Elevated Ornithine Decarboxylase Levels Activate ATM - DNA Damage Signaling in Normal Keratinocytes

doi:10.1158/0008-5472.CAN-07-5030

Cancer Res. Author manuscript; available in PMC 2009 April 1.

Published in final edited form as:

Cancer Res. 2008 April 1; 68(7): 2214–2222.

doi: 10.1158/0008-5472.CAN-07-5030

PMCID: PMC2392890

NIHMSID: NIHMS48343

Elevated Ornithine Decarboxylase Levels Activate ATM - DNA Damage Signaling in Normal Keratinocytes

Gang Wei,¹ Karen DeFeo,¹ Candace S. Hayes,¹ Patrick M. Woster,² Laura Mandik-Nayak,¹ and Susan K. Gilmour^1,³

¹Lankenau Institute for Medical Research 100 Lancaster Avenue Wynnewood, Pennsylvania 19096

²Department of Pharmaceutical Sciences Wayne State University Detroit, MI 48202

³To whom requests for reprints should be addressed, at Lankenau Institute for Medical Research, 100 Lancaster Avenue, Wynnewood, PA 19096 USA; Telephone: (610) 645−8429; Fax: (610) 645−2205; E-mail: gilmours/at/mlhs.org.

The publisher's final edited version of this article is available free at Cancer Res

See other articles in PMC that cite the published article.

Abstract

We examined the effect of increased expression of ornithine decarboxylase (ODC), a key rate-limiting enzyme in polyamine biosynthesis, on cell survival in primary cultures of keratinocytes isolated from the skin of K6/ODC transgenic mice (Ker/ODC) and their normal littermates (Ker/Norm). Although elevated levels of ODC and polyamines stimulate proliferation of keratinocytes, Ker/ODC undergo apoptotic cell death within days of primary culture unlike Ker/Norm that continue to proliferate. Phosphorylation of ATM and its substrate p53 are significantly induced both in Ker/ODC and in K6/ODC transgenic skin. ChIP analyses show that the increased level of p53 in Ker/ODC is accompanied by increased recruitment of p53 to the Bax proximal promoter. ATM activation is polyamine-dependent since DFMO, a specific inhibitor of ODC activity, blocks its phosphorylation. Ker/ODC also display increased generation of H₂O₂, acrolein-lysine conjugates, and protein oxidation products as well as polyamine-dependent DNA damage, as measured by the comet assay and the expression of the phosphorylated form of the histone variant γH2AX. Both ROS generation and apoptotic cell death of Ker/ODC may, at least in part, be due to induction of a polyamine catabolic pathway that generates both H₂O₂ and cytotoxic aldehydes, since spermine oxidase (SMO) levels are induced in Ker/ODC. In addition, treatment with MDL 72,527, an inhibitor of SMO, blocks the production of H₂O₂ and increases the survival of Ker/ODC. These results demonstrate a novel activation of the ATM/DNA damage signaling pathway in response to increased ODC activity in nontumorigenic keratinocytes.

Keywords: p53, polyamines, ornithine decarboxylase, reactive oxygen species, ATM activation, spermine oxidase

Introduction

Previous reports have demonstrated that overexpression of ODC enzyme targeted to the skin of K6/ODC transgenic mice stimulates cellular proliferation in the epithelial cells (1), and promotes the development of tumors in carcinogen-initiated skin (2). While not sufficient to lead to tumor formation, overexpression of ODC in the skin of K6/ODC transgenic mice cooperates with oncogenes such as a mutated H-ras to produce spontaneous skin carcinomas in ODC/Ras double transgenic mice (3). Whereas elevated ODC activity provides a strong proliferative stimulus, it can also induce the expression of inhibitory proteins such as p53, p21^WAF1, and p27^KIP1 as well as evidence of apoptosis in nontumor-bearing skin of K6/ODC transgenic mice (1). Conversely, polyamine depletion via inhibition of ODC or the induction of polyamine catabolic enzymes leads to enhanced expression of inhibitory proteins and inhibition of cell proliferation as well (4-6). These observations support the little understood view that tightly regulated intracellular levels of polyamines are required to maintain cell growth and normal cellular homeostasis. Indeed, polyamines play an important role in a variety of cellular processes including DNA replication, transcription, and translation.

Accumulation of p53 is unusual in normal nontumorigenic tissue since p53 has a short half-life and is normally maintained at low levels in unstressed mammalian cells. Levels of p53 protein are upregulated in response to DNA damage and other cellular stress signals such as oncogenic signaling (7). Various forms of environmental and intracellular stress including ultraviolet and ionizing radiation, DNA-damaging drugs, hypoxia, and hyperproliferation rapidly induce a transient increase in p53 protein with little or no effect on the steady-state level of p53 mRNA (8). Although the function of the p53 protein has proven to be very intricate, it is generally agreed that an important function of p53 is to trigger apoptosis in order to ensure that damaged DNA is not propagated to daughter cells (7). Because of its pivotal role in cell cycle control, it is not surprising that the p53 tumor suppressor gene is the most frequent target for genetic alterations in human cancers, with mutations occurring in almost 50% of all human tumors (9).

ATM (ataxia telangiectasia mutated) kinase plays an essential role in maintaining genome integrity by coordinating cell cycle arrest, apoptosis, and DNA damage repair (10). DNA damage triggers the phosphorylation of ATM at serine 1981 (ATM pSer1981), and this activation of ATM results in the subsequent phosphorylation of H2AX Ser139 (γH2AX), and p53 Ser15 (p53pSer15) (11, 12). The ATM-mediated phosphorylation of p53 inhibits Mdm2 binding and leads to accumulation and increased transcriptional activation capacity of p53 (11). Recent reports have demonstrated that the ATM-DNA damage response pathways are activated early by a number of proliferative or oncogenic factors, such as Myc, E2F1 and cyclin E (13-15).

This study investigates the apparent contradiction of the widely accepted role of ODC as a strong tumor promoting stimulus with the induction of cell death in a normal epithelial cell type that express elevated levels of ODC. We show that elevated ODC activity and increased biosynthesis of polyamines serve as a novel stimulus to induce the ATM/DNA damage signaling pathway and cell death in normal keratinocytes.

Materials and Methods

Transgenic Animals

K6/ODC transgenic mice in which a keratin 6 promoter directs the expression of ODC to the outer root sheath cells of hair follicles in the skin were used as previously described (1-3). K6/ODC transgenic mice were bred with p53^−/− mice (obtained from Jackson Laboratories, Bar Harbor, Maine) to generate p53^−/− mice with expressing the ODC transgene.

Primary cultures of epidermal cells

Primary cultures of epidermal cells were isolated from 3- to 4-day old K6/ODC transgenic newborn pups and their normal littermates by a trypsin flotation procedure. K6/ODC transgenic pups were distinguished from their normal littermates by PCR genotyping for the K6/ODC transgene. Cells were plated at 3.2 × 10⁶ cells per 60 mm dish or onto glass coverslips in low calcium keratinocyte media (EMEM without calcium, Cambrex, Walkersville, MD) supplemented with 8% chelex-treated fetal bovine serum, 0.05mM calcium, EGF, aminoguanidine and gentamycin and grown at 35°C with 5% CO₂. Some cells were treated with 3 mM DFMO (α-difluoromethylornithine) or 25 μM MDL 72,527 (N, N'-bis(2,3-butadienyl)-1,4-butanediamine) after plating. DFMO was obtained from ILEX Oncology (San Antonio, TX), and MDL 72,527 was synthesized in the laboratory of Dr. Patrick Woster.

Protein Extraction and Immunoblot Analyses

Keratinocytes were homogenized in either RIPA buffer (50 mM Tris-HCl, pH 7.4, 150 mM NaCl, 0.25% (w/v) deoxycholic acid, 1% (w/v) NP-40, 1 mM EDTA, containing 1 μg/mL each of aprotonin, leupeptin, pepstatin, 1 mM sodium orthovanadate, 1 mM sodium fluoride and 1 mM pefabloc), or Laemmli buffer (125 mM Tris-HCl, pH 6.8, 20% glycerol, 4% SDS, containing same protease inhibitors as RIPA buffer) and passed through a syringe needle multiple times preceding a 45 min incubation on ice. Lysates were clarified by centrifugation at 14,000 × g for 10 min and the protein content was determined using the Bio-Rad D/C protein assay kit (Bio-Rad Laboratories, Hercules, CA). Nuclear extracts were prepared using NE-PER kit (Pierce, Rockford, IL). Total skin tissues excised from K6/ODC transgenic and normal littermate mice were frozen in liquid nitrogen, pulverized and stored at −80°C. Ground skin tissue was homogenized in RIPA-DTT buffer (50 mM Tris-HCl, pH 7.5; 1% NP-40; 0.25% sodium deoxycholate; 0.25% SDS; 150 mM NaCl; 1 mM EGTA and 1 mM DTT) containing 2 μg/μl each of aprotinin, leupeptin, and pepstatin, 1 mM sodium fluoride, 1 mM sodium orthovanadate, and 1 mM Pefabloc, by passing through a syringe needle and incubating 30 minutes on ice. Debris was removed by centrifugation at 13000 rpm for 10 min. Protein content was determined using the Bio-Rad D/C protein assay kit.

Protein lysates were separated by SDS-PAGE, transferred to polyvinylidene difluoride (PVDF) membranes (Millipore, Temecula, CA), and briefly stained with Ponceau S (Sigma, St. Louis, MO) to verify efficient transfer. Immunoblots were incubated overnight at 4°C in blocking solution (phosphate-buffered saline (PBS) with 5% non-fat dry milk and 0.05% Tween 20) followed by 2 h incubation with the primary antibody diluted in PBS-Tween. Blots were probed with antibodies directed against PCNA (PC10), Lamin B (M-20) and p21 (C-19 (Santa Cruz, Santa Cruz, CA)); p53 (1C12) and phospho-p53 (Ser15) (16G8) (Cell Signaling Technology, Danvers, MA); phospho-ATM (S1981) (Rockland, Gilbertsville, PA); ATM (Genetex, San Antonio, TX); phospho-histone H2AX (Ser139), Bax and Bcl-2 (Upstate Biotechnology, Lake Placid, NY); p19^ARF (Calbiochem, San Diego, CA); and spermine oxidase (a kind gift from Bob Casero, Johns Hopkins University, Baltimore, MD) were used with the appropriate secondary antibody conjugated to horseradish peroxidase. Antibody binding was detected by enhanced chemiluminescence (ECL Plus Western Blotting Detection System, Amersham/GE Healthcare, Piscataway, NJ). Filters were reprobed with an antibody against tubulin (Calbiochem, San Diego, CA) to verify equal loading of protein.

Immunofluorescence

Formaldehyde-fixed, paraffin-embedded mouse skin sections were deparaffinized, steamed in 0.1 mM sodium citrate, pH 6.0 for 10 minutes, and incubated overnight at 4°C with antibodies specific for ATM pS1981 (Rockland Immunochemicals, Inc., Gilbertsville, PA) or ATM (GeneTex, Inc., San Antonio, TX), followed by incubation with secondary antibody conjugated to Cy3 (Jackson ImmunoResearch Laboratories, Inc., West Grove, PA). Sections were covered with coverslips mounted with Vectashield mounting medium containing DAPI (Vector Labs, Burlingame, CA) to counterstain DNA and to visualize the nuclei of all cells. Immunostained sections were imaged by fluorescence microscopy using a Zeiss Axioplan microscope powered by Axiovision 3.1 software and an Axiocam digital camera.

Single-Cell Gel Electrophoresis (Comet) Assay

Primary keratinocytes, at a concentration of 2 × 10⁵ cells per mL, were embedded in low-melting-point agarose on a glass slide using the Comet Assay kit and the manufacturer's protocol (Trevigen, Gaithersburg, MD). The embedded cells were incubated overnight at 4°C in the lysis solution provided. The following morning slides were incubated in alkaline solution for 40 min to denature the DNA. The samples were then washed twice in TBE buffer and electrophoresed at 19V for 10 min in 1X TBE buffer. The samples were stained with 50 μL of SYBR Green, and nuclei were visualized by fluorescent microscopy. Tail length and olive tail moment of at least 250 nuclei were scored using COMETSCORE software (TriTek, Morrisville, VA). (Student's t test was used to derive p values.) Tail moment is the product of the tail length and the fraction of total DNA in the tail, which gives a measure of the extent of DNA damage.

Detection of reactive oxygen species

Cells were trypsinized, collected in PBS and spun down for 4 min at 1000 rpm at 4°C. H₂O₂ generation was determined by incubating cells with 10 μM CM-H₂DCFdA (Molecular Probes, Eugene, Oregon) in 0.8 mL PBS at 37 °C on a nutator for 25 min. Samples were spun again for 4 min at 1000 rpm at 4°C and resuspended in 1 mL of PBS before being immediately read on a BD FACSCanto II flow cytometer and analyzed using BD FACS Diva software (Becton Dickinson, San Francisco, CA).

Detection of oxidative proteins and acrolein-conjugated proteins

The Oxyblot protein oxidation detection kit (Chemicon, Temecula, CA) based on reaction of protein carbonyl groups with 2,4-dinitrophenylhydrazine was used to perform the assay following the manufacturer's directions. For detection of acrolein-conjugated protein, PBS cell lysates were assayed by a direct NWLSS™ ACRL01 ELISA using a monoclonal antibody to acrolein-lysine (Northwest Life Science Specialties, Vancouver, WA).

Immunohistochemistry

Primary keratinocytes grown on glass coverslips were washed with cold PBS and fixed for 20 min with 4% p-formaldehyde in PBS. Slides were incubated with a primary antibody specific to the p20 subunit of Caspase 3 (R&D Systems, Minneapolis, MN). Slides then incubated with a biotinylated secondary antibody and then an avidin- biotinylated horseradish peroxidase complex (Vectastain Elite ABC kit, Vector Laboratories, Burlingame, CA). Immunoreactive cells were detected using diaminobenzidine chromagen solution and then counterstained with hematoxylin. At least 1000 cells were counted for each group and the percent of stained cells was reported.

Chromatin immunoprecipitation (ChIP) analysis

Experiments were performed using the Chromatin Immunoprecipitation Assay Kit (Upstate Biotechnology Inc., Charlottesville, VA) with some modification. Cells were fixed in 1% formaldehyde in PBS and rotated at room temperature for 15 minutes. The crosslinking reaction was stopped by adding glycine to a final concentration of 0.125 M with continued rotation for 5 minutes. Samples were centrifuged at low speed, washed once with cold PBS, incubated in PIPES buffer (5 mM Pipes, pH 8.0; 85 mM KCl; 0.5% NP-40; 10 mM sodium butyrate and inhibitor cocktail) on ice for 10 minutes, and homogenized on ice using a polytron homogenizer. Following low-speed centrifugation, the pellet was resuspended in Nuclei lysis buffer (50 mM Tris-HCl, pH 8.1; 10 mM EDTA; 1% SDS and inhibitors), incubated on ice for 20 minutes, and centrifuged. The pelleted material was resuspended in ChIP lysis buffer and the chromatin was sonicated to an average length of 800−600 bp. After clearance by centrifugation at maximum speed for 10 minutes at 4°C, the supernatant was diluted 10-fold in ChIP dilution buffer and incubated with salmon sperm DNA/protein A agarose for 30 minutes at 4°C with agitation. The precleared lysate was then incubated with polyclonal antibody p53 (FL-393) at 4°C overnight. The immunocomplexes were captured by salmon sperm DNA adsorbed/protein A beads. After sequential washings, the immunocomplexes were eluted from the beads, and DNA-protein crosslinks were reversed by incubating for 6 hours at 65°C. DNA was purified using the MinElute PCR cleanup kit (Qiagen, Valencia, CA). The following primers were used to amplify the proximal promoter of the BAX gene: sense primer 5’- GAT GTT GTA GCC ACC GCG TAC AGC C -3’; antisense primer 5’- TTC ATG GTA GAG AGC ACT AAG GAG G -3’.

RNA isolation and reverse transcription-PCR

Total RNA was isolated from skin tissue using TriReagent (Molecular Research Center, Cincinnati, OH). Total RNA (2μg) was reverse transcribed using random hexamer primers at 42°C for 1 hour. Duplicate PCR amplification reactions contained 200 μmol/L deoxynucleotide triphosphates, 0.04 to 0.5 μmol/L forward and reverse primers, 1 mol/L betaine, and 1 unit of polymerase. A constitutively expressed gene, glyceraldehyde 3-phosphate dehydrogenase (GAPDH), was simultaneously amplified as an internal control. Twenty μL of PCR products were electrophoresed on a 1.5% agarose gel. The primers used for PCR were SMO forward primer 5’-CAC GTG ATT GTG ACC GTT TC-3’and reverse primer 5’- TGG GTA GGT GAG GGT ACA GTC -3’; SSAT forward primer 5’- GAC CCC TGA AGG ACA TAG CA-3’ and reverse primer 5’-CCG AAG CAC CTC TTC TTT TG-3’; APAO forward primer 5’-CTT TTC CAG GGG AGA CCT TC-3’ and reverse primer 5’- CAC ACC ACC TGG ATG AAC TG-3’; AdoMetDC forward primer 5’-GACA TTAGCTAGCG CTCGCTCAAC-3’ and reverse primer 5’-CAGACCTCCAGCAGTTTCTCCGTCCCTTCG-3’; and GAPDH forward primer 5’-TGC TGA GTA TGT CGT GGA GTC-3’ and reverse primer 5’-AGT GGG AGT TGC TGT TGA AGT-3’.

Results

Polyamine-Dependent p53 Protein Accumulation and Apoptotic Cell Death in ODC-Overexpressing Primary Keratinocytes

In order to investigate the effect of elevated ODC activity on normal epithelial cell function, we cultured primary keratinocytes from the skin of K6/ODC transgenic mice (Ker/ODC) and their normal littermates (Ker/Norm). In agreement with previous reports that increased ODC activity directed to various subpopulations of epidermal cells stimulates cell proliferation both in vivo (1, 16) and in primary keratinocyte cultures (16), the proliferation marker PCNA remains elevated in Ker/ODC (Fig. 1A). However, expression of proteins associated with cell growth inhibition, such as p53 and p21^Waf1, also increases in Ker/ODC compared to Ker/Norm (Fig. 1A). Treatment with DFMO prevents these changes in Ker/ODC, and normalizes the cells. Indeed, Ker/ODC undergo early cell death within a week of culture unlike Ker/Norm that remain viable (Fig. 1B). Viability of Ker/ODC appears to be dependent upon cell density since plating both Ker/ODC and Ker/Norm at near confluent density prolongs the survival of Ker/ODC, albeit only delaying the earlier death of Ker/ODC compared to that of Ker/Norm. This early cell death is dependent upon polyamine biosynthesis since treatment of Ker/ODC with α-difluoromethylornithine (DFMO), a specific inhibitor of ODC enzyme activity, blocks cell death. Cell death in ODC-overexpressing keratinocytes appears to be due to apoptosis as evidenced by a significant increase in numbers of Ker/ODC positive for the activated cleaved form of caspase-3 compared to that seen in Ker/Norm or in DFMO-treated Ker/ODC (Fig. 1C). In addition, the expression of the proapoptotic protein, Bax, increased in Ker/ODC with no significant change in the pro-survival protein Bcl-2, and this was prevented when Ker/ODC were cultured in medium containing DFMO to inhibit ODC activity (Fig. 1A).

Figure 1

Polyamine-dependent p53 protein accumulation and apoptotic cell death in ODC-overexpressing primary keratinocytes

In order to confirm whether accumulated and, therefore stabilized, p53 may be regulating the expression of the pro-apoptotic gene Bax, we investigated whether more p53 is bound to the Bax promoter using crosslinked chromatin from Ker/Norm, Ker/ODC, and DFMO-treated Ker/ODC using a chromatin immunoprecipitation assay. Figure 1D shows enhanced binding of p53 protein to the Bax promoter in ODC overexpressing keratinocytes, and inhibition of this binding in Ker/ODC treated with DFMO. These findings suggest that polyamine-dependent p53 accumulation plays a role in the induction of apoptosis in ODC-overexpressing keratinocytes.

ODC overexpression activates ATM in the DNA damage signaling pathway

Post-translational modification of p53, including phosphorylation, plays an essential role in both stabilization and activation of the normally short-lived p53 protein (11, 17). Since p53 protein accumulates in keratinocytes with elevated ODC activity, we analyzed nuclear extracts of Ker/ODC and Ker/Norm for p53 phosphorylated at Ser15. Phosphorylation of serine-15 in p53 was induced in Ker/ODC, and the ODC-induction of p53 phosphorylation was blocked by DFMO (Fig. 2A). There was no change in lamin B indicating equal extraction of nuclear protein. Phosphorylation and activation of ATM leads to the phosphorylation of several ATM targets including Ser15 in p53 as well as Mdm2 and γH2AX, the phosphorylated form of the histone variant H2AX (18). Immunoblot analyses of cell lysates from Ker/ODC and Ker/Norm revealed not only elevated phosphorylation of ATM at Ser1981 but also increased phosphorylation of the ATM substrate, γH2AX (Fig. 2A) and Mdm2 (data not shown). Similar to p53 phosphorylation, DFMO treatment suppressed both the ATM and γH2AX phosphorylation, indicating that elevated levels of ODC leads to ATM activation and subsequent phosphorylation and activation of p53.

Figure 2

ODC overexpression activates ATM in primary keratinocytes and in K6/ODC transgenic skin

Stabilization of p53 can also be mediated through the Arf-mdm2-p53 pathway that is activated by growth-promoting stimuli such as oncoproteins. For example, constitutive and simultaneous activation of multiple signaling pathways by oncogenic Myc induces p19^ARF, that blocks Mdm2-mediated inhibition of p53 and stabilizes p53 (19). Although ODC is known to be transactivated by c-Myc, immunoblot analyses revealed no change in the levels of p19^Arf expression in Ker/ODC compared to Ker/Norm (Fig. 2A).

To determine if elevated polyamine biosynthesis activates the ATM pathway in vivo, we examined the skin of K6/ODC transgenic mice, in which ODC is targeted to the outer root sheath cells of hair follicles with a keratin 6 promoter (1). Immunofluorescent staining was performed on skin sections from K6/ODC transgenic mice and their normal littermates. ATM phosphorylated at serine-1891 was detected in the epithelial cells lining follicular cysts in the dermis of K6/ODC transgenic skin (Fig. 2B), which corresponds to the staining pattern for ODC protein. Phospho-ATM staining was completely inhibited with the addition of phospho-ATM peptide (Fig. 2B). In contrast, there was no significant difference in the ATM staining pattern in skin sections from K6/ODC transgenic mice and normal littermates (data not shown). Phosphorylation of serine-15 in p53 was significantly induced in K6/ODC transgenic skin compared to normal littermate skin (Fig. 2C). These combined results suggest that elevated ODC is a novel stress signal that activates the ATM response pathway.

DNA damage induced by elevated ODC activity in primary keratinocytes

Whereas γH2AX has been reported to be a sensitive marker for detecting DNA damage (20), the Comet assay was also used to confirm that elevated ODC activity in primary cultures of keratinocytes induces DNA damage. In contrast to wild type keratinocytes, the majority of Ker/ODC demonstrated comet tails, indicating DNA damage (Fig. 3). Although some tails were also detected in DFMO-treated Ker/ODC, the number of positive cells and the average length of the comet tails were similar to that seen with Ker/Norm and significantly depressed compared to nontreated Ker/ODC. Measurements of the average tail length and tail moment confirmed that Ker/ODC had significantly (p < 0.0001) more DNA damage compared with normal littermate keratinocytes and that inhibition of polyamine biosynthesis with DFMO blocked the induction of DNA damage (Fig. 3).

Figure 3

DNA damage induced by elevated ODC activity in primary keratinocytes

Increased Reactive Oxygen Species with Elevated ODC activity

The induction of polyamine catabolic pathways leads to the production of H₂O₂ and cytotoxic aldehydes (6, 21). The back-conversion of the polyamines spermine and spermidine can be mediated by two pathways, both involving oxidases that generate H₂O₂(22-25). Spermine can be directly converted to spermidine, H₂O₂, and 3-aminopropanal by spermine oxidase (SMO). In addition, spermine or spermidine can first be acetylated by spermidine/spermine N¹-acetyltransferase (SSAT) and then oxidized by acetylpolyamine oxidase (APAO) to produce H₂O₂ as a by-product. The effect of elevated ODC activity on possible induction of SMO, SSAT, and APAO mRNA was examined using semiquantitative RT-PCR. Although SSAT and APAO mRNA were not induced in Ker/ODC, SMO mRNA levels were elevated in keratinocytes with increased ODC activity (Fig. 4B). Immunoblot analyses of keratinocyte lysates revealed that SMO protein is induced in ODC overexpressing keratinocytes and inhibited with DFMO (Fig. 4A). However, we found no evidence of increased APAO protein levels or increased SSAT activity in Ker/ODC compared to Ker/Norm (data not shown). Moreover, although HPLC analysis of intracellular polyamines revealed increased levels of putrescine in Ker/ODC, acetylated polyamines were not detected and spermine levels were decreased (Fig. 4C). Consistent with the small rise in spermidine and the lack of increase in spermine levels in Ker/ODC, we found no increased expression of S-adenosylmethionine decarboxylase (AdoMetDC), the rate-limiting enzyme in the biosynthesis of spermidine and spermine (Fig. 4B). These data suggest that increased ODC activity results in dramatic increases in putrescine levels and reduced spermine levels due to induction of the catabolic enzyme spermine oxidase.

Figure 4

Elevated ODC activity induces spermine oxidase

Since reactive oxygen species (ROS) induce oxidative damage of DNA resulting in DNA breaks that can activate the ATM-DNA damage response pathway (26, 27), we investigated whether ROS play a role in the activation of the ATM/DNA damage pathway in ODC overexpressing primary keratinocytes. ROS activity was measured in Ker/Norm and Ker/ODC via fluorescence measured by flow cytometry. Figure 5A shows a significant increase in the ROS production as indicated by the shift to the right of the fluorescence peaks in the presence of CM-H₂DCFDA, an oxidation-sensitive fluorescent probe. Spermine oxidation by SMO produces H₂O₂ and 3-aminopropanal that spontaneously forms the highly reactive and toxic compound acrolein (28). Protein-conjugated acrolein levels as determined by ELISA assay were significantly elevated in Ker/ODC compared to Ker/Norm, and the accumulation of acrolein protein conjugates was prevented with DFMO treatment (Fig. 5B). Additional evidence of ROS production included a 2-fold increase in protein carbonyl levels, or protein oxidation products, in Ker/ODC lysates compared to that of Ker/Norm or DFMO-treated Ker/ODC (Fig. 5C). All together, these results suggest that elevated ODC activity induces spermine catabolism via SMO, subsequently leading to increased ROS activity in primary cultures of keratinocytes.

Figure 5

Elevated ODC activity leads to increased ROS generation

Inhibition of ODC or Polyamine Catabolic Enzymes Increases Survival of ODC Overexpressing Keratinocytes

To determine if polyamine catabolism is the source of ODC-induced H₂O₂ production, Ker/ODC were cultured with MDL 72,527, an inhibitor of the polyamine catabolic enzymes spermine oxidase and polyamine oxidase (25). Similar to culture with DFMO, treatment with 25 μM MDL 72,527 attenuated the shift to the right in fluorescence in the presence of CM-H₂DCFDS in Ker/ODC compared with Ker/Norm (Fig. 6A). Since MDL 72,527 inhibits ROS generation in Ker/ODC, the cells were cultured with MDL 72,527 to compare their survival with non-treated Ker/ODC. Most of the ODC-overexpressing keratinocytes died by 7 days following plating, but the Ker/ODC treated with MDL 72,527 remained viable similar to the Ker/Norm or DFMO-treated Ker/ODC even after 2 weeks in culture (Fig. 6B). Thus, MDL 72,527 inhibition of polyamine catabolic oxidase activity and its associated generation of ROS prevent the early apoptotic death of ODC-overexpressing keratinocytes.

Figure 6

DFMO and MDL72,527 prevent H₂O₂ generation in primary keratinocytes and increase survival of Ker/ODC

In an attempt to determine whether the ODC-induced apoptosis of primary keratinocytes is p53-dependent, K6/ODC transgenic mice were bred with p53^−/− knockout mice. Primary keratinocytes were cultured from the skin of p53^−/− knockout mice in which the ODC transgene is expressed and compared with p53^−/− keratinocytes with no ODC transgene expression. Both Ker/ODC and Ker/Norm with p53^−/− continued to proliferate 2 weeks following plating (Fig. 6B, lower panels) unlike the Ker/ODC with wild-type p53 that all died by 7 days of cell culture (Fig. 6B, top right panel). Thus, these data demonstrate that loss of p53 function confers increased survival in Ker/ODC.

Discussion

Although ATM is stimulated in response to a variety of oncogenic signals and DNA damage (29), we show that elevated levels of ODC activity stimulate ROS production and the ATM-DNA damage response pathway leading to apoptotic cell death of nontumorigenic epithelial cells. Our studies with primary keratinocytes isolated from p53^−/− null mice demonstrate that a loss of p53 function confers increased survival in Ker/ODC, suggesting that the ODC-induction of cell death in primary keratinocytes is p53-dependent. Normal cells are well protected against malignant transformation by the tumor suppressive activity of p53 that regulates the transcription of genes required for cell cycle arrest, DNA repair, and apoptosis. In addition to DNA damage, oncogenic signaling activates p53 through ARF, which interacts with MDM2 to inhibit its p53 ubiquitin ligase activity (19). However, we found no evidence of increased expression of p19^Arf in primary keratinocytes with elevated ODC. Our studies show that the activation of ATM and phosphorylation of the ATM substrates p53 and γH2AX are induced in both K6/ODC transgenic skin and in ODC overexpressing primary keratinocytes. In addition, previous studies have shown that levels of the Tip60 HAT enzyme, reported to acetylate and activate ATM (30), are also substantially elevated in the skin of ODC-overexpressing mice (31).

Since oncogenes such as c-Myc can transactivate and upregulate ODC expression (32), it is possible that activation of ATM by oncogenes such as c-Myc (15) is, at least in part, due to increased polyamine metabolism and production of ROS and DNA damage. This study adds ODC to the list of growth promoting stimuli, including oncogenes such as Myc or E2F1, that have been reported to induce the ATM signaling pathway (13, 15). DNA replication stress has been suggested to be a trigger for the ATM response pathway, which has been found to be activated in precancerous lesions (33, 34). Oncogenic activation may generate DNA damage through the production of reactive oxygen species and/or through the aberrant firing of replication origins (13, 35, 36). That elevated polyamine biosynthesis acts as a strong proliferative and tumor promoting stimulus while also inducing p53-mediated tumor suppressive activity presents a seeming paradox. However, a similar precedence has been reported for a variety of proliferative signals including the oncogenes c-Myc, Ras, and E2F1 (13, 15, 37). Although the immediate result is protective via cell cycle arrest and apoptosis of aberrantly growing cells that still retain a functional p53 (Fig. 6), it can also create a selection pressure for inactivation of ATM or p53, thus leading to genetic instability and tumor progression (14, 33, 34). It is likely that elevated ODC activity in primary cultures of proliferating keratinocytes is a greater stress than in relatively quiescent keratinocytes in intact skin. Although ATM is activated and p53 levels accumulate in both ODC-overexpressing keratinocyte cultures and in ODC transgenic skin, massive apoptosis is only observed in Ker/ODC cultured at subconfluent density. Thus, p53-dependent apoptotic cell death eliminates cells that have acquired ROS-induced damage that is too severe to be repairable or that may be oncogenic. Since ODC overexpressing keratinocytes exhibit both increased ROS production as well as increased DNA damage, ODC-induced apoptosis of cells with a functional p53 may play an important role in promoting tumorigenesis by contributing to a mutator phenotype. Indeed Wallon et al. (38) reported that overexpression of ODC enzyme targeted to the skin of K6/ODC transgenic mice may increase susceptibility to mutation following carcinogen exposure. In addition, recent studies have shown that while DNA damage-induction of p53 can produce a strong apoptotic response, it is not necessary for p53-mediated tumor suppression which requires ARF signaling in response to oncogene activation (7, 39). Thus, the lack of signaling through the ARF pathway, which is critical for p53-mediated tumor suppression, may leave the tissue more susceptible to genetic instability and tumor progression.

With increased ODC activity, stimulation of polyamine biosynthesis and subsequent increased intracellular polyamine levels induce the activity of normal polyamine catabolic pathways. We have shown that elevated ODC activity in normal keratinocytes results in the early induction of spermine oxidase that generates both 3-aminopropanal/acrolein and H₂O₂, leads to increased DNA damage, and activates ATM signaling. This novel activation of ATM and stabilization of p53 is dependent upon polyamine biosynthesis since specific inhibition of ODC activity with DFMO prevents both the generation of ROS and the subsequent activation of the ATM-DNA damage response pathway. Moreover, inhibition of spermine oxidase activity with MDL 72,527 treatment also inhibits ROS generation and subsequent cell death in ODC overexpressing keratinocytes. We found no evidence for ODC induction of polyamine catabolism via the SSAT/APAO pathway since there was no increase in SSAT activity, no acetylated polyamines detected, and no increase in APAO mRNA or protein levels in Ker/ODC. Indeed, a recent report (6) that SSAT overexpression leads to DNA damage and G₂ arrest concluded that the primary driving mechanism was due to the depletion of cellular polyamines with increased H₂O₂ production playing only a secondary role in the reduced cell proliferation. Furthermore, they found that spermine oxidase activity was not induced with SSAT overexpression, and the cells did not undergo apoptotic cell death despite the presence of damaged DNA (6). The decreased spermine levels detected in ODC overexpressing keratinocytes and skin likely results from the increased spermine oxidase activity. Although increased activity of polyamine catabolic oxidases, including both APAO and SMO, have been shown to lead to oxidative stress (21, 22, 25), our data suggest that induction of SMO is primarily responsible for the increased H₂O₂ and acrolein accumulation in Ker/ODC. Igarashi et al. (28, 40) have shown that acrolein is the major toxic compound produced from spermine by spermine oxidase. We have shown by a direct ELISA assay that there is a significant increase in acrolein-conjugated lysine in Ker/ODC cell lysates compared to Ker/Norm and that this can be blocked with DFMO. Since acrolein has been reported to cause DNA damage and cell damage in a variety of cell types (40, 41), it is likely that both H₂O₂ and aldehyde/acrolein produced via spermine oxidase activity are responsible for the induction of the DNA damage response observed in keratinocytes with elevated ODC activity.

Previous reports have also shown that alterations in intracellular polyamine levels can lead to apoptotic cell death. In particular, accumulation of putrescine, as a result of increased ODC activity or increased uptake from the medium, can provoke apoptosis in various cell types (42, 43). Putrescine induction of oxidative stress has been implicated to mediate apoptotic cell death induced by ODC (44), but the signaling pathways involved have not been defined prior to this study. Conversely, DFMO depletion of polyamines has also been reported by Wang et al.(45) to induce p53 gene expression and growth inhibition but not apoptosis in intestinal epithelial cells. Similarly, treatment of cells with polyamine analogues also results in decreased intracellular polyamines but, in some cases, cells undergo apoptosis (46, 47). However, unlike DFMO depletion of polyamines, polyamine analogues induce the activity of polyamine catabolic enzymes including spermine oxidase and polyamine oxidase, that generate H₂O₂ and toxic aldehyde/acrolein (21{Sakata, 2003 #1597, 48)}. The induction of polyamine catabolic oxidases and its associated H₂O₂ generation appears to be responsible for the anti-tumor activity of a variety of polyamine analogues (21). We have observed that treatment of ODC-overexpressing primary keratinocytes with the polyamine analogues, BENSpm or CPENSpm, accelerates their apoptotic cell death (data not shown). Thus, ODC-overexpressing keratinocytes are more sensitive to agents, such as the polyamine analogues, that cause additional ROS generation.

In summary, we demonstrate that apoptotic cell death is induced in normal keratinocytes with elevated ODC activity via the induced generation of reactive aldehydes and H₂O₂, at least in part due to induction of spermine oxidase, followed by the subsequent activation of the ATM-DNA damage response pathway. Since elevated ODC is a common characteristic of tumor cells, it is possible that cells with high ODC activity will be selectively sensitized to die when exposed to further oxidative insults by radiation or agents that cause further ROS stress. On the other hand, further studies are needed to explore the possibility that ODC-upregulation of polyamine catabolic oxidation and production of mutagenic ROS contributes to a malignant phenotype. Recent studies have shown that ROS production by inflammatory cells and its association with tumor development appears to be mediated in some cases by the induction of spermine oxidase either in response to pathogens such as H. pylori (49) or via a direct induction of spermine oxidase by TNFα (50). Accordingly, spermine oxidase may be a promising target for anti-neoplastic intervention in premalignant tissue with elevated ODC activity.

Acknowledgements

We are grateful to Dr. Robert Casero for his generous gift of spermine oxidase antibody and for his many insightful suggestions. We thank Dr. Slavoljub Vujcic and Paula Diegelman for their excellent technical assistance. We thank Drs. Debora Kramer, Ira Ayene and Alex Muller for helpful discussions and valuable comments on the manuscript. We would also like to thank Kate Ciavarelli for editorial assistance. This work was supported by NIH grants CA95592 and CA70739 (S.K.G.)

References

1. Gilmour SK, Birchler M, Smith MK, Rayca K, Mostochuk J. Effect of elevated levels of ornithine decarboxylase on cell cycle progression in skin. Cell Growth Differ. 1999;10:739–48. [PubMed]

2. O'Brien TG, Megosh LC, Gilliard G, Soler AP. Ornithine decarboxylase overexpression is a sufficient condition for tumor promotion in mouse skin. Cancer Res. 1997;57(13):2630–7. [PubMed]

3. Smith MK, Trempus CS, Gilmour SK. Co-operation between follicular ornithine decarboxylase and v-Ha-ras induces spontaneous papillomas and malignant conversion in transgenic skin. Carcinogenesis. 1998;19(8):1409–15. [PubMed]

4. Ray RM, Zimmerman BJ, McCormack SA, Patel TB, Johnson LR. Polyamine depletion arrests cell cycle and induces inhibitors p21(Waf1/Cip1), p27(Kip1), and p53 in IEC-6 cells. Am J Physiol. 1999;276(3 Pt 1):C684–C91. [PubMed]

5. Kramer DL, Vujcic S, Diegelman P, et al. Polyamine analogue induction of the p53-p21WAF1/CIP1-Rb pathway and G1 arrest in human melanoma cells. Cancer Res. 1999;59(6):1278–86. [PubMed]

6. Zahedi K, Bissler JJ, Wang Z, et al. Spermidine/spermine N1-acetyltransferase overexpression in kidney epithelial cells disrupts polyamine homeostasis, leads to DNA damage, and causes G2 arrest. Am J Physiol Cell Physiol. 2007;292(3):C1204–C15. [PubMed]

7. Efeyan A, Serrano M. p53: guardian of the genome and policeman of the oncogenes. Cell Cycle. 2007;6(9):1006–10. [PubMed]

8. Prives C, Hall PA. The p53 pathway. J Pathol. 1999;187(1):112–26. [PubMed]

9. Hollstein M, Shomer B, Greenblatt M, et al. Somatic point mutations in the p53 gene of human tumors and cell lines: updated compilation. Nucleic Acids Res. 1996;24(1):141–6. [PMC free article] [PubMed]

10. Bakkenist CJ, Kastan MB. Initiating cellular stress responses. Cell. 2004;118(1):9–17. [PubMed]

11. Appella E, Anderson CW. Post-translational modifications and activation of p53 by genotoxic stresses. Eur J Biochem. 2001;268(10):2764–72. [PubMed]

12. Kang J, Ferguson D, Song H, et al. Functional interaction of H2AX, NBS1, and p53 in ATM-dependent DNA damage responses and tumor suppression. Mol Cell Biol. 2005;25(2):661–70. [PMC free article] [PubMed]

13. Vafa O, Wade M, Kern S, et al. c-Myc can induce DNA damage, increase reactive oxygen species, and mitigate p53 function: a mechanism for oncogene-induced genetic instability. Mol Cell. 2002;9(5):1031–44. [PubMed]

14. Hong S, Pusapati RV, Powers JT, Johnson DG. Oncogenes and the DNA Damage Response: Myc and E2F1 Engage the ATM Signaling Pathway to Activate p53 and Induce Apoptosis. Cell Cycle. 2006;5(8):801–3. [PubMed]

15. Pusapati RV, Rounbehler RJ, Hong S, et al. ATM promotes apoptosis and suppresses tumorigenesis in response to Myc. Proc Natl Acad Sci U S A. 2006;103(5):1446–51. [PubMed]

16. Lan L, Hayes CS, Laury-Kleintop L, Gilmour S. Suprabasal induction of ornithine decarboxylase in adult mouse skin is sufficient to activate keratinocytes. J Invest Dermatol. 2005;124:602–14. [PubMed]

17. Brooks CL, Gu W. Ubiquitination, phosphorylation and acetylation: the molecular basis for p53 regulation. Curr Opin Cell Biol. 2003;15(2):164–71. [PubMed]

18. Banin S, Moyal L, Shieh S, et al. Enhanced phosphorylation of p53 by ATM in response to DNA damage. Science. 1998;281(5383):1674–7. [PubMed]

19. Sherr CJ. The INK4a/ARF network in tumour suppression. Nat Rev Mol Cell Biol. 2001;2(10):731–7. [PubMed]

20. Rogakou EP, Pilch DR, Orr AH, Ivanova VS, Bonner WM. DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139. J Biol Chem. 1998;273(10):5858–68. [PubMed]

21. Pledgie A, Huang Y, Hacker A, et al. Spermine oxidase SMO(PAOh1), Not N1-acetylpolyamine oxidase PAO, is the primary source of cytotoxic H2O2 in polyamine analogue-treated human breast cancer cell lines. J Biol Chem. 2005;280(48):39843–51. [PubMed]

22. Vujcic S, Diegelman P, Bacchi CJ, Kramer DL, Porter CW. Identification and characterization of a novel flavin-containing spermine oxidase of mammalian cell origin. Biochem J. 2002;367(Pt 3):665–75. [PubMed]

23. Vujcic S, Liang P, Diegelman P, Kramer DL, Porter CW. Genomic identification and biochemical characterization of the mammalian polyamine oxidase involved in polyamine back-conversion. Biochem J. 2003;370(Pt 1):19–28. [PubMed]

24. Wang Y, Devereux W, Woster PM, Stewart TM, Hacker A, Casero RA., Jr Cloning and characterization of a human polyamine oxidase that is inducible by polyamine analogue exposure. Cancer Res. 2001;61(14):5370–3. [PubMed]

25. Wang Y, Murray-Stewart T, Devereux W, et al. Properties of purified recombinant human polyamine oxidase, PAOh1/SMO. Biochem Biophys Res Commun. 2003;304(4):605–11. [PubMed]

26. Barzilai A, Yamamoto K. DNA damage responses to oxidative stress. DNA Repair (Amst) 2004;3(8−9):1109–15. [PubMed]

27. Tanaka T, Halicka HD, Huang X, Traganos F, Darzynkiewicz Z. Constitutive histone H2AX phosphorylation and ATM activation, the reporters of DNA damage by endogenous oxidants. Cell Cycle. 2006;5(17):1940–5. [PubMed]

28. Sakata K, Kashiwagi K, Sharmin S, Ueda S, Igarashi K. Acrolein produced from polyamines as one of the uraemic toxins. Biochem Soc Trans. 2003;31(2):371–4. [PubMed]

29. Bakkenist CJ, Kastan MB. DNA damage activates ATM through intermolecular autophosphorylation and dimer dissociation. Nature. 2003;421(6922):499–506. [PubMed]

30. Sun Y, Jiang X, Chen S, Fernandes N, Price BD. A role for the Tip60 histone acetyltransferase in the acetylation and activation of ATM. Proc Natl Acad Sci U S A. 2005;102(37):13182–7. [PubMed]

31. Hobbs CA, Wei G, Defeo K, Paul B, Hayes CS, Gilmour SK. Tip60 Protein Isoforms and Altered Function in Skin and Tumors that Overexpress Ornithine Decarboxylase. Cancer Res. 2006;66(16):8116–22. [PubMed]

32. Bello-Fernandez C, Packham G, Cleveland JL. The ornithine decarboxylase gene is a transcriptional target of c-Myc. Proc Natl Acad Sci USA. 1993;90:7804–8. [PubMed]

33. Bartkova J, Horejsi Z, Koed K, et al. DNA damage response as a candidate anti-cancer barrier in early human tumorigenesis. Nature. 2005;434(7035):864–70. [PubMed]

34. Gorgoulis VG, Vassiliou LV, Karakaidos P, et al. Activation of the DNA damage checkpoint and genomic instability in human precancerous lesions. Nature. 2005;434(7035):907–13. [PubMed]

35. Di Micco R, Fumagalli M, Cicalese A, et al. Oncogene-induced senescence is a DNA damage response triggered by DNA hyper-replication. Nature. 2006;444(7119):638–42. [PubMed]

36. Lee AC, Fenster BE, Ito H, et al. Ras proteins induce senescence by altering the intracellular levels of reactive oxygen species. J Biol Chem. 1999;274(12):7936–40. [PubMed]

37. Zhao Y, Chaiswing L, Bakthavatchalu V, Oberley TD, St Clair DK. Ras mutation promotes p53 activation and apoptosis of skin keratinocytes. Carcinogenesis. 2006;27(8):1692–8. [PubMed]

38. Wallon UM, O'Brien TG. Polyamines modulate carcinogen-induced mutagenesis in vivo. Environ Mol Mutagen. 2005;45(1):62–9. [PubMed]

39. Christophorou MA, Ringshausen I, Finch AJ, Swigart LB, Evan GI. The pathological response to DNA damage does not contribute to p53-mediated tumour suppression. Nature. 2006;443(7108):214–7. [PubMed]

40. Igarashi K, Ueda S, Yoshida K, Kashiwagi K. Polyamines in renal failure. Amino Acids. 2006;31(4):477–83. [PubMed]

41. Feng Z, Hu W, Hu Y, Tang MS. Acrolein is a major cigarette-related lung cancer agent: Preferential binding at p53 mutational hotspots and inhibition of DNA repair. Proc Natl Acad Sci U S A. 2006;103(42):15404–9. [PubMed]

42. Tobias KE, Kahana C. Exposure to ornithine results in excessive accumulation of putrescine and apoptotic cell death in ornithine decarboxylase overproducing mouse myeloma cells. Cell Growth Differ. 1995;6:1279–85. [PubMed]

43. Tome ME, Fiser SM, Payne CM, Gerner EW. Excess putrescine accumulation inhibits the formation of modified eukaryotic initiation factor 5A (eIF-5A) and induces apoptosis. Biochem J. 1997;328(Pt 3):847–54. [PubMed]

44. Erez O, Goldstaub D, Friedman J, Kahana C. Putrescine activates oxidative stress dependent apoptotic death in ornithine decarboxylase overproducing mouse myeloma cells. Exp Cell Res. 2002;281(1):148–56. [PubMed]

45. Li L, Li J, Rao JN, Li M, Bass BL, Wang JY. Inhibition of polyamine synthesis induces p53 gene expression but not apoptosis. Am J Physiol. 1999;276(4 Pt 1):C946–C54. [PubMed]

46. Kramer DL, Fogel-Petrovic M, Miller J, Diegelman P, McManis JS, Bergeron RJ, Porter CW. Effects of novel spermine analogs on cell cycle progression and apoptosis in MALME-3M human melanoma cells. Cancer Res. 1997;57:5521–7. [PubMed]

47. Casero RA, Jr., Frydman B, Stewart TM, Woster PM. Significance of targeting polyamine metabolism as an antineoplastic strategy: unique targets for polyamine analogues. Proc West Pharmacol Soc. 2005;48:24–30. [PubMed]

48. Devereux W, Wang Y, Stewart TM, et al. Induction of the PAOh1/SMO polyamine oxidase by polyamine analogues in human lung carcinoma cells. Cancer Chemother Pharmacol. 2003;52(5):383–90. [PubMed]

49. Xu H, Chaturvedi R, Cheng Y, et al. Spermine oxidation induced by Helicobacter pylori results in apoptosis and DNA damage: implications for gastric carcinogenesis. Cancer Res. 2004;64(23):8521–5. [PubMed]

50. Babbar N, Casero RA., Jr Tumor necrosis factor-alpha increases reactive oxygen species by inducing spermine oxidase in human lung epithelial cells: a potential mechanism for inflammation-induced carcinogenesis. Cancer Res. 2006;66(23):11125–30. [PubMed]