Advanced stages of neuroblastoma, the most common extracranial malignant solid tumor of the central nervous system in infants and children, are refractive to therapy. Ectopic expression of melanoma differentiation-associated gene-7/interleukin-24 (mda-7/IL-24) promotes broad-spectrum antitumor activity in vitro, in vivo in preclinical animal models, and in a phase I clinical trial in patients with advanced cancers without harming normal cells. mda-7/IL-24 exerts cancer-specific toxicity (apoptosis or toxic autophagy) by promoting endoplasmic reticulum stress and modulating multiple signal transduction pathways regulating cancer cell growth, invasion, metastasis, survival, and angiogenesis. To enhance cancer-selective expression and targeted anticancer activity of mda-7/IL-24, we created a tropism-modified cancer terminator virus (Ad.5/3-CTV), which selectively replicates in cancer cells producing robust expression of mda-7/IL-24. We now show that Ad.5/3-CTV induces profound neuroblastoma antiproliferative activity and apoptosis in a caspase-3/9–independent manner, both in vitro and in vivo in a tumor xenograft model. Ad.5/3-CTV promotes these effects through a unique pathway involving apoptosis-inducing factor (AIF) translocation into the nucleus. Inhibiting AIF rescued neuroblastoma cells from Ad.5/3-CTV–induced cell death, whereas pan-caspase inhibition failed to promote survival. Ad.5/3-CTV infection of neuroblastoma cells increased ATM phosphorylation instigating nuclear translocation and increased γ-H2AX, triggering nuclear translocation and intensified expression of AIF. These results were validated further using two ATM small-molecule inhibitors that attenuated PARP cleavage by inhibiting γ-H2AX, which in turn inhibited AIF changes in Ad.5/3-CTV–infected neuroblastoma cells. Taken together, we elucidate a novel pathway for mda-7/IL-24–induced caspase-independent apoptosis in neuroblastoma cells mediated through modulation of AIF, ATM, and γ-H2AX. Cancer Res; 76(12); 3572–82. ©2016 AACR.

Neuroblastoma is the most frequent extracranial solid tumor in children under five years of age, affecting 1 in 7,000 children. It is speculated that these tumors develop as a result of rapid proliferation of neuroblasts during fetal growth (1). Neuroblastoma arises along the sympathetic nervous system and adrenal medulla (2) from neural crest cells of sympathetic origin. They represent heterogeneous masses, both clinically and biologically. When occurring in infants, neuroblastoma may relapse unpredictably in a majority of cases, whereas in older patients, these tumors frequently persist as benign ganglioneuromas (2). At the time of diagnosis, approximately half of the patients are assumed to be high risk due to distant metastasis. Neuroblastoma can be classified into four stages. In stages I and II, disease is confined to the primary lesion. Stages III and IV are characterized by disease outside the primary lesion. Once neuroblastoma attains advanced stage (III or IV), it expands persistently even when subjected to rigorous multimodal therapies (1, 3). Presentation of tumors at advanced stages combined with the absence of surgical options culminates in very poor patient prognosis. Although some improvements in the overall cure rate of neuroblastomas have been realized using intensive multimodality therapies, these therapies promote significant short- and long-term toxicities (1, 3, 4). Only about 2% of neuroblastoma patients with stage III or IV remain disease free with relapse occurring shortly after completing chemotherapy, indicating a negligible effect of these agents long term (5). Therapy failures are believed to be a consequence of development of resistance, underscoring the need for less toxic and more efficient therapeutic strategies (6). Accordingly, a comprehensive knowledge of mechanisms governing proliferation, differentiation, and cell death may expand our understanding of the molecular pathogenesis of neuroblastoma, which may result in novel biologically based therapies diminishing toxicity and maximizing efficacy.

mda-7/IL-24 is a unique member of the IL10-related cytokine gene family (7), displaying wide spectrum antitumor activity in diverse cancers without harming normal cells or tissues (8, 9). mda-7/IL-24 was initially cloned using subtraction hybridization combined with induction of cancer cell terminal differentiation (10). Forced expression of mda-7/IL-24 in cancer cells promotes direct cancer toxicity through induction of apoptosis or toxic autophagy (11) and indirect antitumor effects through inhibition of angiogenesis (8, 12), promoting antitumor immune responses (8), sensitization of cancer cells to radiotherapy- and chemotherapy-induced killing (13), and by promoting potent “antitumor bystander activity” through autocrine/paracrine secretion (14). mda-7/IL-24 displays nearly universal antitumor properties in vitro and in vivo in almost every cancer context (15, 16), which led to successful entry into clinical trials (17, 18). These properties of mda-7/IL-24 make it a potential candidate gene for the treatment of neuroblastoma, where adenovirus administration in a single human neuroblastoma cell line (SH-SY5Y) inhibited both in vitro and in vivo xenograft growth (19). To enhance the utility of mda-7/IL-24 for gene therapy of cancer, we are employing a conditionally replication-competent adenovirus carrying mda-7/IL-24 (20). In this cancer terminator virus (CTV; ref. 21) adenoviral replication is controlled by the promoter of a cancer-selective rodent gene, progression elevated gene-3 (PEG-3; ref. 22). To enhance even further the utility of the CTV, we have engineered the adenovirus to more effectively infect cancer cells, creating tropism-modified chimeric CTVs (23).

Adenoviruses (Ad) use CAR (coxsackie–adenovirus receptors) to infect normal and cancer cells; however, cancer cells express varying levels of CAR on their cell surface. To improve the low efficiency of Ad infection of tumor cells, “tropism modification” approaches have been developed (23). One such vector Ad.5/3 displayed equal efficacy when compared with wild-type Ad.5, thereby providing an expanded range of utility for Ad.5/3, in both low and high CAR-expressing cells (23, 24). For that reason, we used a modified Ad.5/3-CTV (Ad.5/3-PEG-E1A-mda-7) to evaluate therapeutic applications in human neuroblastoma cells.

We presently describe a previously unrecognized pathway involved in mda-7/IL-24–mediated induction of caspase-independent apoptosis induction in neuroblastoma cells. This pathway involves modulation of apoptosis-inducing factor (AIF) expression and translocation into the nucleus of neuroblastoma cells that is mediated through induction of ATM followed by phosphorylation and nuclear translocation of γ-H2AX into the nucleus. These findings provide new insights into the mechanism of action of a near ubiquitous cancer-suppressing gene supporting its applications for potential therapy of neuroblastoma.

Cells and reagents

Human neuroblastoma cancer cell lines SK-N-AS and SK-N-SH were obtained from the ATCC, and NB1691 cells were obtained from Dr. Alan Houghton of St. Jude Children's Research Hospital (Memphis, TN). NB1691 cell line was authenticated using the “CellCheck” service provided by the Research Animal Diagnostic Laboratory and compared with initial short tandem repeat profile generated by the collaborator (IDEXX BioResearch). The cumulative culture length of the cells (SK-N-SH and SK-N-AS) was less than 6 months after recovery. Early passage cells were used for all experiments. All the cell lines were frequently tested for mycoplasma contamination using a mycoplasma detection kit from Sigma. SK-N-AS cells were cultured in DMEM with nonessential amino acids, SK-N-SH cells were cultured with RPMI 1640, and NB1691 cells were cultured with DMEM (Invitrogen) supplemented with 10% FBS, 50 units/mL penicillin, and 50 μg/mL streptomycin (Life Technologies Inc.). Cells were incubated in a humidified 5% CO2 atmosphere at 37°C. The antibodies specific for AIF (#4642), ATM (#2873), pATM (ser 1981, #13050), BCL-2 (#2876), BAX (2772), PARP (#9542), caspase-3 (#9662), caspase-8 (#9746), H2AX (#7631), and γ-H2AX (ser 139, #9718; Cell Signaling Technology), MDA-7/IL-24 (#K101; GenHunter), horseradish peroxidase (HRP)–conjugated secondary antibodies (Dako), β-actin (#NB600-501; Novus Biologicals, Inc.) were used in this study. The other materials used in this study were the Transcriptor First Strand cDNA Synthesis Kit, In Situ Cell Death Detection Kit, Fluorescein (#11684795910; Roche Applied Science), and MTT cell growth assay Kit (#CT02; Millipore Corporation). KU60019 (#SML1416) and KU-55933 (#SML-1109; Sigma).

Transfection with plasmids

All transfection experiments were performed with FuGene HD transfection reagent according to the manufacturer's protocol (Roche). Briefly, plasmid/siRNA was mixed with FuGene HD reagent (1:3 ratio) in 500 μL of serum-free medium and left for 30 minutes to allow for complex formation. The complex was then added to the 100-mm plates, which had 2.5 mL of serum-free medium (2 μg plasmid per mL of medium). After 6 hours of transfection, complete medium was added, and cells were cultured for another 24 hours (1).

Cell proliferation assay (MTT assay)

Cell growth rate was determined using a modified 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay as a measurement of mitochondrial metabolic activity as described earlier (8). Cells were treated with mock, Ad.5/3-Null, Ad.5/3-E1A, or the indicated doses of Ad.5/3-CTV and incubated at 37°C. After 0 to 96 hours, MTT reagent was added, and cells were incubated for 4 hours at 37°C. After removing the medium, formazan crystals were dissolved in DMSO, absorbance at 550 nm was read using a microplate spectrophotometer, and the results were expressed graphically.

Terminal deoxy nucleotidyl transferase-mediated nick-end labeling assay

Induction of apoptosis in neuroblastoma cancer cells as well as in xenograft tumor tissue sections of mice treated with mock, Ad.5/3-Null, Ad.5/3-E1A, or Ad.5/3-CTV was evaluated using terminal deoxynucleotidyl transferase–mediated dUTP nick end labeling (TUNEL) enzyme reagent following the manufacturer's instructions and as described previously (25). Briefly, 5 × 103 neuroblastoma cancer cells were cultured and treated with mock, Ad.5/3-Null, Ad.5/3-E1A, or Ad.5/3-CTV for 72 hours, fixed in 4% paraformaldehyde in PBS for 1 hour at room temperature, and permeabilized with 0.1% Triton-X 100 in 0.1% sodium citrate in PBS for 2 minutes (for cells) or 10 minutes (for tissue sections) on ice. The samples were incubated in TUNEL reaction mixture in a humidified atmosphere at 37°C for 1 hour in the dark. Images were captured with an Olympus research fluorescence microscope attached to a CCD camera, and cells were counted. The positive-staining apoptotic cells were counted from 5 microscopic fields per tumor tissue from 3 animals per treatment.

Western blotting

Western blotting analysis was performed as described previously (25). Briefly, Mock, Ad.5/3-Null, Ad.5/3-E1A, or Ad.5/3-CTV–treated neuroblastoma cancer cells were lysed in radioimmunoprecipitation assay lysis buffer containing 1 mmol/L sodium orthovanadate, 0.5 mmol/L PMSF, 10 μg/mL aprotinin, and 10 μg/mL leupeptin. Equal amounts of total protein fractions of lysates were resolved by SDS-PAGE and transferred to PVDF membranes. The blot was blocked with 5% non-fat dry milk/5% BSA and probed overnight with primary antibodies followed by HRP-conjugated secondary antibodies. An ECL system was used to detect chemiluminescent signals. All blots were reprobed with β-actin antibody to confirm equal loading.

In vivo studies

To directly evaluate the effect of Mock, Ad.5/3-Null, Ad.5/3-E1A, or Ad.5/3-CTV on tumor growth in vivo, we subcutaneously implanted 5 × 106 NB1691 cells on both flanks of 4- to 6-week-old athymic nude mice. The tumors on the left flank were challenged with 8 intratumoral injections of Mock, Ad.5/3-Null, Ad.5/3-E1A, or Ad.5/3-CTV for 3 weeks (3 injections for 2 weeks and 2 injections in the last week) 7 days after tumor cell implantation when the tumors reached palpable sizes. Tumor growth was monitored in mice by measuring tumor size with calipers on each flank every alternate day until completion of the experiment. Each treatment group had two sets of animals. One set was sacrificed 2 days after the final dose of treatment (1 mouse from each group), and another set (N = 5) was followed until the control tumor group reached a point where it needed to be sacrificed according to our Institutional Animal Care and Use Committee protocol. After completion of the experiment, the tumors were fixed and the sections were used for immunohistochemical analysis.

Statistical analysis

All data are presented as mean ± SD of at least three independent experiments, each performed at least in triplicate. One-way ANOVA combined with the Tukey post hoc test of means was used for multiple comparisons. Statistical differences are presented at probability levels of P < 0.05, P < 0.01, and P < 0.001.

CTV expressing mda-7/IL-24 inhibits neuroblastoma cell proliferation in vitro

To examine mda-7/IL-24 overexpression on neuroblastoma tumor growth in vitro and in vivo, a genetic approach was used with a tropism-modified cancer terminator virus (Ad.5/3-CTV; refs. 23, 26), i.e., a conditionally replicating adenovirus that ectopically expresses mda-7/IL-24. Adenovirus entry is cell surface receptor dependent so we determined receptor status of CAR (for Ad.5), desmoglein, and CD46 (for Ad.3) of the three neuroblastoma cell lines, SK-N-AS, NB1691, and SK-N-SH, used in this study. CAR expression was variable with similar lower levels in SK-N-AS and NB1691 cells and higher levels in SK-N-SH cells (Supplementary Fig. S1). CD46 was expressed at a comparable level in all three cell lines, and Desmoglein levels followed a similar pattern as CAR, with highest expression in SK-N-SH cells. When transgene expression was monitored (MDA-7/IL-24 and E1A) following Ad.5/3-CTV infection, all three neuroblastoma cell lines expressed the expected transgenes as compared with mock and Ad.5/3-Null–infected cells (Fig. 1A). A dose-dependent increase in MDA-7/IL-24 protein levels was seen in Ad.5/3-CTV–infected cells compared with controls. To confirm that the increased levels of MDA-7/IL-24 protein represented an upregulation of mda-7/IL-24 mRNA transcription, we assessed mRNA transcript levels in the Ad.5/3-CTV–treated cells. Ad.5/3-CTV–treated neuroblastoma cells showed a strong increase in mda-7/IL-24 mRNA levels when compared with mock, Ad.5/3-Null, or Ad.5/3-E1A–treated cells (data not shown). Next, we assessed the effects of Ad.5/3-CTV on neuroblastoma cell growth using MTT assays. Although Ad.5/3-E1A inhibited cell proliferation to some extent through its oncolytic activity, forced expression of mda-7/IL-24 using Ad.5/3-CTV resulted in the greatest dose-dependent decrease in cell proliferation compared with other treatments (Fig. 1B).

Ad.5/3-CTV induces cell death in neuroblastoma cells

Ectopic expression of mda-7/IL-24 induces apoptosis in a wide array of cancer types (16). Overexpression of mda-7/IL-24 in the neuroblastoma cell lines increased TUNEL-positive cells compared with that of cells treated with mock, Ad.5/3-Null, or Ad.5/3-E1A treatment (Fig. 2A). Further confirmation of apoptosis induction was shown by FACS analysis where the sub-G1 population (DNA content) was enhanced in Ad.5/3-CTV–infected cells. DNA frequency distribution histograms in which the sub-G1 region corresponded to apoptotic cells indicated that Ad.5/3-CTV increased the number of apoptotic cells to 40% to 50% in SK-N-AS, 35% to 50% in SK-N-SH, and 40% to 50% in NB1691 cells, as compared with 5% in Ad.5/3-Null–infected controls or approximately 20% in Ad.5/3-E1A–infected cells (Fig. 2B). PARP cleavage was also evident by Western blotting analysis predominantly in Ad.5/3-CTV–infected neuroblastoma cells (Fig. 2C). We also analyzed the expression of mda-7/IL-24–downstream molecules and signals involved in cell death following infection of neuroblastoma cells with Ad.5/3-CTV. In many cancers, mda-7/IL-24 is known to enhance proapoptotic genes and decrease antiapoptotic genes in the Bcl-2 family of proteins (27). A similar expression profile was found in neuroblastoma cells following Ad.5/3-CTV infection, i.e., enhancement of BAX and P-JNK (proapoptotic proteins) and decreased expression of BCL-2 and BCL-xL (antiapoptotic proteins; Supplementary Fig. S2). Of note, these changes were only evident following Ad.5/3-CTV infection and not with Ad.5/3-Null or Ad.5/3-E1A infection of neuroblastoma cells.

mda-7/IL-24 induces caspase-independent apoptosis in vitro in neuroblastoma cells

Although mda-7/IL-24 has well-established tumor-suppressor and apoptosis-promoting properties in a broad spectrum of human cancer cells, the molecular mechanism by which mda-7/IL-24 induces apoptosis is quite diverge and involves different pathways depending on the tumor type (27). Caspase-dependent apoptosis is the common modality of programmed cell death (28), so we determined whether mda-7/IL-24–induced cell death in neuroblastoma was caspase dependent. Treatment of neuroblastoma cells with Ad.5/3-CTV did not induce caspase-3 or caspase-9 activation when analyzed by Western blotting or using a luminescence-based assay (Fig. 3A and B). To determine a potential involvement of the extrinsic apoptosis pathway, we monitored caspase-8 expression following Ad.5/3-CTV infection and found no activation in these cell lines (Supplementary Fig. S3). In an additional confirmatory study, neuroblastoma cells were treated with z-vad fmk, a pan-caspase inhibitor, prior to Ad.5/3-CTV infection and cultured for an additional 48 hours. The cells were then analyzed via Western blotting for PARP cleavage, which demonstrated similar PARP cleavage with or without treatment with the pan-caspase inhibitor prior to Ad.5/3-CTV infection (Fig. 3C). This result further supports the caspase-independent cell death mechanism following ectopic expression of MDA-7/IL-24 in neuroblastoma cells.

mda-7/IL-24–mediated apoptosis in neuroblastoma involves AIF activation and nuclear translocation

The tumor-suppressor p53 plays an important role in suppressing tumorigenesis by inducing genomic stability, cell-cycle arrest, or apoptosis (29). AIF is a mitochondrial protein, which, when translocated to the nucleus, results in apoptosis, mainly in a caspase-independent context through the induction of chromatin condensation and DNA fragmentation (30). p53 is an established regulator of AIF in caspase-independent cell death, and AIF can contribute to p53-mediated cell death (31). p53 levels were modestly increased in a dose-dependent manner following Ad.5/3-CTV infection as compared with the mock or Ad.5/3-Null–infected cells (Supplementary Fig. S4). AIF levels were increased in a dose-dependent manner in Ad.5/3-CTV–infected neuroblastoma cells (Fig. 4A), suggesting the potential involvement of AIF in caspase-independent cell death.

Previous studies suggest that BCL-2 proteins facilitate the insertion of BAK or BAX into the mitochondrial membrane to form functional oligomers, which result in depolarization of the inner mitochondrial membrane and subsequent AIF nuclear translocation, which promotes caspase-independent apoptosis (28). To determine if mda-7/IL-24 exerts similar effects on AIF nuclear translocation, immunostaining and cell fractionation methods were used. AIF displayed a granular pattern in the mitochondria of untreated controls, whereas after treatment with Ad.5/3-CTV, AIF was detected in the nucleus (Fig. 4B). We confirmed this result using cellular fractionation, which clearly showed AIF accumulation in nuclear lysates and concomitant decreased levels in the cytoplasmic fraction following infection with Ad.5/3-CTV (Fig. 4C).

Ad.5/3-CTV–induced, AIF-mediated cell death in neuroblastoma cells was confirmed using an AIF inhibitor, N-Phenylmaleimide. Treatment with the AIF inhibitor at a concentration of 50 μmol/L for 1 hour prior to treatment with Ad.5/3-CTV for 48 hours reduced cell death as monitored by FACS analysis (data not shown). This phenomenon was further confirmed by Western blotting analysis for PARP cleavage. Treatment with an AIF-inhibitor prior to Ad.5/3-CTV infection resulted in decreased PARP cleavage (Fig. 4D). Collectively, these results indicate that Ad.5/3-CTV induces caspase-independent AIF-mediated apoptosis in neuroblastoma cells.

ATM-γ−H2AX axis mediates AIF-induced cell death in neuroblastoma cells

The mechanism that regulates AIF induction and nuclear translocation leading to caspase-independent apoptotic functions is not well understood. Previous studies suggest that γ-H2AX plays a pivotal role in AIF-mediated necroptosis in mouse embryonic fibroblasts (32). To test this hypothesis, we checked the effects of Ad.5/3-CTV on expression and activation of H2AX in SK-N-AS and NB1691 neuroblastoma cells. Ad.5/3-CTV infection increased the levels of H2AX as well as phosphorylation of H2AX (γ-H2AX) when compared with control, Ad.5/3-Null, or Ad.5/3-E1A–infected cells (Fig. 5A and Supplementary Fig. S5). To further decipher the molecular mechanism of H2AX phosphorylation, we evaluated the levels and activation of ATM in Ad.5/3-CTV–treated SK-N-AS, SK-N-SH, and NB1691 neuroblastoma cells, which showed increased ATM levels as well as phosphorylation of ATM when compared with control, Ad.5/3-Null, or Ad.5/3-E1A–treated cells (Fig. 5B and Supplementary Fig. S6). In total, these results indicate that AIF-mediated caspase-independent apoptosis requires ATM-induced histone H2AX phosphorylation in Ad.5/3-CTV–treated neuroblastoma cells.

To confirm further the involvement of ATM as an upstream regulator of H2AX- and AIF-mediated cell death in Ad.5/3-CTV–treated neuroblastoma cells, we used small-molecule ATM inhibitors, KU-60019 and KU-55933, to block the ATM kinase. ATM phosphorylates numerous proteins at specific positions, including H2AX at S139 (γ-H2AX). Neuroblastoma cells were treated over night with either KU-60019 (3 μmol/L) or KU-55933 (5 μmol/L; Supplementary Fig. S7) prior to Ad.5/3-CTV infection. Treatment with KU60019 prior to Ad.5/3-CTV infection inhibited the phosphorylation of ATM, thereby inhibiting γ-H2AX in SK-N-AS and NB1691 cells (Fig. 5C). This also resulted in decreased PARP cleavage reflecting decreased apoptosis, which was confirmed by TUNEL assay (Fig. 5E and Supplementary Fig. S7). Taken together, these results indicate that ATM acts as an upstream regulator of H2AX phosphorylation, which results in AIF-mediated cell death in neuroblastoma cells following treatment with Ad.5/3-CTV.

mda-7/IL-24 inhibits neuroblastoma tumor growth in vivo

To directly evaluate the effect of mda-7/IL-24 delivered by Ad.5/3-CTV on tumor growth in vivo, we implanted NB1691 cells subcutaneously on both sides of nude mice. The tumors on the left flank were challenged with intratumoral injections of Ad.5/3-Null, Ad.5/3-E1A, or Ad.5/3-CTV. Tumor growth was monitored in mice by measuring tumors every alternate day with Vernier calipers. There was a significant decrease in tumor volume in mice treated with Ad.5/3-CTV compared with mice treated with Ad.5/3-Null or Ad.5/3-E1A (Fig. 6A). Although Ad.5/3-E1A reduced tumor growth to some extent on the injected left side, it was evident that “bystander” activity in the noninjected right tumor was only observed in animals in which the left tumors were treated with Ad.5/3-CTV (Fig. 6). These results confirm previously published data that MDA-7/IL-24 exhibits potent antitumor “bystander” activity. To determine whether MDA-7/IL-24 caused AIF-mediated apoptosis in vivo, tumor sections were immunoassayed for MDA-7/IL-24, pATM, γ−H2AX, and AIF. Apoptotic content was determined by TUNEL analysis. Consistent with our in vitro observations, tumor sections from Ad.5/3-CTV–treated mice showed increased staining for MDA-7/IL-24, pATM, γ-H2AX, and AIF (Fig. 6C). Furthermore, the apoptotic index of tumor cells quantified by the number of TUNEL staining-positive cells increased with Ad.5/3-CTV treatment (Fig. 6B).

Neuroblastoma is a heterogeneous clinical entity, ranging from subgroups that have a very favorable prognosis with a high probability of spontaneous regression to those that display a very poor prognosis despite aggressive therapies (1, 33). Considering this conundrum and the high incidence of recurrence in advanced stages of neuroblastoma (stages III and IV; refs. 4, 6), defining appropriate strategies for treating this cancer particularly in advanced stages is a priority. Presently, we evaluated a broad-spectrum antitumor protein MDA-7/IL-24 (11, 12, 16) delivered by a tropism-modified chimeric Ad.5/3-CTV (23, 26) in neuroblastoma cells. Ad.5/3-CTV induced decreased neuroblastoma cell growth and increased apoptosis in vitro and decreased tumor growth in vivo, supporting potential applications for the therapy of this cancer. Mechanistic studies uncovered a new pathway by which mda-7/IL-24 can promote apoptosis in cancer cells, i.e., through induction and translocation of AIF into the nucleus.

mda-7/IL-24 shows potent antitumor activity that is mediated through multiple pathways in diverse cancers (7, 16). Mechanisms of mda-7/IL-24 toxicity include ER stress and tumoral cell apoptosis by suppression of antiapoptotic Bcl-2 family members (27, 34), which was also evident in this study. Previously, MDA-7/IL-24 treatment has been shown to increase ROS production in many cancer types (18, 35). It is well known that ROS generation is closely associated with early stages of apoptosis and mitochondrial dysfunction (36). Earlier reports suggest that ROS generation, together with Cyt C release from mitochondria, promote cell death (37, 38). This results in increased permeability of the outer mitochondrial membrane, decreasing transmembrane potential, and activation of AIF (32) eventually inducing caspase-independent apoptosis (39). Ad.5/3-CTV–delivered mda-7/IL-24 to neuroblastoma cells increased the levels of AIF. Our results show, in agreement with previously published data, that AIF is translocated into the nucleus inducing caspase-independent cell death in mda-7/IL-24–overexpressed neuroblastoma cells. This was further confirmed using AIF and pan-caspase inhibitors. Inhibition of AIF by small-molecule inhibitor attenuated PARP cleavage, inhibiting cell death in neuroblastoma cells upon treatment with Ad.5/3-CTV. In addition, applying a pan-caspase inhibitor did not alter mda-7/IL-24–induced PARP cleavage, further validating caspase-independent cell death induced by this cytokine in neuroblastoma cells.

Cells respond to DNA damage by phosphorylating a variant of the H2A protein family, H2AX (40). H2AX assists chromatin to facilitate DNA repair by providing binding sites for downstream repair factors (41). AIF is a flavoprotein that is in the mitochondrial inter-membrane space and performs a major role in mediating caspase-independent cell death (42, 43). Upon receiving a cell death stimuli, AIF is cleaved within the mitochondria by calpains and cathepsins (44), released into the cytosol possibly through a mitochondrial permeability transition pore, and translocated into the nucleus where it induces chromatin condensation and DNA fragmentation through complex formation with H2AX and cyclophilin A (45). A variety of apoptotic stimuli have been documented to induce AIF mitochondria-to-nucleus translocation, including DNA-damaging agents, hypoxia/ischemia, oxidative stress, and excitotoxins (such as glutamate; ref. 46). However, the signaling pathways that cause AIF nuclear translocation have not been fully elucidated. In this regard, we studied the effects of Ad.5/3-CTV on key apoptotic proteins, AIF and poly (ADP-ribose) polymerase-1 (PARP1), which constitutes a relatively novel, yet, crucial pathway of caspase-independent apoptosis in MDA-7/IL-24 treatment.

H2AX, a member of the histone H2A family is characterized by a phosphorylable SQE motif in its C-terminal tail (32, 47). It is also established that DNA fragmentation induces phosphorylation of H2AX histone at serine 139 (48). Even though H2AX is mainly associated with DNA-damage repair and DNA packaging, it is also a key regulator of programmed cell death (32, 49). To decipher the mechanism by which MDA-7/IL-24 leads to AIF nuclear translocation, we assessed the levels of γ-H2AX in Ad.5/3-CTV–treated cells and found increased activation levels of H2AX. It is known that ATM is a primary kinase involved in the phosphorylation of H2AX and also that ATM is one of the earliest kinases to be activated in the cellular response to double-strand breaks. We found activation of ATM, H2AX, and AIF translocation following Ad.5/3-CTV treatment, and these cellular modifications were confirmed by pharmacologic inhibition of ATM and AIF. Data obtained through our studies indicate that ATM activation is important in triggering H2AX phosphorylation and AIF activation, leading to caspase-independent cell death in Ad.5/3-CTV–treated neuroblastoma cells. In contrast with neuroblastoma cells, infection of human breast cancer (MDA-MB-231 and ZR-751) and melanoma (C8161 and SK-Mel) cells with Ad.5/3-CTV did not enhance AIF expression (Supplementary Fig. S8). Precisely, how ATM is activated in MDA-7/IL-24–mediated apoptosis in neuroblastoma cells is a key question requiring further experimentation. One recent study by Baritaud and colleagues revealed the significance of ATM and DNA-PK in regulating γ-H2AX in AIF-mediated caspase-independent necroptosis (32). In particular, they showed that ATM inhibition prevents the H2AX phosphorylation observed after MNNG addition and, subsequently, blocked AIF-mediated cell death. This is in agreement with our observations, which show that ATM small-molecule inhibitors attenuated Ad.5/3-CTV–induced PARP cleavage and H2AX phosphorylation, and inhibited AIF changes in neuroblastoma cells (Fig. 5C). Conversely, an AIF small-molecule inhibitor reduced Ad.5/3-CTV–induced ATM phosphorylation and cell death (Figs. 4D and 5D) in neuroblastoma cells. Taken together, our results suggest that ATM and AIF are functionally related in a positive feedback loop in which they regulate each other in neuroblastoma cells following Ad.5/3-CTV infection (Fig. 7). Another recent study reported that treatment with pro-oxidant resulted in caspase-independent, AIF-dependent apoptosis in ATM-null primary CLL tumors (50). These results from others and us suggest that ATM and AIF can work independently or together to induce caspase-independent cell death.

In conclusion, we demonstrate for the first time a new cell death pathway triggered by mda-7/IL-24 through ATM-mediated activation of H2AX and AIF resulting in caspase-independent apoptosis (Fig. 7) that appears unique to neuroblastoma cells, because this effect was not evident in human breast carcinoma or melanoma cells (Supplementary Fig. S8). Support for this stems from three lines of experimental evidence: (i) inhibition of AIF using AIF inhibitors decreased MDA-7/IL-24–mediated apoptosis; (ii) inhibition of caspases using a pan-caspase inhibitor did not block MDA-7/IL-24–induced cell death; and (iii) inhibition of ATM altered the levels of AIF, resulting in inhibition of cell death in MDA-7/IL-24–overexpressing neuroblastoma cells. Accordingly, the use of Ad.5/3-CTV, which displays cancer-specific viral replication combined with robust production and secretion of MDA-7/IL-24, to selectively induce cytolysis in neuroblastoma cells may represent a potentially viable treatment option for this aggressive cancer.

No potential conflicts of interest were disclosed.

Conception and design: P. Bhoopathi, P.B. Fisher

Development of methodology: P. Bhoopathi, A.K. Pradhan

Acquisition of data (provided animals, acquired and managed patients, provided facilities, etc.): P. Bhoopathi, A.K. Pradhan

Analysis and interpretation of data (e.g., statistical analysis, biostatistics, computational analysis): P. Bhoopathi, S.K. Das, L. Emdad, P.B. Fisher

Writing, review, and/or revision of the manuscript: P. Bhoopathi, N. Lee, S.K. Das, D. Sarkar, P.B. Fisher

Administrative, technical, or material support (i.e., reporting or organizing data, constructing databases): L. Emdad

Study supervision: D. Sarkar, L. Emdad, P.B. Fisher

This study was supported in part by NCI grant R01 CA097318 (P.B. Fisher), the National Foundation for Cancer Research (P.B. Fisher), a VCU Massey Cancer Center (MCC) development award (P.B. Fisher), and NCI Cancer Center Support Grant to VCU Massey Cancer Center P30 CA016059 (S.K. Das, D. Sarkar, L. Emdad, and P.B. Fisher). D. Sarkar is a Harrison Scholar in the MCC, and P.B. Fisher holds the Thelma Newmeyer Corman Chair in Cancer Research.

The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

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