Lack of efficacy of blueberry in nutritional prevention of azoxymethane-initiated cancers of rat small intestine and colon
© Simmen et al; licensee BioMed Central Ltd. 2009
Received: 18 March 2009
Accepted: 16 September 2009
Published: 16 September 2009
Blueberries may lower relative risk for cancers of the gastrointestinal tract. Previous work indicated an inhibitory effect of consumed blueberry (BB) on formation of aberrant crypt foci (ACF) in colons of male Fisher F344 rats (inbred strain). However, effects of BB on colon tumors and in both genders are unknown.
We examined efficacy of BB in inhibition of azoxymethane (AOM)-induced colon ACF and intestine tumors in male and female Sprague-Dawley rats (outbred strain). Pregnant rats were fed a diet with or without 10% BB powder; progeny were weaned to the same diet as their dam and received AOM as young adults.
Male and female rats on control diet had similar numbers of ACF at 6 weeks after AOM administration. BB increased (P < 0.05) ACF numbers within the distal colon of female but not male rats. There was a significant (P < 0.05) diet by gender interaction with respect to total colon ACF number. Colon and duodenum tumor incidences were less in females than males at 17 weeks after AOM. BB tended (0.1 > P > 0.05) to reduce overall gastrointestinal tract tumor incidence in males, however, tumor incidence in females was unaffected (P > 0.1) by BB. There was a tendency (0.1 > P > 0.05) for fewer adenocarcinomas (relative to total of adenomatous polyps plus adenocarcinomas) in colons of female than male tumor-bearing rats; in small intestine, this gender difference was significant (P < 0.05). BB favored (P < 0.05) fewer adenocarcinomas and more adenomatous polyps (as a proportion of total tumor number) in female rat small intestine.
Results did not indicate robust cancer-preventive effects of BB. Blueberry influenced ACF occurrence in distal colon and tumor progression in duodenum, in gender-specific fashion. Data indicate the potential for slowing tumor progression (adenomatous polyp to adenocarcinoma) by BB.
Epidemiological findings generally indicate a lowering of relative risk of colorectal cancers in humans who regularly consume large amounts of fruits [1–7]. Conversely, individuals consuming relatively small amounts of fruits may have increased risk of colon cancer . Fruit consumption lowers relative risk for cancers of the colon [7, 9, 10], rectum , and small intestine . Protective effects of fruits may be more robust for cancers of the colon than rectum [2, 10, 13], may be stronger in distal than proximal colon sub-sites [2, 13, 14], and in at least one study were more prominent in men than women . Adenomatous polyps (adenomas), the precursors to colorectal adenocarcinomas, are less prevalent in high fruit consumers [13, 15]. In addition, colorectal adenoma growth was inversely associated with consumption of fruits and berries . In spite of the above, there are few epidemiological studies that have examined for effects of specific types of fruits and in particular berries on human colorectal cancer risk.
Berry fruits contain a diverse array of phytochemicals that may have human health benefits . The possible colon cancer-preventive actions of berries have received recent interest . Extracts of berries inhibited, in dose-dependent fashion, proliferation of human cancer cell lines . Among the phenolic compounds of the blueberry (BB), the anthocyanins were shown to be the most potent inhibitors of cell proliferation and inducers of apoptosis when tested, in relatively pure form, on colon cancer cell lines [20, 21]. In humans consuming blueberries, a significant portion of the ingested anthocyanins reach the colon  where they may contribute to tissue anti-oxidant capacity and hence, to anti-carcinogenesis. Additionally, consumption of BB results in postprandial increases in plasma antioxidant level in humans . Pterostilbene, another phytochemical constituent of blueberry, impedes advancement of the cell cycle and induces apoptosis of human cancer cell lines in vitro .
In vivo studies of the colon cancer-preventive actions of berries have used the AOM-administered male Fisher 344 rat or the Apcmin mutant mouse. Freeze-dried black raspberries in the diet inhibited the size (and therefore development) of colon aberrant crypt foci (ACF) as well as tumor multiplicity in male Fisher 344 rats . In this same animal model, blueberry suppressed the total number of colon ACF per rat , similar to that observed with 40 ppm of pterostilbene added to diet . In the Apcmin mouse model, the blackberry anthocyanin, cyanidin-3-glucoside, as well as an anthocyanin enriched extract of bilberry decreased numbers of small intestine adenomas . Also in Apcmin mice, supplementation of diet with bilberry, lingonberry or cloudberry led to reductions in overall number and size of intestinal adenomas . Feeding tart cherries or anthocyanin extract of cherries to Apcmin mice inhibited the frequency and size of intestine adenomas [30, 31]. Thus, suppressive effects of berries on small intestine adenomas in Apcmin mice appear to be robust and consistent between studies.
Despite the above support for preventive effects of fruits and berries on colorectal cancers, several caveats remain. The in vitro studies typically observed effects of anthocyanins in the micromolar range, concentrations that may never be reached systemically or within the lumens of the small intestine or colon. The Apcmin mouse does not model sporadic colon cancers, the most frequent type of colorectal cancer. The AOM-treated, inbred Fisher 344 male rat is highly sensitive to dietary and chemical manipulation of colon carcinogenesis and many structurally diverse molecules have been shown to inhibit or promote ACF and/or tumors in this model . Therefore, results from the above animal models should be examined in outbred rat strains and in both genders.
Insulin and insulin resistance have been positively linked with AOM-induced carcinogenesis in rats [33, 34]. Serum C-peptide, a bio-marker of insulin secretion, is positively associated with colorectal cancer risk in humans  and is regulated by dietary factors ; however, relevance of insulin to suppressive effects of fruit consumption on colorectal cancer development is unclear. In this study, we used a validated, AOM-treated Sprague-Dawley (outbred) rat model (males and females) to evaluate effects of BB on intestine tumor genesis and serum C-peptide. Results did not provide strong support for cancer-preventive effects of BB in the rat colon.
Experimental AIN-93G diets
AIN93G Mineral Mix
AIN93G Vitamin Mix
Tumors and ACF
AOM (Midwest Research Institute; Kansas City, MO) was administered subcutaneously (15 mg/kg body weight) to offspring at PND 53 and again at PND 60. Animals were weighed weekly throughout the duration of the experiment. ACF are observed in the colon mucosa during AOM-induced colon tumorigenesis and are used as an intermediate end point to evaluate cancer-prevention by nutritional and chemo-preventive factors . Colons were obtained from 15 randomly selected animals of each diet group and gender at 6 weeks after the second AOM administration and used for visualization of ACF. Each colon was divided into three equal-length segments, designated as proximal, mid or distal. Segments were stained with 0.2% methylene blue in PBS for 3-5 minutes, rinsed with phosphate-buffered saline (PBS) for 1-2 minutes, and placed in 0.4% formalin-PBS. ACF were visualized using a Nikon AMZ800 stereoscope (40 × magnification) by a single observer blinded to treatment. ACF were elevated (single or multiple clustered) crypts with elongated and enlarged openings. The regional assignment of each ACF and number of crypts per ACF were recorded .
At 16 weeks post-AOM, a group of 10 animals from each diet group and gender were randomly chosen and subjected to necropsy for confirmation of tumor presence. At 17 weeks post-AOM, the liver, stomach, spleen, small intestine, cecum, colon and rectum from 73 or 74 animals of each diet group and gender were obtained and inspected for presence of tumors. Tumor location was determined relative to the distal end of the colon or small intestine. Tumors were removed, weighed, marked on the serosal surface with India ink, and placed in formalin. Serum was prepared from each animal. Pancreas and liver weights were recorded.
Small intestine and colon tumors were classified as adenomatous polyp (adenomatous polyp or adenomatous polyp with carcinoma in situ) or adenocarcinoma (invasive adenocarcinoma, invasive mucinous carcinoma, or metastatic adenocarcinoma with signet ring features) as described previously . Diagnostic features of adenomatous polyps were well differentiated epithelial cells with low mitotic rate and absence of invasion. Adenocarcinomas were poorly differentiated, with cellular and nuclear pleomorphism, high mitotic rate, and evidence of invasion. Some colons manifested nodules which had a tumor-like appearance on gross examination, but which were comprised of focal areas/aggregates of lymphoid B and T cells . These lesions, as well as the few observed mammary, liver, spleen, stomach, cecal and rectal tumors were excluded from statistical analysis.
Serum C-peptide levels were measured using a rat C-peptide radioimmunoassay (Linco Research, Inc, St. Charles, MO). Sera (100 μl) from n = 12 to 14 animals of each diet group and each gender at 17 weeks post-AOM were assayed in duplicate in two replicate assays. Sensitivity of the assay was 25 pM and the inter-assay variation was less than 10%.
Statistical analysis was performed using SigmaStat for Windows, version 3.11 (Systat Software, Inc., Richmond, CA). BB effects on AOM-induced tumor incidence at 17 weeks post-AOM were examined by χ 2 analysis. Tumor pathology was compared for effects of diet and gender using Fisher's Exact Test. The effects of BB on colon ACF number and ACF crypt multiplicity (number of crypts per ACF) were evaluated by Student's t test or the Mann-Whitney rank sum test, the latter when data were not normally distributed. The interaction between effects of diet and gender on ACF was determined using two-way ANOVA. Effects of BB on serum C-peptide concentration were evaluated using Student's t test. All values are presented as means ± S.E.M. Differences between means were considered to be significant at P < 0.05, whereas 0.1 > P > 0.05 was considered to represent a tendency for a difference.
Colon ACF number (per rat) at 6 weeks after second carcinogen treatment.
1.9 ± 0.6
2.2 ± 0.7
2.4 ± 0.8
2.7 ± 0.8
92.7 ± 12.6
74.3 ± 9.0
77.7 ± 11.8
103.1 ± 9.9
47.1 ± 5.6
34.7 ± 3.0
42.1 ± 5.4 a
58.1 ± 5.3 b
Colon ACF number and multiplicity at 6 weeks post-AOM *
Number of Small ACF
129.5 ± 15.4
117.6 ± 15.1 a
99.9 ± 8.9
152.8 ± 11.9 b
Interaction between diet and gender
P = 0.016
Number of Large ACF
12.2 ± 2.4
7.1 ± 2.5
8.1 ± 1.7
10.1 ± 2.2
Interaction between diet and gender
Total Number of ACF
141.7 ± 16.7 a
124.7 ± 15.2 a
107.9 ± 10.0 b
162.8 ± 12.8 b
Interaction between diet and gender
P = 0.012
ACF Crypt Multiplicity
2.1 ± 0.1
1.9 ± 0.1
2.0 ± 0.1
1.9 ± 0.1
Interaction between diet and gender
Incidence of AOM-induced tumors at 17 weeks post-AOM *
# rats per group
P < 0.001
P < 0.01
P < 0.001
Proximal SI **
P < 0.01
P < 0.01
Colon + SI
56.2 (41) a
41.8 (31) b
P < 0.001
Our results did not provide strong support for a beneficial role of BB in inhibition of AOM-induced intestinal cancers in Sprague-Dawley rats. BB only tended to reduce the total number of colon ACF and overall intestine tumor incidence and only in males. In female rats, BB augmented ACF numbers in distal colon, contrary to the hypothesized protective action. The non-significant tendency for a reduced number of ACF in male Sprague-Dawley rats consuming BB diet somewhat agrees with findings by Boateng et al., 2007 , who studied male Fisher 344 rats. However, the latter group reported a statistically significant and robust suppression of ACF by BB diet, in contrast to that observed here. This difference between studies may reflect the two rat strains used, the differences in group size (n = 6 animals for previous study, n = 15 animals for present study), and/or the differing amounts of blueberry incorporated in the diet (10% in the present study, 5% in the previous study). With regard to differences in dietary content of blueberry, we do not consider this a likely cause of the study differences, since anthocyanins suppressed adenoma formation in a linear dose-dependent fashion in Apcmin mice . It is plausible that Sprague-Dawley rats are less susceptible (and/or individually more variable) to dietary influences on AOM-induced ACF and tumor formation than inbred Fisher 344 rats, which also may contribute to differences between studies. In marked contrast to these findings was the significant increase in ACF occurrence in distal colon of female rats consuming BB. The basis for this novel, gender-specific response to BB is unknown, albeit, we speculate that this may involve functional interactions of BB constituent(s) with female sex hormones and/or receptors.
Regional distribution of adenocarcinomas closely followed that for ACF, as in our prior studies [36, 37, 39]. Specifically, ACF and tumors were more prevalent in mid > distal > proximal colon. Several epidemiological studies reported more pronounced cancer-protective effects of fruits in distal rather than proximal colon of humans [2, 13, 14]. The functional correspondence of the mid colon of the rat to one or more sub-sites of the human colon is not known; anatomically, it corresponds to transverse and upper distal regions of the human colon. The lack of inhibitory effect of BB on tumorigenesis in the rat colon may suggest that BB will not be preventive for human colon cancers, although epidemiological studies are necessary to resolve this question.
The similar ACF numbers for male and female rats on control diet, but less frequently occurring colon tumors in females relative to males, were noted. Thus, progression of ACF to adenomatous polyps may be slowed or partially blocked in female rats or alternatively, ACF in female rats may regress to a greater extent during the later stages of tumorigenesis, also leading to fewer polyps. Such mechanisms have a precedent in the case of AOM-treated AKR/J mice which are resistant to colon tumor-formation but manifest ACF in their colons . Striking differences in tumor incidence with gender were maintained across the three regions of the colon as well as proximal small intestine (duodenum). This is consistent with previous observations of greater tumor incidence in male than female rats after administration of colon carcinogens [41–43]. Since ACF numbers were similar for males and female Sprague-Dawley rats on control diet, liver activation of AOM to the proximate carcinogen, methylazoxymethanol  likely does not differ with gender. Rather, the involvement of systemic or local factor(s) that affect post-initiation phases of intestinal tumorigenesis and which exhibit sexual dimorphism is suggested. We speculate that insulin may be one such factor, since C-peptide levels were significantly lower in female rats (presumably as a consequence of their increased insulin sensitivity) and insulin (and insulin resistance) have been positively linked with AOM carcinogenesis in rats [33, 34]. Interestingly, incidence of colorectal cancer is slightly lower in women than men . Thus, a further understanding of how gender affects tumorigenesis in this animal model may be relevant to elucidating endocrine and other influences on human colorectal cancer incidence rates.
Regional differences in tumor incidence within the colon and small intestine have been reported [36, 37, 39, 46, 47] and were confirmed here. Another laboratory has shown in male Sprague-Dawley rats that AOM induces DNA modifications (alkylation) to similar extents in proximal and distal halves of the colon; however, the distal half of the colon responds to these DNA modifications with a greater degree of apoptosis and DNA repair, compared to proximal colon . In view of the known apoptosis-inducing effects of anthocyanins and stilbenes in vitro, we hypothesized that these molecules, when provided via BB diet, would promote apoptosis of colon epithelial cells whose DNA was newly modified by AOM during initiation of carcinogenesis, thus resulting in fewer ACF and tumors. However, our ACF and tumor results did not support this hypothesized action. Perhaps, the levels of these bio-active factors within the microenvironment of the colonic crypt and luminal epithelium were limiting.
Consumption of fruits may protect against cancer development in human small intestine . Indeed, we observed that BB inhibited the adenoma-adenocarcinoma transition in female rat duodenum. This is generally concordant with the reported inhibition, by fruit consumption, of colorectal adenoma growth in humans [13, 15, 16] and the rather consistent inhibition by berries of adenoma growth in Apcmin mice [29–31]. In the latter model, adenomas are common in small intestine. Thus, collective findings highlight the potential for use of berries and fruits in dietary prevention of small intestine tumors.
In vitro and in vivo studies implicate anthocyanins and other phytochemicals in growth-inhibition of cancerous cells [20, 21, 24, 27]. Such molecules may have estrogenic or anti-estrogenic actions  which may pertain to the gender-specificity of effects observed, although this is speculative. Further studies that examine how BB components affect the adenoma-adenocarcinoma transition, and how this is affected by gender, may yet reveal approaches for cancer-prevention using whole BB or its constituent(s), alone or in combination with other colon cancer-preventive foods or factors.
Results did not demonstrate robust cancer-preventive effects of BB but identified marked gender differences in incidence of AOM-induced tumors. Blueberry influenced, in gender-specific fashion, ACF occurrence in distal colon and tumor progression in duodenum. These findings illustrate the complex interplay of bio-active dietary factors, gender, tissue sub-site, and endocrine status in intestinal carcinogenesis and neoplasia.
aberrant crypt foci
Dr. Rosalia C.M. Simmen provided many helpful suggestions during the course of this work and a critical review of the manuscript. This work was supported by the U.S. Department of Agriculture (CRIS 6251-51000-005-03S). Research was performed, in part, using compound(s) provided by the National Cancer Institute's Chemical Carcinogen Reference Standards Repository operated under contract by Midwest Research Institute, no. N02-CB-07008.
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