- Research Article
- Open Access
Iodine Uptake and Prostate Cancer in the TRAMP Mouse Model
Molecular Medicine volume 19, pages409–416(2013)
Iodine supplementation exerts antitumor effects in several types of cancer. Iodide (I−) and Iodine (I2) reduce cell proliferation and induce apoptosis in human prostate cancer cells (LNCaP and DU-145). Both chemical species decrease tumor growth in athymic mice xenografted with DU-145 cells. The aim of this study was to analyze the uptake and effects of iodine in a preclinical model of prostate cancer (transgenic adenocarcinoma of the mouse prostate [TRAMP] mice/SV40-TAG antigens), which develops cancer by 12 wks of age. 125I− and 125I2 uptake was analyzed in prostates from wild-type and TRAMP mice of 12 and 24 wks in the presence of perchlorate (inhibitor of the Na+/I− symporter [NIS]). NIS expression was quantified by quantitative polymerase chain reaction (qPCR). Mice (6 wks old) were supplemented with 0.125 mg I− plus 0.062 mg I2/mouse/day for 12 or 24 wks. The weight of the genitourinary tract (GUT), the number of acini with lesions, cell proliferation (levels of proliferating cell nuclear antigen [PCNA] by immunohistochemistry), p53 and p21 expression (by qPCR) and apoptosis (relative amount of nucleosomes by enzyme-linked immunosorbent assay) were evaluated. In both age-groups, normal and tumoral prostates take up both forms of iodine, but only I− uptake was blocked by perchlorate. Iodine supplementation prevented the overexpression of NIS in the TRAMP mice, but had no effect on the GUT weight, cell phenotype, proliferation or apoptosis. In TRAMP mice, iodine increased p53 expression but had no effect on p21 (a p53-dependent gene). Our data corroborate NIS involvement in I− uptake and support the notion that another transporter mediates I2 uptake. Iodine did not prevent cancer progression. This result could be explained by a strong inactivation of the p53 pathway by TAG antigens.
Prostate cancer is the second most frequently diagnosed cancer in men worldwide, with an incidence significantly lower in Japan than in the United States (22.7 versus 83.8/100,000 per year, respectively) (1). This lower risk has been associated with lifestyle factors such as diet. The traditional Japanese diet is high in fish (rich in omega-3 fatty acids), soybeans (isoflavones) and seaweeds (iodine) (2). Epidemiological studies show a possible association between high iodine intake and low risk of prostate cancer, given that the daily intake of iodine in Japan is 25-fold higher than in Western countries (5), 280 µg in Japan versus 209 µg in the US) (3,4).
This chemoprotection by iodine is also evident in thyroid and breast cancer, and it seems to be related to the ability of these tissues to take up and metabolize iodide (I−) and/or molecular iodine (I2) (5). It is well established that I− uptake depends on the Na+/I− symporter (NIS), whereas the uptake of I2 is probably mediated by facilitated diffusion (6–8). I2 supplementation exerts antitumor effects in thyroid, breast, neuroblastoma and lung carcinoma by arresting the cell cycle (increases p53 and p21 proteins), inducing apoptosis (dissipates mitochondrial membrane potential and increases Bax, caspases 3 and 7) and reducing mRNA expression of invasion genes (vascular endothelial growth factor [VEGF] and urokinase-type plasminogen activator [uPA]) (9–14). For I− to exert some of these effects, it must be converted to an oxidized species of iodine by specific peroxidases (thyro-, lacto- or myeloperoxidase) (15–17).
The pathways by which I2 inhibits the carcinogenic process are not fully understood, but contributions of both direct (anti- or prooxidant) and indirect mechanisms (generation of iodolipids, iodinated derivatives of arachidonic acid) have been proposed (5). 6-Iodolactone (6-IL) is an iodolipid that reproduces some of the antitumorogenic effects mentioned above, and it has been suggested that 6-IL could function as a ligand/activator for peroxisome proliferator-activated receptors (12,13,18–20).
There is evidence that prostate epithelium is an iodine-responsive target. In several species, NIS mRNA was detected in normal and cancerous prostate (21–23). In humans, NIS protein is present in 50–70% of adenocarcinomas (24). With regard to the effects of iodine, in vitro studies show that LNCaP and DU-145 prostate cancer cells take up both I− and I2, and treatment with either chemical species reduces cell proliferation and induces apoptosis (Bax capsases). Consistent with these results, supplementation in nude mice with both chemical species consistently reduces tumor growth of DU-145 xenografts (25). The aims of this study were to analyze the uptake and potential antineoplasic effects of a mixture of iodine and iodide in transgenic adenocarcinoma of the mouse prostate (TRAMP) mice, a preclinical model of prostate cancer.
Materials and Methods
The TRAMP mice were obtained from The Jackson Laboratory (Bar Harbor, ME, USA). Heterozygous (TRAMP+/−) females were crossed with nontransgenic C57BL/6 males to generate heterozygous transgenic male offspring. In the TRAMP model, expression of SV40 early genes (TAG) is driven by the prostate-specific promoter probasin. Long and short antigens inactivate p53 and Rb proteins as well as protein phosphatase 2, respectively, leading to the development of intraepithelial neoplasia (prostatic intraepithelial neoplasia [PIN]) and both well-differentiated and poorly differentiated cancer. Tail deoxyribonucleic acid (DNA) was used to determine the presence of the transgene by polymerase chain reaction (PCR). Experiments were approved by the Committee on Bioethics from the Universidad Nacional Autónoma de México, and procedures were carried out according to guidelines of the Norma Oficial Mexicana NOM-062-ZOO-1999 (26).
Radio-Iodine Uptake Assay
Prostate tissue from wild-type and TRAMP mice of 12 and 24 wks was used to characterize the uptake of I− and I2 by using 125I as a tracer (Na125I; PerkinElmer, Waltham, MA, USA; specific activity: ∼17 Ci [629 GBq]/mg). Oxidation of 125I− to 125I2 was carried out according to the method described by McAlpine (27). Mice received intraperitoneal doses of 125I− or 125I2 (0.001 Ci/kg body weight) and were euthanized after 5, 10, 15, 30, 60, 120 and 180 min. Thyroid gland was used as an internal positive control.
To analyze NIS involvement in iodine uptake, one group each of wild-type and TRAMP mice received intraperitoneal physiological saline solution or 25 mg perchlorate (ClO4−) (specific inhibitor of NIS) per kilogram body weight. Two hours after the ClO4− injection, mice were injected with 125I− or 125I2, and after another 2 h, they were killed. This dose of ClO4− inhibits >80% of iodide uptake in thyroid gland (positive control) (28). Thyroid, prostate and liver were collected, and the radiolabel was measured in counts per minute (cpm) in a γ-counter (Packard, Palo Alto, CA, USA). Radioactive iodine uptake by thyroid and prostate was normalized to liver uptake (negative control). Data are expressed as cpm per milligram thyroid or cpm per milligram prostate/cpm per milligram liver (23).
Effects of Iodine Supplementation on Prostate Cancer Development
Male wild-type and TRAMP mice (6 wks old) were given drinking water supplemented with a mixture of iodine (0.125 mg I− plus 0.062 mg I2/day/mouse) for 12 or 24 wks. Body weight was registered every 2 wks. At the end of the experiments, mice were anesthetized with a ketamine and xylazine mixture (Cheminova, Mexico City, Mexico; 8 and 0.6 mg, respectively, per 100-g body weight) and killed by decapitation. The genitourinary tract (GUT) (prostate, bladder, seminal vesicles and urethra) was weighed, and the prostate was dissected. Prostate tissue was fixed in 10% neutral buffered formalin (Sigma-Aldrich, St. Louis, MO, USA) for histopathology and immunohistochemistry or frozen and stored at −70°C to measure expression of the NIS, p53 and p21 genes by reverse transcriptase-quantitative polymerase chain reaction (RT-qPCR). Blood was collected to determine the circulating levels of triiodothyronine (T3). At the time of necropsy, all organs were examined for gross abnormalities.
Histopathology and Immunohistochemistry
The 5-µm, paraffin-embedded sections of the dorso-lateral lobes were stained with hematoxylin-eosin for histopathology or were processed for immunohistochemical analysis. The pathological grading system used was that proposed by Kaplan-Lefko, which considers several criteria such as epithelial cytoarchitecture and the presence of mitosis, apoptosis and inflammation (28). The percentages of normal and pathological acini were registered. The analysis was carried out by quantifying the whole field of three animals per group at 20× magnification.
Immunodetection of proliferating cell nuclear antigen (PCNA) was used as an indicator of cell proliferation. Briefly, paraffin tissue sections were deparaffinized, rehydrated and heated in citrate buffer (pH 6.0). Sections were blocked with peroxidase block solution from DakoCytomation (Dako, Glostrup, Denmark), followed by bovine serum albumin and then incubated overnight at 4°C with the anti-PCNA rabbit polyclonal primary antibody (1:50; Santa Cruz Biotechnology, Santa Cruz, CA, USA). Slides were then reacted with biotin-labeled anti-rabbit IgG/anti-mouse IgG and developed in diaminobenzidine (DAB) (DakoCytomation). Sections were counterstained with hematoxylin, dehydrated and mounted. Tissue sections without primary antibody were used as negative control. The analysis was carried out under light microscopy (Leica DM 2500), and images were acquired with a Leica DFC 420 camera. The percentage of PCNA-positive cells was defined as the number of brown-stained cells divided by the total number of cells in three randomly selected fields at 40× magnification. The quantification of cells was performed with the Leica Application Suite (version 2.8.1).
Circulating T3 Levels
To verify thyroid status, serum T3 levels were measured by a homologous radioimmunoassay previously standardized in our laboratory (30).
Apoptosis was measured by enzymelinked immunosorbent assay (ELISA) by using a cell death detection kit (Roche Diagnostics, Mannheim, Germany). This assay detects the relative amounts of mono- and oligo-nucleosomes. Data were normalized to DNA concentration. All samples exhibited at least twice the absorbance of the blank. The percent change of apoptosis was calculated, considering the prostatic levels of the nonsupplemented wild-type mice as 100%.
RT-qPCR (Real Time)
Total RNA was extracted by using the SV Total Isolation System (Promega, Madison, WI, USA) and was reverse-transcribed by using oligo-deoxythymine. The sequence detector system Rotor-Gene 3000 (Corbett Research, Mortlake, Australia) was used to perform qPCR with SYBRgreen. The reaction contained 2 µg cDNA template and the Maxima SYBR Green/ROX qPCR Master Mix (Fermentas, CA, USA), using 40 cycles of three-step amplification (95°C for 30 s, 55–60°C for 30 s and 72°C for 30 s). Table 1 shows the primers used in this study. PCR generated only the expected specific amplicon, which was demonstrated in each case by the melting temperature profile and by electrophoresis of the PCR product through a 2% agarose gel containing ethidium bromide in Tris-acetate-EDTA buffer. No PCR products were observed in the absence of template. Gene expression was calculated by using a standard curve and normalized to the content of β-actin. The coefficient of variation for this gene was <15%.
The data are shown as mean ± standard error of the mean (SEM). Differences between groups were analyzed by using a two-way analysis of variance (ANOVA) with a Bonferroni post hoc test and Student t test. Results were analyzed by using the statistical package GraphPad Prism 4 (GraphPad, San Diego, CA, USA).
Time Course of Iodine Uptake
Figure 1 shows that normal prostate of 12- and 24-wk-old mice takes up 125I− and 125I2 within the first 5 min. For both iodine types, sustained but not statistically significant increases were observed in 24-wk-old mice after 10 min.
Expression of NIS and Its Involvement in Iodide Uptake
Figure 2A shows that both chemical species of iodine are taken up by normal and cancerous prostate of 12- and 24-wk-old mice. In all groups, 125I− uptake was significantly inhibited by ClO4−. In contrast, ClO4− administration did not modify 125I2 uptake in any group. Figure 2B shows NIS expression in prostates from wild-type and TRAMP mice of 30 wks. TRAMP mice exhibited high NIS expression compared to wild-type mice. Chronic iodine supplementation (24 wks) decreased TRAMP NIS overexpression to values similar to those of the wild-type mice.
Effect of Iodine Supplementation on the Development of Prostate Cancer
Figure 3 shows that iodine supplementation for 12 or 24 wks had no effect on body weight. The data show a significant increase in the GUT weight of TRAMP mice in comparison to wild-type mice at both ages. Iodine supplementation had no effect on the GUT weight or circulating levels of T3 (data not shown).
As expected, wild-type mice showed a normal histological phenotype, whereas TRAMP mice exhibited a well-differentiated cancer (Figure 4). A detailed analysis in TRAMP mice showed that around 40% of acini had a normal phenotype, whereas 5–10% of acini exhibited a high-grade PIN (epithelial stratification, cribiform structures, nuclear pleomorphism, hypercromatic nuclei), and around 50% exhibited a well-differentiated cancer (loss of intraductal spaces and invasion of basal membrane). However, iodine supplementation for 12 or 24 wks did not modify the normal (wild type) or tumor phenotype (TRAMP).
In relation to indicators of cell proliferation, our data showed a higher number of PCNA-positive cells in prostate tumors (TRAMP) than in normal prostate (wild type) (Figure 5). However, iodine supplementation for 12 or 24 wks did not modify the PCNA levels in any group. Figure 6 shows that iodine supplementation significantly increased p53 mRNA expression but had no effect on p21 expression in tumors from 24-wk-old TRAMP mice. We found no differences in apoptosis between control and iodine-supplemented groups of normal and cancerous prostate (Figure 7).
The present study was designed to explore if continued supplementation with iodine inhibits or delays the development of prostate cancer in the TRAMP model. Our data showed that, although cancerous prostate takes up both I− and I2, supplementation with a mixture of the two species of iodine for 12 or 24 wks does not reproduce the antitumor effects previously reported in an in vitro model of prostate cancer (25).
This study shows the ability of cancerous prostate to take up I− and I2. NIS expression and the inhibition of I− uptake by ClO4− (specific inhibitor of NIS symporter) in normal and cancerous prostate confirm that iodide uptake is NIS dependent. These data are in accord with a clinical study indicating that around 50% of human prostate tumors express NIS protein (24), but they differ with studies in LNCaP and DU-145 cells showing that I− uptake is NIS independent (25). This mechanistic difference between in vivo and in vitro models could be explained by the tumor heterogeneity. Our data show that cancerous prostate overexpresses NIS, but this increase is not functionally associated with higher I− influx. This dissociation between NIS transcription and iodide uptake has also been reported to occur in other cancers as part of the tumorogenic process. Well-differentiated thyroid and breast cancers express high levels of NIS compared with their normal counterparts; however, this expression decreases to undetectable levels when the cancer becomes undifferentiated (16,31–34). Our data show that iodine supplementation for 24 wks does not modify the basal expression of NIS in normal prostate, but it prevents the overexpression in cancerous prostate. In contrast, studies in breast tumors have shown that iodine supplementation induces NIS expression. These studies discussed the possibility that NIS upregulation by iodine might be associated with tumor redifferentiation (16,30).
With regard to I2 uptake, no significant blockade by ClO4− was observed in any group, corroborating an NIS-independent mechanism. These data agree with studies in human cell lines of prostate and breast cancer (8,25). There is evidence that I2 uptake depends on protein synthesis, independent of ATP and Na+/K− ATPase (8). A NIS-independent mechanism for I2 uptake has also been demonstrated in sea urchin larvae and seaweeds (7,35), suggesting that this mechanism could be widespread in nature.
The functional relevance of iodine for the prostate gland is still unknown, but data from our group have shown anti-growth effects in models of prostatic diseases (25,36). The present study showed that iodine supplementation for 12 or 24 wks did not modify the GUT weight, incidence of lesions, cell proliferation or apoptosis in wild-type or TRAMP mice. This insensitivity to iodine contrasts with studies in benign prostate hyperplasia or cancer prostate cells that show (a) I− or I2 supplementation prevents prostate hyperplasia induced by sexual hormones in rats (36); (b) I− or I2 treatments reduce cell proliferation and induce apoptosis by a BAX caspase pathway in LNCaP and DU-145 cells; and (c) iodine supplementation (same schedule of administration used in the current study) reduces the tumor growth in nude mice xenografted with DU-145 cells (25). These data support the notion that the null response observed in TRAMP mice is not associated with the chemical species or schedule of administration of iodine or with the origin of prostatic cells (rodents versus human). Instead, the insensitivity to iodine seems to be related to the mechanisms underlying the carcinogenic process in the TRAMP model. Studies in breast cancer cells (MCF-7) show a significant increase of p53 protein and, consequently, increased levels of p21 and Bax proteins as part of the anti-tumor mechanism of I2 (11,12). In the current study we found an increase of p53 expression but no increase of its target gene p21. The functional inhibition of p53 has been described in the TRAMP model as a consequence of the strong constitutive expression of the oncoprotein TAG, which directly inactivates antitumoral proteins such as p53 and Rb. There are controversies related to the sensitivity of prostate toward chemotherapeutic agents in the TRAMP model; some studies have validated its efficacy (37), but others have concluded that it represents an aggressive model of carcinogenesis (diffuse tumor, invasion of seminal vesicles and fast transition from low- to high-grade invasion) (38). Some antiinflammatory drugs such as celecoxib or exisulind exhibit important protection against development of early lesions (PIN), but they do not prevent the transition to adenocarcinoma. This partial protection has been explained as a coordinated activation of p53-dependent (p21/Bax) and p53-independent pathways (inhibition of nuclear factor κ-light-chain enhancer of activated B cells [NF-κB], cyclooxygenase-2, phosphatidylinositide 3-kinase [PI3K]/serine threonine kinase [AKT]/p27). Moreover, in studies using different compounds or diet conditions (low fat, energy restriction) whose action mechanisms involve the inhibition of p53-independent pathways (androgen receptor, NF-κB, PI3K/AKT, protein kinase Cε, and so on), these drugs have only a modest antitumor effect on this model (39–41).
On the other hand, there is evidence that iodine could also act against cancer progression, by preventing or delaying the acquisition of invasion mechanisms. In breast cancer models, it has been shown that iodine supplementation inhibits expression of the VEGF and uPA genes (13,14). Our study shows that none of the TRAMP mice (control or iodine supplemented) developed a phenotype of undifferentiated cancer at 18 or 30 wks. Nevertheless, in the TRAMP model, it was found that prostate cancer could progress to an invasive neuroendocrine phenotype (42,43). It would be interesting to analyze the role of iodine in the acquisition of the neuroendocrine phenotype, since recent studies in neuroblastoma cells show that I2 induces antiproliferative effects and sensitizes these cells to the differentiating effects of retinoic acid (9,44).
Our data show that although normal and cancerous prostate take up both I− and I2, the supplementation with a mixture of these two forms of iodine does not modify the physiopathology of the prostate. The inability of iodine to induce cell arrest or apoptosis could be explained by continued and exacerbated expression of TAG-oncoprotein (inhibitor of p53 and Rb) in the TRAMP model. Studies in less aggressive preclinical models, whose action mechanism does not involve a direct inactivation of p53, will be necessary to better understand the iodine effects on prostate tumor biology.
The authors declare that they have no competing interests as defined by Molecular Medicine, or other interests that might be perceived to influence the results and discussion reported in this paper.
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This study was supported by grants from Programa de Apoyo a Proyectos de Investigación e Inovación Tecnológica. Universidad Nacional Autónoma de México (PAPIIT-UNAM; IN202513, IN200813) and Consejo Nacional de Ciencia y Tecnología (CONACYT; 127368, 176911). P Olvera-Caltzontzin was a graduate student of the Programa de Doctorado en Ciencias Biomédicas, UNAM, and received a scholarship from CONACYT (215709). The authors thank Martín García, Alejandra Castilla, and Moisés Pérez-Mendoza for technical assistance; Francisco Valles, Leonor Casanova and Lourdes Lara for academic support; Ramon Martínez, Alberto Lara and Omar González for computer assistance; and Dr. Dorothy Pless for proofreading.
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Olvera-Caltzontzin, P., Delgado, G., Aceves, C. et al. Iodine Uptake and Prostate Cancer in the TRAMP Mouse Model. Mol Med 19, 409–416 (2013). https://doi.org/10.2119/molmed.2013.00093