Kg (n = 3) and ZnCl2 10mg/Kg (n = 7). Arrows represent the days of ZnCl2 or saline (control) IP injection. The percentage increase compared to day 0 was calculated and the mean ± SEM plotted. Statistical analysis was calculated by two-way ANOVA. #p < 0.05, ZnCl2 3 mg/Kg versus control.
Accumulation and utilisation of Zn2+ is a significant property of prostate epithelial cells. We investigated the effect of Zn2+ on PC cell proliferation in vitro and in vivo. A low well tolerated dose of ZnCl2 (10 μM) was selected for a long-term (72 hour) MTT cell proliferation assay. At 72 hours relative cell numbers increased 3.8 ± 0.5 fold in Zn2+-treated PC3 cells, and the increase was significantly lower than in untreated cells which increased by 6.6 ± 0.8 fold (p < 0.001) (Figure 3B). Exposure to Zn2+ had a significant effect on proliferation of PNT1A but no effect on LNCaP cells (Figure 3C and 3D). The possibility that serum starvation might affect the viability was confirmed in the case of normal prostate PNT1A cells as viability was decreased at the 72 hr time point under serum starvation either in the presence or absence of zinc (Ctrl). In contrast cancer ous LNCaP and PC3 cells maintained viability over 72 hr.
To supplement the in vitro observations of the effects of Zn2+ on PC cell proliferation, SCID mice with established PC3 xenograft tumours were injected twice weekly with ZnCl2 (3 mg/kg or 10 mg/kg) (Figure 3E). Mice were randomised (up to n = 7 per group) to either Zn2+-treated or control groups. Tumour volumes (mm3) were measured daily with micro-callipers and the values expressed as percentage increase compared to day zero. No significant difference in tumour volume was observed over the 2 week treatment period. In addition, treatment with the Zn2+ chelator TPEN at 3 mg/Kg or 10 mg/Kg had no effect on tumour growth. Thus Zn2+ does not stimulate or inhibit prostate tumour growth in vivo. Furthermore a higher dose of Zn2+ (20 mg/Kg) was toxic and all mice in this treatment group were culled after a maximum of 2 doses (data not presented). A higher dose of TPEN (20 mg/Kg) also resulted in toxicity.
Zn2+ augments resistance of PC3 cells to oxidative stress
Our previously published study revealed that LNCaP cells, which contain low free Zn2+, are more sensitive to oxidative stress than PC3 cells, which contain high free Zn2+ . Therefore, we hypothesized that the higher free Zn2+ concentration in CPRC-like DU145 and PC3 cells, compared to either normal prostate PNT1A cells or androgen sensitive LNCaP cells, may be responsible for the increased resistance of CRPC-like cells to various stresses. Indeed the basal IC50 value for resistance to H2O2 was significantly higher at 45.3 μM for PC3 cells compared to 1.8 μM in PNT1A cells (Figure 4A). Furthermore exogenous Zn2+ can further increase resistance to oxidative stress by H2O2 in PC3 cells (with a maximal 2.3 fold greater survival at 10μM Zn2+) (Figure 4B), but not in benign PNT1A cells (Figure 4C).
Figure 4: Zn2+ mediated protection against oxidative stress injury in PC3 cells. (A) Cell survival/proliferation was measured by MTT assay. The data demonstrates increased resilience in PC3 cells compared to PNT1A under oxidative stress induced by increasing concentrations of H2O2. Cell survival was measured by MTT assay in (B) PC3 and (C) PNT1A cells preconditioned with the indicated concentrations of ZnCl2 for 4 hours followed by oxidative stress (75 μM H2O2 for 24 hours). Values are expressed as the mean ± SEM of at least three separate experiments.
Zn2+ induces HIF1α in prostate cancer cells
HIF1α is a transcription factor that initiates molecular responses to protect against cellular injury. Expression of HIF1α is upregulated by hypoxia and also by Zn2+ ions . We have previously demonstrated that HIF1α is overexpressed in PC3 compared to LNCaP cells under normoxic conditions and that it contributes to resistance to H2O2 and chemotherapeutics such as 5-fluorouracil . Therefore in this study, the basal expression of HIF1α in PNT1A cells, which contain low concentrations of free Zn2+, was compared to PC3 cells. Basal expression of HIF1α was significantly greater (21 ± 5 fold) in PC3 cells compared to LNCaP cells (p < 0.01) (Figure 5A). Interestingly, normal PNT1A cells expressed up to 4.5 ± 2.3 fold more HIF1α protein than LNCaP cells, and another CRPC-like cell line (DU145) expressed 12.0 ± 3.6 fold higher HIF1α protein. Overall there was a linear correlation (r2 = 0.97) between HIF1α expression and concentration of free Zn2+ in untreated normal prostate epithelial and PC cell lines (Figure 5B). Exogenous Zn2+ further increased expression of HIF1α in a dose- and time-dependent manner in PC3 cells, with a maximal increase of 8.9 ± 2.4 fold at 10 μM Zn2+ (Figure 5C). Maximal stimulation of HIF1α expression was observed in PNT1A cells at 50 μM Zn2+, a concentration which was cytotoxic to PC3 cells (Figure 5D). HIF1α stimulation by Zn2+ in PC3 cells was time dependent and occurred as rapidly as 2 h post-exposure (Figure 5E). Increased HIF1α expression was only seen after 24 h in PNT1A cells (Figure 5F).
Figure 5: Zn2+ induces HIF1α protein expression in PC3 cells in a time- and dose-dependent manner. (A) Baseline normoxic HIF1α expression is high and (B) correlates with free Zn2+ concentration in PC cells. HIF1α protein expression following treatment with increasing concentrations of ZnCl2 for 24 hours was analysed by Western blot in (C) PC3 and (D) PNT1A cells. Zinc ion-stimulated HIF1α protein expression was measured at the indicated times by Western blot in (E) PC3 and (F) PNT1A cells. *p < 0.05, **p < 0.01 and ***p < 0.001. Values are expressed as the mean ± SEM of at least three separate experiments.
Resistance to oxidative stress in PC3 cells is regulated by HIF1α
Having observed a protective effect of exogenous Zn2+ in wild-type PC3 cells, in order to test the hypothesis that this protection was HIF1α dependent, the ability of Zn2+ to protect against oxidative stress was examined in a clone of PC3 cells which had been transfected with HIF1α shRNA (HIF1α knock-down or HIF1α-KD cells) . As demonstrated in Figure 6A, HIF1α expression in the HIF1α-KD cell line was reduced by nearly 50% to 0.50 ± 0.06 fold compared to wild-type PC3 cells. Pre-conditioning with ZnCl2 (10 μM for 4 hours) significantly increased HIF1α expression by 15.4 ± 3.5 fold in PC3 cells (p < 0.001) (Figure 6B). A smaller fold increase in HIF1α expression of 4.5 ± 1.5 was observed in HIF1α-KD PC3 cells. Furthermore, in the HIF1α-KD PC3 cell line a significant protective effect of Zn2+ pre-conditioning against oxidative injury was not observed (Figure 6C), unlike the previous results in wild-type PC3 cells (Figure 4B). The reduction in the protection conferred by Zn2+ in HIF1α-KD cells implies that HIF1α is an important component of the Zn2+-dependent protective mechanism present in PC3 cells. However, as there was some protection still evident in the Zn2+-pre-conditioned HIF1α-KD cells, Zn2+ ions might be activating alternate mechanisms.
Figure 6: The protective role of Zn2+ against oxidative injury in PC3 cells is HIF1α dependent. A HIF1α knock-down PC3 cell line (HIF1α-KD) was created by transfection of a shRNA vector expressing HIF1α into wild-type (WT) PC3 cells resulting in (A) suppression of HIF1α expression on Western blot. (B) HIF1α protein expression in PC3-WT and PC3-HIF1α-KD cells following pre-treatment with 10μM ZnCl2 for 4 hours was measured by Western blot. (C) Survival/proliferation was measured by MTT assay in HIF1α-KD cells following preconditioning with ZnCl2 for 4 hours then exposure to oxidative stress (75 μM H2O2 for 24 hours). Values are expressed as the mean ± SEM of at least three separate experiments.
Zn2+ ions competitively inhibit HIF1α degradation by displacing Fe2+ ions
In many cell types HIF1α is degraded under normoxic conditions by two key sequential processes: firstly the hydroxylation of HIF-α subunits, by prolyl-hydroxylase (PHD) enzymes in an oxygen- and iron (Fe2+)-dependent reaction, promotes binding to the pVHL-E3-ubiquitin complex, and secondly HIF1α is destroyed by proteasomal degradation . However, in PC cells under normoxia HIF1α degradation is minimal and there is no decrease in HIF1α translational activity. The exact mechanism is unknown but the available evidence suggests that Zn2+ ions compete with Fe2+ ions for binding at the active sites of PHDs [13, 14]. In agreement with this hypothesis treatment of CRPC-like cells, which in normoxic conditions over-express HIF1α, with ammonium ferric citrate (AFC) resulted in the degradation of HIF1α to 29% and 20% in DU145 and PC3 cells, respectively, compared to untreated control cells (Figure 7A). More importantly, in the presence of iron, Zn2+ rescued HIF1α expression by 3.5 ± 0.95 fold compared to virtually complete degradation of the HIF1α protein in cells treated with AFC alone (p < 0.05) (Figure 7B). These observations are consistent with the above hypothesis that Zn2+ ions stabilise the HIF1α protein in the presence of oxygen in PC cells by competing with Fe2+ ions for binding at the PHD active site (Figure 7D).
Figure 7: Zn2+ ions competitively inhibit HIF1α degradation by displacing Fe2+ ions. (A) HIF1α protein was degraded in the presence of ammonium ferric citrate (AFC) in DU145 and PC3 cells. (B) The reduction in HIF1α expression in the presence of iron was partially reversed by Zn2+ in PC3 cells. Values are expressed as the mean ± SEM of at least three separate experiments. (C) In a normal prostate epithelial cell (PNT1A) under normoxic conditions, the pathway for HIF1α degradation pathway is activated. Proteasomal degradation is achieved by binding to the pVHL-E3-ubiquitin complex mediated by prolyl-hydroxylase (PHD) enzymes which require the co-factors iron (Fe2+), ascorbate and 2-oxoglutarate. (D) In CRPC cells (PC3) under the same normoxic conditions the HIF1α pathway is inhibited by Zn2+ ions, which substitute for Fe2+ ions at the PHD binding site, and also potentially reduce the co-factor 2-oxoglutarate via mAC inhibition in the citric acid cycle. Ultimately HIF1α is overexpressed in CRPC leading to increased transcription of genes responsible for glucose metabolism, proteolysis, cell survival, erythropoiesis and angiogenesis.
Zn2+ is essential for cell proliferation and especially for the regulation of DNA synthesis and mitosis, and Zn2+ deficiency leads to inhibition of growth [15, 16]. Zn2+ stimulates Hep-2 tumour cell proliferation and mitogenic signalling , and conversely inhibits proliferation and invasion/migration in some cells including prostate cancer cells . In this study, we have demonstrated that exogenous Zn2+ (greater than 15μM) is cytotoxic to prostate cancer cells in vitro. Furthermore as normal PNT1A prostate cells had higher IC50 values for Zn2+ toxicity compared to prostate cancer PC3 cells we concluded that prostate cancer cells are more sensitive to the cytotoxic effect of Zn2+ compared to normal cells. In another study, IC50 values of Zn2+ treatments were 194 μM for non-tumour PNT1A cells and 94 μM for PC3 tumour cells . The discrepancy in IC50 values between the two studies may be attributed to the fact that MTT assays in the Masarik et al. study were carried out in the presence of FBS which would confer a putative survival advantage [20, 21]. Our results are in agreement with a previous study where CRPC-like DU145 cells were shown to be more sensitive to Zn2+ than another normal prostate cancer cell line RWPE-1 . Overall, these observations suggest Zn2+ has a cytotoxic effect on prostate cancer cells in vitro and, because of this anti-proliferative effect, Zn2+ has been hypothesised to be a tumour suppressor in prostate cancer .
However, if Zn2+ is to be effective as an anti-cancer therapy, its cytotoxic effects need to be observed in vivo. Shah et al.  injected zinc acetate directly into PC3 xenograft tumours and observed a significant reduction in tumour volume. The concentration of Zn2+ administered in the Shah et al. study  equates to 3mM ZnCl2, which would immediately be toxic to both normal and cancerous cells, as demonstrated in vitro in (Figure 3A). Although intra-tumoural injection in a mouse xenograft tumour model is achievable, the multifocal nature of prostate tumours limits its application in the clinic. Previously a mouse xenograft study using PC3 cells demonstrated that a sustained subcutaneous dosage of zinc sulfate (0.51 mg elemental Zn over 28 days) increased the plasma Zn2+ concentration by ~90%, and resulted in ~50% inhibition (P < 0.05) of tumour growth [25, 26]. In contrast, our results demonstrated that 10 mg/kg ZnCl2 (0.4 mg elemental Zn over 14 days) treatment has neither an accelerating nor inhibiting effect on tumour growth (Figure 3E). Previously a single intra-peritoneal injection of 10 mg/kg ZnCl2 into SCID mice has been shown to increase free intracellular Zn2+ and induce gastrin gene expression in colon cancer cells grown as xenograft tumours  and two subcutaneous injections of 10 mg/kg ZnCl2 into rats protects against renal ischemia reperfusion injury . This suggests that ZnCl2 at a10 mg/kg dose is able to stimulate a multitude of biological effects without any toxicity. It could be argued that the 10 mg/kg ZnCl2 dose was not enough to cause anti-tumour effects and that a higher Zn2+ dose would have reduced tumour growth. However the fact that 20 mg/kg ZnCl2 resulted in severe toxicity in mice precludes the use of high doses of Zn2+.
Interstitial fluid normally contains 2 to 5μM Zn2+, and a cytotoxic effect of Zn2+ is observed at concentrations significantly higher than this normal range [24, 27–30]. A lower non-toxic dose of Zn2+ did not affect the proliferation of LNCaP prostate cancer cells (Figure 3D). Interestingly Zn2+ treatment slowed the proliferation of CRPC-like PC3 cells (Figure 3B) to a much greater degree compared to normal prostate PNT1A cells (Figure 3C). However this was not due to any difference in the uptake of Zn2+ because normal PNT1A cells increased intracellular free Zn2+ equally, rapidly and to a greater degree than PC3 cells exposed to 10 μM ZnCl2 (Figure 1C). Furthermore, Masarik et al  and Kriedt et al  demonstrated that PC3 cell viability is compromised at earlier Zn2+ exposure times and lower doses than low grade LNCaP prostate cancer cells. It seems that an increase in intracellular free Zn2+ does not necessarily lead to greater proliferation as previously observed . However the observation that the migration of PC3 and DU145 cells, which contain high intracellular free Zn2+ is high compared to LNCaP cells which contain low free Zn2+  suggests a role of intracellular Zn2+ ions in generation of the non-proliferative but migratory and chemo-resistant phenotype  synonymous with CRPC tumors. Overall these results highlight a distinct effect of Zn2+ on CRPC-like cells and suggest that the increase in extracellular Zn2+ may not be as important as how the cells regulate and cope with a rapid increase in intracellular Zn2+. The possibility that Zn2+ homeostasis is altered in CRPC-like cancer cells compared to normal cells needs to be investigated.
In human prostate specimens’ total Zn2+ concentrations decrease with PC development [2, 33–35]. In vitro, although the mean endogenous concentration of Zn2+ in LNCaP cells was higher than in PC3 cells, the Zn2+ concentrations were not compared to normal prostate cells . A previous study by Qin et al.  reported a significant reduction in total Zn2+ in LNCaP cells compared to normal epithelial RWPE1 cells using ICP-MS. However, the fact that RWPE1 cells were cultured in keratinocyte serum-free medium (KSFM) which contains 0.7 μM Zn2+ , while LNCaP cells were grown in RPMI which does not contain any detectable amount of Zn2+ questions the validity of such results. To overcome these limitations in the current study total Zn2+ concentrations were compared by ICP-MS in four prostate cell lines (PNT1A, LNCaP, DU145 and PC3) which were all cultured in the same media (RPMI), and in the absence of any serum which may influence total Zn2+ concentrations [20, 21]. The ICP-MS data suggests that there is no correlation between normal and cancerous PC cells in vitro in terms of total Zn2+ concentrations, although LNCaP cells did contain higher Zn2+ than PC3 cells as published previously .
In a normal cell, a large proportion of intracellular Zn2+ is bound and only a very small proportion is free. An increase in intracellular free Zn2+ ions (the “Zn wave”) may therefore be more relevant in orchestrating downstream biological effects such as increased survival or migration [31, 39]. Interestingly, recent studies have revealed that while total Zn2+ is reduced in prostate cancer cells, cytosolic free Zn2+ is actually higher, emphasizing the importance of measuring free Zn2+ . Such an increase in free cytosolic Zn2+ can be attained either by activation of receptors [31, 40, 41] or by increased uptake via Zn2+ transporters/channels. Measurement of free (also called labile or loosely bound) Zn2+ using the Zn2+-specific fluorescent probe FluoZin-3 demonstrated that at baseline CRPC-like PC3 and DU145 cells contained a significantly higher concentration of free Zn2+ than normal PNT1A cells or low grade androgen-sensitive LNCaP cells. Furthermore calculation of Pearson’s coefficient for the fluorescence microscopy studies indicated that, while both PC3 and PNT1A cells increased Zn2+ in the mitochondria in the first 30 min of treatment with exogenous Zn2+, only PC3 cells maintained Zn2+ in the mitochondria at 4h post initiation of the treatment. It has been suggested that Zn2+ may be sequestered in the mitochondria to prevent cytotoxicity . If so, then Zn2+ should have been less toxic to PC3 cells compared to PNT1A cells, which was not the case. Overall the hypothesis of Zn2+ dys-homeostasis in PC is supported by data from Masarik et al.  who demonstrated that the free-to-bound Zn2+ ratio was much higher in untreated PC3 cells compared to PNT1A cells. Masarik et al. also noted that Zn2+ was localised in and around nuclei and in the inner part of the cytoplasm in the form of ‘spots’ in PC3 cells which were not seen in PNT1A cells.
Accumulation of high mitochondrial Zn2+ concentrations in specific prostate cells results in the induction of apoptosis and the inhibition of cell growth . The opposing notions of the observed ability of Zn2+ to be either anti-apoptotic or pro-apoptotic may in part be due to the ability or lack thereof of the mitochondria in different cells to respond directly to the effects of Zn2+ . Zn2+ ions decrease cell viability and mitochondrial succinate dehydrogenase activity in CRPC-like PC3 cells and benign prostatic hyperplasia epithelial BPH-1 cells . Further mitochondrial Zn2+ accumulation has been shown not only to severely impede mitochondrial enzymes such as aconitase, 2-oxoglutarate dehydrogenase, NAD+-dependent isocitrate dehydrogenase, and succinate dehydrogenase, but also to induce oxidative stress [45, 46]. These studies raised the possibility that as PC3 cells accumulate greater amounts of Zn2+ for a longer period in the mitochondria they may be more sensitive to oxidative stress compared to PNT1A cells. On the contrary, CRPC-like PC3 cells are more resistant to H2O2 treatment than PNT1A cells, and also exogenous Zn2+ at a non-toxic dose can increase further the resistance to oxidative stress. Previously, we have shown that the survival rates of PC3 cells following treatment with either H2O2 or the chemotherapeutic 5-fluorouracil were significantly greater compared to LNCaP cells via a HIF-dependent mechanism .
Hypoxia inducible transcription factors induce diverse genes involved in cell survival, angiogenesis, glucose metabolism and invasion and play an important role in cancer progression . HIF1α degradation normally occurs via oxygen- and iron-dependent prolyl-hydroxylation by prolyl hydroxylase domain-containing protein (PHD) . CRPCs by their nature are extremely resistant to chemotherapy, and we have previously shown an association between HIF1α and resistance to cytotoxic agents [9, 48]. The observation made nearly two decades ago by Zhong and co-workers that PC3 cells overexpress HIF1α even in the presence of oxygen [49, 50] is a very reproducible and robust phenotypic characteristic of CRPC-like cells although the mechanism is unclear. Further the role of Zn2+ in HIF1α expression is unclear. Nardinocchi et al  showed that exogenous Zn2+ suppressed both HIF1α and HIF2α protein expression. In contrast, Jeong et al.  reported a Zn2+-mediated dose dependent stimulation of HIF1α protein expression in DU145 and PC3 cells and that HIF1α plays a crucial role in the regulation of zinc resistance [52, 53]. More recently, we have shown that Zn2+ induces expression of HIF1α in normal HK-2 renal tubular cells as well as in ACHN renal cancer cells . In this study we have shown a strong correlation between the concentration of free Zn2+ and HIF1α expression in prostate cells (Figure 5B) but, more importantly, that exogenous Zn2+ stimulates HIF1α expression in a time- and dose-dependent manner in PC3 cells with a simultaneous increase in resistance to cytotoxics such as H2O2 (Figure 4A). Furthermore, as knockdown of HIF1α reduced survival of PC3 cells, even in the presence of Zn2+, we concluded that the Zn2+-dependent increase in resistance to oxidative stress may in part be via a HIF1α-dependent mechanism in CRPC-like cells.
Our current study using CRPC-like DU145 and PC3 cells confirms previous observation by Knowles et al  that HIF1α protein expression in reduced in the presence of exogenous iron. More importantly we have establish that exogenous Zn2+ was able to reverse the reduction in HIF1α expression in the presence of exogenous iron in PC3 cells (Figure 7B). Overall we postulate that increased free Zn2+ in CRPC-like PC3 and DU145 cells may displace the Fe2+ binding at the PHD site and thereby results in increased stabilization of the HIF1α protein under normal oxygen conditions.
The role of zinc in prostate cancer has been investigated because of changes in the total amount of zinc compared to the normal prostate. Based on the evidence that in prostate cancer the amount of Zn is reduced, it was postulated that re-establishing normal intracellular Zn2+ concentrations in prostatic tumours might restore a benign phenotype in malignant prostate cells. However, in contrast Kratochvilova et al. and Holubova et al. have convincingly showed that exogenous Zn2+ drives tumour cells towards a more aggressive and resistant phenotype [53, 55].
In conclusion, a state of Zn2+ dys-homeostasis in PC exists as demonstrated by the increased availability and subcellular distribution of free Zn2+ in PC3 cells. Expression of basal HIF1α correlates with free Zn2+ concentration in PC cell lines. HIF1α protein can be further increased by exogenous Zn2+ in a dose- and time-dependent manner in PC3 cells. Zn2+ enhances PC3 cell survival under oxidative stress, an effect not seen in PNT1A cells or in a HIF1α-KD PC3 cell model. Therefore HIF1α is an integral component of a Zn2+-dependent protective mechanism in PC3 cells. Based on these findings it can be hypothesized that free Zn2+ is more relevant especially in CRPC. Furthermore there are no studies which have specifically looked at the role of Zn2+ in the chemo-resistant phenotype of CRPC, although the role of HIF1α as a downstream mediator of Zn2+ is well established in CRPC . Further studies will be required to establish firstly, if such Zn2+ dys-homeostasis may be clinically significant through its contribution to castrate-resistant PC survival and secondly, whether or not Zn2+ chelation therapies are effective in counteracting the resistance to treatment of CRPC.
MATERIALS AND METHODS
Cell culture and treatment
Normal prostate epithelial cells (PNT1A) were purchased from The European Collection of Cell Cultures (ECACC). Three human prostate cancer cell lines (PC3, DU145 and LNCaP) were purchased from the American Type Culture Collection (Manassas, VA). All cell lines were cultured in Roswell Park Memorial Institute (RPMI) medium (Scoresby, VIC) which was supplemented with 7.5% Fetal Bovine Serum (FBS), 0.4% Penicillin-Streptomycin and 2% HEPES. HIF1α knock-down PC3 cells (HIF1α-KD) were used as previously described  .
HIF1α protein was analysed by Western blot using the method previously described  with a primary HIF1α purified mouse anti-human antibody at dilution 1:1000 (BD Biosciences, USA) followed by a secondary anti-mouse horseradish peroxidase-conjugated antibody (1:5000, Bio-Rad). GAPDH was assayed as a loading control with a rabbit monoclonal GAPDH antibody (1:10000, Cell Signaling, USA).
MTT cell proliferation assay
Cells were cultured as described above and trypsinised at 80% confluency. For the MTT cell survival assay cells were plated into a 96-well plate (1.0 × 104 cells/well) and incubated in media containing 7.5% serum for 24 hours. For Zn2+ treatment ZnCl2 in serum free media (SFM) was added to 12.5 μM, 25 μM or 50 μM, and the cells were incubated for 48 h. For long-term cell proliferation assays cells were plated in four 24-well plates (2.5 × 104 cells/well) representative of each time point (0, 24, 48 and 72 hour) and incubated in SM for 24 h. Next day a MTT assay was performed on one plate to determine the relative cell numbers prior to the start of zinc treatment. The values were recorded as the 0 hr absorbance reading. Cells in the rest of the plates were treated with either 10 μM ZnCl2 (10 μM in SFM) or serum free medium only and incubated for 24, 48 or 72 hours. MTT stock solution (5 mg/ml) (Sigma Aldrich, USA) was prepared in 1× PBS and 10 μL/well added. After incubation with MTT solution for 1 h and following the solubilization of formazan crystals in acidified isopropanol the absorbance, which is directly proportional to cell numbers, was measured at a wavelength of 570 nm with background subtraction at 620 nm using a FLUOstar Optima Microplate Reader (BMG Labtech, Mornington, VIC). Data are expressed as a percentage of the 0 hr reading taken just prior to zinc treatment.
H2O2 survival assay
Cells were plated on a 12-well plate (1.2 × 105 cells/well) and incubated in culture medium for 24 h. For Zn2+ pre-conditioning ZnCl2 in SFM was added to the indicated final concentrations between 0.1 μM to 50 μM, and the cells were incubated for 4 h, and the media was then replaced with H2O2 (25 μM, 50 μM, 75 μM or 100 μM) in SFM for 24 h. MTT analysis was performed as described above.
FluoZin-3 free Zn2+ assay
Cells were plated on a black 96-well plate (1.0 × 104 cells/well) and incubated overnight. Zn2+ (10 μM or 50 μM ZnCl2 in SFM) was added for 1, 4 or 24 h. 10 μM TPEN or 500 μM ZnCl2 were added for 1 h for measurement of Fmin or Fmax, respectively. FluoZin-3 (AM, cell permeant, F-24195, Life Technologies) was added to a final concentration of 5 μM (50 μl/well) and the 96 well plates were covered with foil to protect them from light. Samples were equilibrated for 30 min before the dye was removed and replaced by Hank’s balanced salt solution (HBSS) for 15 min. The resulting fluorescence was recorded on a FLUOstar Optima Microplate Reader (BMG Labtech, Mornington, VIC). Free Zn2+ (nM) was calculated according to the manufacturer’s instructions with the formula: Zn2+ = Kd × (F-Fmin)/(Fmax-F), where the Kd for FluoZin-3 is 15 nM.
Fluorescence microscopy (FM)
PNT1A and PC3 cells were mounted onto coverslips overnight then ZnCl2 (10 μM in SFM) was added for 30, 60, 120 or 240 min. FluoZin-3 (2.5 μM), MitoTracker Red FM (50nM) or Hoechst 33342 (0.2 μg/mL) was added for 45 min at 37°C in the dark and then fixed by treatment with 4% paraformaldehyde for 3 min. A Nikon DS-Qi 1Mc camera and NIS Nikon Elements Software were used to take separate and composite images, from which mean Pearson correlation coefficient (PCC) values were calculated from 10 images per treatment per cell line.
Metal analysis by Inductively Coupled Plasma Mass Spectroscopy (ICP-MS)
For measurement of total zinc 5.0 × 105 cells for each cell line (PNT1A, LNCaP, DU145 and PC3) were cultured in 60mm cell culture dishes in 5mls serum media overnight. Next day serum media was aspirated and cells were washed briefly for 10–20 seconds with 2mLs of Milli-Q water. A final volume of 500μL of Milli-Q water was added and cells were scraped and the lysate collected into a 1.5 mL eppendorf tube. Cell lysates were freeze-dried, nitric acid (50 μL of 65%, Suprapur, Merck) was added to each cell pellet, and the pellets were digested overnight at room temperature. The samples were heated using a heating block at 90°C for 20 min to a volume of ~40 μL. To each sample 460μL of 1% (v/v) of nitric acid diluent was added to a final Volume of 0.5 mL. Measurements were made using an Agilent 7700 series ICP-MS instrument under routine multi-element operating conditions using a helium reaction gas cell. The instrument was calibrated using 0, 5, 10, 50, 100 and 500 ppb of certified multi- element ICP-MS standard calibration solutions (ICP-MS-CAL2-1, ICP-MS-CAL-3 and ICP-MS-CAL-4, Accustandard) for a range of elements. A certified internal standard solution containing 200 ppb of Yttrium (Y89) was used as an internal control (ICP- MS-IS-MIX1-1, Accustandard).
In vivo study
The animal studies (project number A2014/05210) were approved by the Animal Ethics Committees of Austin Health, Victoria, Australia, in accordance with the guidelines laid down by the National Health and Medical Research Council of Australia’s Code of Practice for the Care and Use of Animals for Experimental Purposes. Certified severe combined immunodeficiency (SCID) male mice, aged > 4 weeks were purchased from the Animal Resource Centre (Perth, Australia) and housed in the BioResources Facility (Austin Health). PC3 cells were injected into the flanks of the mice and xenograft tumours were allowed to develop. Tumour volumes were measured daily and mice were randomised to treatment or control groups when the tumour volume was > 200 mm3. Treatment consisted of twice-weekly intra-peritoneal injections of ZnCl2 or the Zn2+ chelator TPEN (Sigma-Aldrich, Australia) (3 mg/Kg, 10 mg/Kg or 20 mg/Kg) until the tumour volume exceeded 1000 mm3. Xenograft tissue was harvested for immunohistochemistry (IHC) and Zn2+ analysis. Zinc chloride was dissolved in 0.1% HCL in injection water and diluted to a final concentration of 1 μg/μL in saline. TPEN (Sigma-Aldrich) was dissolved in DMSO and diluted with saline to a final concentration of 1 μg/μL. The final DMSO concentration w as < 4.0 %.
Statistics were analysed with GraphPad Prism (Version 7). All experiments were repeated in triplicate. Values are expressed as mean ± standard error of the mean (SEM). Statistical significance for single comparisons of normally distributed data was determined by a two-way Student’s t test. For multiple comparisons, one-way ANOVAs followed by the Bonferroni correction were performed. Statistical significance was determined by p value < 0.05 (borderline significant), p < 0.01 (moderately significant) and p < 0.001 (strongly significant).
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