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Urothelial genotoxicity of environmental chemicals detected in the urine of healthy dogs and their owners

Published online by Cambridge University Press:  24 October 2024

Hannah M. Peterson ,
Jenna C. Holler ,
Abby Boswell  and
Lauren A. Trepanier Open the ORCID record for Lauren A. Trepanier [Opens in a new window]
Hannah M. Peterson
Affiliation:
Department of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, USA
Jenna C. Holler
Affiliation:
Department of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, USA
Abby Boswell
Affiliation:
Department of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, USA
Lauren A. Trepanier*
Affiliation:
Department of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, USA
*
Corresponding author: L. A. Trepanier; Email: [email protected]
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Abstract

Introduction:

Major risk factors for urothelial cell carcinoma (UCC) in people are smoking and occupational exposures. However, up to 30% of human UCC risk is still unexplained. Pet dogs develop UCC that models the clinical behavior of muscle-invasive human UCC. Dogs may therefore provide a useful model for non-tobacco, nonoccupational UCC risk. We previously found that nonsmoking human subjects and their pet dogs share exposures to the urothelial carcinogens acrolein and arsenic. We hypothesized that these urinary exposures would reach genotoxic concentrations in some individuals.

Methods:

We exposed immortal and primary human and canine urothelial cells in vitro to acrolein and inorganic arsenic and used the γ-H2AX and comet assays to measure DNA damage.

Results:

For acrolein, we found a genotoxic threshold of 1.1–4.4 μM in human cells and a threshold of 20.0–55.6 μM in canine cells. These findings are consistent with potentially genotoxic urinary acrolein exposures in 51% of healthy human subjects and 17% of pet dogs previously surveyed. For inorganic arsenic, we found a genotoxic threshold of ≥10 μM in canine and human cell lines. No healthy human or canine subject reached these urinary inorganic arsenic exposures when assayed at a single time point.

Conclusions:

Non-tobacco, nonoccupational acrolein exposures could increase the risk of early urothelial DNA damage in both people and pet dogs. Ongoing studies will assess these chemical exposures in the setting of UCC in both human and canine patients.

Keywords

Bladder canceracroleinarsenicenvironmental chemicalsurothelial carcinoma risk
Type
Research Article
Information
Journal of Clinical and Translational Science , Volume 8 , Issue 1 , 2024 , e172
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2024. Published by Cambridge University Press on behalf of Association for Clinical and Translational Science

Introduction

Urothelial cell carcinoma (UCC) is an environmental cancer in human patients. Up to 30% of cases are high-grade muscle invasive UCC, which has a 5-year mortality rate of about 50% [Reference Zhang, Zhou and Ding1]. Smoking and occupational exposures are known major risk factors, with only minor contributions from hereditary or medical factors [Reference Czerniak, Dinney and McConkey2]. Almost one-third of environmental risk for UCC is not well understood in human patients, which makes preventative measures difficult to implement. Part of this remaining UCC risk could be due to chronic chemical exposures in the household environment.

Pet dogs develop UCC that models the clinical presentation, molecular features, and poor prognosis of human muscle invasive UCC [Reference Knapp, Ramos-Vara, Moore, Dhawan, Bonney and Young3,Reference Knapp, Dhawan and Ramos-Vara4]. This makes the pet dog with UCC a potentially useful model for non-tobacco, nonoccupational UCC risk. Pet dogs develop UCC at an earlier absolute age of onset (median 11 years) [Reference Knapp, Glickman, DeNicola, Bonney, Lin and Glickman5]. compared to humans (median 65–70 years) [Reference Kirkali, Chan and Manoharan6]. This compressed life span, along with potentially intensified exposures compared with humans, could make it easier to identify relevant chemical exposure risk factors [Reference Knapp, Dhawan and Ostrander7]. While some breeds of dogs have a higher risk for UCC [Reference Knapp, Glickman, DeNicola, Bonney, Lin and Glickman5], environmental factors can influence UCC development even among these high-risk breeds [Reference Glickman, Raghavan, Knapp, Bonney and Dawson8]. Environmental tobacco smoke has not been shown to be a risk factor for canine UCC [Reference Glickman, Schofer, McKee, Reif and Goldschmidt9,Reference Luethcke, Ekena, Chun and Trepanier10], and occupational exposures are uncommon in pet dogs. Therefore, we hypothesize that household chemical exposures could be important in canine UCC risk and might be a relevant model for non-tobacco, nonoccupational bladder cancer risk in people.

As a first step in assessing relevant household chemical exposures in dogs and people, we measured concentrations of several known or suspected urothelial carcinogens in the urine of healthy pet dogs and their owners [Reference Craun, Luethcke and Shafer11]. We found that urinary metabolites of acrolein and inorganic arsenic were readily detectable in both species (Figure 1) and were correlated across dogs and their owners in the same household, which suggested shared exposure sources [Reference Craun, Luethcke and Shafer11]. We further hypothesize that urinary chemical exposures to acrolein and inorganic arsenic might reach genotoxic concentrations in some healthy dogs and their owners.

Figure 1. Previously measured acrolein (as its stable metabolite, 3-HPMA; Panel A) and urinary inorganic arsenic (iAs; the sum of As [III], As[V], dimethylarsinic acid, and monomethylarsonic acid; Panel B) in the urine of healthy pet dogs and their owners [Reference Craun, Luethcke and Shafer11].

The aim of this study was to determine whether acrolein and inorganic arsenic exposures, previously observed as stable metabolites in the urine of healthy pet dogs and their owners, reached genotoxic concentrations in some individuals, when tested in vitro in canine and human urothelial cell lines using the γ-H2AX and comet assays as measures of DNA damage.

Materials and Methods

Cell culture of immortalized urothelial cell lines

Canine K9TCC-AxC and K9TCC-SH cells, derived from two female dogs with intermediate to high-grade muscle-invasive UCC [Reference Dhawan, Ramos-Vara, Stewart, Zheng and Knapp12], were a gift from Dr Deborah Knapp at Purdue University. Fetal bovine serum (FBS) was purchased from Sigma-Aldrich. Dulbecco’s modified Eagle medium nutrient mix (DMEM) and dimethyl sulfoxide (DMSO) were purchased from Fisher Scientific. The cells were maintained in DMEM with L-glutamine and phenol red supplemented with 10% FBS. Cells were at passage 35 (K9TCC-AxC) and 39 (K9TCC-SH) when received and were expanded to passages 42 and 44, respectively, and banked in liquid nitrogen with 10% DMSO prior to experimental use.

Human adherent urothelial carcinoma cell lines, HT-1376 (CRL-1472TM) and T24 (HTB-4TM), were purchased from ATCC (Manassas, VA) and maintained in minimum essential medium (MEM) with phenol red supplemented with 10% FBS and L-glutamine at a final concentration of 2 mM or McCoy’s 5A Medium modified with 10% FBS, respectively. Cells were received at passages 43 (HT-1376) and 38 (T24) were grown to passages 50 and 45, respectively, and were banked in 10% DMSO in liquid nitrogen prior to experimental use. L-glutamine and MEM were purchased from Sigma-Aldrich. McCoy’s 5A medium was purchased from Fisher Scientific.

Prior to chemical exposures, urothelial cells were thawed and passaged twice to ∼70% confluence. Experiments were performed at passage 44 for K9TCC-AxC, passage 46 for K9TCC SH, passage 52 for HT-1376, and passage 47 for T24 cells. Cells destined for the γ-H2AX assay were counted and transferred to chamber slides (Lab-Tek II 4-Well Chamber Glass Slides, Thermo Fisher, Rochester, NY) at 2.5 × 104 cells/well and left overnight for 18 h to adhere, in an incubation chamber at 37 °C with 5% CO2. Cells used for the CometChip assay were immediately utilized after reaching ∼70% confluence.

Cell culture of primary urothelial cell lines

Canine primary urothelial cells were obtained from Creative Bioarray (Cat No: CSC-C9111J, Donor ID 363633) and maintained in SuperCult® bladder epithelial cell medium (Cat No: CM-C9111J). Cells were received at passage 2, seeded in gelatin-coated flasks at 5,000 cells per cm2, and grown to passage 4 before immediate use in experiments.

Human primary urothelial cells were obtained from ATCC (Cat No: PCS-420-010, Donor ID 80203232). They were maintained in complete bladder epithelial cell basal medium supplemented with growth kit components purchased from ATCC (Cat No: PCS-420-032 and PCS-420-042). Cells were received at passage 2, seeded at 5,000 cells per cm2, and expanded to passage 3 before immediate use in experiments.

Chemical exposures

Previous urinary chemical concentrations in 42 healthy dogs and their 42 owners, reported in ng/mg creatinine [Reference Craun, Luethcke and Shafer11], were converted to direct μM concentrations based on each chemical’s molecular weight. Urinary exposures to acrolein were extrapolated from its measured stable urine metabolite, 3-hydroxypropylmercapturic acid (3-HPMA), on an equivalent molar basis (Figure 1A) since 3-HPMA was not available commercially. Urinary exposures to inorganic arsenic were determined as the molar sum of all measured inorganic arsenic species: iAs(V), iAs (III), dimethylarsinic acid, and monomethylarsinic acid (Figure 1B) [Reference Craun, Luethcke and Shafer11].

Human and canine immortal and primary urothelial cells were incubated with either acrolein or with inorganic arsenic as sodium arsenite. Acrolein was procured from Restek (Bellafonta, Pennsylvania), while sodium arsenite was purchased from Sigma-Aldrich (St. Louis, Missouri). For each chemical and cell line combination, time course experiments were performed over 24 h at 37 °C (5% CO2) to determine time to peak genotoxicity at the highest observed in vivo urinary concentrations for each species. Concentration-dependent genotoxicity experiments, encompassing the range of observed urinary concentrations, were then performed at these peak times for each chemical/cell line combination. Peak genotoxicity was observed at 6 h for all cell lines with either acrolein or iAs (III) (data not shown). Each concentration-dependent genotoxicity experiment was performed in triplicate on at least two separate occasions.

Immunocytochemistry for γ-H2AX

For immortal cell lines, DNA damage was assessed using both the γ-H2AX assay, which detects a histone protein, H2AX, that is, phosphorylated in response to single- and double-stranded DNA damage [Reference Kopp, Khoury and Audebert13]. and the comet assay, which detects single- and double-stranded DNA damage more directly.

Cells destined for the γ-H2AX assay were washed after chemical incubations with prewarmed 1X phosphate- buffered solution (PBS), fixed on slides with 4% formaldehyde, and washed in 1X PBS. Slides were kept at 4oC for no more than 1 week prior to the γ-H2AX assay.

Immunocytochemistry for γ-H2AX was performed with an anti-phospho-histone H2A.X [Ser139] mouse monoclonal antibody (Abcam, Cambridge, MA) and an anti-mouse IgG Fab2 Alexa Fluor® 488 antibody (Cell Signaling Technology, Danvers, MA), as previously described [Reference Peterson, Manley, Trepanier and Pritchard14]. Slides were counterstained with DAPI (Thermo Scientific, Rockford, IL) to detect cell nuclei. Imaging for γ-H2AX foci was performed with a Leica TCS SP8 laser scanning confocal microscope (Leica Microsystems, Wetzlar, Germany), equipped with a 63x oil-immersion objective. Two channels were acquired sequentially with the following parameters: 488 nm for the secondary antibody and 405 nm for DAPI [Reference Peterson, Manley, Trepanier and Pritchard14]. The γ-H2AX foci were quantified using open access software (FoCo, MATLAB), which is robust and reliable for automated counting of nuclear foci in single-cell images [Reference Lapytsko, Kollarovic, Ivanova, Studencka and Schaber15]. At least 100 cells were counted per replicate, and data were expressed as mean γ-H2AX foci/nucleus.

Alkaline CometChip assay

We also assessed DNA damage using the traditional alkaline comet assay, using a high-throughput adaptation, the CometChip [Reference Sykora, Chiari, Heaton, Moreno, Glaberman and Sobol16]. The CometChip uses a 96 well format that contains hundreds of microwells per well to improve cell distribution, reduce cell clumping, and minimize inter- and intra-assay variability [Reference Sykora, Chiari, Heaton, Moreno, Glaberman and Sobol16]. We fabricated CometChips using a 30-micron stamp gifted to our lab from Dr Bevin Engelward at the Massachusetts Institute of Technology, using a protocol developed in her laboratory [Reference Sykora, Chiari, Heaton, Moreno, Glaberman and Sobol16].

In preparation for the CometChip assay, immortal or primary urothelial cells were counted and passed through a 40 mm filter to remove any clumps. Then 100 mL of cell solution (∼100,000 cells) was added to each well. Cells were incubated at 37°C with 5% CO2 for 30 min to allow them to settle into the microwells. Wells were washed with 1X PBS, overlaid with 1% low-melting point agarose in 1X TBE buffer, and allowed to solidify. Concentrations of sodium arsenite or acrolein were added to each well and incubated for 6 h for each cell line. After dosing, chips were immersed in an alkaline lysis solution (2.5 M NaCl, 100 mM Na2EDTA, 10 mM Trizma® Base, and 1% Triton X-100, adjusted to pH 10) at 4°C overnight. Chips were then immersed in an alkaline unwinding buffer (0.3 M NaOH and 1 mM Na2EDTA) for 40 min at 4°C. The DNA was electrophoresed in the same buffer for 30 min at 1 V/cm and ∼ 300 mA. Chips were submerged twice in neutralization buffer (0.4 M Trizma® base at pH 7.5) for 15 min each, washed with deionized water and then 70% ethanol, and dried overnight before imaging.

Cellular DNA in the CometChip wells was stained for 30 min at room temperature with 2X SYBR™ Gold in 1X TBE buffer. Imaging was performed with the Leica TCS SP8 laser scanning confocal microscope with a 4X dry objective with a 495 nm excitation filter. Percent DNA in the comet tails were quantified using CometAssay Analysis Software (Bio-Techne, Minneapolis, MN). At least 50 cells were counted per replicate. Each experiment was performed in triplicate on two separate occasions. Data were expressed as mean percent DNA in the comet tail [Reference Collins17].

Statistical analyses

DNA damage as mean γ-H2AX foci/nucleus or percent tail DNA was compared between vehicle and chemical concentrations using one-way ANOVA, followed by Dunnett’s multiple comparison tests. Statistical analyses were performed using commercial software (Prism 9, GraphPad Software LLC). P < 0.05 was considered statistically significant.

Results

Acrolein

The highest extrapolated acrolein exposure previously observed in healthy canine urine was 55.6 μM (12,300 ng/mL 3-HPMA; Figure 1A). Using the γ-H2AX assay, acrolein led to significant DNA damage over vehicle at 55.6 μM in K9TCC-AxC cells (Figure 2A) and at 35.7 μM in K9TCC SH cells (7,892 ng/mL 3-HPMA; Figure 2B).

Figure 2. Genotoxicity of acrolein using the γ-H2AX assay in canine urothelial cell lines K9TCC-AxC (Panel A; *** P = 0.0001) and K9TCC-SH (Panel B; * P = 0.014).

Using the comet assay, the same thresholds for DNA damage were observed in the canine immortal cell lines (55.6 μM for K9TCC-AxC cells (Figure 3A) and 35.7 μM for K9TCC SH cells (Figure 3B). The genotoxic threshold for acrolein in primary canine urothelial cells was 20.0 μM (Figure 3C). Using 20 μM as a threshold for acrolein genotoxicity, 7 of 41 healthy dogs (17%) previously screened [Reference Craun, Luethcke and Shafer11] had potentially genotoxic urinary exposures to acrolein at a single time point (Figure 1A).

Figure 3. Genotoxicity of acrolein using the CometChip assay in canine urothelial cell lines K9TCC-AxC (Panel A; *** P = 0.0001) and K9TCC-SH (Panel B; * P = 0.013; ** P = 0.009), and in primary canine urothelial cells (Panel C; * P = 0.02; ** P = 0.006; *** P ≤ 0.004).

In healthy human urine [Reference Craun, Luethcke and Shafer11], the highest extrapolated acrolein exposure was 4.5 μM (984 ng/mL 3-HPMA; Figure 1A). Using the γ-H2AX assay, acrolein showed significant concentration-dependent DNA damage over vehicle at concentrations ≥1.8 μM (394 ng/mL 3-HPMA) in HT-1376 cells (Figure 4A), and at 4.4 μM (973 3-HPMA ng/mL) in T24 cells (P = 0.008; Figure 4B).

Figure 4. Genotoxicity of acrolein using the γ-H2AX assay in human urothelial cell lines HT-1376 (Panel A; *** P ≤ 0.0009) and T24 (Panel B; ** P = 0.008).

Using the comet assay, DNA damage thresholds for acrolein were ≥2.1 μM for HT-1376 cells and ≥2.9 μM for T24 cells (Figure 5A and 5B). The threshold for acrolein genotoxicity in primary human urothelial cells was ≥1.1 μM (Figure 5C). Using 1.1 μM as a possible threshold for genotoxicity, 21 of 41 human subjects previously screened (51%) had potentially genotoxic urinary exposures to acrolein at a single time point (Figure 1A).

Figure 5. Genotoxicity of acrolein using the CometChip assay in human urothelial cell lines HT-1376 (Panel A; ** P ≤ 0.005; *** P < 0.0001) and T24 (Panel B; ** P = 0.003; *** P < 0.0001), and in human primary urothelial cells (Panel C; * P = 0.007; *** P < 0.0001).

Total inorganic arsenic

In initial experiments performed with urothelial cells exposed to iAs and assayed for DNA damage using the γ-H2AX assay, arsenic-induced DNA damage was not detectable (data not shown). On review of the literature, we found that iAs can indirectly inhibit H2AX phosphorylation by blocking upstream activation of the DNA repair protein ataxia telangiectasia mutated (ATM) [Reference Nail, McCaffrey, Banerjee, Ferragut Cardoso and States18]. Therefore, we are only reporting DNA damage from iAs using the alkaline CometChip assay, which directly assesses DNA strand damage without need for activation of this pathway.

Total measured inorganic arsenic species in healthy canine urine ranged from 0.02 to 2.18 μM (Figure 1B). Using the comet assay, inorganic arsenic led to significant DNA damage compared to vehicle at ≥10 μM in K9TCC-SH cells and only at 75 μM in K9TCC-AxC cells, (Figure 6A–B). In primary canine urothelial cells, the genotoxic threshold for inorganic arsenic was also 10 μM (Figure 6C). No healthy dogs reached this urinary inorganic arsenic concentration when screened at a single time point.

Figure 6. Genotoxicity of inorganic arsenic (as sodium arsenite) using the CometChip assay in canine urothelial cell lines K9TCC-AxC (Panel A; *** P < 0.0001) and K9TCC-SH (Panel B; * P = 0.026; *** P < 0.0001), and in canine primary urothelial cells (Panel C; * P = 0.04; *** P < 0.0001).

In healthy human subjects, total measured urinary inorganic arsenic ranged from 0.01 to 0.18 μM (Figure 1B). Inorganic arsenic led to significant DNA damage compared to vehicle only at 75 μM in both immortal human cell lines (P < 0.0001; Figure 7A and B) and at 10 μM in human primary urothelial cells (Figure 7C). No healthy human subjects reached this urinary inorganic arsenic concentration when screened at a single time point.

Figure 7. Genotoxicity of inorganic arsenic (as sodium arsenite) using the CometChip assay in human urothelial cell lines HT-1376 (Panel A) and T24 (Panel B) *** P < 0.0001, and in human primary urothelial cells (Panel C; * P = 0.005; ** P = 0.0006; *** P < 0.0001).

Discussion

In our previous study, we found that healthy pet dogs had significantly higher urinary concentrations of the acrolein metabolite 3-HPMA and total inorganic arsenic compared to their human owners sharing the same household, with wide individual variability within species [Reference Craun, Luethcke and Shafer11]. The goal of the current study was to assess the genotoxic potential of these urinary exposures in both dogs and people.

Acrolein was genotoxic to immortal and primary human urothelial cell lines with thresholds of 1.8 and 1.1 μM, respectively. These data are consistent with a previously reported threshold of 2.5 μM acrolein for mutagenic transformation of human urothelial cells [Reference Lee, Wang and Weng19]. In our immortal and primary canine urothelial cell lines, acrolein had a genotoxic threshold of ≥20 μM, which was nearly 20-fold higher than in human urothelial cells. It is unclear whether canine urothelial cells are truly less sensitive to DNA damage from acrolein in vivo, or whether this is sampling bias from the cell lines chosen. While median acrolein exposures were more than eightfold higher in pet dogs (Figure 1), predicted in vivo genotoxic exposures were reached in a relatively lower proportion of dogs (17%) compared to people (51%).

We used urinary exposures to the stable metabolite 3-HPMA as a surrogate for urinary acrolein exposures. However, it is unclear whether 3-HPMA concentrations reflect direct urothelial exposures to acrolein, and because of its volatility, acrolein itself cannot be directly measured. Acrolein does reach urothelial cells however, as genotoxic and mutagenic DNA adducts have been detected in healthy human bladder mucosa [Reference Lee, Wang and Weng20]. Follow-up studies could include measurement of acrolein–protein conjugates in the peripheral blood of enrolled subjects or acrolein-DNA adducts in bladder biopsy samples.

For inorganic arsenic, we found that the γ-H2AX assay was insensitive to DNA damage from iAs. We attribute this to the observation that iAs inhibits ATM, a vital component of the pathway that leads to phosphorylation of H2AX [Reference Nail, McCaffrey, Banerjee, Ferragut Cardoso and States18], which would lead to false-negative results from iAs in the γ-H2AX assay. We, therefore, utilized the alkaline CometChip assay to directly measure both single- and double-stranded DNA breaks and added additional parallel experiments using the CometChip assay for acrolein [Reference Sykora, Chiari, Heaton, Moreno, Glaberman and Sobol16]. We found that inorganic arsenic reached a genotoxic threshold of 10 μM in K9TCC-SH cells and in both primary canine and human urothelial cell lines. Similarly, a genotoxic threshold of 10 μM was reported for sodium arsenite in human HUC-RAS cells [Reference Liao, Chen and Lee21], whereas concentrations of 1–10 μM led to increases in urothelial p53 mutations [Reference Chai, Huang, Hung, Kang and Chen22]. No healthy canine or human subjects reached the 10 μM urinary threshold in our previous in vivo study [Reference Craun, Luethcke and Shafer11].

In another study, sodium arsenite led to modest but significant increases in comet tails in human SV-HUC urothelial cells at 1 μM, albeit with a 48-h incubation period [Reference Chai, Huang, Hung, Kang and Chen22]. Using a 1 μM threshold, no human subjects, but 5 of 37 healthy dogs (∼14%) would have had potentially genotoxic urothelial exposures to iAs.

Limitations of these experiments include the use of only one primary and two immortal cell lines per species and the uncertainties of extrapolation from cell lines to urothelial cells in vivo. Immortal cell lines do not replicate in vivo heterogeneity and can vary greatly in their gene and protein expression patterns [Reference Pinto-Leite, Carreira and Melo23,Reference Zuiverloon, de Jong, Costello and Theodorescu24], which could include differences in DNA repair mechanisms. Primary cells better represent normal urothelium but may not generate a normal urothelial barrier. Follow-up studies could further incorporate human and canine urinary organoids, which may better recapitulate the cellular heterogeneity and biologic behavior of urothelial cells of origin [Reference Elbadawy, Usui and Mori25,Reference Minoli, Cantore and Hanhart26]. In addition, indirect mechanisms of chemically induced DNA damage, such as oxidative stress, could be evaluated by adding formamidopyrimidine DNA glycosylase prior to electrophoresis in the CometChip assay [Reference Marsà, Cortés, Hernández and Marcos27]. This additional step unveils sites of oxidative damage to purines, which may occur independently of DNA strand breaks [Reference Marsà, Cortés, Hernández and Marcos27]. Finally, our experiments reflect only acute chemical exposures, and longer incubation of urothelial cells with acrolein or arsenic would better reflect the effects of chronic in vivo urothelial exposures.

Overall, the results of this study suggest that healthy individuals and their pet dogs, in the absence of known occupational exposures, may have potentially genotoxic concentrations of acrolein in their urine, which could increase the risk of urothelial DNA damage. We are currently assessing urinary acrolein and inorganic arsenic levels in casecontrol studies in both human patients and pet dogs with UCC. The overall goal of these studies is to identify non-tobacco, non-occupational sources of exposure to genotoxic urothelial carcinogens in the household, so that evidence-based prevention measures can be considered.

Acknowledgements

The authors thank Dr Deborah Knapp at Purdue University for kindly sharing the canine urothelial cell lines and Dr Bevin Engelward and Joshua Corrigan at the Massachusetts Institute of Technology for graciously proving a stamp to generate CometChips.

Author Contributions

Conception and design: HMP, LAT; generation of data: HMP, JCT, AB; analysis of data: HMP, LAT; manuscript draft: HMP, JCH, LAT; final manuscript approval: HMP, JCH, AB, LAT.

Funding statement

This project was supported by the Melita Grunow Family Professorship in Companion Animal Health and by a generous donation from Mr. Duncan Alexander.

Competing interests

The authors have no conflicts of interest to declare.

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Figure 0

Figure 1. Previously measured acrolein (as its stable metabolite, 3-HPMA; Panel A) and urinary inorganic arsenic (iAs; the sum of As [III], As[V], dimethylarsinic acid, and monomethylarsonic acid; Panel B) in the urine of healthy pet dogs and their owners [11].

Figure 1

Figure 2. Genotoxicity of acrolein using the γ-H2AX assay in canine urothelial cell lines K9TCC-AxC (Panel A; *** P = 0.0001) and K9TCC-SH (Panel B; * P = 0.014).

Figure 2

Figure 3. Genotoxicity of acrolein using the CometChip assay in canine urothelial cell lines K9TCC-AxC (Panel A; *** P = 0.0001) and K9TCC-SH (Panel B; * P = 0.013; ** P = 0.009), and in primary canine urothelial cells (Panel C; * P = 0.02; ** P = 0.006; *** P ≤ 0.004).

Figure 3

Figure 4. Genotoxicity of acrolein using the γ-H2AX assay in human urothelial cell lines HT-1376 (Panel A; *** P ≤ 0.0009) and T24 (Panel B; ** P = 0.008).

Figure 4

Figure 5. Genotoxicity of acrolein using the CometChip assay in human urothelial cell lines HT-1376 (Panel A; ** P ≤ 0.005; *** P < 0.0001) and T24 (Panel B; ** P = 0.003; *** P < 0.0001), and in human primary urothelial cells (Panel C; * P = 0.007; *** P < 0.0001).

Figure 5

Figure 6. Genotoxicity of inorganic arsenic (as sodium arsenite) using the CometChip assay in canine urothelial cell lines K9TCC-AxC (Panel A; *** P < 0.0001) and K9TCC-SH (Panel B; * P = 0.026; *** P < 0.0001), and in canine primary urothelial cells (Panel C; * P = 0.04; *** P < 0.0001).

Figure 6

Figure 7. Genotoxicity of inorganic arsenic (as sodium arsenite) using the CometChip assay in human urothelial cell lines HT-1376 (Panel A) and T24 (Panel B) *** P < 0.0001, and in human primary urothelial cells (Panel C; * P = 0.005; ** P = 0.0006; *** P < 0.0001).