2-Deoxy-D-glucose enhances TRAIL-induced apoptosis in human melanoma cells through XBP-1-mediated up-regulation of TRAIL-R2
Molecular Cancervolume 8, Article number: 122 (2009)
Past studies have shown that sensitivity of melanoma cells to TRAIL-induced apoptosis is largely correlated with the expression levels of TRAIL death receptors on the cell surface. However, fresh melanoma isolates and melanoma tissue sections express generally low levels of death receptors for TRAIL. The clinical potential of TRAIL in the treatment of melanoma may therefore be limited unless given with agents that increase the cell surface expression of TRAIL death receptors. 2-Deoxy-D-glucose (2-DG) is a synthetic glucose analogue that inhibits glycolysis and glycosylation and blocks cell growth. It has been in clinical evaluation for its potential use as an anticancer agent. In this study, we have examined whether 2-DG and TRAIL interact to enhance their cytotoxicity towards melanoma cells.
2-DG did not kill melanoma cells, but enhanced TRAIL-induced apoptosis in cultured melanoma cells and fresh melanoma isolates. This was associated with increased activation of the caspase cascade and mitochondrial apoptotic pathway, and was blocked by inhibition of TRAIL-R2, and to a lesser extent, inhibition of TRAIL-R1. Treatment with 2-DG up-regulated TRAIL death receptors, in particular, TRAIL-R2, on the melanoma cell surface. Up-regulation of TRAIL-R2 was due to increased transcription that was not dependent on the transcription factors, p53 and CHOP. Instead, the IRE1α and ATF6 pathways of the unfolded protein response that were activated by 2-DG appeared to be involved. Moreover, XBP-1, which is known to be transcriptionally regulated by ATF6 and functionally activated by IRE1α, was found to play an important role in 2-DG-mediated transcriptional up-regulation of TRAIL-R2 in melanoma cells.
These results indicate that 2-DG sensitizes human melanoma cells to TRAIL-induced apoptosis by up-regulation of TRAIL-2 via the ATF6/IRE1α/XBP-1 axis of the unfolded protein response. They suggest that 2-DG is a promising agent to increase the therapeutic response to TRAIL in melanoma.
TNF-related apoptosis-inducing ligand (TRAIL) appears to be a promising candidate for cancer therapeutics because of its ability to preferentially induce apoptosis in malignant cells [1–3]. The potential significance of TRAIL as an anti-cancer agent has been supported by studies in animal models showing selective toxicity to human tumor xenografts but not normal tissues [4, 5]. Induction of apoptosis by TRAIL is mediated by its interaction with two death domain containing receptors, TRAIL-R1 and -R2 [1–3]. This in turn orchestrates the assembly of the death-inducing signaling complex (DISC) that contains adapter components such as Fas associated death domain (FADD) that activates initiator caspases, caspase-8 and -10, leading eventually to activation of effector caspases such as caspase-3 and to apoptosis [1–3]. TRAIL and agonistic antibodies against its death receptors are currently in clinical evaluation for the treatment of various cancers [6–8].
We have previously shown that sensitivity of cultured melanoma cells to TRAIL-induced apoptosis is in general correlated with the levels of the cell surface expression of TRAIL death receptors, in particular, TRAIL-R2 [9, 10]. Subsequent studies demonstrated that fresh melanoma isolates are relatively resistant to TRAIL-induced apoptosis due to low levels of TRAIL-death receptor expression . Moreover, melanoma cells selected for TRAIL resistance by prolonged exposure to TRAIL express substantially reduced levels of TRAIL-R2 on their surface [12, 13]. Studies on melanoma tissue sections revealed that reduced TRAIL-R2 expression is associated with disease progression and a poor prognosis . Taken together, these studies indicate that melanoma may not respond to treatment with TRAIL unless given with agents that increase the cell surface expression of TRAIL death receptors, in particular, TRAIL-R2.
Cancer cells exhibit increased glycolysis and depend on this metabolic pathway for ATP production [15–17]. As a consequence, they need a high uptake of glucose and accelerated rates of glycolysis to survive. This metabolic feature has evoked much interest in development of glycolytic inhibitors as potential anticancer agents [16, 17]. Among them, 2-Deoxy-D-glucose (2-DG) is a synthetic glucose analogue that is phosphorylated by hexokinase upon transport into cells, but can not be fully metabolized [16–18]. 2-DG-6 phosphate accumulates in cells and interferes with glycolysis primarily by inhibition of phosphorylation of glucose by hexokinase, thus causing a depletion of ATP [16, 18]. 2-DG can also cause inhibition of protein glycosylation that induces endoplasmic reticulum (ER) stress and gives rise to activation of the unfolded protein response (UPR) [19, 20]. As a single agent, 2-DG has been shown to inhibit cell growth in a number of cancers, and to enhance the therapeutic efficacy of chemotherapeutic drugs in human cancer xenografts [21–23]. On the other hand, 2-DG has been reported to protect cancer cells from death by activation of the Akt and mitogen-activated protein kinase (MAPK) pathways .
The cellular response to ER stress, the UPR, consists of three distinct yet coordinated signaling pathways initiated respectively by inositol-requiring transmembrane kinase and endonuclease 1α (IRE1α), activation of transcription factor 6 (ATF6), and protein kinase-like ER kinase (PERK) [25–27]. As an adaptive response, the UPR is orchestrated by transcriptional activation of multiple genes mediated by IRE1α and ATF6, and a general decrease in translation initiation mediated by PERK, to alleviate the stress condition [25–27]. However, excessive and prolonged activation of the UPR can lead to apoptosis [25–27]. We have previously shown that, although melanoma cells are not sensitive to ER stress-induced apoptosis, activation of the UPR by the glycosylation inhibitor tunicamycin (TM), or the ER Ca2+ ATPases inhibitor thapsigargin (TG), up-regulates TRAIL-R2 and enhances TRAIL-induced apoptosis in melanoma cells [28–30].
In view of the potential application of 2-DG and TRAIL in the treatment of melanoma, we have examined whether they interact to enhance their toxic effect on melanoma cells. We show in this report that the combination of 2-DG and TRAIL enhanced TRAIL-induced apoptosis in melanoma cell lines and fresh melanoma isolates. This was primarily due to up-regulation of TRAIL death receptors, in particular, TRAIL-R2 on the melanoma cell surface. Moreover, we demonstrate that up-regulation of TRAIL-R2 by 2-DG was due to an increase in transcription, but this is not mediated by p53 or CCAAT/enhancer-binding protein-homologous protein (CHOP). Instead, the XBP-1 pathway of the UPR plays an important role in 2-DG-mediated up-regulation of TRAIL-R2 in melanoma cells.
2-DG sensitizes melanoma cells to TRAIL-induced apoptosis
Our initial studies on two melanoma cell lines, Mel-RM and MM200, indicated that 2-DG alone did not induce notable apoptosis, although it inhibited cell proliferation (Figures 1A & 1B). Nevertheless, studies on its effect on TRAIL-induced apoptosis showed that the combination of 2-DG and TRAIL enhanced sensitivity of the cells to apoptosis-induced by TRAIL (Figures 1B & 1C). The increase in TRAIL-induced apoptosis in the presence of 2-DG was observed as early as 16 hours and reached a peak at 36 hours after treatment (Figure 1B). In association with this, co-treatment with 2-DG enhanced TRAIL-induced activation of caspase-8, reduction in ΔΨm, mitochondrial release of cytochrome c, activation of caspase-3 and cleavage of its substrate PARP (Figures 1D & Figure 2A). It is of note that the cleaved products of caspase-8 were hardly detected in MM200 presumably due to relatively low concentrations within the cells (Figure 1D). Increased activation of caspase-3 was shown by both decreased cleavage of the pro-enzyme of caspase-3, and reduced conversion of the larger cleaved fragment to smaller ones (Figure 1D).
A summary of studies on the effect of 2-DG on TRAIL-induced apoptosis in a panel of melanoma cell lines and cultured melanocytes and fibroblasts is shown in Figure 2B. As expected, co-treatment with 2-DG enhanced TRAIL-induced apoptosis in all the melanoma lines (p < 0.05). Neither TRAIL nor 2-DG alone induced apoptosis in melanocytes and fibroblasts, but the combination of TRAIL and 2-DG resulted in an increase in apoptosis in both types of normal cells, even though the overall levels of apoptosis remained low (< 20%) (Figure 2B).
2-DG up-regulates TRAIL-R2 in melanoma cells
Having found that 2-DG enhances TRAIL-induced activation of caspase-8 (Figure 1D), we examined whether it regulates the cell surface expression of TRAIL receptors in melanoma cells. As shown in Figures 3A & 3B, 2-DG up-regulated the expression of TRAIL-R2 on the surface of Mel-RM and MM200 cells, with a significant increase being detected at 16 hours, and further increases at 24 and 36 hours after exposure to the compound. The levels of TRAIL-R1 on the cell surface were also increased by 2-DG, albeit to a lesser extent, in both cell lines (Figure 3A). In contrast, 2-DG did not induce any change in the expression of TRAIL-R3 and -4 on the cell surface (data not shown). Up-regulation of the cell surface expression of TRAIL death receptors by 2-DG was confirmed in a panel of melanoma cell lines (Figure 3C). Treatment with 2-DG resulted in slight increases in TRAIL-R2 and -R1 on the surface of melanocytes and fibroblasts (Figure 3C).
TRAIL-induced apoptosis of melanoma cells is primarily correlated with the levels of TRAIL-R2 expression on the cell surface [9, 10]. We therefore focused on investigation of the mechanism by which TRAIL-R2 is up-regulated by 2-DG. To this end, we examined if 2-DG regulates TRAIL-R2 total protein and mRNA levels by Western blotting and Real time PCR, respectively. As shown in Figure 3D, 2-DG increased the levels of the TRAIL-R2 total protein that could be detected by 16 hours after treatment. Figure 3E shows that treatment with 2-DG up-regulated the levels of TRAIL-R2 mRNA in both cell lines. The increase in TRAIL-R2 mRNA levels induced by 2-DG could be inhibited by pretreatment with actinomycin D (Figure 3E), suggesting that this was due to a transcriptional increase, rather than a change in the mRNA stability. Taken together, these results suggest that up-regulation of the cell surface expression of TRAIL-R2 by 2-DG results from increased TRAIL-R2 transcription in melanoma cells.
Sensitization of melanoma cells to TRAIL-induced apoptosis by 2-DG is largely mediated by up-regulation of TRAIL-R2
The role of up-regulation of TRAIL-R2 in sensitization of melanoma cells to TRAIL-induced apoptosis by 2-DG was studied by inhibition of the interaction between TRAIL and TRAIL-R2 using a TRAIL-R2/Fc chimeric protein. Figure 4A shows that the TRAIL-R2/Fc chimera significantly inhibited TRAIL-induced apoptosis in both Mel-RM and MM200 cells in the absence or presence of 2-DG (p < 0.05). Similarly, 2-DG-mediated sensitization of melanoma cells to TRAIL-induced apoptosis was blocked by either the general caspase inhibitor z-VAD-fmk, or the caspase-8 specific inhibitor z-IETD-fmk (p < 0.05) (Figure 4B & data not shown). In contrast, a TRAIL-R1/Fc chimeric protein displayed only minimal inhibitory effects on sensitization of Mel-RM and MM200 cells to TRAIL-induced apoptosis (Figure 4C).
To confirm the predominant role of up-regulation of TRAIL-R2 in sensitization of melanoma cells to TRAIL-induced apoptosis by 2-DG, we transfected a TRAIL-R2 specific siRNA pool into Mel-RM and MM200 cells. While TRAIL-R2 siRNA markedly inhibited TRAIL-R2 expression even in the presence of 2-DG, it inhibited TRAIL-induced apoptosis in the absence or presence of 2-DG (p < 0.05) (Figure 4D). Collectively, these results indicate that up-regulation of TRAIL-R2 on the cell surface is the main cause of sensitization of melanoma cells to TRAIL-induced apoptosis by 2-DG.
2-DG-mediated activation of TRAIL-R2 is independent of p53 and CHOP
TRAIL-R2 is a transcriptional target of p53 . However, up-regulation of TRAIL-R2 by 2-DG in the melanoma cell lines, ME4405 that lacks p53 expression  and Sk-Mel-28 that harbors mutated p53 , suggested that 2-DG-mediated up-regulation of TRAIL-R2 was independent of p53 (Figure 2B). To confirm this, we transfected a siRNA pool for p53 into Mel-RM and MM200 cells. As shown in Figure 5A, the cells transfected with the p53 siRNA, but not those with the control siRNA, displayed markedly lower levels of p53 expression. The reduced expression of p53 did not have any appreciable effect on 2-DG-mediated up-regulation of TRAIL-R2 on the cell surface and at the mRNA levels in both cell lines (Figure 5B).
Another transcription factor that is known to regulate TRAIL-R2 transcription in many cell types is CHOP [33, 34]. We examined if CHOP contributes to 2-DG-mediated up-regulation of TRAIL-R2 in Mel-RM and MM200 cells with CHOP stably knocked down by lentiviral infections (Figure 5C). Deficiency in CHOP did not appear to significantly impact on the increase in TRAIL-R2 induced by 2-DG at both the protein and mRNA levels (Figure 5D). Together, these results indicate that neither p53 nor CHOP plays a role in 2-DG-mediated up-regulation of TRAIL-R2 in melanoma cells.
2-DG-mediated up-regulation of TRAIL-R2 is mediated by XBP-1
We have previously shown that the IRE1α and ATF6 pathways of the UPR are involved in transcriptional up-regulation of TRAIL-R2 by the classic ER stress inducers TM and TG [29, 30]. We tested if 2-DG impinges on ER stress and activates the UPR in melanoma cells. As shown in Figure 6A, 2-DG up-regulated glucose-regulated protein 78 (GRP78) and the active form of x-box-binding protein-1 (XBP-1) mRNA, two commonly used markers of activation of the UPR [35, 36].
To examine whether any of the UPR signaling pathways plays a role in up-regulation of TRAIL-R2 by 2-DG, we transfected siRNA pools for IRE1α, ATF6, and PERK into Mel-RM and MM200 cells, respectively (Figure 6B). As shown in Figure 6C, while the basal level of TRAIL-R2 expression was not impacted, up-regulation of TRAIL-R2 by 2-DG on the cell surface was partially inhibited in cells transfected with the siRNA for IRE1α and ATF6. In contrast, inhibition of PERK by siRNA did not alter the expression of TRAIL-R2 before and after treatment with 2-DG (Figure 6C).
The IRE1α and ATF6 signaling pathways of the UPR converge on the UPR effector XBP-1, as XBP-1 is transcriptionally regulated by ATF6, and its activation is mediated by IRE1α [25–27]. We therefore envisaged that XBP-1 plays a role in up-regulation of TRAIL-R2 by 2-DG in melanoma cells. To test this, we examined the effect of 2-DG on TRAIL-R2 expression in XBP-1-deficient melanoma cell lines established by stable knockdown with shRNA by lentiviral infections. Deficiency in XBP-1 inhibited 2-DG-induced up-regulation of TRAIL-R2 on the cell surface (Figures 6D & 6E). Similarly, it blocked the increase in TRAIL-R2 transcription induced by 2-DG (Figures 6D & 6E). Collectively, these results indicate that up-regulation of TRAIL-R2 by 2-DG is mediated by XBP-1 as a consequence of activation of the ATF6 and IRE1α pathways of the UPR.
2-DG up-regulates TRAIL-R2 and enhances TRAIL-induced apoptosis in fresh melanoma isolates
Our previous studies have shown that fresh melanoma isolates, which may reflect more closely the in vivo situation, are relatively resistance to TRAIL-induced apoptosis due to low levels of expression of TRAIL death receptors . We studied if 2-DG can also up-regulate TRAIL-R2 in fresh melanoma isolates. Freshly isolated melanoma cells, Mel-CA and Mel-MC were treated with 2-DG for 24 hours. As shown in Figures 7A and 7B, treatment with 2-DG increased the levels of TRAIL-R2 on the cell surface as measured in flow cytometry, and the TRAIL-R2 total protein levels as detected in Western blot analysis, in both Mel-CA and Mel-MC cells. Figure 7C shows that neither 2-DG nor TRAIL induced significant levels of apoptosis (< 20% apoptotic cells) in a panel of fresh melanoma isolates. However, co-treatment with 2-DG and TRAIL resulted in increases in the percentages of apoptotic cells (p < 0.05). Sensitization of fresh melanoma isolates to TRAIL-induced apoptosis by 2-DG was substantially inhibited by a recombinant TRAIL-R2/Fc chimera (p < 0.05) (Figure 7D), indicating that the effect of 2-DG on TRAIL-induced apoptosis in fresh melanoma isolates is largely accounted for by the increase in TRAIL-R2 expression on the cell surface.
The above results show that the combination of 2-DG and TRAIL, two promising anticancer agents, results in enhanced killing in cultured melanoma cell lines and fresh melanoma isolates. This is primarily due to up-regulation of TRAIL-R2 on the melanoma cell surface. Moreover, they demonstrate that 2-DG-mediated up-regulation of TRAIL-R2 is due to increased transcription, but this is not dependent on p53 and CHOP. Instead, the ATF6/IRE1α/XBP-1 axis of the UPR appears to play an important role in up-regulation of TRAIL-R2 induced by 2-DG in melanoma cells.
TRAIL is currently in clinical evaluation for the treatment of various cancers . However, our past studies have shown that fresh isolates of melanoma and melanoma in tissue sections frequently had low TRAIL death receptor expression and therefore may be unresponsive to TRAIL [11, 14]. Unlike studies in many other solid cancers, in which TRAIL-death receptors could be up-regulated by other clinically relevant therapeutic drugs [37–40], we have not found these to increase TRAIL death receptor expression in melanoma. Agents tested have included DNA-damaging agents, microtubulin-targeting agents, histone deacetylase inhibitors, and MEK inhibitors [, & data not shown]. Nevertheless, the classic ER stress inducers, the glycosylation inhibitor TM and the ER Ca2+ ATPases inhibitor TG have been shown to enhance TRAIL-induced apoptosis in melanoma cells by up-regulation of TRAIL-R2 via activation of the UPR [29, 30], but these compounds are not clinically applicable due to their toxicity towards normal tissues. The ability of 2-DG to up-regulate TRAIL death receptors in melanoma is therefore of particular interest, in that fluorodeoxyglucose is commonly used in clinical imaging, eg. positron emission tomography (PET) . In addition, 2-DG alone or in combination with other therapeutics has been shown to inhibit tumor cell growth and has been in clinical trial for its potential as an anticancer agent [16, 20–23].
Up-regulation of TRAIL death receptors by 2-DG was associated with enhanced apoptotic signaling induced by TRAIL. This was evidenced by increased activation of caspase-8, reduction in ΔΨm, mitochondrial release of cytochrome C, activation of caspase-3 and cleavage of its substrate PARP. Caspase-8 and -3 are the major initiator and effector caspase, respectively, in TRAIL-induced apoptosis of melanoma cells [2, 3, 10], whereas the mitochondrial apoptotic pathway is known to play an important role in TRAIL-induced apoptosis of melanoma [10, 43]. In agreement with our previous finding that TRAIL-R2 is the dominant TRAIL death receptor in melanoma cells [9, 10], inhibition of the interaction of TRAIL with TRAIL-R2, but not with TRAIL-R1, markedly blocked sensitization of melanoma cells to TRAIL-induced apoptosis by 2-DG, indicating that up-regulation of TRAIL-R2 was the main cause of sensitization of melanoma cells to TRAIL-induced apoptosis, even though both TRAIL-R1 and -R2 were increased by 2-DG. It is of note, however, the overall levels of TRAIL-R1 expression on the melanoma cell surface were lower than those of TRAIL-2 before and after treatment with 2-DG. Therefore, our results do not negate a potential role of TRAIL-R1 in mediating TRAIL-induced apoptosis in melanoma cells when it is expressed at relatively higher levels .
2-DG-mediated up-regulation of TRAIL-R2 on the melanoma cell surface was associated with elevated TRAIL-R2 total protein levels and increased TRAIL-R2 gene transcription. However, p53, which is known to mediate TRAIL-R2 transcription under many conditions [31, 37], did not appear to play a part in up-regulation of TRAIL-R2 by 2-DG in melanoma cells. This was initially suggested by the finding that a p53-null melanoma cell line (ME4405), and a melanoma cell line carrying mutated p53 (Sk-Mel-28) displayed increased TRAIL-R2 in response to 2-DG. Further studies with siRNA knockdown of p53 in melanoma cell lines with wide-type p53 confirmed that inhibition of p53 did not impact on the up-regulation of TRAIL-R2 by 2-DG. These results, along with our previous observations that DNA-damaging agents such as cisplatin and adriamycin that increased the levels of p53 but did not up-regulate TRAL-R2 in melanoma cells [, & data not shown], suggest that p53 may not be functionally active in melanoma cells in regard to regulation of TRAIL-R2 expression. We have found that p53 in melanoma cells are frequently expressed as the smaller isoforms that aberrantly impact on the transcriptional activity of p53 .
We have previously shown that the ER stress inducers TM and TG could up-regulateTRAIL-R2 via the ATF6 and IRE1α pathways of the UPR independently of p53 [29, 30]. In addition, the transcription factor CHOP that is an effector of the UPR also plays a part in up-regulation of TRAIL-R2 by TM and TG [29, 30]. In this study, both the GRP78 protein and the active form of XBP-1 mRNA, two commonly used markers of activation of the UPR, were induced by 2-DG, indicating that, consistent with its inhibitory effect on glycolysis and glycosylation, 2-DG activated the UPR in melanoma cells. These results also suggest that the increase in TRAIL-R2 gene transcription might be the consequence of activation of UPR target genes. However, CHOP did not appear to contribute to increased TRAIL-R2 transcription, as deficiency in CHOP did not block up-regulation of TRAIL-R2 by 2-DG. It is unclear why CHOP played a role in up-regulation of TRAIL-R2 by TM and TG, but failed to do so in 2-DG-mediated up-regulation of TRAIL-R2, whereas all these compounds seemingly activated the UPR to comparable levels in melanoma cells [29, 30]. A possible cause for this is that the cofactor(s) required by CHOP to trigger TRAIL-R2 transcription is not activated by 2-DG in melanoma cells. CHOP-mediated activation of Bim transcription is known to require the formation of CHOP-C/EBP heterodimers .
As with TM and TG, 2-DG-induced up-regulation of TRAIL-R2 in melanoma cells was partially inhibited by siRNA knockdown of IRE1α or ATF6, indicating that these pathways of the UPR are involved in up-regulation of TRAIL-R2 by 2-DG. Because XBP-1 is transcriptionally regulated by ATF6, and is activated by IRE1α [25–27], it seemed that XBP-1 may play a part in up-regulation of TRAIL-R2 mediated by these pathways of the UPR. In this study, deficiency in XBP-1 markedly blocked up-regulation of TRAIL-R2 in melanoma cells, verifying a role of XBP-1 in 2-DG-mediated up-regulation of TRAIL-R2. However, the UPR element (UPRE) or ER stress response element (ERSE) consensus sequence, which is characteristic of promoters of UPR target genes, could not be identified in the promoter region of the TRAIL-R2 gene (data not shown). This argues against a direct role of XBP-1 in activation of transcription of TRAIL-R2 in melanoma cells. It is conceivable that XBP-1 may activate TRAIL-R2 transcription indirectly via activation of an unknown transcription factor(s). Alternatively, XBP-1-mediated signaling may cause relief of transcriptional repression on the TRAIL-R2 promoter. In this regard, inactivation of the transcription repressor Yin Yang 1 (YY1) has been shown to lead to up-regulation of TRAIL-R2 in various types of cells . Interestingly, YY1 is known to be regulated by O-Linked N-Acetylglucosaminylation (O-GlcNacylatiioioin), which was proposed to be connected with the pathway of glucose metabolism .
The finding that 2-DG could sensitize fresh melanoma isolates to TRAIL-induced apoptosis by up-regulation of TRAIL-R2 is of particular importance, for it is known that fresh melanoma isolates are relatively resistant to TRAIL-induced apoptosis due to low levels of TRAIL death receptor expression . This may reflect more closely the in-vivo status of TRAIL death receptor expression in melanoma cells and their susceptibility to TRAIL-induced apoptosis. However, treatment with 2-DG also resulted in a small increase in TRAIL-R2 in normal cells such as melanocytes and fibroblasts, and caused increased toxicity towards the cells, suggesting that careful evaluation of low dose of 2-DG or its analogues in combination with low concentrations of TRAIL is required before investigations in patients are carried out.
This study shows that 2-DG, a synthetic glucose analogue that inhibits glycolysis and glycosylation, up-regulates TRAIL death receptors and enhances TRAIL-induced apoptosis in cultured human melanoma cell lines and fresh melanoma isolates. Moreover, the study demonstrates that 2-DG-induced up-regulation of TRAIL-R2 is mediated by the ATF6/IRE1α/XBP-1 axis of the unfolded protein response independently of p53 and CHOP. Collectively, our data indicate that 2-DG is a promising agent to increase the therapeutic response of melanoma to TRAIL.
Human melanoma cell lines Mel-RM, MM200, IgR3, Mel-CV, Mel-FH, Sk-Mel-28, Sk-Mel-110, and ME4405, have been described previously . They were cultured in DMEM containing 5% FCS (Commonwealth Serum Laboratories, Melbourne, Australia). The cultured human melanocyte line HEMn-MP was purchased from Banksia Scientific (Bulimba, Qld, Australia) and the cells were cultured in medium supplied by Clonetics (Edward Kellar, Vic., Australia). Human embryonic fibroblasts (FLOW 2000) were cultured in DMEM containing 5% FCS as described previously .
Fresh Melanoma Isolates
Isolation of melanoma cells from fresh surgical specimens was carried out as described previously .
Antibodies, Recombinant Proteins, and Other Reagents
2-DG was purchased from Sigma Chemical Co. (Castle Hill, Australia). It was dissolved in DMSO to make up a stock solution of 1 mM. Recombinant human TRAIL and the TRAIL-R2/Fc chimera were supplied by Genentech Inc. (San Francisco, CA). The mouse MAbs against TRAIL-R1, -R2, -R3, and -R4 were also supplied by Genentech Inc. (San Francisco, CA). The cell-permeable general caspase inhibitor Z-Val-Ala-Asp(OMe)-CH2F (z-VAD-fmk) and the caspase-8 specific inhibitor Z-lle-Glu(Ome)-Thr-Asp(Ome)-CH2F (z-IETD-fmk) were purchased from Calbiochem (La Jolla, CA). The rabbit polyclonal Abs against caspase-3 and -8 were from Stressgen (Victoria, BC, Canada). The rabbit polyclonal Ab against against cleaved form of PARP was from Cell Signaling Technology (Beverly, MA). The rabbit mAbs against GRP78, XBP-1, IRE1α, ATF6, PERK, and CHOP, were purchased from Santa Cruz Biotechnology (Santa Cruz, CA). Isotype control Abs used were the ID4.5 (mouse IgG2α) mAb against Salmonella typhi supplied by Dr. L. Ashman (Institute for Medical and Veterinary Science, Adelaide, Australia), the 107.3 mouse IgG1 MAb purchased from PharMingen (San Diego, CA), and rabbit IgG from Sigma Chemical Co (Castle Hill, Australia).
Quantitation of apoptotic cells by measurement of sub-G1 DNA content using the propidium iodide (PI) method or by Annexin-V staining was carried out as described elsewhere .
Mitochondrial Membrane Potential (ΔΨm)
Melanoma cells were seeded at 1 × 105 cells/well in 24-well plates and allowed to reach exponential growth for 24 hours before treatment. Changes in ΔΨm were studied by staining the cells with the cationic dye, JC-1, according to the manufacture's instructions (Molecular Probes, Eugene, OR) as described previously .
Western Blot Analysis
Western blot analysis was carried out as described previously [29, 30]. Labeled bands were detected by Immun-Star™ HRP Chemiluminescent Kit, and images were captured and the intensity of the bands was quantitated with the Bio-Rad VersaDoc™ image system (Bio-Rad, Regents Park, NSW, Australia).
Preparation of Mitochondrial and Cytosolic Fractions
Methods used for subcellular fraction were similar to the methods described previously .
XBP-1 mRNA Splicin
The method used for detection of unspliced and spliced XBP-1 mRNAs was as described previously . Briefly, RT-PCR products of XBP-1 mRNA were obtained from total RNA extracted using primers 5'-cggtgcgcggtgcgtagtctgga-3' (sense) and 5'-tgaggggctgagaggtgcttcct-3' (anti-sense). Because a 26 bp fragment containing an Apa-LI site is spliced upon activation of XBP-1 mRNA, the RT-PCR products were digested with Apa-LI to distinguish the active spliced form from the inactive unspliced form. Subsequent electrophoresis revealed the inactive form as two cleaved fragments and the active form as a non-cleaved fragment.
Quantitation of TRAIL-R2 mRNA expression using Real-Time PCR was performed as described previously. Briefly, total RNA was isolated, and reverse transcription PCR was carried out. The resulting cDNA products were used as templates for real-time PCR assays. Real-time PCR was performed using the ABI Prism 7700 sequence detection system (Applied Biosystems, Foster City, CA). For TRAIL-R2, Twenty-five μl mixtures were used for reaction, which contains 5 μl cDNA sample (0.5-1 μg/μl), 300 nM forward primers for TRAIL-R2 (CGCTGCACCAGGTGTGATT), 300 nM reverse primers for TRAIL-R2 (GTGCCGGCTTCGCACTGACA), 200 nM probes for TRAIL-R2 (6FAM-CCCTGCACCACGACCAGAAACACAG-TAMRA), and 9 mM MgCI2. Analysis of cDNA for β-actin was included as a control. The threshold cycle value (Ct) was normalized against β-actin cycle numbers. The relative abundance of mRNA expression of a control sample was arbitrarily designated as 1, and the values of the relative abundance of mRNA of other samples were calculated accordingly.
Small RNA Interference (siRNA)
Melanoma cells were seeded at 3.5 × 104 cells/well in 24-well plates and allowed to reach approximately 50% confluence on the day of transfection. The siRNA constructs used were obtained as the siGENOME SMARTpool reagents (Dharmacon, Lafayette, CO). The siGENOME SMARTpool IRE1α (M-004951-01-0010), the siGENOME SMARTpool ATF6 (M-009917-01-0010), the siGENOME SMARTpool PERK (M-004883-01-0010), the siGENOME SMARTpool TRAIL-R2 (M-004819-01-0010), the siGENOME SMARTpool p53 (L-003329-00-0005), and the non-targeting siRNA control, SiConTRolNon-targeting SiRNA pool (D-001206-13-20) were obtained from Dharmacon. Cells were transfected with 50-100 nM siRNA in Opti-MEM medium (Invitrogen, Carlsbad, CA) with 5% fetal calf serum using Oligofectamine reagent (Invitrogen, Carlsbad, CA) according to the manufacturer's transfection protocol. Efficiency of siRNA was measured by Western blot analysis 24 hours after transfection.
Short Hairpin RNA (shRNA) Knockdown
Melanoma cell lines were seeded at 1 × 104 per well in 96 well plates and left to attach overnight. Sigma MISSION® Lentiviral Transduction Particles for shRNA-mediated knockdown of CHOP (SHVRS-NM-000100) and Sigma MISSION® Lentiviral Transduction Particles for shRNA-mediated knockdown of XBP-1 (SHVRS-NM-000100)were applied to ~70% confluent cells in the presence of polybrene (4 or 8 μg/ml) at MOIs of 0.5, 1 or 5 in 100 μl DMEM. After 16 - 24 hours, the culture medium was replaced and cells were left another 24 hours. Cells were selected with 2 μg/ml puromycin for 3 days until mock-transduced controls (polybrene only) were completely dead. For each transduced melanoma cell line, up to 4 wells of cells per lentiviral clone were tested for knockdown via Western Analysis. Cells with lowest CHOP or XBP-1 levels were expanded for experimental use.
The significance of differences between experimental data was determined using the two-tailed student's t test for unpaired observations with Microsoft Excel 2000 software.
tumor necrosis factor-related apoptosis-inducing ligand
the unfolded protein response
inositol-requiring transmembrane kinase and endonuclease 1α
activation of transcription factor 6
protein kinase-like ER kinase
x-box-binding protein-1. CHOP: CCAAT/enhancer-binding protein-homologous protein
glucose-regulated protein 78
death-inducing signaling complex
Fas-associated death domain
mitochondrial membrane potential
small RNA interference
Short hairpin RNA.
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This work was supported by the NSW State Cancer Council, the Melanoma and Skin Cancer Research Institute Sydney, the Hunter Melanoma Foundation, NSW, and the National Health and Medical Research Council (NHMRC), Australia. X.D. Zhang is a Cancer Institute NSW Fellow.
The authors declare that they have no competing interests.
HL, CCJ, CJL, AC, HYT, FY, and KHT performed the experiments, and analyzed the experiments results. PH and XDZ conceived the study, designed experiments, interpreted the findings and drafted the manuscript. All authors read and approved the final manuscript.
Hao Liu, Chen Chen Jiang contributed equally to this work.