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I.Rusyn et al.
polymerases and ligases in livers of rats (Fisher 344) and mice(C57Bl/6) treated with peroxisome proliferators. To assemblea comprehensive set of liver tissues, a combination of samplesfrom several different studies performed at the University ofNorth Carolina at Chapel Hill, Chemical Industry Instituteof Toxicology, or by the National Toxicology Program hasbeen used.
WY-14,643 causes a dose-dependent increase in expression
of DNA BER enzymes in rodent liver
Mammalian N-methylpurine-DNA glycosylase (MPG) hasbroad substrate specificity and primarily is capable of hydro-lysis of 3-methyladenine. It has also been shown to hydrolyze1,N6-ethenoadenine in vitro and weak activity towards 8-OH-dG has been reported (19). A quantitative reverse transcriptasePCR assay (19) was used to test the hypothesis that peroxisomeproliferators induce expression of MPG in rat liver. The useof in vitro synthesized reference RNA allowed quantitation ofthe PCR products (MPG and standard) after gel electrophoresisand autoradiography (Figure 1A). The effect of a 21 daytreatment with WY-14,643 (1000 p.p.m.) on MPG mRNA inwhole rat liver is shown in Figure 1B. In livers of animals feda regular chow diet, expression of MPG mRNA was low (89 ⫾ 16 fg/µg total RNA), however, it was elevated 2-fold aftertreatment with WY-14,643 (164 ⫾ 21 fg/µg total RNA).
Moreover, a dose-dependent increase in expression of MPGwas observed in rats treated with WY-14,643 for 90 days(Figure 1C). The amount of MPG mRNA was 2- or 6.5-foldhigher in livers of rats treated with 100 or 500 p.p.m. WY-14,643, respectively, than in control animals. Collectively,these results support the hypothesis that potent peroxisomeproliferators (i.e. WY-14,643) may inflict DNA damage andthat levels of DNA repair gene expression could be used toestablish a gene response profile after exposure to thesechemicals.
Next, we used a recently developed multi-probe RNase protection assay for BER enzymes. This approach distinguishesthe presence of multiple expressed DNA repair genes simultan-eously from a single sample, which allows comparative analysisof different mRNA products both within and between samples.
This is a highly sensitive and specific approach for detection Fig. 1. MPG mRNA is induced in rat liver by dietary feeding of WY-
and quantitation of gene expression at the mRNA level. It 14,643. (A) An autoradiogram of PCR products of native mRNA and
synthetic MPG RNA (a kind gift of Dr S. Mitra, University of Texas,
should be noted, however, that the RNase protection assay Galveston, TX) after EcoRI digestion is shown. Fisher 344 rats were fed template sets (a kind gift of BD PharMingen, San Diego, CA) either control diet (NIH-07) or diet containing WY-14,643 (1000 p.p.m. for used here for rat and mouse tissues were under development 21 days). Total cellular RNA was isolated using a QuickPrep extraction kit and differed slightly in the composition of DNA repair genes (Amersham Pharmacia Biotech) and RT–PCR was performed as describedin Roy et al. (19). Three 1:2 serial dilutions of each sample mixture evaluated. Total mRNA was isolated from livers of rats fed containing 2 µg total cellular RNA and 540 fg synthetic RNA standard were control or WY-14,643 (1000 p.p.m.)-containing diet for up to made, amplified by PCR and resolved on 6% polyacrylamide gels. The 471 22 weeks. A time-dependent 3- to 12-fold increase in mRNA bp product of cellular MPG amplification and 366 bp product of reference for OGG1, APE, MPG and Pol β was observed (Figure 2).
RNA amplification after enzymatic cleavage of the 105 bp non-radioactive Importantly, expression of several enzymes that are not related fragment are indicated. Representative autoradiogram. (B) Data shown are
results of densitometry analysis of images from the experiment detailed in
to oxidative DNA damage (e.g. O6-methylguanine-DNA (A). (C) As above but rats were given 0 (Control), 100 or 500 p.p.m. WY-
methyltransferase and polymerase δ) was not changed. It 14,643 for 90 days. Data reported as means ⫾ SEM from four separate should be noted that our findings of an increased expression experiments. Asterisks (*) denote statistical differences (P ⬍ 0.05) from the of mRNA for BER proteins were corroborated recently when control group by one way ANOVA and Student–Newman–Keuls post hoctest.
it was reported that Pol β and APE protein levels wereincreased markedly after treatment with WY-14,643 for 6days (20).
patch' repair pathway, was induced in mouse liver after dietary The single nucleotide BER pathway is a favorable mechan- treatment with WY-14,643 (500 p.p.m.) for 7 days (Figure 3).
ism for removal of oxidized bases and is dependent upon the Similar to what was observed in rats, WY-14,643 (500 p.p.m.) interaction between DNA Pol β and DNA ligase I (21). Indeed, caused an 3-fold increase in mRNA for OGG1, TDG, APE, only ligase I, but not ligase III or other enzymes of the ‘long MPG and Nth1 in mouse liver (data not shown). These findings

Peroxisome proliferators induce DNA repair
Fig. 3. Expression of ligase I is induced in mouse liver by WY-14,643.
Mice (C57Bl/6) were fed a diet containing the potent carcinogen WY-
14,643 (WY, 500 p.p.m.) for 7 days. Total RNA was isolated from liver
samples and used in the RNase protection assay as detailed in Figure 2.
Representative autoradiograms from three separate experiments.
carcinogens from this group of compounds have similar effectson DNA repair enzymes, rats were fed WY-14,643 or theweaker carcinogens di(2-ethyhexyl)phthalate (DEHP) and clo-fibric acid for 22 weeks. Both DEHP (12000 p.p.m.) andclofibric acid (5000 p.p.m.) increased expression of mRNAfor OGG1, APE, MPG and Pol β by 2- to 3-fold, however, Fig. 2. WY-14,643 causes a time-dependent increase in expression of base
these effects fell short of the profound changes caused by excision DNA repair enzymes in rat liver. (A) Total RNA was isolated from
WY-14,643 (1000 p.p.m.) (Figure 4). It should be noted that livers of rats treated with WY-14,643 (1000 p.p.m.) for up to 22 weeks since WY-14,643, DEHP and clofibric acid cause a similar using a QuickPrep extraction kit (Amersham Pharmacia Biotech) anddissolved in RNase-free water. Expression of base excision DNA repair initial increase in cell proliferation, the differences in expres- enzymes was analyzed with an RNase protection assay using rodent multi- sion of DNA repair enzymes observed here are not due to a nucleotide RNA probe template sets (a generous gift of BD PharMingen).
rapid growth of liver mass. Furthermore, when WY-14,643 Riboprobes were synthesized in the presence of [32P]dUTP to yield labeled (1000 p.p.m.) and DEHP (12000 p.p.m.) were administered to antisense RNA probes. The RNase protection assay was performed on 40 rats for 7 days, induction of OGG1 APE and Nth1 was µg of individual RNA samples using a RiboQuant multi-probe RNaseprotection assay kit (BD PharMingen). Protected fragments were separated observed only in WY-14,643-treated animals (data not shown).
on QuickPoint nucleic acid separation gels (Novex, San Diego, CA), dried Similar effects were observed with gemfibrozil, another potent and exposed to X-ray film. Representative autoradiogram from three rodent carcinogen, but not with the weak carcinogen dibutyl separate experiments. (B) Data shown are results of densitometry analysis of
phthalate (Figure 5). Specifically, both WY-14,643 (500 p.p.m.) images from the experiment detailed in (A). The intensity of protectedbands was quantified using an image analyzer and normalized to the and gemfibrozil (16000 p.p.m.) administered to rats for 90 intensity of housekeeping genes L32 and GAPDH.
days increased expression of DNA BER enzymes, while dibutylphthalate (10000 p.p.m.) had no effect.
are important because they show that WY-14,643 induces It has been hypothesized that the hepatocarcinogenicity of expression of the whole pathway responsible for the repair of peroxisome proliferators is due to oxidative stress. At least oxidative DNA damage, DNA glycosylases, APE, Pol β and two possible sources of oxidants following administration of peroxisome proliferators have been proposed: (i) peroxisomalacyl CoA oxidase in parenchymal cells; (ii) NADPH oxidase Potent carcinogens are more potent inducers of BER
in Kupffer cells (reviewed in ref. 22). The data presented here enzymes gene expression
are important for mechanistically based risk assessment of WY-14,643 is one of the most potent carcinogens among peroxisome proliferators for several reasons. First, further the peroxisome proliferators. To test whether less potent evidence supporting the role of oxidative DNA damage in the

I.Rusyn et al.
mechanism of action of peroxisome proliferators is provided.
Specifically, we suggest that DNA BER may be an importantfactor in peroxisome proliferator-induced carcinogenesis andthat induction of DNA repair reflects an increase in oxidizedbases following treatment with these compounds. The smalland inconsistent increases in oxidative DNA damage observedin previous studies may be due to an inability to observe realincreases due to the artifactual formation of oxidative DNAdamage during DNA isolation. Most of the studies havereported 8-OH-dG values in control rat livers of 2 per 10–5bp. These values can be dramatically reduced through the useof free radical trapping reagents and antioxidants (23, 24).
Reductions in artifactual 8-OH-dG are likely to increase thelevel of detectable oxidative DNA damage resulting fromexposure to peroxisome proliferators.
Second, overexpression of DNA repair enzymes per se may play an important role in the mechanism of action of peroxi-some proliferators. For instance, Pol β is normally expressedat low levels and has high infidelity in replicating DNA (25).
Recently it was shown that overexpression of Pol β may resultin increased spontaneous mutagenesis (26). Moreover, it washypothesized that an excess of Pol β may disrupt functions ofother DNA polymerases by introducing illegitimate deoxyri-bonucleotides or mutagenic base analogs like those producedby oxidative stress (27).
In addition, APE (Ref-1) is a multifunctional protein that stimulates DNA binding by a number of transcription factors,such as NF-κB and AP-1 (28). Interestingly, peroxisomeproliferators increase the activity of NF-κB in rodent liver andit was hypothesized that NF-κB activation plays a role in Fig. 4. Chronic treatment with peroxisome proliferators that are potent
increased cell proliferation induced by these compounds carcinogens induces increases in DNA BER enzymes expression. TotalRNA was isolated from livers of rats treated with DEHP (1.2% w/w), (reviewed in ref. 22). Therefore, the marked increase in clofibric acid (Cl. A., 0.5% w/w) or WY-14,643 (WY, 0.1% w/w) for 22 APE expression observed here might be important for the weeks and used in the RNase protection assay as detailed in Figure 2.
promotional activity of peroxisome proliferators. On the other Representative autoradiogram from three separate experiments.
hand, APE is known to regulate transactivation of p53 (29).
This transactivation only requires the C-terminus and has beensuggested to delay the G1/S transition and enhance BER (29).
Given that p53 has been shown to enhance BER (30), it ispossible that up-regulation of APE expression by peroxisomeproliferators leads to enhanced p53-dependent BER. Thesignificance of APE transactivation of the pro-apoptotic func-tions of p53 is unclear, since peroxisome proliferators areknown to decrease apoptosis in liver (31).
An additional concern is that DNA repair enzymes could be up-regulated unevenly, so that a state of imbalanced DNArepair may exist. Indeed, imbalanced DNA repair may lead toformation of both mutagenic and clastogenic lesions. In thecase of oxidative DNA damage, if glycosylase and APE areoverabundant (relative to DNA polymerase or DNA ligase) thenDNA strand breaks might accumulate that could consequentlyinfluence cell viability and induce chromosomal damage (32).
Whether peroxisome proliferators cause imbalanced repair hasyet to be determined.
Finally, since current risk assessment of peroxisome pro- liferators is based on important differences between humansand rodents in expression of PPARα (reviewed in ref. 3), the Fig. 5. Sub-chronic treatment with the potent carcinogens WY-14,643 and
approach of analyzing expression of DNA repair enzymes can gemfibrozil, but not with the weak carcinogen dibutyl phthalate, increasesexpression of DNA excision repair enzymes. Total RNA was isolated from be used in further studies to assess whether or not BER livers of rats treated with WY-14,643 (WY, 500 p.p.m.), dibutyl phthalate enzymes, as a biomarker of oxidative stress, are induced by (D.P., 10000 p.p.m.) or gemfibrozil (Gemf., 16000 p.p.m.) for 90 days and WY-14,643 in PPARα knockout mice.
used in the RNase protection assay as detailed in Figure 2. Data shown are In summary, the results of this study provide new information results of densitometry analysis and the intensity of protected bands was that supports a role of oxidative stress as a mechanism of quantified using an image analyzer and normalized to the intensity ofhousekeeping genes L32 and GAPDH.
carcinogenesis for peroxisome proliferators. It demonstrates a Peroxisome proliferators induce DNA repair
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16. Tsurudome,Y., Hirano,T., Yamato,H., Tanaka,I., Sagai,M., Hirano,H., Received on July 26, 2000; revised on September 22, 2000; accepted on September 25, 2000

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