A complex network of interactions between the stroma, the extracellular matrix and the epithelium drives mammary gland development and function. Two main assumptions in chemical carcinogenesis of the mammary gland have been that carcinogens induce neoplasia by causing mutations in the DNA of the epithelial cells and that the alterations of tissue architecture observed in neoplasms are a consequence of this primary mutational event. Here, we use a rat mammary tissue recombination model and the chemical carcinogen N-nitrosomethylurea (NMU) to determine whether the primary target of the carcinogen is the epithelium, the stroma or both tissue compartments. Mammary epithelial cells were exposed in vitro either to the carcinogen or vehicle before being transplanted into the cleared fat pads of rats exposed to carcinogen or vehicle. We observed that neoplastic transformation of these mammary epithelial cells occurred only when the stroma was exposed in vivo to NMU, regardless of whether or not the epithelial cells were exposed to the carcinogen. Mammary epithelial cells exposed in vitro to the carcinogen formed phenotypically normal ducts when injected into a non-treated stroma. Mutation in the Ha-ras-1 gene did not correlate with initiation of neoplasia. Not only was it often found in both cleared mammary fat pads of vehicle-treated animals and intact mammary glands of untreated animals, but it was also absent in some tumors. Our results suggest that the stroma is a crucial target of the carcinogen and that mutation in the Ha-ras-1 gene is neither necessary nor sufficient for tumor initiation.
A comprehensive understanding of carcinogenesis in general, and in the rat mammary gland in particular, has been delayed because of epistemological issues. It has been obvious to many of us working in the field of carcinogenesis that we lack a consistently reliable set of premises on which we can base a solid rationale to conduct research (Sonnenschein and Soto, 1999a; Sonnenschein and Soto, 2000; Moss, 2003). For almost a century, a majority of researchers have followed the lead provided by Theodor Boveri in 1914, favoring the notion that carcinogenesis occurs at the cellular level of biological organization (Boveri, 1929). After a number of course corrections to accommodate lacks of fit, Boveri's ideas have coalesced into what is now generally accepted as the Somatic Mutation Theory of carcinogenesis (Hanahan and Weinberg, 2000; Mastorides and Maronpot, 2002). Throughout the twentieth century, this theory has been challenged by others, who proposed instead that carcinogenesis takes place at the tissue level of biological organization (Orr, 1958; Smithers, 1962; Hodges et al., 1977; Sonnenschein and Soto, 2000). In the past decade, attempts to find a synthetic position that would incorporate claims from both theoretical approaches have also been advanced (Folkman et al., 2000; Bissell and Radisky, 2001; Thiery, 2002). Objectively, however, the identification of the target(s) upon which the carcinogenic agents act in order to initiate neoplastic transformation has, so far, remained elusive.
The development of mammary cancer in susceptible rodent strains following administration of N-nitrosomethylurea (NMU) is a widely accepted model for the study of chemical carcinogenesis (Gullino et al., 1975). The majority of NMU-induced rat mammary tumors are carcinomas or adenocarcinomas, that is tumors of presumed epithelial origin (Thompson, H. J. et al., 2000a). According to the Somatic Mutation Theory, a neoplastic outcome would result from accumulated NMU-induced mutations in one of the epithelial cells of this gland (Guzman et al., 1992; Gould, 1995). Although these carcinomas show an altered organization of both the epithelium and the stroma, when examined through a light microscope, changes observed in the stroma have been assumed to be a secondary effect of the primary mutational events in the epithelium.
An alternative theory considers that carcinogenesis is a process akin to development gone awry (Pierce et al., 1978; Sonnenschein and Soto, 1999a). The Tissue Organization Field Theory proposes that carcinogens alter stromal-epithelial interactions and that proliferation is the default state of all cells (Sonnenschein and Soto, 1999b; Sonnenschein and Soto, 2000). Carcinogenesis would therefore be an emergent phenomenon that takes place at the tissue level of biological organization. As mentioned above, several authors have proposed synthetic approaches that straddle both theories as applied to mammary carcinogenesis (Bissell and Radisky, 2001; Wiseman and Werb, 2002; Thiery, 2002).
In an effort to deal comprehensively and simultaneously with all the competing theories, we decided to use a rat mammary tissue recombination model. This model affords an easy surgical separation of stroma and epithelium such that each compartment might be exclusively exposed to the carcinogen. We chose NMU because it is a direct carcinogen in that it does not need to be metabolized in order to form DNA adducts and has a very short half-life (Swann, 1968). This minimizes the risk of inadvertent indirect exposure of epithelial cells to the carcinogen when recombining them with the stroma. The outcome of the proposed experimental design would determine whether the primary target of NMU is the epithelium (as suggested by the Somatic Mutation Theory), the stroma (as implied by the Tissue Organization Field Theory), or both tissue compartments.
Materials and Methods
Chemicals and cell culture reagents
NMU (CAS #684-93-5), insulin, penicillin, progesterone, prolactin, fatty acid-free fraction V bovine serum albumin (BSA), hydrocortisone, human transferrin, ascorbic acid, gentamicin, aluminum potassium sulfate and methyl salicylate were purchased from Sigma-Aldrich. Human epidermal growth factor (EGF) and Matrigel™ were obtained from Becton Dickinson. Phenol red-free DMEM/F12 medium and trypsin were obtained from Gibco. Collagenase was purchased from Worthington Biochemical Corporation and pronase from Calbiochem. Percoll™ was obtained from Amersham Pharmacia Biotech and Carmine from Fisher Scientific.
Wistar-Furth rats were purchased from Harlan and housed with food and water ad libitum. Animals were maintained on a 14:10 hours light:dark cycle and care was in accordance with the Guidelines for the Care and Use of Animals and the Tufts-New England Medical Center Institutional Animal Care and Use Committee. When the animals were 21 days old, the mammary epithelium was surgically removed from the 4th and 5th inguinal mammary glands according to procedures outlined previously (DeOme et al., 1959). In each of the animals used in these experiments, the excised epithelium was whole-mounted and observed microscopically to assure that the ductal tree was removed in its entirety and that only a small portion of the fat pad remained attached to it (Fig. 1A).
Tissue recombination experimental design
The animals with cleared fat pads were distributed into experimental Groups 1-4. At 52 days of age, animals from Groups 1 and 2 received a single intraperitoneal dose of 50 mg NMU/kg body weight dissolved in warm 0.85 g/l NaCl solution (vehicle), pH 5.0; by contrast, Groups 3 and 4 were exposed to just the vehicle. Five days later, 50,000 mammary epithelial cells were injected into the cleared fat pads according to the following experimental design: animals from Groups 1 and 4 received vehicle-treated mammary epithelial cells, and animals from Groups 2 and 3 received NMU-treated mammary epithelial cells. Positive and negative control groups were used. These control groups were intact virgin animals that were age-matched to the animals in Groups 1 to 4. They were not subjected to any surgical manipulation. These animals were treated at 52 days of age with NMU and vehicle, respectively. They were injected at the same time with the animals used in Groups 1 to 4. Intact animals injected with NMU were considered as the positive control for tumor incidence and histopathology of the tumors (Group 5). Animals injected with vehicle were considered as the control for spontaneous tumors and for the normal architecture of the mammary gland (Group 6). Four experiments were performed where all the experimental groups were represented. Animals were excluded from the analyses when no epithelial outgrowths were found in the whole mounts (`no takes') or if they died as a result of surgical complications. The initial (i) and final (f) sample sizes at 9 months after the NMU injection were as follows: Group 1, i=14, f=13; Group 2, i=10, f=8; Group 3, i=12, f=10; Group 4, i=11, f=6.
Cleared fat pad repopulation
A second set of animals with cleared fat pads was transplanted with 50,000 mammary epithelial cells at 52 days of age. The recombinants were inspected 30, 60 and 90 days later.
Mammary epithelial cell culture
Mammary epithelial cells were isolated from 50-60-day-old virgin female Wistar-Furth rats using a combination of two previously described protocols (Hahm and Ip, 1990; Imagawa et al., 2000). Briefly, the 4th and 5th inguinal mammary glands were bilaterally excised, minced and digested in phenol red-free DMEM containing 0.15% collagenase III at 37°C for 2 hours with agitation. This digest was centrifuged and the pellet was then treated with 0.05% pronase for 30 minutes at 37°C with agitation. This suspension was filtered through a 530 μm-pore Nitex® filter (Sefar America) and the filtrate was centrifuged at 100 g for 3 minutes (Hahm and Ip, 1990). The pellet was resuspended in 1-2 ml of serum-free medium (SFM) containing phenol red-free DMEM/F12 plus 10 μg/ml insulin, 1 μg/ml progesterone, 10 ng/ml EGF, 1 μg/ml prolactin, 1 mg/ml BSA, 1 μg/ml hydrocortisone, 5 μg/ml human transferrin, 0.88 μg/ml ascorbic acid and 50 μg/ml gentamicin (Hahm and Ip, 1990). This cell suspension was layered over a pre-made Percoll™ gradient (Imagawa et al., 2000) and centrifuged for 20 minutes at 800 g. Single epithelial cells and organoids were recovered from the gradient, diluted in SFM and similarly centrifuged. The pellet was resuspended in SFM and plated on Matrigel™-coated (100 μg/cm2) 6-well plates (Becton Dickinson). This layer was enough to promote cell attachment but insufficient to facilitate three-dimensional growth. Non-epithelial cells were successfully removed by treating the plates with a 0.025% trypsin and 0.01% EDTA solution. Five days before being transplanted into recipient animals, the mammary epithelial cells were treated with SFM containing either vehicle or 50 μg/ml NMU for 1 hour at 37°C (Miyamoto et al., 1988). The cells were then rinsed twice with SFM and fresh SFM was added. NMU was used within 5 minutes of preparation. A different batch of mammary epithelial cells prepared following this protocol was used for each of the four experiments. The dose of NMU used in the in vitro experiments was selected following Miyamoto et al. (Miyamoto et al., 1988).
Epithelial cell transplantation
After harvesting by trypsinization, the cells were counted in a Coulter Counter Apparatus (Model ZM, Coulter Electronics). The volume of the cell suspension was adjusted in order to inject 50,000 cells in 10 μl into the CFP using a Hamilton syringe. All rats receiving a cell transplant were palpated weekly, starting one month after the mammary epithelial cell inoculation. Thoracic glands were used as internal controls for the carcinogen and were equally palpated. Animals were sacrificed when inguinal tumors reached 1 cm in diameter or 9 months after cell transplant, whichever came first.
DNA extraction and analysis of Ha-ras-1 gene mutation
DNA was extracted from mammary neoplastic lesions, fat pads and whole mammary glands from virgin rats using the DNeasy kit (Quiagen), following the manufacturer's instructions. We used the mismatch amplification mutation assay (MAMA) described by Cha et al. (Cha et al., 1996) with some modifications. The MAMA is specific for the codon 12 GGA to GAA mutation in Ha-ras-1 gene. Briefly, this method uses two sets of primers; one targets the mutation and the other a control area in the genomic DNA. The mutant-specific mismatch primer PAA (5′-CTTGTGGTGGTGGGCGCTGAA-3′), the Pmnl2 (5′-ACTCGTCCACAAAATGGTTC-3′) and the control primers (P1: 5′-CCTGGTTTGGCAACCCCTGT-3′; and Pmnl2: 5′-ACTCGTCCACAAAATGGTTC-3′) were used at a 40 ng/μl concentration. The PCR was performed using Platinum Supermix (Invitrogen). The PCR products were run in a 2% agarose gel (Gibco). The expected size of the non-mutated Ha-ras-1 gene is 128 bp, whereas the mutated Ha-ras-1 gene is 74 bp.
Whole mounts and histology
Whole mounts were prepared following protocols described by the Laboratory of Genetics and Physiology at the National Institute of Diabetes, Digestive and Kidney Diseases within the National Institutes of Health (http://mammary.nih.gov), and Thompson et al. (Thompson et al., 1995). The mammary glands were removed and spread on a 75×50×1 mm glass slide (Fisher Scientific), fixed overnight in 10% phosphate-buffered formalin, dehydrated in 70%, 95% and 100% alcohols, cleared in toluene, rehydrated and stained with Carmine Alum. After staining, the whole mounts were dehydrated as described above, cleared in xylene, and bagged in Kpak® SealPak heat-seal pouches in methyl salicylate. The whole mounts were analyzed under a stereomicroscope for microscopic lesions. Tumors larger than 0.5 cm were removed before whole mounts were prepared and separately fixed as described above. Microscopic lesions were removed and embedded in paraffin for histological analysis. Images were captured with an AxioCam HR color digital camera (Carl Zeiss) attached to a Stemi 2000 stereomicroscope (Carl Zeiss).
An antigen-retrieval method based on microwave pretreatment and 0.01 M sodium citrate buffer (pH 6) was used as previously described (Maffini et al., 2001). Mouse monoclonal anti-pan cytokeratin (Sigma-Aldrich), anti-vimentin (Novocastra) and anti-desmin (Novocastra) were used at 1:700, 1:100 and 1:100 dilutions, respectively. The antigen-antibody reaction was visualized using the streptavidin-peroxidase complex, with diaminobenzidine tetrahydrochloride (Sigma-Aldrich) as the chromogen. Counterstaining was performed with Harris' hematoxylin. For the double-staining immunofluorescence technique, cytokeratin and vimentin were detected using a previously described technique (Maffini et al., 2002). The primary antibodies were used at 1:100 dilutions in 4% BSA supplemented with 10% normal goat serum. Secondary antibodies and streptavidin-Alexa 594 and 488 (Molecular Probes) were used at 1:100 dilutions. Cell nuclei were counterstained with Hoechst 33258. Images were captured with an AxioCam HR color digital camera (Carl Zeiss) attached to an Axioskop 2 plus microscope (Carl Zeiss).
Statistical significance of the incidence of neoplastic lesions and Ha-ras-1 gene mutation were determined using the χ2 Test. The Mann-Whitney and Kruskal-Wallis tests were used to compare the latency periods and the number of lesions in inguinal and thoracic mammary glands between groups. To compare the latency of pectoral and inguinal lesions in the same animal within each treatment group, we used the Wilcoxon signed ranks test, and treated the pectoral and inguinal latency for each animal as a pair.
Normal ducts developed from cultured mammary epithelial cells
The tissue recombination components were mammary gland stroma (cleared fat pad) and mammary epithelial cells grown in vitro (Fig. 2A). We observed the phenotype of the ductal outgrowth and the repopulation dynamics in the cleared fat pads after transplantation of 50,000 mammary epithelial cells. The ductal outgrowths were phenotypically normal and, 90 days after mammary epithelial cell transplantation, the ductal tree covered a third of the fat pad (Fig. 2B-E).
Neoplastic transformation of mammary epithelial cells
We observed that only those animals whose stroma was exposed to NMU developed neoplasms, regardless of whether or not the transplanted mammary epithelial cells were exposed to the carcinogen (Fig. 3A). The incidence of neoplastic lesions in Groups 1 and 2 was 76.9% (10/13) and 75% (6/8), respectively (Fig. 3B). The positive control Group 5 had 100% incidence (6/6). There were no significant differences in neoplastic incidence between Groups 1 and 2 (P=0.920) or between Groups 1 or 2 and Group 5 (P=0.200 and P=0.186, respectively). By contrast, the animals whose stroma was exposed to vehicle developed no neoplasms, regardless of whether the mammary epithelial cells were exposed in vitro to NMU (Group 3, 0/10) or to vehicle (Group 4, 0/6). The negative control Group 6 had 0% incidence (0/6). Group 3 was significantly different from Group 1 (P<0.001) and Group 2 (P=0.001). Group 4 was also significantly different from Group 1 (P=0.002) and Group 2 (P=0.005).
Multiple neoplastic lesions were found
Multiple lesions were observed in the inguinal mammary glands of rats in Groups 1, 2 and 5 (Fig. 4A), suggesting that the neoplasms found in these groups were not a consequence of mechanical injury resulting from the injection procedure. The inguinal glands of Group 5 had twice as many lesions as those in Groups 1 and 2 (P=0.013 and P=0.001, respectively) (Fig. 4A). This difference might have been owing to the fact that the intact mammary glands in Group 5 had a full complement of epithelium whereas Groups 1 and 2 had an initial population of only 50,000 mammary epithelial cells. The incidence of neoplastic lesions in the thoracic mammary glands of NMU-treated rats from Groups 1, 2 and 5 was comparable (P=0.622) (Fig. 4A). There was no significant difference among Groups 1, 2 and 5 regarding inguinal tumor latency periods (P=0.147). The latency period was similar in the thoracic and inguinal mammary glands within the same experimental groups (Group 1: P=0.276; Group 2: P=0.414; Group 5: P=0.684) (Fig. 4B).
We performed the histopathological analyses of the neoplastic lesions following the classification described by Russo et al. (Russo et al., 1990). Carcinomas were seen in 53.8% of the animals from Group 1, 25% of Group 2 and 66.7% of Group 5 (Fig. 3B), and represented 70%, 33% and 66.7% of the neoplasms found in these groups, respectively (Table 1). The most frequent type of neoplastic lesion was papillary carcinoma (Fig. 5B, Table 1). All the tumors were of epithelial origin; the neoplastic cells were cytokeratin positive, and vimentin and desmin negative (Fig. 5C). Regardless of whether or not the mammary epithelial cells had been exposed to NMU, the tissue-recombined mammary glands of animals that did not develop tumors appeared histologically similar to a normal mammary gland (Fig. 5A).
Mutated Ha-ras-1 does not correlate with neoplasia
We analyzed the DNA of neoplastic lesions from Groups 1 and 2 and observed that 2 out of 11 neoplasms from Group 1, and 1 out of 6 from Group 2, lacked the G-A mutation in the codon 12 of the Ha-ras-1 gene. Similarly, DNA taken from the neoplastic lesions in the positive control (Group 5) showed that 1 out of 7 lacked the point mutation (Fig. 6). No statistically significant difference was found between the groups (P=0.977). In order to test whether any correlation existed between the presence of the mutated Ha-ras-1 gene and the initiation of neoplasia, we analyzed DNA extracted from the stroma of animals treated with vehicle (i.e. Groups 3 and 4). All stroma samples from Groups 3 (7 out of 7) and 4 (6 out of 6) showed the mutation. Thus, we now report that this Ha-ras-1 gene mutation was present in the mammary gland fat pad of rats exposed to vehicle. Moreover, DNA harvested from whole mammary glands of intact rats randomly taken from our colony (4 out of 4) also showed the mutation, which agrees with previous findings (Cha et al., 1996). The incidence of mutated Ha-ras-1 gene was not significantly different between animals that were or were not exposed to NMU (P=0.604). Finally, the mutation was also assessed in DNA isolated from mammary epithelial cells, mammary fibroblasts, and mammary pre-adipocytes collected from intact virgin rats and grown in vitro. All these different types of cells were collected at different times during the course of 2 years. DNA was extracted from frozen cells, vehicle-treated cells and NMU-treated cells. The presence of the mutation did not correlate with cell type, culture conditions or carcinogen treatment (data not shown).
Our results regarding the role of histoarchitecture in carcinogenesis are consistent with previous findings stemming from the use of diverse rodent models. Barcellos-Hoff and Ravani showed that radiation-induced changes in the stromal microenvironment contributed to the neoplastic progression of non-irradiated, quasi-normal, established COMMA-1 mammary epithelial cells (Barcellos-Hoff and Ravani, 2000). Sternlicht et al. observed that overexpression of the matrix metalloproteinase stromelysin-1 can induce carcinogenesis in mouse mammary glands (Sternlicht et al., 1999). Also, using tissue recombinant techniques, Olumi et al. concluded that `primary, phenotypically normal fibroblasts associated with a human epithelial malignancy can stimulate progression of a nontumorigenic (prostate) epithelial cell' (Olumi et al., 1999). Thompson et al. have also used a tissue recombination model, the mouse prostate reconstitution model system, and observed that `intrinsic properties of the BALB/c mesenchyme can arrest the progression of ras+myc-initiated C57BL/6 epithelium from benign hyperplasia to malignant carcinoma' (Thompson et al., 1993).
Our experiments, designed to explore simultaneously the competing theories mentioned in the introduction, suggest that the stroma is a target of NMU in mammary carcinogenesis. We were concerned, of course, that inadvertent technical mishaps might have influenced our data. For instance, epithelial cells might have remained in the fat pads after the clearing procedure and could have been exposed in vivo to NMU. We addressed this possibility by microscopically examining the tissue containing the ductal tree after clearing the fat pads at 21 days of age and verifying that the margins contained no epithelial cells (Fig. 1A). In addition, we also cleared the 5th mammary gland to prevent the migration of indigenous epithelial cells into the 4th cleared fat pad. Therefore, we consider it unlikely that epithelial cells were present after clearing. It was also reassuring to observe that cleared fat pads not injected with mammary epithelial cells remained free of epithelium at the end of the experiment (Fig. 1B).
Several research groups have used experimental rodent models to explore the concept that epithelial cells are the targets of carcinogens, as implied by the Somatic Mutation Theory. Miyamoto et al. reported tumor formation after mammary epithelial cells were exposed to NMU in vitro and injected into cleared fat pads (Miyamoto et al., 1988). These authors used a cell inoculum one order of magnitude higher than the one we used and a different cell purification method. Also, they added the NMU when the cultures were 3 days old and made no reference to the degree of fibroblast contamination. It is conceivable that, in their experiments, fibroblasts exposed to NMU in vitro could have played a role in the carcinogenic process. On the contrary, we repeatedly trypsinized and subcultured the mammary epithelial cells to enrich this pool of cells and reduce fibroblast contamination. In essence, we exposed a highly enriched mammary epithelial cell population to NMU (Fig. 2A). Furthermore, Miyamoto et al. injected the mammary epithelial cells into fat pads immediately after clearing, while in the midst of wound healing (Miyamoto et al., 1988). In this context, it has been shown that carcinogenesis is promoted by a wounded stroma (Konstantinidis et al., 1982; Sieweke et al., 1990). Their data and those by Guzman et al. do not suggest a positive correlation between tumor yield and either NMU concentration or the number of exposures to this carcinogen in vitro. Moreover, normal epithelial outgrowths were observed at all NMU doses (Guzman et al., 1987; Miyamoto et al., 1988). Using yet another protocol, Kamiya et al. showed that NMU- or radiation-exposed mammary epithelial cells yielded mammary carcinomas when grafted into rat fat pads that were `cleared' by injecting 70% ethanol (Kamiya et al., 1995). They interpreted these data as evidence that tumor formation was due to undefined epigenetic factors rather than to mutations. They also observed that tumor incidence diminished as the number of cells injected increased, an outcome inconsistent with the Somatic Mutation Theory.
These experiments dealing with in vitro exposure to NMU were based on the premise that NMU acted directly on the epithelial cells and, therefore, under this rationale, no attempt was made to evaluate the role of the stroma in tumor formation (Greiner et al., 1983; Guzman et al., 1987; Miyamoto et al., 1988; Delp et al., 1990). The novelty of our observations stems from the fact that a carcinogen-treated stroma was able to transform vehicle-treated cells into neoplastic tissues comparable with those seen in intact NMU-exposed rats (positive control Group 5) (Fig. 5 and Table 1).
The prevalent hypothesis that NMU exposure results in carcinogenesis because of NMU-induced point mutations in the codon 12 of the Ha-ras-1 gene of mammary epithelial cells (Zarbl et al., 1985) has been challenged. As shown in our results and in the literature (Cha et al., 1994; Cha et al., 1996; Swanson et al., 1996; Shirai et al., 1997; Thompson, T. A. et al., 2000b), not all NMU-induced mammary neoplasms express this mutation. Also, Korkola and Archer have observed comparable results in NMU-induced pre-neoplastic lesions (Korkola and Archer, 1999). Equally important, this mutation is present in mammary glands from non-exposed animals (Cha et al., 1996). Here, we confirm these findings and show that the frequency of tumors expressing mutated Ha-ras-1 is statistically similar in the positive controls (Group 5) and recombinants from NMU-exposed stroma (Groups 1 and 2). Moreover, we also observed that mutated Ha-ras-1 is also present in the cleared mammary fat pad of vehicle-exposed animals. Furthermore, Zhang et al. demonstrated that increasing the dose of NMU increased total tumor yield but reduced the frequency of mammary tumors expressing mutated Ha-ras-1 (Zhang et al., 1990). In sum, these data suggest that the Ha-ras-1 gene mutation appears to be neither necessary nor sufficient for neoplastic transformation and that it is not exclusively present in the epithelial cells.
The concept that altered tissue architecture is at the core of carcinogenesis was pioneered by Waddington (Waddington, 1935), Orr (Orr, 1958) and, more recently, by Bissell and Radisky (Bissell and Radisky, 2001) and others (Sonnenschein and Soto, 2000; Moss, 2003, Weaver and Gilbert, 2004). Altogether, our data and those of others challenge the long-held notion that carcinogens induce mammary cancer by causing mutations in the DNA of an epithelial cell (Fearon and Vogelstein, 1990; Mastorides and Maronpot, 2002). These results suggest the need to explore the roles that the stroma components [i.e. the cells (fibroblasts, adipocytes, mast cells, etc.)] and the extracellular matrix play in rodent mammary carcinogenesis. Efforts should also be directed at exploring the role of the stroma in experimental models for carcinogenesis involving organs other than the mammary gland (i.e. skin, prostate, liver, bladder). To accommodate a novel perspective on the role of the stroma in carcinogenesis, a rigorous analysis of concepts, definitions and experimental approaches is now needed. This will facilitate the identification of the mediators responsible for the altered tissue phenotype in cancers and of ways to reverse their effect by adopting a solid epigenetic perspective.
A report on these findings was made at the 12th International Conference of the International Society of Differentiation, 14-17 September 2002, at Lyon, France. This research was supported primarily by the Bradshaw Foundation (Geneva, Switzerland), by the USA Department of Defense grant 17-01-1-0654 and by the Massachusetts Department of Public Health. Dr Will Rand's statistical advice is appreciated, as is the technical help of Dr Peter Geck, Jenny Lenkowski, Cheryl Michaelson and Carise Wieloch. The authors also thank Drs D. Radinsky, P. Kenny, T. Shioda and J. Russo for their critical reading of the manuscript.
- Accepted November 20, 2003.
- © The Company of Biologists Limited 2004