Effects of high-isoflavone soy diet vs. casein protein diet and obesity on DMBA-induced mammary tumor development

  • Authors:
    • Reza Hakkak
    • Saied Shaaf
    • Chan Hee Jo
    • Stewart MacLeod
    • Soheila Korourian
  • View Affiliations

  • Published online on: November 8, 2010     https://doi.org/10.3892/ol.2010.202
  • Pages: 29-36
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Abstract

Obesity and elevated serum insulin growth factor-1 (IGF-1) level are major risk factors in the development of breast cancer. We investigated the long-term effects of high-isoflavone soy intake and obesity on 7,12-dimethylbenz(a)anthracene (DMBA)-induced mammary tumor development and on serum IGF-1 and binding protein (IGFBP-3) levels. Lean and obese female Zucker rats fed casein or high-isoflavone soy protein were orally gavaged at age 50 days with DMBA and sacrificed after 147 days. The majority of lean casein-fed rats (69%) developed mammary tumors compared to 50% in lean soy-fed rats (P=0.176). In the obese groups, 76% of soy-fed rats developed mammary tumors compared to 15% of obese casein-fed rats (P<0.001). At age 43 days, IGFBP-3 was increased in the lean soy-fed rats compared to the lean casein-fed rats (P<0.05). At age 99 days, soy- and obese casein-fed rats exhibited increased serum IGF-1 compared to the lean rats and this increase was maintained for the rest of the experiment (P<0.05). Obese rats fed casein exhibited increased IGFBP-3 levels (P<0.001). However, obese rats fed soy exhibited a significant decrease in IGFBP-3 levels compared to the lean soy-fed rats (P<0.001) and a significant decrease in IGFBP-3 levels compared to the obese casein-fed rats (P<0.001). At age 197 days, IGFBP-3 levels were increased in obese casein- and soy-fed rats (P<0.001). The results suggest that female Zucker rats fed casein diets are protected against DMBA-induced mammary tumors, which is not the case for those on high-isoflavone soy diet, and changes in the concentration of serum IGFBP-3 may contribute to the incidence of DMBA-induced mammary tumors.

Introduction

Breast cancer is the most common malignant tumor among women and, of all cancers, it is the second leading cause of mortality in women in the United States. In 2010, an estimated 207,090 women are likely to be diagnosed with invasive breast cancer and 39,840 women are likely to succumb to this disease (1). Obesity has been epidemic in the United States for more than two decades and the proportion of overweight and obese adults in the population continues to rise. In an investigation of the role of overweight and obesity in carcinogenesis, Calle et al documented not only an association between body mass index (BMI) and mortality from various types of cancer, but also provided a reliable estimate of the contribution of overweight and obesity to the total mortality from cancer (2). The authors reported that women with the highest BMI (40 kg/m2) had mortality rates from all types of cancer combined that were 62% higher (with a relative risk of death of 1.62) than the rates of women of normal weight. These authors reported a significant trend whereby individuals with a higher BMI exhibited an increased risk of succumbing to cancers of the breast, uterus, cervix and ovary.

Numerous studies suggest health benefits from soy consumption, including its role in the reduction of cardiovascular disease and certain types of cancer (3,4). Soybeans and soy protein products are a major source of phytoestrogen, plant-based estrogen-like substances. Soybeans contain isoflavones, which are structurally similar to mammalian estrogens, have estrogenic properties and are potential anticarcinogens (5). The most common dietary isoflavones are genistein, daidzein and glycitein, also known as isoflavonoids (6). Gut flora metabolizes daidzein into equol, a non-steroidal estrogen (6). It has been proposed that a high consumption of soy foods is partially responsible for the observed lower breast cancer rate in Asian women (7). However, results of these studies conflict with those of studies concluding that certain components of soy are estrogenic and therefore increase the breast cancer risk.

Certain studies are available regarding the protective effects of soy on breast cancer, while findings of other studies report the adverse effects of soy. For example, soy intake has been found to increase spontaneous mammary gland tumors in mice (8). Moreover, the use of a soy protein supplement for 2 weeks by women with benign or malignant breast disease was found to have estrogenic effects on the breasts of these individuals (9). On the other hand, in a large cohort study of British women no effects of dietary isoflavone intake and breast cancer risk were found among either pre- or post-menopausal women (10). Experimental studies showed variable results on breast cancer reduction by soy or the soy isoflavone genistein (1115). For example, it was reported that genistein reduces the growth of tumors that arise from inoculated human or mouse breast cancer carcinoma cells in pre-menopausal mouse models (16,17). On the other hand, isolated genistein was found to promote MNU-induced estrogen-dependent mammary tumorigenesis and growth of the MCF-7 estrogen receptor (ER)-positive human breast cancer cell line implanted in ovariectomized rats and mice as a model for postmenopausal status (18,19). Data on the effects of soy consumption on breast health, particularly in obese women, are lacking.

A number of epidemiological studies showed that elevated levels of serum insulin-like growth factor-1 (IGF-1), a mitogenic and antiapoptotic protein, are related to an increased risk of breast cancer (2027). IGF-1 levels are increased in obese individuals and at least part of the greater risk of breast cancer in obese women may be due to IGF-1 growth stimulation of breast cells. IGF-1 activity is modulated by a family of IGF-binding proteins, IGFBPs 1–6. These proteins bind and reduce the availability of IGF-1 in serum. Increased IGFBP levels are associated with lower bioavailable IGF-1 and are involved in the antiproliferative effects of antiestrogens in human breast cancer cell lines (28,29). IGF-1 and estrogen function as growth factors for mammary epithelial cells and for mammary tumor cell lines, operating to increase proliferation in breast cancer cell lines. Additionally, IGF-1 is required for maximum ER activation in these cells (28,29). Higher insulin levels are also associated with obesity and may enhance cellular proliferation leading to the development of breast cancer (30).

Of the IGFBPs, IGFBP-3 exhibits the highest concentration in serum and the majority of IGF-1 in serum are bound by IGFBP-3. IGFBP-3 with bound IGF-1 is thought to be inactive, but IGFBP-3 can be degraded by proteases in tumor cells, thereby releasing IGF-1 and increasing local IGF-1 bioavailability. Human data regarding IGFBP-3 levels and breast cancer risk have been inconclusive. Some studies show a relationship between breast cancer risk and IGFBP-3 concentrations (23,24,26), whereas in other studies a protective effect (22) or no association at all (31) was noted.

The Zucker rat (fa/fa) is the best known, most widely used rat model for genetic obesity. Obesity in the Zucker rat is inherited as an autosomal recessive trait caused by a mutation (fa) in the leptin receptor gene (32,33), discovered by Zucker and Zucker (34,35). Animals homozygous for the fa allele were notably obese by 3–5 weeks of age and by 14 weeks of age their body composition was >40% lipid (36). A number of investigators have used this model to study the development, etiology, associated pathogenesis, possible treatment and putative mechanisms of severe obesity (37). Obese Zucker rats develop hyperinsulinemia and insulin resistance prior to the development of obesity-associated non-insulin-dependent diabetes mellitus (NIDDM) in a manner similar to that in humans (38). Lean Zucker rats, by contrast, exhibit normal metabolic function and are considered ideal controls. Consequently, this model can be used to investigate the impact of soy consumption on mammary tumor development in an obese animal model. No published data are currently available regarding the effects of soy diet and obesity on mammary tumor development in obese animals.

Material and methods

Experimental design

The animal protocols were approved by the Institutional Animal Care and Use Committee (IACUC) at the University of Arkansas for Medical Sciences. A total of 99 five-week-old female Zucker rats (45 obese fa/fa and 54 lean) were purchased from Harlan Industries (Indianapolis, IN, USA). Harlan Industries performed genotyping to identify fa/fa and lean/lean rats at the age of 24 days. After 1 week of acclimation (age 42 days), rats were randomly assigned to groups: i) lean, casein diet; ii) obese, casein diet; iii) lean, soy protein diet; and iv) obese, soy protein diet. The rats were housed 2 per cage with ad libitum access to water and a semi-purified diet similar to the AIN-93G diet (Harlan Teklad, Madison, WI, USA) prepared with dietary protein, either casein (control) or an enzymatically treated soy protein isolate with high isoflavones [3.24 mg total isoflavones/g protein (1.88 aglycone equivalents/g protein), Lot no. M330024462; Solae LLC, St. Louis, MO, USA]. The compositions of the two diets are described in Table I. At age 50 days the rats received 65 mg DMBA/kg body weight (Sigma Chemical Co., St. Louis, MO, USA) in sesame oil, via gavage. Blood samples were drawn from the tail vein at various ages (43, 99 and 197 days) to measure serum IGF-1 using ELISA kit (IDS, Fountain Hills, AZ, USA) and IGFBP-3 ELISA kit (DSL, Webster, TX, USA). Beginning 4 weeks after DMBA treatment, the rats were palpated twice weekly for mammary tumor detection. The detection date and location of each mammary tumor were recorded for each rat. The rats were sacrificed 147 days post-DMBA treatment. The mammary tumors were excised, counted and weighed. Three rats with tumor masses >2.5 cm in diameter were sacrificed early according to our IACUC-approved animal protocol. The tumor sections were placed in 10% neutral-buffered formalin for histopathologic analysis. Sections (4 μm) of the paraffin-embedded tumors were stained with hematoxylin and eosin for light microscopic evaluation.

Table I

Composition of study diets.

Table I

Composition of study diets.

IngredientsCasein (g/kg)aSoy protein (g/kg)
Casein200.0-
Isolated soy protein-202.0
L-Cystine3.0-
L-Methionine-2.5
L-Cystine-1.3
L-Tryptophan-0.4
L-Threonine-0.3
Corn starch397.5409.0
Maltodextrin132.0132.0
Sucrose100.0108.0
Corn oilb70.063.0
Cellulose50.050.0
AIN-93G mineral mix35.035.0
AIN-93G vitamin mix10.010.0
Choline bitartrate2.52.5
TBHQ, antioxidant0.0140.014

a Measurements are g of ingredient/kg of diet.

b The amount of corn oil was adjusted in the soy protein diet to account for the fat contribution from soy protein.

Pathology

A board-certified anatomic pathologist (S.K.) evaluated the tumors in a blinded protocol. The tumors were classified as benign (essentially unremarkable breast parenchyma with non-proliferative fibrocystic changes); intraductal proliferation (IDP), characterized by epithelial proliferation or presence or multiple papillomas; ductal carcinoma in situ (DCIS), uniform proliferation of tumor cells within pre-existing structures without evidence of invasion to the surrounding tissue; invasive ductal and lobular carcinoma (IDC), showing an invasive (infiltrative) pattern of neoplastic cells; or Phyllodes, characterized by a relatively well-demarcated fibroepithelial mass showing marked stromal cellularity and numerous stromal mitosis, similar to the pattern of the Phyllodes tumor observed in female individuals.

Statistical analysis

A Kruskal-Wallis test was used to analyze the four treatment groups, followed by between-group comparisons using the Mann-Whitney U test due to unequal variances in the groups. A two-way ANOVA was used to measure serum IGF-1 and IGFBP-3 levels, followed by Tukey’s post-hoc test. A Kaplan-Meier analysis of tumor latency was performed. A log-rank test was used to compare the median tumor-free times. Fisher’s exact test was used to compare the percentage of rats with tumors and tumor histology in each group. The median number of tumors per tumor-bearing rat (multiplicity) for each group was compared using the non-parametric Kruskal-Wallis test for overall differences and the Mann-Whitney U test for group comparisons. Statistical significance was set at P<0.05 and the P-values were not adjusted for multiple comparisons. For the rats that were sacrificed early due to tumor burden, the number of tumors was assumed to have remained constant until the end of the study. Data analyses were generated and the plots were constructed using SPSS© version 17.0 for Windows (SPSS Inc., Chicago, IL, USA) and SAS version 9.0 (SAS Inc., Cary, NC, USA).

Results

Body weight

All of the rats gained weight during the course of the experiment (Fig. 1A). Obese rats gained significantly (P<0.001) more weight than lean rats. Obese soy protein-fed rats were significantly heavier than obese casein rats (543±11 vs. 484±8) (P<0.001). The lean soy protein-fed rats also exhibited a higher body weight than the lean casein-fed rats (300±5 vs. 283±4) (P=0.024).

Serum IGF and IGFBP-3 levels

At age 43 days, no differences were found in the serum IGF-1 levels among the groups, but IGFBP-3 was increased in the high-isoflavone soy protein-fed lean group compared to the casein-fed lean rats (Table II). At age 99 days, obese rats fed a casein diet exhibited increased IGFBP-3 levels (P<0.001), but obese rats fed soy protein exhibited a significant decrease in IGFBP-3 levels compared to the lean soy protein-fed group (P<0.001). Moreover, obese soy protein-fed rats exhibited a significant decrease in IGFBP-3 levels compared to obese casein-fed rats (P<0.001). At the end of the experiment, IGFBP-3 levels were increased in the obese casein- and soy protein-fed rats (P<0.001).

Table II

Serum levels of IGF-1 and IGFBP-3 (mean ± standard error).

Table II

Serum levels of IGF-1 and IGFBP-3 (mean ± standard error).

L/C (n=26)L/S (n=28)O/C (n=20)O/S (n=25)
IGF-1
 Age (days)431.327±541.422±571.309±521.472±65
991.129±27a,c1.213±321.705±76b,d1.528±67b,e
197816±18834±201.652±67b,d1.433±84b,e
IGFBP-3
 Age (days)4369±2b,c79±178±2b,d78±1
9944±246±159±3b,d40±1b,e,f
19716±219±240±5b,d30±3b,e

{ label (or @symbol) needed for fn[@id='tfn3-ol-02-01-0029'] } L/C, lean casein; L/S, lean soy protein; O/C, obese casein; O/S, obese soy protein.

a P<0.05;

b P<0.001;

c L/C vs. L/S;

d L/C vs. O/C;

e L/S vs. O/S;

f O/C vs. O/S.

Time course for tumor formation, latency and multiplicity

The time course of palpable mammary tumor detection is shown in Fig. 1B and the data are presented in Table III.

Table III

Characteristics of DMBA-induced mammary tumors.

Table III

Characteristics of DMBA-induced mammary tumors.

L/C (n=26)L/S (n=28)O/C (n=20)O/S (n=25)
Tumor onset
 Day of first tumora88469588
 Day at 25% tumorsb124116N/A106
Tumor incidence
 Rats with tumors (%)c69f,g501576f,h
Multiplicityd1 (1–4)1 (1–2)11 (1–3)
Total tumors (n=82)e30 (37%)18 (21%)3 (4%)31 (38%)
 Benign2 (7%)0 (0%)0 (0%)2 (6%)
 IDP6 (20%)0 (0%)0 (0%)0 (0%)
 DCIS21 (70%)9 (50%)2 (67%)16 (52%)
 IDC0 (0%)6 (33%)1 (33%)11 (35%)
 Phyllodes1 (3%)3 (17%)0 (0%)2 (7%)

{ label (or @symbol) needed for fn[@id='tfn10-ol-02-01-0029'] } L/C, lean casein; L/S, lean soy protein; O/C, obese casein; O/S, obese soy protein; N/A, not applicable.

a Post-DMBA day at which the first mammary tumor was detectable by palpation.

b Post-DMBA treatment at which the probability of tumor development was 25%.

c Percentage of rats with at least one mammary tumor.

d Median number of tumors in tumor-bearing rats (minimum and maximum in parentheses).

e Number and percentage of total mammary tumors graded as benign, intraductal proliferation (IDP), ductal carcinoma in situ (DCIS), invasive ductal and lobular carcinoma (IDC) or Phyllodes.

f P<0.001.

g L/C vs. O/C;

h O/C vs. O/S.

Tumor latency (the number of days post-DMBA treatment until the detection of the first mammary tumor) was longer in the obese casein-fed rats than the remaining three groups. The first mammary tumor detected in lean soy protein-fed rats was 46 days post-DMBA treatment compared to 88 days in lean casein-fed rats. For the obese soy protein-fed rats, the first mammary tumor was detected 88 days post-DMBA treatment, compared to 95 days in obese casein-fed rats. In addition, 25% of the lean soy protein-fed rats developed mammary tumors 116 days post-DMBA treatment, compared to 124 days for the lean casein-fed rats and 106 days for the obese soy protein-fed rats. By the end of the experiment, 69% of the lean casein rats developed mammary tumors, compared to 50% in the lean high-isoflavone soy protein group. However, this difference was not statistically significant (P=0.176). In the obese group, 76% of the high-isoflavone soy protein-fed rats developed mammary tumors, compared to 15% of the obese casein-fed rats (P<0.001). The lean casein-fed group had a higher incidence of mammary tumor development than that of the obese casein rats (69 vs. 15%) (P<0.001). A higher incidence of mammary tumors was noted in the obese soy protein-fed rats than in the lean soy protein-fed rats. However, this result was not statistically significant (76 vs. 50%) (P=0.088). The median number of mammary tumors per tumor-bearing rat (multiplicity) was compared. No statistically significant difference was found among the four groups. In regards to multiplicity, the lean soy protein-fed rats had a range of 1–2 tumors per rat, compared to a range of 1–4 tumors per rat in the lean casein-fed group. The tumor multiplicity for obese casein-fed rats (1 tumor per rat) was lower compared to the obese soy protein-fed rats (1–3 tumors per rat) (Table III).

Mammary tumor characteristics

Mammary tumor histology data are presented in Table III. A total of 82 mammary tumors were detected in the study. Table III shows the light microscopic classification of these mammary tumors in the four groups. A total of 30 masses were detected (37% of the total tumors) in the lean casein-fed group compared to 18 tumors (21%) in the lean soy protein-fed group, 31 tumors (38%) in the obese soy protein-fed rats and only 3 tumors (4%) in the obese casein-fed rats. Pathological analysis of the 30 tumors in the lean casein-fed group showed the following classification: 2 (7%) benign, 6 (20%) IDP, 21 (70%) DCIS and 1 (3%) Phyllodes. Of the 18 mammary tumors in the lean soy protein-fed group 9 were DCIS (50%), 6 IDC (33%) and 3 Phyllodes (17%). For the obese casein-fed group, 2 tumors were classified as DCIS and 1 tumor as IDC. Mammary tumors in the obese soy protein-fed group included 2 (6%) benign, 16 (52%) DCIS, 11 (35%) IDC and 2 (7%) Phyllodes. While tumors classified as benign, IDP, DCIS and IDC were observed in the author’s previously published study on obesity and breast cancer in female Zucker rats (39,40), tumors with the morphologic characteristics of Phyllodes tumors have not been observed in prior studies. A tumor classified as Phyllodes from this study is shown in Fig. 2.

Discussion

This study aimed to compare the effects of long-term high-isoflavone soy protein to those of long-term casein protein intake and obesity on DMBA-induced mammary tumor development, as well as to investigate the effects of high-isoflavone soy protein and obesity on serum IGF-1 and IGFBP-3 levels.

Results of the present study showed that obese soy protein-fed rats gained significantly more weight than obese casein-fed rats (P<0.001) and the lean soy protein-fed rats exhibited a slightly higher body weight than their lean casein-fed counterparts (P=0.057). In the lean groups, 69% of the casein-fed rats developed mammary tumors compared to 50% (P<0.08) of the soy protein-fed rats. In the obese groups, 76% of the soy protein-fed rats developed mammary tumors compared to 15% (P<0.05) of the obese casein-fed rats. At age 99 days, obese rats fed a casein diet exhibited increased IGFBP-3 levels (P<0.001), but obese rats fed soy protein exhibited a significant decrease in IGFBP-3 levels compared to the lean soy protein-fed group (P<0.001). Additionally, IGFBP-3 levels in obese soy protein-fed rats were significantly decreased compared to obese casein-fed rats (P<0.001). At the end of the experiment, the IGFBP-3 levels were found to have increased in obese casein- and soy protein-fed rats (P<0.001).

Our observations regarding weight increase of obese soy protein-fed compared to obese casein-fed rats (P<0.001) are agreement with those of Tovar et al (41). These authors found that obese ZDF fa/fa rats fed either a casein or soy protein diet gained weight at a similar rate until day 140, but after day 150, rats fed the casein diet began to lose weight compared to rats fed the soy protein diet (P=0.004). By day 160 post-treatment, Tovar et al observed that the casein-fed rats weighed significantly less than the soy-fed rats. These authors concluded that the difference in weight gain between groups is explained by a physical deterioration observed in rats fed the casein diet in the last days of the study. Another study reported that among obese rats fed either casein or soy diets, casein-fed rats gained significantly less weight than soy-fed rats, probably due to their physical deterioration (42). In their study, Mezei et al reported that when female obese Zucker rats were fed with high- or low-isoflavone soy diets, the high-isoflavone soy-fed rats gained more body weight than the low-isoflavone soy-fed and casein-fed rats (P<0.05) (43).

Our results for casein-fed obese rats showing that obesity protected against DMBA-induced mammary tumor development are in agreement with epidemiological data showing that obesity protects against breast cancer development in obese pre-menopausal women (4446).

Our results show that in obese Zucker rats, a soy protein diet containing high isoflavone levels promoted DMBA-induced mammary tumor development compared to a casein-based diet. We found that lean and obese rats fed soy protein diets developed more advanced mammary tumors, graded IDC, than their respective controls in the casein group. Simmen et al reported that when Sprague-Dawley rats were fed AIN-93G diets with either casein or soy protein as the source of protein and treated with N-methyl nitrosourea, rats on soy protein diets developed more advanced grade tumors (47). The mechanism underlying the higher grade tumors elicited by soy diet has yet to be determined.

The presence of dietary isoflavones may affect the development of mammary tumors, as previously reported (19,48). For this reason, we used the purified diet AIN-93G, which contains no soy or soy isoflavones. In our previous study (39), the standard natural ingredient diet 2018 was employed. The 2018 diet contains soybean meal with the isoflavone levels ranging from 150 to 250 mg/kg diet, depending on the batch. The presence of soy isoflavones in this diet may explain the differences in mammary tumor induction observed in other sutdies (39).

Meta-analyses on soy intake and breast cancer risk have been reported. Epidemiological studies have showed that soy consumption was associated with a reduction in breast cancer risk in pre-but not postmenopausal women in Singapore (49). Another meta-analysis found an inverse association between soy intake and breast cancer risk among pre-menopausal women, but no effect was noted among postmenopausal women (50). A meta-analysis of 18 epidemiological studies has shown that a high soy intake may be associated with a small reduction of breast cancer risk, but this association was not significant among women in Asian countries and the reduction was more significant in pre-compared to postmenopausal women (51). The inverse association between soy food intake and breast cancer risk was mainly noted in Asian women, with only one study reporting such a correlation in women of Caucasian descent (52). The correlation of adolescent and adult soy food intake with breast cancer risk was evaluated in a cohort of 73,223 Chinese women who participated in the Shanghai Women’s Health Study. A protective effect of soy food intake against pre-menopausal breast cancer was noted (53). A recent meta-analysis of the literature (a total of 34 studies) on the relationship between dietary soy intake and breast cancer risk has concluded that the intake of naturally occurring dietary soy food or its components appears to be safe for women without breast cancer. However, the safety of high levels of consumption of soy containing supplements or soy components was less certain (54).

Experimental studies in non-obese animal models have shown an association between serum IGF-1 concentrations and mammary cancer risk. For example, liver IGF-1 deficient mice, which have hepatic IGF-1 gene deletion, show a 75% reduction in serum IGF-1 levels, but normal growth and development. These mice have shown delays in the onset of chemically-and genetically-induced mammary tumors. Wu et al (55) used an IGF-1 gene-deleted mouse model to show that the lack of IGF-1 in these mice resulted in a significant delay in the onset of DMBA-induced mammary tumors. These data indicate that tumor development can be induced by IGF-1. Thus, modulation of IGF-1 and IGFPB-3 concentration is a crucial strategy for determining the effects of the incidence of breast cancer in obese Zucker rats. Clinical studies on the effects of soy on IGF-1 levels were found to be inconclusive, with some studies showing that soy increases IGF-1 levels (56,57). However, these studies used subjects with normal body weight and not obese ones. By contrast, other studies have shown decreases in serum IGF-1 levels (58,59). Our preliminary data using obese Zucker rats have shown that obesity increases the serum IGF-1 levels (60). The impact of dietary factors on IGF-1 levels in humans is limited to a number of observational epidemiological studies (6172). Thus, no data regarding the effect of specific factors, such as soy or isoflavones, are available. Since obesity is likely to increase serum IGF-1 levels, and a soy diet with a high isoflavone content modulates serum IGF-1 levels, we investigated the effects of a soy-based diet with isoflavones on serum IGF-1 and IGFBP-3 levels and its effect on DMBA-induced mammary tumors. Elevated IGF-1 has been shown to be a risk factor for breast cancer in women (22,26,73). It is thought that increased IGFBP-3 levels may be play a protective role in breast cancer by decreasing the levels of bioavailable IGF-1 (24,74).

For these reasons, we measured IGF-1 and IGFBP-3 serum levels at three time points in lean and obese casein- and soy protein-fed rats. Lean soy protein-fed rats exhibited increased IGFBP-3 levels compared to casein-fed rats. After 1 day on the diets (Day 43), the lean soy protein-fed rats exhibited higher IGFBP-3 levels compared to their lean casein-fed counterparts. Short-term dietary intervention with soy isoflavones is known to result in rapid changes in serum IGFBP-3 levels (75). Increased IGFBP-3 may reduce the bioavailability of IGF-1 and be partially responsible for the observed lower incidence (non-significant) of tumors in lean soy protein-fed rats. However, in the obese groups, IGFBP-3 levels were increased in casein-fed rats, while much lower levels were noted in soy-fed rats. Our results clearly show that obesity increased serum IGF-1 levels for casein-and soy protein-fed rats compared to lean rats fed with either diet. By age 99 days, the obese casein-fed rats exhibited increased IGFBP-3 levels compared to their soy protein-fed counterparts. This increase in IGFBP-3 and the resultant decrease in bioavailable IGF-1 may be the mechanism responsible for the lower tumor numbers observed in obese casein-fed compared to obese soy protein-fed animals.

To the best of our knowledge, this report is the first to show that intact obese vs. lean Zucker female rats fed semi-purified diets are protected against DMBA-induced mammary tumors for a longer period of time while on casein vs. high-isoflavone soy protein diets. The majority of the observed tumors were epithelial in nature resembling the invasive and in situ carcinoma observed in female individuals. However, we have observed another rare tumor which mimics the Phyllodes tumors found in women. Phyllodes are in general rare tumors and their etiology has yet to be elucidated.

Our results suggest that the dietary protein source affects serum IGFBP-3 levels in obese female Zucker rats. Furthermore, changes in the concentration of IGFBP-3 may contribute to the reduction of the incidence of DMBA-induced mammary tumors.

Acknowledgements

The authors wish to thank John Gregan and Phaedra Yount for valuable assistance in the preparation of this manuscript on behalf of the Arkansas Children’s Hospital Research Institute. This study was supported by the U.S. Department of Agriculture and the Arkansas Biosciences Institute. R.H. applied for and received funding, designed and supervised the study, and participated in the collection of tumor data and the writing of the manuscript. S.S. coordinated and performed the daily activities regarding overseeing the animals, recording data and processing the samples. S.M. participated in the study design, interpretation of study results and participated in discussions involving the findings. C.H.J. participated in the study design and performed the statistical analyses. S.K. provided expertise in classifying and analyzing all of the mammary tumors and participated in the interpretation of study results and writing of this manuscript. The authors read and approved the final manuscript.

Abbreviations:

DMBA

7,12-dimethylbenz(a)anthracene

BMI

body mass index

ER

estrogen receptor

IGF-1

insulin growth factor-1

IGFBP-3

insulin growth factor binding protein-3

NIDDM

non-insulin-dependent diabetes mellitus

IACUC

Institutional Animal Care and Use Committee

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January-February 2011
Volume 2 Issue 1

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Spandidos Publications style
Hakkak R, Shaaf S, Jo CH, MacLeod S and Korourian S: Effects of high-isoflavone soy diet vs. casein protein diet and obesity on DMBA-induced mammary tumor development. Oncol Lett 2: 29-36, 2011.
APA
Hakkak, R., Shaaf, S., Jo, C.H., MacLeod, S., & Korourian, S. (2011). Effects of high-isoflavone soy diet vs. casein protein diet and obesity on DMBA-induced mammary tumor development. Oncology Letters, 2, 29-36. https://doi.org/10.3892/ol.2010.202
MLA
Hakkak, R., Shaaf, S., Jo, C. H., MacLeod, S., Korourian, S."Effects of high-isoflavone soy diet vs. casein protein diet and obesity on DMBA-induced mammary tumor development". Oncology Letters 2.1 (2011): 29-36.
Chicago
Hakkak, R., Shaaf, S., Jo, C. H., MacLeod, S., Korourian, S."Effects of high-isoflavone soy diet vs. casein protein diet and obesity on DMBA-induced mammary tumor development". Oncology Letters 2, no. 1 (2011): 29-36. https://doi.org/10.3892/ol.2010.202