Background
Pancreatic cancer is one of the leading causes of cancer death in many countries, including the United States. Pancreatic ductal adenocarcinoma (PDAC) constitutes approximately 90% of all primary malignant tumors arising from the pancreatic gland. Of all gastrointestinal malignancies, pancreatic adenocarcinoma is the second most common cause of death from cancer [
1‐
3]. Pancreatic cancer is an aggressive malignant cancer with a high metastatic rate and is an almost uniformly lethal disease in humans [
3‐
5]. Of affected patients, 60% have liver metastasis, malignant ascites, or other evidence of tumor spread at the time of diagnosis [
6]. The 5-year survival rate in the United States is less than 5% [
3].
The renin-angiotensin system is one of the phylogenetic hormone systems and plays a key role in the regulation of cardiovascular homeostasis, which maintains arterial blood pressure and fluid and electrolyte homeostasis [
7,
8]. Angiotensin II (Ang II), an octapeptide hormone, is the key effector in the renin-angiotensin system. Ang II has two well-defined receptors: Ang II type 1 (AT
1) and type 2 (AT
2) receptor [
9]. The AT
1 receptor is widely expressed in a variety of adult tissues. AT
1 receptor-mediated signaling is responsible for most Ang II-dependent actions in cardiovascular and renal tissues. Responses of the AT
1 receptor are typically associated with stimulation of growth factor receptors leading to cell growth, proliferation, cell migration, apoptosis, and gene expression [
10,
11]. These effects are executed through a heterotrimeric G protein-coupled receptor, which mediates Ang II transactivated epidermal growth factor (EGF)-induced activation of MEK (MAPK kinase 1) and ERK [
12]. The AT
2 receptor, the second major isoform of the Ang II receptor, is primarily expressed in the mesenchyme of the fetus and to a limited extent in adult tissues [
13]. It is, however, inducible and functional under pathophysiologic conditions [
14‐
17]. The AT
2 receptor mediates signals that counteract the AT
1 receptor-mediated biological actions [
18‐
20]. In addition, the AT
2 receptor is known to inhibit cell proliferation and stimulate apoptosis in cardiovascular and neuronal tissues
in vitro [
21]. However, the relationship between the AT
2 receptor and cancer has yet to be clarified. Our previous studies revealed that chemical carcinogen-induced tumorigenesis in mouse colon [
22] and lung [
15] was significantly attenuated by AT
2 receptor deficiency. Since AT
2 receptor expression has been noted in various stromal fibroblasts [
23,
24] and is inducible in the pancreas in pathological conditions [
25], AT
2 receptor deficiency may also influence pancreatic cancer growth. In addition, Ang II receptor antagonists and angiotensin I-converting enzyme inhibitors currently used for human clinical hypertension treatment attenuate growth of human cancer cells in experimental animals [
26‐
30] and may reduce the risk of several human cancers[
31]. This suggests that AT
2 receptor expression potentially plays an important role in cancer.
In the present study, we subcutaneously inoculated pancreatic ductal carcinoma cells in syngeneic AT2-KO and wild type mice and examined tumor growth, cell proliferation, and apoptosis. In addition to the in vivo study, we also studied the effect of stromal fibroblasts, which were prepared from either AT2-KO or control wild type mice, on PAN02 cancer cell growth in vitro. These studies revealed that Ang II AT2 receptor signaling in stromal cells plays an important regulatory role in the growth of pancreatic carcinoma cells.
Methods
Materials
Ang II was purchased from Peninsula Laboratories Inc. (San Carlos, CA). The AT1 receptor blocker Losartan was a gift from Dr. Tadashi Inagami (Vanderbilt University Medical Center); the AT2 receptor blocker PD123319 was purchased from Sigma Chemical Co. (St. Louis, MO). Rabbit anti-human von Willebrand factor (vWF) and rat anti-mouse Ki-67 antibodies were purchased from DakoCytomation (Glostrup, Denmark). Rabbit anti-human vascular endothelial cell growth factor (VEGF) and rabbit anti-human GAPDH antibodies were from Santa Cruz Biotechnology, Inc. (Santa Cruz, CA). A biotin-conjugated secondary antibody was purchased from Jackson ImmunoResearch (West Grove, PA). Avidin-biotin peroxidase complex (ABC) reagents was from Vector Laboratories (Burlingame, CA). ApopTag® Plus Peroxidase In Situ Apoptosis Detection Kit was from Chemicon International, Inc. (Tokyo, Japan). Bio-αRat biotin-conjugated secondary antibody was from Jackson ImmunoResearch, (West Grove, PA). A horseradish peroxidase-conjugated anti-rabbit IgG secondary antibody was from Amersham Biosciences (Piscataway, NJ). All other chemicals were of analytical grade.
Cell culture
The PAN02 murine pancreatic adenocarcinoma cell line was obtained from the National Cancer Institute and maintained in RPMI-1640 medium supplemented with 10% fetal bovine serum (FBS), 2 mM L-glutamine, 100 U/ml penicillin, and 100 μg/ml streptomycin.
Primary cultured mouse skin fibroblasts (MSFs) from wild type and AT
2-KO mice were prepared from 24 to 48 hour old C57BL/6J mouse pups following an established method [
14]. MSFs were cultured in DMEM/Ham's F-12 medium (1:1) supplemented with 10% FBS, 100 U/ml penicillin, and 100 μg/ml streptomycin. All cells were incubated in 5% CO
2 humidified air at 37°C.
Animals and genotyping
Hemizygous AT
2-KO mutant (Agtr2-/y) mice were generated as described previously [
15]. These mice were backcrossed with wild type C57BL/6J (The Jackson Laboratory, Bar Harbor, MA) for 17 generations such that the genetic background of the mice is susceptible to our pancreatic cancer syngeneic model. Wild type littermates served as controls. Genotypes were confirmed by the PCR method using extracted tail DNA. Briefly, published sequences [
19,
32] were used to synthesize primers for the AT
2 receptor (forward 5'-CACCAGCAGAAACATTAC-3' and reverse 5'-AACACAGCTGTTGAATCC-3') and the neomycin resistance (Neo-r) gene product (forward 5'-AGCCAACGCTATGTCCTGAT-3' and reverse 5'-AGACAATCGGCTGCTCTGAT-3'). Extracted tail DNA (10-20 ng) was amplified (35 cycles) at 95°C for 1 minute (denaturation), at 58°C for 1 minute (annealing), and at 72°C for 1 minute (elongation) with 0.5 nmol/L of each primer, 1.25 units DNA polymerase, and 0.2 mmol/L deoxynucleotide triphosphates in PCR buffer. PCR products of the AT
2 receptor (478 bp) and Neo-r gene product (593 bp) were visualized by 1% agarose gel electrophoresis. AT
2 (+) and Neo-r (-), AT
2 (+) and Neo-r (+), and AT
2 (-) and Neo-r (+) were assigned as wild type, heterozygote, and AT
2-KO, respectively. All animals were maintained in a humidity- and temperature-controlled room on 12-hour light/dark cycles. All procedures for handling animals were approved by the Institutional Committee for Animal Care and Use of Kansas State University.
Pancreatic cancer syngeneic model
Seven to nine week-old AT
2-KO/C57BL/6J mice and wild-type littermates were anesthetized with isoflurane. Cells were trypsinized and washed with PBS. Five million cells in 200 μl PBS were subcutaneously inoculated into each flank using a 1 ml syringe with a 27G needle [
16]. The tumor size was measured by caliper every three days and the volume was calculated using the formula (short diameter)
2 × (long diameter) × 0.5 [
17].
At the end of the experiments, the mice were sacrificed by cervical dislocation under anesthesia. The tumors were dissected and weighed. For histological assessment, the specimens were fixed in 10% formalin, embedded in paraffin, and sectioned for histopathological analysis.
Immunohistochemical analysis
Tissue sections of 4 μm thickness were prepared for all staining. Slides were dewaxed and rehydrated before staining. The heat-induced antigen unmasking was performed in Citra Plus Solution, pH 6.0 (BioGenex, San Ramon, CA) for 5-10 minutes using an autoclave oven. Sections were then incubated with 0.3% hydrogen peroxide in methanol for 20 minutes to block endogenous peroxide activity. The dilution of antibodies for Ki-67, von Willebrand factor (vWF) and VEGF was 1:50, 1:100, and 1:50, respectively. Sections were incubated with the primary antibodies for 60 minutes at room temperature. In immunostaining for Ki-67, sections were incubated with biotin-conjugated secondary antibody (Jackson ImmunoResearch, West Grove, PA) followed by reaction with the avidin-biotin peroxidase complex (ABC) reagent (Vector Laboratories, Burlingame, CA) for 30 minutes at room temperature. In immunostaining for vWF, an ABC kit (Vector Laboratories) was used. Peroxidase activity was visualized with 3,3'-diaminobenzodine tetrahydrochloride (Sigma Chemical Co). Sections were lightly counterstained with Hematoxylin solution (Merck KGaA, Darmstadt, Germany).
TUNEL assay
To determine cell death, apoptotic cells in paraffin sections were detected by TUNEL (Terminal Deoxynucleotidyltransferase-Mediated dUTP Nick End Labeling) assay using the Apop Taq Plus Peroxidase In Situ Apoptosis Detection Kit (Millipore Corporation, Billerica, MA) according to the manufacturer's instructions. Sections were counterstained with Methyl green solution (Nacalai Tesque, Inc., Kyoto, Japan).
Image analysis
Ki-67 or TUNEL positive cell numbers and whole cell numbers (as background) in five randomly selected fields were counted by two independent observers. The VEGF positive cell area in five randomly selected fields was evaluated using NIH digital-image analyzing software, Image J 1.37v, (NIH, Bethesda, MD).
Evaluation of the effect of angiotensin II and fibroblasts on the growth of PAN02 cells
Primary cultured MSFs (100 cells/well, 96-well plate) from wild type or AT2-KO mice were incubated in serum-free medium in 5% CO2 humidified air at 37°C. Following 24 hours incubation, PAN02 cells (400 cells/well) were added to the culture plate and co-cultured with the wild-type or AT2-KO MSFs in DMEM/Ham's F12 medium (1:1) containing 10% FBS. One day after co-culture, the cells were treated with Ang II (10 nM) for 48 hours in the presence of the AT2 receptor-specific antagonist PD123319 (10 μM). The degree of cell proliferation was evaluated by MTT assay. In brief, 10 μl MTT solution (5 mg/ml) was added to each well 4 hours prior the end of the incubation. Formazan crystals formed in the cells were dissolved by adding 100 μl of MTT solvent (0.01 N HCl in 10% SDS). The absorbance was measured at 550 nm by spectrometer 24 hours after incubation at 37°C with the MTT solvent.
Evaluation of the effect of AT2receptor over-expression in fibroblasts on co-cultured PAN02 cell growth
MSFs from wild type or AT2-KO mice were seeded in T25 flasks. After cell attachment, the medium was changed to serum-free DMEM. After three hours in the serum-free medium, the medium was changed to 875 μl DMEM containing 5% FBS and either adenoviral AT2 receptor (Ad-AT2, 25 MOI) or adenoviral Lac Z (Ad-Lac Z, 25 MOI). The cells were incubated in 5% CO2 at 37°C; the flasks were rocked every 15 minutes for 3 hours. After incubation with the vectors, DMEM/Ham's F12 (1:1) containing 10% FBS was added and the cells were further incubated for an additional 24 hours at 37°C in 5% CO2. Both untransfected and transfected MSFs were co-cultured with PAN02 cells (400 cells/well) as described above. The extent of cell proliferation was evaluated by MTT assay.
Gene expression analysis using real-time PCR
Total RNA was extracted from cells using TRIzol reagent (Invitrogen). Genomic and complementary DNA was removed using RQ1 RNase-free DNase (Promega, Madison, WI) according to the manufacturer's instructions. Real-time PCR was carried out using an iScript One-Step RT-PCR Kit with SYBR Green (Bio-Rad, Hercules, CA), and the reactions were conducted on the real-time PCR detection system iCycler (Bio-Rad). The results were quantified as Ct values, where Ct is defined as the threshold cycle of PCR at which the amplified product is first detected and signifies relative gene expression (the ratio of target/control). The AT2 primers were 5'-AGC CAA GGC CAG ATT GAA GA-3' (forward) and 5'-GCC ACC AGC AGA AAC ATT ACC-3' (reverse), the AT1 primers were 5'-GGC AGC ATC GGA CTA AAT GG-3' (forward) and 5'-CCA GCT CCT GAC TTG TCC TTG-3' (reverse), and the 18S ribosome RNA primers were 5'-TCG CTC CAC CAA CTA AGA AC-3' (forward) and 5'-GAG GTT CGA AGA CGA TCA GA-3' (reverse).
Western blot analysis
Total cellular protein was prepared according to our routinely used protocol [
33]. The membrane was incubated with the antibody against VEGF at a 1:250 dilution in TBST with 0.1% nonfat dry milk for 1 hr at room temperature. Then, the membrane was incubated with a horseradish peroxidase-conjugated anti-rabbit IgG secondary antibody at a 1:2000 dilution in TBST with 0.1% nonfat dry milk for 1 hr at room temperature. The protein expression signal was detected with Pierce SuperSignal Western Blotting substrate. GAPDH was used as the loading control of sample by reprobing with an anti-GAPDH antibody at a 1:12000 dilution.
Statistical analysis
Results are expressed as mean ± standard error of the mean (SEM). For statistical analysis, a Microsoft Excel Data Analysis tool, t-test, was used. The critical value was 95%, and significance was defined as p < 0.05.
Discussion
Increasing evidence suggests that Ang II signaling plays an important role in carcinogenesis [
15,
19,
22,
35‐
37]. While AT
1 receptor over-expression has been implicated in many types of cancers including pancreatic cáncer [
11,
12,
38,
39], the specific role of the AT
2 receptor in carcinogenesis has not been rigorously elucidated. We have previously demonstrated the pro-oncogenic role of the AT
2 receptor in carcinogen-induced colon and lung tumorigenesis in the mouse. In these models, the AT
2 receptor appears to enhance carcinogen metabolism and increase tumorigenesis. However, the effect of AT
2 receptor-mediated signaling on tumor growth is unknown. Since Ang II has been shown to stimulate tumor growth through the AT
1 receptor [
35,
39,
40], and since the AT
2 receptor antagonizes the AT
1 receptor [
41,
42], it is relevant to study the role of the AT
2 receptor in tumor growth. Therefore, in this study we sought to evaluate the role of AT
2 receptor expression in stroma in the growth of pancreatic ductal adenocarcinoma, the most common form of pancreatic cancer.
In the first study, we have examined the growth of PAN02 adenocarcinoma cells in AT
2-KO and wild type mice and found that the growth of PAN02 xenografts is significantly faster in AT
2-KO mice than in wild type mice (Figure
1). The degree of cell proliferation and the index of apoptosis were measured by anti-Ki-67 staining and TUNEL assay, respectively. It was found that anti-Ki-67 positive staining was significantly higher in AT
2-KO mouse tumors than in wild type mouse tumors (Figure
2). It was also observed that the index of apoptosis is slightly higher in the wild type mouse tumors than in AT
2-KO mouse tumors, although there was no statistical difference between the two groups (Figure
3). In addition, tumor vessel density was significantly higher in AT
2-KO mice than in wild type mice (Figure
4). At a glance, the
in vivo results show that growth of PAN02 cells was significantly faster in the AT
2-KO environment than in the wild type environment, most likely due to a high degree of cell proliferation. Higher tumor vessel density may also be associated with faster tumor growth in the AT
2-KO mice.
Following the
in vivo mouse study,
in vitro studies were carried out to determine the mechanism by which AT
2 receptor expression in stromal cells modifies the growth of pancreatic carcinoma cells. In the first
in vitro experiment, the effect of AT
2 receptor over-expression in either wild type or AT
2-KO MSFs was evaluated in co-culture with PAN02 cells. Results clearly indicate that AT
2 receptor over-expression significantly attenuates growth of co-cultured PAN02 cells. However, this attenuation was completely abolished by the addition of a low concentration of Ang II in the presence of the AT
2 receptor-specific blocker PD123319 (Figure
5). Since the contribution of MSFs to cell proliferation is approximately one third of the total cell proliferation (MSF + PAN02), since MSF cell proliferation was not influenced by the status of AT
2 receptor expression (Figure
5) nor by the presence of Ang II or the AT
2 antagonist (data not shown), and since PAN02 cells do not express Ang II receptors, the growth of PAN02 cells appears to be indirectly regulated by the MSFs. This experiment nicely recapitulates results obtained from the mouse study (Figure
1). Furthermore, VEGF expression in MSFs was shown to be suppressed by Ang II-AT
2 receptor signaling (Figure
6), implying that AT
2 receptor expression-dependent growth attenuation may be mediated by the attenuation of VEGF production in stromal fibroblasts. In support of this, the VEGF positive cell numbers were higher in AT
2-KO mouse tumors than in the wild type mouse tumors (Figure
4). Taken together, these results strongly suggest that AT
2 receptor signaling in stromal cells plays an important role in inhibition of tumor growth. As this research shows, tumor growth regulation is indirectly controlled through stromal cells. The significance of tumor stromal cells in tumor growth is widely accepted [
43] and further emphasized by another recent report [
44]. The mechanism by which tumor stromal fibroblasts regulate tumor growth has not been rigorously studied. However, Sugimoto
et al. suggest that hepatocyte growth factor produced in fibroblasts controls tumor growth[
45]. Since Ang II is known to be produced in fibroblasts and acts as a local cell growth regulator [
10,
15], it is reasonable to speculate that Ang II also plays a role as a local mediator for tumor growth. In support of this speculation, Fujimoto
et al. [
39] have reported AT
1 receptor over-expression in human pancreatic cancer tissues and AT
1 receptor-mediated growth regulation in pancreatic cancer cells. Furthermore, Anandanadesan has also reported that Ang II stimulates VEGF expression in a panel of human pancreatic cancer cell lines [
38]. The present study also indicates that tumor stromal fibroblasts appear to be a rich source of VEGF (Figure
4).
It is well known that the Ang II receptor has two major isoforms, and their signaling is associated with cell proliferation and apoptosis [
20]. The major isoform, the AT
1 receptor, is expressed in a wide variety of tissues, and its signaling functions in a variety of pathophysiological reactions, including constriction of blood vessels, induction of cell proliferation and expression of proto-oncogenes such as c-fos, c-myc and c-jun [
46]. The second major isoform, the AT
2 receptor, is abundantly expressed in fetal tissues, but its expression declines rapidly after birth [
14]. Multiple studies have shown that AT
2 receptor signaling counteracts the biological effects mediated by AT1 receptor signaling, including inhibition of cell proliferation [
41,
42,
47]. Therefore, the delicate balance between the activities of these two receptors plays an important role in the pathophysiology of various diseases[
20]. Accordingly, AT
2 receptor-deficiency-induced tumor growth stimulation may be mediated at least in part through Ang II-AT
1 receptor signaling in either stromal cells or cancer cells. Indeed, it has been well documented that Ang II, besides its conventional physiological actions, displays characteristics of a growth factor [
48]. The AT
2 receptor signaling-dependent cell growth attenuation reported here is in good agreement with earlier studies [
41,
49]. In these studies, growth of vascular endothelial cells and smooth muscle cells were shown to be attenuated by AT
2 receptor-mediated Ang II signaling. Although these studies did not clarify the potential second messenger that controls cell growth, the present study suggests that AT2 receptor-mediated attenuation of VEGF production is a potential mechanism for AT
2 receptor expression-dependent growth attenuation of pancreatic carcinoma.
Based on observations by other researchers[
20,
21,
48,
50,
51] and findings in the present study, it is clear that the AT
2 receptor plays an important role in tumor growth in rodents. To the best of our knowledge, this is the first report to describe the involvement of AT
2 receptor mediated signaling in controlling the growth of pancreatic adenocarcinoma at least in part by attenuating stromal fibroblast-dependent VEGF production. However, whether AT
2 receptor expression indeed plays an important role in human pancreatic cancer growth must be clarified by human clinical studies.
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
CD, NE and AK equally contributed to this study. CD, NE, AK, NO, DU, RA, LP, YI and MT were responsible for the study design, experimental work, data evaluation and analysis, and drafting the manuscript. DKM, DT, and ST were consulted extensively in the experimental design and interpretation of results, as well as in the preparation of the manuscript. MT was the research supervisor and participated in the study design, assessment of the results, and drafting the manuscript. All authors read and approved the manuscript.