Antineoplastic effect of iodine in mammary cancer: participation of 6-iodolactone (6-IL) and peroxisome proliferator-activated receptors (PPAR)
© Aceves et al; licensee BioMed Central Ltd. 2009
Received: 03 February 2009
Accepted: 06 June 2009
Published: 06 June 2009
Studies in mammary cancer demonstrated that moderately high concentrations of molecular iodine (I2) have a antiproliferative and apoptotic effect either in vivo as in vitro, however the cellular intermediated involved in these effects has not been elucidated.
Virgin Sprague-Dawley rats were treated with methyl-nitrosourea (MNU: single dose ip, 50 mg/Kg bw) and the participation of arachidonic acid (AA) and PPAR receptors in the antineoplasic effect of I2 where analyzed.
I2-treated rats for four weeks exhibited a significant reduction in the incidence (62.5 vs. 100%) and size (0.87 ± 0.98 vs 1.96 ± 1.5 cm3) of mammary tumors. HPLC analysis showed that tumoral but not normal mammary tissue contained an elevated basal concentration of AA and significantly more AA-iodinated called 6-iodolactone (6-IL) after chronic I2 treatment. Tumors from I2-treated rats showed fewer cells positive to proliferating cell nuclear antigen, lower blood vessel density, as well as decreases in vascular endothelial growth factor, urokinase-type plasminogen activator, and PPAR type alpha (PPARα). These same tumors showed increases in the cell death markers, TUNEL-positive cells (p < 0.05) and the enzyme caspase-3 (trend), as well as significant induction of PPAR type gamma (PPARγ).
Together, these data demonstrate that the antineoplasic effect of iodine involves 6-IL formation and PPARγ induction.
In recent years, it has become evident that molecular iodine (I2) participates in the physiology and/or pathology of extrathyroidal organs like mammary gland, stomach, prostate, etc. [1–3]. In mammary gland I2 but not iodide (I-) supplementation alleviates human mastalgia and exerts a potent antineoplasic effect on pharmaco-induced mammary tumoral progression in rats [4–7]. In thyroid gland, I- has an apoptotic effect that is mediated by derivatives of arachidonic acid (AA) or eicosapentaenoic acid such as 6-iodo-5-hydroxy-8,11,14-eicosatrienoic acid, also called 6-iodolactone (6-IL), or alpha-iodohexadecanal, respectively [8–10]. The formation of these iodolipids requires, in addition to iodide uptake by specific transporters, its oxidation by thyroperoxidase (TPO). The oxidized iodine intermediate has not been identified, but one of the candidates is I2 [11, 12]. We reported that mammary glands of virgin rats and MNU-induced tumors take up 125I2 by mechanisms independent of the sodium iodine symporter (NIS) or pendrin (PEN) . These findings were corroborated in the human tumoral cell line MCF-7, where we found that 125I2 is taken up by a facilitated diffusion system and covalently bound to lipids similar to 6-IL in both the presence or absence of peroxidase inhibitors, indicating that the oxidized iodine form I2 is organified in the absence of peroxidases . Our data also shows that cancerous cells are more sensitive than the normal mammary cells to the apoptotic effect of I2, but they are equally sensitive to 6-IL; this suggests the presence of abundant 6-IL precursor in tumoral cells . 6-IL is formed by the iodination of AA, which is an essential membrane lipid, and elevated AA has been widely implicated in tumoral process [16, 17]. Although the cellular mechanism involved in the 6-IL apoptotic effect has not yet been elucidated, we have proposed that the peroxisome proliferator-activated receptors (PPAR) could be the mediator . These ligand-dependent transcription factors are involved in regulating cell cycle control and apoptosis of several cancer cells [18, 19]. Recently, our laboratory showed that 6-IL is a specific ligand of PPARs with almost 6-fold higher affinity than AA, which is one of the endogenous ligands of these receptors . In the present work we analysed, in an in vivo model, the presence of AA and formation of its 6-IL derivative in normal and tumoral mammary gland after chronic supplement of I2. We also characterized the cellular pathways involved in the antineoplasic effect of I2 treatment.
Our data show that tumoral tissue contains 5-fold more AA and produce 12 times more 6-IL than normal mammary tissue, and that this increase in 6-IL is accompanied by decreases in invasive signals as well as increases in apoptosis indicators. In normal mammary gland from I2-treated rats, these parameters have not shown any changes compared to untreated rats. Together, these data demonstrated that the antineoplasic effect of iodine involves the formation of 6-IL and PPARγ induction.
Materials and methods
Virgin, female Sprague-Dawley rats, 5 weeks of age, were obtained from the vivarium of the Instituto de Neurobiología, UNAM-Juriquilla. Rats were housed in a temperature-controlled room (21 ± 1°C) with a 12-h light/dark schedule. They were provided with food (Purina rat chow; Ralston Purina Co., St. Louis, Missouri, USA) and water ad libitum. All of the procedures followed UNAM Animal Care and Use Committee guidelines.
Iodine treatment and carcinogenesis induction
At 5 weeks old, rats were sorted into 2 experimental groups using a randomization process, and iodine treatment was started. The experimental groups were: a) Control and b) 0.05% I2 in drinking water (I2). Distilled water was used for drinking water and for all solutions. A saturating solution of I2 (1.33 × 10-3 M) was prepared, and the concentration of 0.05% was confirmed by titration with sodium thiosulfate (Kenkel, 1994). Treatments were continued until 16 weeks after carcinogen injection. Two weeks after the I2 treatment began, subgroups of rats (control and I2 treatment) were anesthetized with a mixture of ketamine and xylazine (Cheminova, México, 30 mg and 6 mg, respectively, per Kg bw) and given a single intraperitoneal injection of 50 mg of MNU (Sigma, St. Louis, Missouri, USA) per Kg bw. MNU was dissolved and activated by heating to 50–60°C in 0.9% saline, pH 5.0 .
Evaluation of mammary gland carcinogenesis
Rats were weighed and palpated for tumors every week beginning 4 weeks after and ending 16 weeks after MNU administration. A tumor was defined as a discrete, palpable mass recorded for at least 2 consecutive weeks. Tumor incidence was calculated as the percentage of animals with one or more palpable tumors. Tumor multiplicity was calculated as the average number of tumors per animal in each treatment group. The mean latency of tumor onset for each treatment group was calculated as the mean time interval (in weeks) from MNU injection to the appearance of the first palpable tumor. At the end of the experiment the rats from each group were sacrificed by decapitation. Tumor sizes were measured using a caliper, and the volumes were calculated by the ellipsoid formula . If the tumors reached the ethically maximal size of 3 cm3 (1.5 × 2.0 cm), rats were anesthetized with the ketamine/xylazine mixture, and the tumors were surgically removed even before the end of the experiment. Normal or tumoral mammary glands were fixed in 10% neutral buffered formalin or frozen in dry ice and kept at -70°C. Blood was collected to determine T3 circulating levels.
T3 circulating levels
Serum T3 levels were measured by the homologous RIA method previously described .
Fixed mammary tumors were embedded in paraffin blocks. Sections of 5-μm thickness were cut from each block and placed on slides that had been treated with 3-aminopropyltriethoxysilane. Sections were deparaffinized in xylene, rehydrated in descending grades of ethanol, and stained with hematoxylin and eosin. Tumors were classified according to criteria published by Russo & Russo .
Arachidonic acid (AA) and 6-iodolactone (6-IL) identification
Normal and tumoral mammary tissues were collected and stored frozen; 500 mg tissue samples were used for neutral lipid extraction according to the procedure described by Boeynaems and Hubbard (1980), and the extracts were evaporated to dryness under a stream of N2 and stored at -80°C. Before HPLC (BIO-RAD 2800, Hercules California, USA) analysis, the neutral lipids were dissolved in 100% EtOH, and a standard curve was constructed with 10–500 nmol of pure AA (Amershan, Arlington Heights, Illinois, USA) or 6-IL dissolved in ethanol. The samples (100 μl) were injected into the μBondapak C18 column (3.9 × 300 mm; particle size, 10 μm; WATERS, Milford, Mississippi, USA) maintained at room temperature. Elution was performed with a mobile phase gradient using solution A (CH3CN-H2O; 1:2, vol/vol) and solution B (CH3CN-H2O; 2:1, vol/vol) at 1 ml/min. Absorption was measured at 206 nm.
Immunohistochemistry of proliferating cell nuclear antigen (PCNA)
Five-μm sections of mammary tumors from rats with or without I2 treatment were deparaffinized, rehydrated, and subjected to antigen retrieval (10 mM sodium citrate) at 80°C for 20 minutes. After cooling at room temperature, sections were treated with 0.3% hydrogen peroxide to block endogenous peroxidase activity. Non-specific binding was blocked with 2% dried fat-free milk in 20% fetal bovine serum-PBS solution (1 hr at 37°C). Sections were incubated at room temperature for 30 min in a humid chamber with mouse monoclonal anti-rat PCNA, clone PC10 (DakoCytomation, Carpinteria, California, USA), diluted 1:150. Immunocomplexes were visualized by goat anti-mouse-immunoglobulin, peroxidase labeled (EnVision™+System, peroxidase, DakoCytomation, Carpinteria, California, USA). Diaminobenzidine (DAB) was used as the chromogen to generate a brown precipitate after reaction with peroxidase. Sections were counterstained with hematoxylin, rinsed, dehydrated, and mounted with Entellan (Merk, Darmstadt, Germany). Cells expressing the antigen were identified by a brown stain over the nucleus. Tumor sections were incubated without either the primary or secondary antibody to test for the specificity of the antibody. PCNA-positive cells were identified by a brown stain over the nucleus. Labeling indices were obtained by counting the number of labeled cells among at least 500 cells per region, and 5 random regions were analyzed.
Quantification of blood vessels
The protocol described was used to prepare the sections for immunofluorescence. Blood vessels were marked using the anti-mouse antibody coupled to fluorescein isothiocyanate (Alexa Fluor 488; Molecular Probes, Eugene, OR). This antibody stained blood vessels in all samples, as confirmed by dual label immunofluorescence studies with anti-PECAM-1 , and the number of stained blood vessels was determined visually (5 areas per slide) with a 10× objective. Images were digitized and evaluated with image-analysis software. Blood vessels were outlined, and their areas were calculated.
Quantification of in situ cell death
Cell death was detected in formalin-fixed, paraffin-embedded tumor sections using the in situ cell death detection kit, fluorescein, POD (Roche Molecular Biochemicals, Mannheim, Germany), which is based on the terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) method. Sections (5 μm) were prepared and treated according to the manufacturer's instructions. DAB was used as the chromogen, and sections were counterstained with hematoxylin. TUNEL-positive cells were identified by a brown stain over the nucleus. Five regions, chosen at random, were analyzed, and labeling indices were obtained by counting the number of labeled cells among at least 500 cells per region and expressed as percentage values.
Caspase-3 activity was measured using a standard colorimetric kit (Sigma, St. Louis, MO). Briefly, frozen mammary tumors were homogenized (1:2) with lysis buffer (50 mM HEPES, pH 7.4, 5 mM CHAPS, 5 mM DTT, 4°C). Samples were centrifuged at 16, 000 g for 20 min, 4°C, and supernatants were collected and stored at -70°C. Protein concentrations were determined by the Bradford method (BIO-RAD protein assay, Richmond, CA), and 100 μg of protein were assayed for caspase activity. The substrate was 200 μM DEVD-pNa, which contains the chromophore p-nitroanilide (pNa) linked to a synthetic tetrapeptide DEVD (acetyl-Asp-Glu-Val-Asp). Final cocktail (300 uL) were incubated in assay buffer (20 mM HEPES, pH 7.4, 2 mM EDTA, 0.01% CHAPS, 5 mM DTT) for 3 h at 37°C with continuous agitation and protected from light in a 96-well plate. Samples were read at 405 nm in an ELISA reader, and caspase activity was expressed as nmol of pNa released/h/mg protein.
Expression of vascular endothelial growth factor (VEGF), urokinase-type plasminogen activator (uPA), and PPAR receptors
Nakamura et al, 1996
The effects of dietary treatments on mammary cancer incidence were analyzed using 2 × 2 contingency tables and a one-tail chi-square with Yates' correction test. The effects of treatments on tumor multiplicity, tumor latency, tumor size, caspase-3 activity, PCNA, TUNEL, and vascular area counts were analyzed using the unpaired t test; for the other variables, two-way ANOVA analysis was performed to determine the significance of differences between groups, followed by Tukey's test for the significance of differences among multiple experimental groups. Values with p < 0.05 were considered statistically significant.
Effect of long-term I2-treatment on mammary tumorigenesis after 16 weeks of MNU administration.
No. of rats with tumors
Tumor latency (weeks)†
Tumors per rat†
11.9 ± 2.8
2.5 ± 1.7
11.6 ± 1.4
2.0 ± 0.9
Body weight gain and T3 levels after 16 weeks of iodine treatment.
Body weight gain (g)
154 ± 15
63.7 ± 10
157 ± 12
67.9 ± 3
Control + I2
152 ± 9
63.2 ± 11
MNU + I2
150 ± 16
60.2 ± 5.6
This report confirms our previous observations that I2 treatment reduces mammary cancer incidence , decreases the proliferative rate (PCNA), and induces apoptosis (TUNEL and caspases) in cancerous mammary cells in vitro [14, 15] or in vivo without any secondary adverse effect on the thyroid or general health . One interesting effect of I2 treatment observed in these tumors was the generalized reduction in proliferation and vasculature, but the regionalized zones with positive apoptotic signaling (TUNEL) suggest the existence of cell populations with differential I2-sensitivity Although we cannot yet explain this pattern, it is well known that tumors are heterogeneous populations of cells. Studies in our laboratory  have shown that cancer cells – either differentiated or not – are more susceptible to the apoptotic effect of I2 than the corresponding normal mammary epithelium (MCF-7 > MDA-MB231 > MCF-12F cells lines, respectively). Indeed, this characteristic pattern of apoptotic zones could account for the lack of significant differences in caspase-3 activity, since it was measured in homogenized pieces of tumors; it may also account for our previous observation that tumor growth resumes if I2 treatment is suspended. . The specific components involved in this I2-sensitivity are not known; however the content of lipids that can be iodinated is an attractive possibility.
The present work demonstrates that tumoral tissue contains significantly higher concentrations of arachidonic acid than normal mammary tissue and that the I2 treatment is accompanied by a 12-fold increase in 6-IL formation. These findings support our earlier hypothesis that the antiproliferative effect of I2 is mediated by the formation of the 6-IL . In thyroid, the apoptotic effect of iodine excess is mediated by 6-IL and/or by iodohexadecanal, both of which are generated by the oxidation and organification of I- by TPO [9, 10]. In this regard, we reported that in thyroid, excess I2 exerts, as I-, an inhibitory effect on NIS, PEN, TPO, and deiodinase type 1 expression, but without the transient decline in circulating thyroid hormone (TH) levels. This finding indicates that I2 can bind to organic components and thereby inhibit gene expression and also generate TH. Moreover, the finding that I2-treated animals supplemented with methimazole preserve the thyroid gene expression pattern of the Wolf-Chaikoff effect supports the proposals that I2, as an oxidized form of iodine does not need TPO for its organification and that a putative iodine-containing organic compound that mediates these effects is generated . These findings agree with previous data obtained in the MCF-7 cell line, where we found that 125I2 is taken up by a facilitated mechanism and that iodinated lipids with a migration similar to that of 6-IL are formed in a process that is not blocked by propylthiouracil (PTU) . It is also interesting that 6-IL is present in I2-treated normal mammary glands, and the possibility that 6-IL at this concentration (0.13 nmol/g) could exert functional effects cannot be dismissed. An analysis investigating this is currently under progress.
Our present data show that I2 treatment significantly reduces PPARα and increases PPARγ expression, findings that could explain the antineoplasic effect of I2. It is well documented that in mammary cancer cells PPARα is over-expressed, and its activation correlates with proliferation [19, 24]. In contrast, in the rat MNU-mammary cancer model dietary treatment with GW7845, an agonist of PPARγ, significantly reduced tumor incidence, tumor number, and tumor weight . Moreover, the significant decrease in vasculature, as well as in VEGF and uPA expression observed in tumors from I2-treated rats, is additional evidence that PPAR receptors participate in the antineoplasic effect of I2. In fact, it has been reported that VEGF is upregulated by PPARα agonists [24, 26], whereas uPA is inhibited by PPARγ activation . VEGF is a potent mitogen with high specificity for endothelia, and it undergoes alternative splicing generating several isoforms . We showed that isoforms 120 and 164, which are the most involved in angiogenesis, are present in MNU-induced tumors and that I2 treatment decreased the expression of both in a similar manner. The inhibition of PPARα expression might explain this effect, although more complex mechanisms could also be involved. Estrogen is known to induce VEGF expression , and recently it was reported that iodine inhibits the expression of several estrogen-responsive genes in MCF-7 cells . Although the detailed mechanism involved in this effect has not been elucidated, PPARγ was shown to exert an inhibitory effect on estrogen-responsive genes via cross-talk with the estrogen receptor binding sites . On the other hand, uPA is a 53-kDa trypsin-like protease that converts the zymogen plasminogen into active plasmin. Although uPA is a relatively specific protease, plasmin acts on a wide variety of protein substrates including metal proteases that destroy the extra cellular matrix (ECM), the degradation of which is a prerequisite for cancer invasion and metastasis . uPA has been used as a specific marker for invasiveness in mammary cancer pathology. The presence of high concentrations of uPA in primary breast cancers correlates with a poor prognosis . I2, after its conversion to 6-IL could, on the one hand, trigger the apoptotic cascades and on the other, decrease the invasive potential of cancer cells by inhibiting the expression of metastatic components like VEGF and uPA, which would account for the antineoplastic effect of I2.
In conclusion, these data support our notion that I2 supplement could be an adjuvant in the therapy of mammary cancer, where the high concentration of AA characteristic of tumoral cells serves as substrate to form 6-IL, which in turn triggers the activation of apoptotic and anti-invasive pathways by modulating PPAR receptors.
The authors are grateful to Drs. Alma Chávez-Blanco, Myrna Doris Arrecillas-Zamora, Teresa Andrea Vela-Chávez from INCAN for advice on tumor classification, to Biol. Felipe Ortíz for technical assistance, Pilar Galarza for bibliographic assistance, and Leonor Casanova for academic support. We also thank Nydia Hernández and Lourdes Lara for image advice and Alberto Lara and Omar González for computer assistance. We thank Dr. Dorothy Pless for proof-reading this manuscript. This work was partially supported by grants: PAPIIT-UNAM IN201207 and CONACYT 78955.
- Cann S, van Netten J, van Netten C: Hypothesis: iodine, selenium and the development of breast cancer. Cancer Causes Control. 2000, 11 (2): 121-127. 10.1023/A:1008925301459.View ArticlePubMedGoogle Scholar
- Venturi S, Donati F, Venturi A, Venturi M, Grossi L, Guidi A: Role of iodine in evolution and carcinogenesis of thyroid, breast and stomach. Adv Clin Path. 2000, 4 (1): 11-17.PubMedGoogle Scholar
- Aceves C, Anguiano B, Delgado G: Is iodine a gatekeeper of the integrity of the mammary gland?. J Mammary Gland Biol Neoplasia. 2005, 10 (2): 189-196. 10.1007/s10911-005-5401-5.View ArticlePubMedGoogle Scholar
- Ghent W, Eskin B, Low D, Hill L: Iodine replacement in fibrocystic disease of the breast. Can J Surg. 1993, 36 (5): 453-460.PubMedGoogle Scholar
- Funahashi H, Imai T, Tanaka Y, Tobinaga J, Wada M, Morita T, Yamada F, Tsukamura K, Oiwa M, Kikumori T: Suppressive effect of iodine on DMBA-induced breast tumor growth in the rat. J Surg Oncol. 1996, 61 (3): 209-213. 10.1002/(SICI)1096-9098(199603)61:3<209::AID-JSO9>3.0.CO;2-F.View ArticlePubMedGoogle Scholar
- Kessler J: The effect of supraphysiologic levels of iodine on patients with cyclic mastalgia. Breast J. 10 (4): 328-336. 10.1111/j.1075-122X.2004.21341.x.Google Scholar
- García-Solís P, Alfaro Y, Anguiano B, Delgado G, Guzman R, Nandi S, Díaz-Muñoz M, Vázquez-Martínez O, Aceves C: Inhibition of N-methyl-N-nitrosourea-induced mammary carcinogenesis by molecular iodine (I2) but not by iodide (I-) treatment Evidence that I2 prevents cancer promotion. Mol Cell Endocrinol. 2005, 236 (1–2): 49-57. 10.1016/j.mce.2005.03.001.View ArticlePubMedGoogle Scholar
- Dugrillon A, Uedelhoven W, Pisarev M, Bechtner G, Gärtner R: Identification of delta-iodolactone in iodide treated human goiter and its inhibitory effect on proliferation of human thyroid follicles. Horm Metab Res. 1994, 26 (10): 465-469. 10.1055/s-2007-1001734.View ArticlePubMedGoogle Scholar
- Pisarev M, Krawiec L, Juvenal G, Bocanera L, Pregliasco L, Sartorio G, Chester H: Studies on the goiter inhibiting action of iodolactones. Eur J Pharmacol. 1994, 258 (1–2): 33-37. 10.1016/0014-2999(94)90054-X.View ArticlePubMedGoogle Scholar
- Langer R, Burzler C, Bechtner G, Gärtner R: Influence of iodide and iodolactones on thyroid apoptosis. Evidence that apoptosis induced by iodide is mediated by iodolactones in intact porcine thyroid follicles. Exp Clin Endocrinol Diabetes. 2003, 111 (6): 325-329. 10.1055/s-2003-42721.View ArticlePubMedGoogle Scholar
- Zhang L, Sharma S, Zhu L, Kogai T, Hershman J, Brent G, Dubinett S, Huang M: Nonradioactive iodide effectively induces apoptosis in genetically modified lung cancer cells. Cancer Res. 2003, 63 (16): 5065-5072.PubMedGoogle Scholar
- Smyth P: Role of iodine in antioxidant defence in thyroid and breast disease. Biofactors. 2003, 19 (3–4): 121-130. 10.1002/biof.5520190304.View ArticlePubMedGoogle Scholar
- Anguiano B, García-Solís P, Delgado G, Aceves Velasco C: Uptake and gene expression with antitumoral doses of iodine in thyroid and mammary gland: evidence that chronic administration has no harmful effects. Thyroid. 2007, 17 (9): 851-859. 10.1089/thy.2007.0122.View ArticlePubMedGoogle Scholar
- Arroyo-Helguera O, Anguiano B, Delgado G, Aceves C: Uptake and antiproliferative effect of molecular iodine in the MCF-7 breast cancer cell line. Endocr Relat Cancer. 2006, 13 (4): 1147-1158. 10.1677/erc.1.01250.View ArticlePubMedGoogle Scholar
- Arroyo-Helguera O, Rojas E, Delgado G, Aceves C: Signaling pathways involved in the antiproliferative effect of molecular iodine in normal and tumoral breast cells: evidence that 6-iodolactone mediates apoptotic effects. Endocr Relat Cancer. 2008, 15 (4): 1003-1011. 10.1677/ERC-08-0125.View ArticlePubMedGoogle Scholar
- Rillema J, Mulder J: Arachidonic acid distribution in lipids of mammary glands and DMBA-induced tumors of rats. Prostaglandins Med. 1978, 1 (1): 31-38. 10.1016/0161-4630(78)90074-5.View ArticlePubMedGoogle Scholar
- Razanamahefa L, Prouff S, Bardon S: Stimulatory effect of arachidonic acid on T-47D human breast cancer cell growth is associated with enhancement of cyclin D1 mRNA expression. Nutr Cancer. 2000, 38 (2): 274-280. 10.1207/S15327914NC382_17.View ArticlePubMedGoogle Scholar
- Berger J, Moller D: The mechanisms of action of PPARs. Annu Rev Med. 2002, 53: 409-435. 10.1146/annurev.med.53.082901.104018.View ArticlePubMedGoogle Scholar
- Michalik L, Desvergne B, Wahli W: Peroxisome-proliferator-activated receptors and cancers: complex stories. Nat Rev Cancer. 2004, 4 (1): 61-70. 10.1038/nrc1254.View ArticlePubMedGoogle Scholar
- Núñez-Anita RE, Arroyo-Helguera O, Cajero-Juárez M, López-Bojorquez L, Aceves C: A complex between 6-iodolactone and the peroxisome proliferator-activated receptor type gamma may mediate the antineoplasic effect of iodine in mammary cancer. Prostaglandins and Other Lipid Mediators. 2009, 89: 34-42. 10.1016/j.prostaglandins.2009.04.001.View ArticlePubMedGoogle Scholar
- Thompson HJ: Methods for the induction of mammary carcinogenesis in the rat using either 7,12-dimethylbenz[a]antracene or 1-methyl-1-nitorosourea. Methods in mammary gland biology and breast cancer research. Edited by: IMaA BB. 2000, New York: Kluwer Academic/Plenum Publishers, 19-29.View ArticleGoogle Scholar
- Russo J, Russo I: Atlas and histologic classification of tumors of the rat mammary gland. J Mammary Gland Biol Neoplasia. 2000, 5 (2): 187-200. 10.1023/A:1026443305758.View ArticlePubMedGoogle Scholar
- Aranda J, Rivera J, Jeziorski M, Riesgo-Escovar J, Nava G, López-Barrera F, Quiróz-Mercado H, Berger P, Martínez de la Escalera G, Clapp C: Prolactins are natural inhibitors of angiogenesis in the retina. Invest Ophthalmol Vis Sci. 2005, 46 (8): 2947-2953. 10.1167/iovs.05-0173.View ArticlePubMedGoogle Scholar
- Suchanek K, May F, Robinson J, Lee W, Holman N, Monteith G, Roberts-Thomson S: Peroxisome proliferator-activated receptor alpha in the human breast cancer cell lines MCF-7 and MDA-MB-231. Mol Carcinog. 2002, 34 (4): 165-171. 10.1002/mc.10061.View ArticlePubMedGoogle Scholar
- Suh N, Wang Y, Williams C, Risingsong R, Gilmer T, Willson T, Sporn M: A new ligand for the peroxisome proliferator-activated receptor-gamma (PPAR-gamma), GW inhibits rat mammary carcinogenesis. Cancer Res. 1999, 59 (22): 5671-5673.PubMedGoogle Scholar
- Biscetti F, Gaetani E, Flex A, Straface G, Pecorini G, Angelini F, Stigliano E, Aprahamian T, Smith R, Castellot J: Peroxisome Proliferator-Activated Receptor Alpha Is Crucial for Iloprost-Induced in vivo Angiogenesis and Vascular Endothelial Growth Factor Upregulation. J Vasc Res. 2008, 46 (2): 103-108. 10.1159/000143793.View ArticlePubMedGoogle Scholar
- Sawai H, Liu J, Reber H, Hines O, Eibl G: Activation of peroxisome proliferator-activated receptor-gamma decreases pancreatic cancer cell invasion through modulation of the plasminogen activator system. Mol Cancer Res. 2006, 4 (3): 159-167. 10.1158/1541-7786.MCR-05-0257.View ArticlePubMedGoogle Scholar
- Houck K, Ferrara N, Winer J, Cachianes G, Li B, Leung D: The vascular endothelial growth factor family: identification of a fourth molecular species and characterization of alternative splicing of RNA. Mol Endocrinol. 1991, 5 (12): 1806-1814. 10.1210/mend-5-12-1806.View ArticlePubMedGoogle Scholar
- Nakamura J, Savinov A, Lu Q, Brodie A: Estrogen regulates vascular endothelial growth/permeability factor expression in 7,12-dimethylbenz(a)anthracene-induced rat mammary tumors. Endocrinology. 1996, 137 (12): 5589-5596. 10.1210/en.137.12.5589.PubMedGoogle Scholar
- Stoddard FR, Brooks A, Eskin B, Johannes G: Iodine alters gene expression in the MCF7 breast cancer cell line: evidence for an anti-estrogen effect of iodine. Int J Med Sci. 2008, 5 (4): 189-196.View ArticlePubMedGoogle Scholar
- Keller H, Givel F, Perroud M, Wahli W: Signaling cross-talk between peroxisome proliferator-activated receptor/retinoid × receptor and estrogen receptor through estrogen response elements. Mol Endocrinol. 1995, 9 (7): 794-804. 10.1210/me.9.7.794.PubMedGoogle Scholar
- Duffy M: Urokinase plasminogen activator and its inhibitor, PAI-1, as prognostic markers in breast cancer: from pilot to level 1 evidence studies. Clin Chem. 2002, 48 (8): 1194-1197.PubMedGoogle Scholar
- Duffy M: Predictive markers in breast and other cancers: a review. Clin Chem. 2005, 51 (3): 494-503. 10.1373/clinchem.2004.046227.View ArticlePubMedGoogle Scholar
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