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Departments of Medicine, Biological Chemistry, and Pharmacology, University of California, Irvine, California 92697
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ABSTRACT |
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 Top ABSTRACT INTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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Purpose and Experimental Design: To determine whether blocking TGF-ß actions would suppress pancreatic cancer cell growth in vivo, we expressed a soluble TßRII, encoding amino acids 1–159 of the extracellular domain in COLO-357 human pancreatic cancer cells. This cell line expresses all of the three mammalian TGF-ß isoforms and is growth inhibited by TGF-ß in vitro.
Results: COLO-357 clones expressing soluble TßRII were no longer growth inhibited by exogenous TGF-ß1 and exhibited a marked decrease in their invasive capacity in vitro. When injected s.c. into athymic mice, these clones exhibited attenuated growth rates and angiogenesis and decreased levels of plasminogen activator inhibitor-1 mRNA as compared with tumors formed by sham-transfected cells.
Conclusions: These results indicate that endogenous TGF-ßs can confer a growth advantage in vivo to a pancreatic cancer cell line that is growth inhibited in vitro and suggest that a soluble receptor approach can be used to block these tumorigenic effects of TGF-ßs.
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INTRODUCTION |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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Human pancreatic cancer is the fifth leading cause of cancer related mortality in the Western industrialized countries. The mortality rate virtually equals its incidence rate (2) . The reasons for this biological aggressiveness are unknown. However, it has been established that these cancers harbor p53 tumor suppressor gene and K-ras oncogene mutations and overexpress multiple mitogenic growth factors and their receptors (3 , 4) . In addition, 50% of these cancers have Smad4 mutations (5) , and many exhibit inactivating mutations or deletions in the p15 and p16 genes (6 , 7) . These mutations may cause these tumors to be resistant to TGF-ß-mediated growth inhibition. However, pancreatic cancers overexpress all of the three TGF-ßs, and this overexpression has been correlated with decreased patient survival (8) . The mechanisms by which TGF-ßs confer a growth advantage to pancreatic cancer cells in vivo have not been elucidated.
In the current study, we used a soluble receptor approach to block the local actions of TGF-ß in a s.c. nude mouse model of pancreatic cancer. To this end, we generated a cDNA encoding a human soluble TßRII receptor and stably transfected this construct into the human pancreatic cancer cell line, COLO-357. These cells express all of the three TGF-ß isoforms and are growth inhibited by TGF-ß1 in vitro in conjunction with increased expression of the mammalian cyclin-dependent kinase inhibitors p15, p21, and p27 (9 , 10) . They also express a functional Smad4 gene, and their TßRI and TßRII genes are not mutated (10, 11, 12) . Furthermore, COLO-357 cells engineered to overexpress inhibitory Smad6 or Smad7 are no longer growth inhibited by TGF-ß1 (13 , 14) . Surprisingly, overexpression of Smad7 is also associated with enhanced anchorage-independent growth and increased tumorigenicity in nude mice (14) , raising the possibility that COLO-357 cell-derived TGF-ßs promote cancer growth in vivo. It is not known, however, whether inhibiting the biological actions of COLO-357 cell-derived TGF-ßs would attenuate the in vivo growth of these cells. We now report that COLO-357 clones expressing the soluble TßRII exhibit attenuated growth inhibition in vitro in response to TGF-ß1 when compared with the sham-transfected cells. These clones also demonstrate a decreased invasive capacity in vitro, as well as a decreased capacity to form tumors in nude mice and attenuated angiogenesis in vivo.
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MATERIALS AND METHODS |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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-32P]dCTP and [
-35S]dATP from Amersham (Arlington Heights, IL), TE Select D G50 columns from 5 Prime
3 Prime, Inc. (Boulder, CO), DNA and protein molecular weight markers, Lipofectamine from Life Technologies, Inc. (Gaithersburg, MD), anti-HA, anti-ERK-2, anti-TßRII antibodies and protein A agarose from Santa Cruz Biotechnology, Inc. (Santa Cruz, CA), biotinylated antihuman TßRII polyclonal antibody from R&D Systems, Inc. (Minneapolis, MN), horseradish peroxidase-conjugated antibodies from Bio-Rad (Hercules, CA), PECAM-1 monoclonal antibody (clone C/70A) from Oncogene Research Products (Cambridge, MA), enhanced chemiluminescence substrate and Restore Stripping Buffer from Pierce (Rockford, IL), Vectastain Universal Elite ABC kit from Vector Labs (Burlingame, CA), Immobilon-P nitrocellulose membranes from Millipore Corp. (Bedford, MA), streptavidin-peroxidase from Kirkegaard and Perry Laboratories, Inc. (Gaithersburg, MD), centriprep concentrators from Amicon Inc. (Beverly, MA), Lab-Tek chamber slides from Nunc Inc. (Naperville, IL), Transwell chambers from Costar (Cambridge, MA), Matrigel from Becton Dickinson (Bedford, MD), and all of the other reagents from Sigma Chemical Co. (St. Louis, MO). COLO-357 human pancreatic cancer cells were a gift from Dr. Richard S. Metzgar (Duke University, Durham, NC). TGF-ß1 was a gift from Genentech, Inc. (South San Francisco, CA). Human dermal microvascular endothelial cells were a gift from Dr. Joyce Bischoff (Children’s Hospital, Harvard University Medical School, Boston, MA) and Dr. Jian Luo (University of California Irvine, Irvine, CA).
Construction of a Mammalian Expression Vector.
The complete cDNA of human TßRII was used as the template for PCR amplification of the coding sequence of the extracellular domain of TßRII (nucleotides 1–477 including the signal sequence). PCR was performed using the sense primer, 5'-AAGCTTGCCGCCGCCATGGGTCG, and antisense primer, 5'-CTGGAATTCGTCAGGATTGCTGG. The sense primer introduced a HindIII restriction site and the consensus Kozak translation initiation start site. The antisense primer introduced an EcoRI site. The PCR fragment was ligated into the PCRZ.1 vector. The soluble TßRII coding fragment was isolated after digestion with HindIII and EcoRV. This gel-purified fragment was subsequently ligated into the HindIII/Eco721-digested pMH expression vector, which is tagged at its COOH terminus with a HA epitope. The constructed vector, pMHsTßRII, contained the open reading frame encoding the human soluble TßRII and nucleotides encoding nine amino acids of HA. The sequence and orientation was confirmed by dideoxy chain termination sequencing. The pMH plasmid containing the G418 resistance gene (neomycin) was used for construction of control clones (sham) expressing the vehicle vector alone.
Cell Culture.
COLO-357 human pancreatic cancer cells were grown in DMEM, supplemented with 8% FBS, penicillin (100 units/ml), and streptomycin (100 µg/ml), and 5% fungazone termed complete medium. Cells were maintained in monolayer cultures at 37°C in humidified air with 5% CO2. The selection medium for the cell lines containing the neomycin resistance gene was supplemented with 0.4 mg/ml G418. For TGF-ß1 experiments, cells were incubated overnight in serum-free medium (DMEM containing 0.1% BSA, 5 µg/ml transferrin, 5 ng/ml sodium selenite, antibiotics, and fungazone). To generate cells expressing the human soluble TßRII, COLO-357 cells were transfected in a stable manner with the pMHsTßRII plasmid (10 µg) using Lipofectamine as reported previously (15)
. After reaching confluence, cells were split 1:10 into selection medium, and single clones were isolated after 3–4 weeks. After expansion of each individual clone, cells from each clone were screened for expression of soluble TßRII by Northern and Western blot analysis. Two clones were selected for additional studies.
Immunoblotting and Immunoprecipitation.
Exponentially growing human pancreatic and dermal microvascular endothelial cells (50–60% confluent) were washed with ice cold 1 x PBS and lysed in buffer containing 1% NP40, 20 mM Tris (pH 8.0), 150 mM NaCl, 1 mM EDTA, 1 mM EGTA, 2.5 mM sodium phosphate, 1 mM ß-glycerophosphate, 1 mM sodium vanadate, 1 µg/ml leupeptin, and 1 mM phenylmethylsulfonyl fluoride. Frozen tumor samples derived from COLO-357 sham-transfected or pMHsTßRII clones were homogenized and lysed in the same buffer. Lysates were subjected to SDS-PAGE and electrotransferred to Immobilon-P membranes for 40–80 min. After blocking with 5% milk (1 x Tris-buffered saline with 0.1% Tween 20), the membranes were incubated with anti-HA monoclonal antibody (1:1200 dilution), anti-CD31 antibody (1:3000 dilution), washed, and incubated with a secondary horseradish peroxidase-conjugated antibody. After washing, bound antibodies were visualized using enhanced chemiluminescence. To confirm equal loading, membranes were stripped for 20 min at room temperature in either Restore stripping buffer or 30 min at 50°C in buffer containing 2% SDS, 62.5 mM Tris (pH 6.7), and 100 mM 2-mercaptoethanol and blotted with an anti-ERK-2 antibody (1:8000 dilution).
For immunoprecipitation with the anti-HA antibody, cells transfected with the soluble TßRII expression construct or sham were grown to 80% confluency in complete medium and then incubated for 24 h in serum-free medium. Conditioned medium from the clones or sham-transfected cells was concentrated by using a Mr 10,000 cutoff filtration membrane. The concentrated medium was incubated for 12 h at 4°C with the anti-HA antibody (2 µg/ml), followed by a 2-h incubation with protein A agarose (50 µl) at 4°C. Precipitates were washed three times with ice-cold PBS, resuspended in 2 x loading buffer, and boiled for 5 min at 100°C. After centrifugation, the supernatants were subjected to Western blotting using the biotinylated antihuman TßRII polyclonal antibody (1:5000 dilution).
Immunohistochemistry.
COLO-357 cells were plated in chamber slides and grown to 70% confluency for 48 h. The cells were fixed in 1.5% paraformaldehyde for 45 min at room temperature and incubated sequentially for 30 min (room temperature) with 0.1% Triton X-100, 30 min (room temperature) with 0.3% hydrogen peroxide/methanol, 30 min (37°C) with 1 mg/ml hyaluronidase, and 40 min (room temperature) with 10% normal goat serum. Cells were then incubated for 16 h (4°C) with the highly specific anti-HA antibody (0.4 µg/ml) recognizing the HA epitope encoded by pMHsTßRII or with the highly specific anti-TßRII antibody (0.2 µg/ml) recognizing the epitope corresponding to the full-length TßRII.
To assess TßRII, HA, and CD31 immunoreactivity, tumors from s.c. lesions were removed and immediately divided. Tissues were fixed in 4% formaldehyde and embedded in paraffin wax. Paraffin-embedded sections (4 µm) from tumor tissue derived from sham-transfected or pMHsTßRII-transfected cells were cut and mounted on poly L-lysine-coated glass slides and air-dried overnight at room temperature. Representative sections of each case were examined by the streptavidin-peroxidase technique using appropriate positive and negative controls. Endogenous peroxidase activity was blocked by incubation for 30 min with 0.3% hydrogen peroxidase in methanol. Tissue sections were incubated for 15 min (room temperature) with 10% normal goat serum and then incubated for 16 h at 4°C with anti-HA antibody (0.4 µg/ml), anti-TßRII antibody (0.2 µg/ml), or anti-platelet endothelial cell adhesion molecule-1 antibody (1:50 dilution) in PBS containing 1% BSA.
For both cell-line and tissue immunohistochemistry, bound TßRII and HA antibodies were detected with biotinylated goat antirabbit IgG secondary antibodies and streptavidin-peroxidase complexes, using diaminobenzidine tetrahydrochloride as the substrate. Sections were counterstained with Mayer’s hematoxylin. Sections incubated with nonimmune rabbit IgG or with secondary antibodies alone did not yield positive immunoreactivity. The frequency of blood vessels in the matrix region of the tumor that was positively stained for PECAM-1 was evaluated morphometrically. Fifty different high-power fields were randomly selected for each specimen, with each high-power field representing 0.25 mm2 on the microscope grid.
RNA Extraction and Northern Blot Analysis.
Total RNA was extracted by the single step acid guanidine thiocyanate-phenol-chloroform method (16)
. RNA was size fractionated on 1.2% agarose/1.8 M formaldehyde gels, electrotransferred onto Genescreen nylon membranes, and cross-linked by UV irradiation (17)
. The blots were prehybridized and hybridized in 0.75 M NaCl, 5 mM EDTA (pH 8.0), 50 mM sodium phosphate, 50% formamide, 5 x Denhardt’s solution, 10% dextran sulfate, 1% SDS, and 100 µg/ml salmon sperm DNA with cDNA probes at 42°C. The cDNA probes included a 500-bp HindIII/EcoRI fragment of the human soluble TßRII, a 500-bp SacII/Pst-1 fragment of the human PAI-1, and a 190-bp BamHI fragment of mouse 7S ribosomal cDNA, which hybridizes with human cytoplasmic RNA. The 7S probe was used to confirm equal RNA loading (17)
. Membranes were washed under high stringency conditions (washed two times in 2 x SSC at room temperature and two times at 55°C in 0.2 x saline-sodium phosphate-EDTA/1% SDS). Blots were exposed to Kodak Biomax MS films in cassettes with BioMax Transcreen-high energy intensifying screens at -80°C.
Cell Growth Assays.
To assess the growth inhibitory effects of TGF-ß, cell growth was determined by the MTT dye reduction assay, which measures the conversion of the MTT tetrazolium salt into MTT formazan by mitochondrial hexosaminidase (18
, 19)
. Cells were seeded at a density of 10,000 cells/well in 96-well plates in DME complete medium and incubated for 24 h before incubation for 72 h in serum-free medium in the absence or presence of TGF-ß1 (10 pM). The assay was initiated by adding MTT solution at a final concentration of 62.5 µg of MTT/well (9
, 10)
. After 4 h, the medium was removed, and the dye crystals were dissolved in acidified isopropanol. The absorbance was measured at 570 nm and 650 nm with an ELISA plate reader (Molecular Devices, Menlo Park, CA). Data were expressed as percentage of unstimulated control cell growth. In pancreatic cancer cells, the results of the MTT assay correspond with results obtained by cell counting with a hemocytometer or by monitoring [3H]-thymidine incorporation into DNA (9)
.
In Vivo Tumorigenicity Assay.
To assess the effect of the soluble TßRII on tumorigenicity, 2 x 106 or 6 x 105 cells expressing the empty vector alone (sham) or soluble TßRII were injected s.c. into two sites in female athymic (nude) mice. The tumor size was measured weekly until mice were sacrificed 56 days after injection. A portion of the tumor tissue was snap frozen in liquid nitrogen and stored for subsequent RNA and protein analysis. Another portion was prepared for immunohistochemistry studies.
Invasion Assay.
The invasive ability of the COL0–357 sham-transfected and soluble TßRII-transfected pancreatic cancer cells were measured as reported previously (20)
with some modifications (21)
. Briefly, polycarbonate membranes (8-µm pore size) of the upper compartment of Transwell chambers were coated with 5% Matrigel. COLO-357 cells that were preincubated for 24 h in serum-free medium containing 0.1% BSA in the absence or presence of 400 pM TGF-ß1 were suspended in 100 µl of serum-free medium containing 0.1% BSA and placed onto this upper compartment. The lower compartment was then filled with 600 µl of serum-free medium containing 0.5% FBS. TGF-ß1 (400 pM) was added to the lower compartment corresponding to chambers that contained cells previously incubated with TGF-ß1. After 16 h, the membranes were fixed in methanol and stained with H&E. Cells on the upper surface of the filter were carefully removed with a cotton swab, and the cells that had migrated through the membrane to the lower surface of the filter were counted in nine different fields using a light microscope (magnification, x200). Invasion assays were performed in triplicate.
Statistics.
Statistical analysis was performed with SigmaStat software (Jandel Scientific, San Raphael, CA) and Prism software (Graphpad Software, Inc., San Diego, CA). Student’s t test was used when indicated. P < 0.05 was taken as the level of significance.
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RESULTS |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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. COLO-357 cells transfected with the pMH empty vector carrying the G418 resistance gene served as the control (sham) and did not express the soluble TßRII (Fig. 1A)
. Immunoblotting of cell lysates with the anti-HA antibody, which recognizes the HA epitope at the COOH terminus of the pMH expression vector, confirmed the expression of the soluble TßRII at the protein level (Fig. 1B)
. To determine whether the soluble TßRII was secreted, conditioned medium from a sham-transfected clone and from clone 1 (C1) was subjected to immunoprecipitation with the anti-HA antibody followed by immunoblotting with the biotinylated antihuman TßRII antibody. A major band (Mr 25,000) representing the soluble TßRII protein was visible in conditioned medium from the C1 clone but not from the sham clone. A minor band (Mr 35,000) was also present in the C1 conditioned medium (Fig. 1C)
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, representing endogenously expressed TßRII. In contrast, there was strong TßRII immunoreactivity in clone 1 cells (Fig. 2B)
and clone 2 (data not shown) expressing the transfected soluble TßRII. When the anti-HA antibody was used, sham-transfected cells were devoid of immunoreactivity (Fig. 2C)
, whereas positive immunostaining for HA was readily evident in the cells transfected with the pMHsTßRII construct (Fig. 2D)
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, as well as in two additional clones (data not shown). TGF-ß1 (400 pM) also significantly increased the invasiveness of sham-transfected COLO-357 cells in an in vitro cell invasion assay (Fig. 3B)
but was without effect in the clones expressing the soluble TßRII (Fig. 3B)
. Thus, expression of soluble TßRII effectively blocked the biological actions of exogenous TGF-ß1.
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. To determine whether tumor growth was also decreased after injection of a lower number of cells, 6 x 105 COLO-357 cells/site were injected next (two sites/mouse). Three mice received injections with sham-transfected COLO-357 cells, and six mice received injections with pMHsTßRII-transfected COLO-357 clones. There was significant inhibition of tumor growth by the transfected clones at 28 days (70%; P < 0.04) and 35 days (75%; P < 0.005) after injection when compared with the respective sham controls (Fig. 4B)
. One site that received injections with the pMHsTßRII C1 cells did not form a tumor, even after 56 days. In contrast, all of the sites that received injections with sham-transfected cells always yielded tumors. After day 35, two mice, each bearing two tumors of the sham-transfected cells, had to be sacrificed because the tumor burden reached the maximum allowable limit by our Institutional Animal Care and Use Committee protocol. The remaining mice bearing tumors from either the pMHsTßRII clones or the sham-transfected cells were allowed to grow until day 56. Even at time of sacrifice (day 56), tumors derived from the clones never became as large as the sham did on day 35. At day 56, the tumors derived from sham-transfected cells were still progressively growing, whereas the growth of the tumors derived from pMHsTßRII cells reached a plateau (Fig. 4B)
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. As expected, these tumors did not exhibit positive immunostaining when the anti-HA antibody was used (Fig. 5C)
. In contrast, strong TßRII (Fig. 5B)
and HA (Fig. 5D)
immunoreactivity was evident in the cancer cells expressing the pMHsTßRII construct. Tumors from both clones expressed high levels of the soluble TßRII mRNA moiety (Fig. 6A)
. In contrast, tumors from sham-transfected cells did not express the soluble TßRII mRNA transcript (Fig. 6A)
. Because PAI-1 has been implicated in pancreatic cancer metastasis in humans (22)
and is overexpressed in this malignancy (23)
, its expression was analyzed next. In the tumors derived from soluble TßRII clones, there was a 67% decrease in PAI-1 mRNA levels when compared with the sham tumors (Fig. 6B)
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revealed a statistically significant decrease in the number of cells that stained positive for anti-PECAM-1 antibody in tumors derived from either clone 1 (6.7 ± 0.35) or clone 2 (5.3 ± 0.37), in comparison with tumors derived from the sham-transfected cells (12.2 ± 0.70). To more clearly assess blood vessel mass, immunoblotting with the anti-PECAM-1 antibody was performed next using frozen tumor tissues derived from both COLO-357 cells. Tumors derived from sham-transfected COLO-357 cells expressed more PECAM-1 then those derived from pMHsTßRII-transfected cells (Fig. 7B)
. Human endothelial cells, which are known to express high levels of PECAM-1, served as a positive control and exhibited a strong PECAM-1 signal.
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DISCUSSION |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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COLO-357 clones expressing the soluble TßRII and sham-transfected COLO-357 cells exhibited similar doubling times in vitro. However, in the pMHsTßRII-expressing clones, the growth inhibitory effect of 10 pM TGF-ß1 was completely blocked, indicating that soluble TßRII efficiently bound and sequestered TGF-ß1. This conclusion is supported by the observation that the stimulatory effect of 400 pM TGF-ß1 on cell invasiveness was also completely blocked by soluble TßRII. The mechanisms by which TGF-ß1 promotes cellular invasion are not known. It has been shown that TGF-ß1 increases Smad2 expression in COLO-357 cells (23) , and elevated levels of Smad2 are known to enhance cellular motility (26) . It has also been established that TGF-ß1 enhances the expression of PAI-1 (10 , 27, 28, 29) , and increased TGF-ß expression correlates with increased PAI-1 levels in pancreatic cancer (23) . PAI-1 is the main inhibitor of the urokinase-type plasminogen activator system. It promotes cancer cell migration by preventing excessive extracellular matrix degradation by plasmin proteolysis (22 , 30) , and its reduced expression correlates with attenuated tumorigenicity in Smad4 reconstituted cancer cells (31) . Therefore, it is possible that TGF-ß1 acts via these mechanisms to promote the motility of COLO-357 cells across a Matrigel membrane. Because pancreatic cancer is a highly invasive malignancy, these observations suggest that TGF-ßs may act directly on pancreatic cancer cells to promote cancer cell invasion.
Multiple s.c. injections of two independent clones expressing soluble TßRII yielded small tumors in nude mice when compared with sham-transfected cells. These tumors expressed the soluble TßRII by Northern analysis and exhibited strong HA and TßRII immunoreactivity, thereby confirming in vivo production of soluble TßRII. These tumors also exhibited attenuated PAI-1 expression by comparison with tumors formed by sham-transfected cells, indicating that soluble TßRII interfered with TGF-ß-mediated induction of PAI-1 in vivo. There was a parallel decrease in tumor angiogenesis as determined by a marked decrease in the number of blood vessels and PECAM-1 levels. Inasmuch as TGF-ß1 and PAI-1 can promote angiogenesis in vivo (32, 33, 34, 35, 36, 37) , these findings suggest that the soluble TßRII interferes with proangiogenic pathways in vivo. This conclusion is supported by our recent observation that this antiangiogenic effect of soluble TßRII also occurs with tumors formed by PANC-1 human pancreatic cancer cells.4
Several different types of experiments have suggested that there is a dissociation between the signaling pathways that mediate the growth suppressive effects of TGF-ßs and their effects on the expression of genes that modulate the extracellular matrix. Thus, in mink lung epithelial cells, expression of a truncated TßRII renders these cells resistant to TGF-ß1-mediated growth inhibitory effects without altering TGF-ß1-mediated induction of PAI-1 (27) . Transfection of these cells with a mutant TßRI that lacks the juxtamembrane region preceding the GS domain leads to TGF-ß1-mediated PAI-1 production but not to growth inhibition (38) . Overexpression of inhibitory Smad7 makes COLO-357 cells resistant to TGF-ß1-mediated growth inhibitory effects without altering TGF-ß1-mediated induction of PAI-1 (14) . Cell lines derived from pulmonary metastases lose TGF-ß1-mediated growth inhibitory responses but still exhibit TGF-ß1-mediated induction of matrix metalloproteinase-9 (29) . In this context, the overexpression of TGF-ßs in pancreatic cancer cells that frequently harbor Smad4 mutations and overexpress inhibitory Smad molecules may provide a mechanism for the activation of autocrine and paracrine pathways that lead to the expression of genes that promote cancer spread and angiogenesis. Indeed, it has been shown recently (39) that the angiogenic potential of TGF-ßs may be enhanced by the presence of Smad4 mutations. Together with the current findings, these observations suggest that soluble TßRII may act to block both paracrine and autocrine pathways that promote the growth of COLO-357 cells in vivo.
Several approaches have been used to suppress the biological actions of TGF-ßs in vivo. These include the use of neutralizing anti-TGF-ß antibodies (34 , 40 , 41) or antisense strategies to inhibit TGF-ß synthesis (33 , 42 , 43) , expression of a mutated TGF-ß1 precursor to inhibit the processing of all of the three TGF-ßs (44) , expression of TßRIII, soluble TßRIII, or soluble TßRII to neutralize TGF-ß activity (25 , 45, 46, 47) , or expression of a dominant-negative version of TßRII to interfere with TGF-ß signaling (32 , 48 , 49) . In the present study, we have used a soluble TßRII strategy to attenuate the invasive and tumorigenic capacity of COLO-357 pancreatic cancer cells, suppress their angiogenic potential, and down-regulate their ability to overexpress PAI-1. Therefore, our findings indicate that this approach can efficiently interfere with multiple TGF-ß-dependent biological activities and paracrine actions in vivo. Inasmuch as PAI-1 is overexpressed in human pancreatic cancer and its overexpression may contribute to tumor invasion and tumor spread (22) , our findings also raise the possibility that soluble TßRII may ultimately have a multifaceted therapeutic role in pancreatic cancer.
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FOOTNOTES |
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1 Partially supported by United States Public Health Service Grant CA-75059, awarded by the National Cancer Institute [to M. K.], and by a postdoctoral fellowship award from the George E. Hewitt Foundation for Medical Research [to M. A. R-G.] 
2 To whom requests for reprints should be addressed, at Division of Endocrinology, Diabetes, and Metabolism, Medical Sciences I, C240, University of California, Irvine, CA 92697. Phone: (949) 824-2272; Fax: (949) 824-1035; E-mail: mkorc{at}uci.edu
3 The abbreviations used are: TGF-ß, transforming growth factor-ß; TßR, TGF ß receptor; FBS, fetal bovine serum; HA, hemagglutinin A; MTT, 3-(4,5-methylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; PAI-1, plasminogen activator inhibitor-1.
4 M. A. Rowland-Goldsmith and M. Korc, unpublished observations.
Received 4/25/01; revised 6/ 7/01; accepted 6/15/01.
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) or presence of 10 pM (
) TGF-ß1 for 72 h. Growth was determined by the MTT assay. Results are expressed as percentage of unstimulated control and are the means (±SE) of eight determinations/experiment from three separate experiments. Error bars for the control groups were exceedingly small. *, P < 0.002 when compared with respective untreated controls. B, effects of TGF-ß1 on invasion. To assess the ability of TGF-ß1 to induce invasion, COLO-357 cells were preincubated for 24 h in serum-free medium containing 0.1% BSA in the absence or presence of 400 pM TGF-ß1. The respective groups of cells (1 x 105/well) were then added to the upper chambers of a 24-well Transwell unit. Medium devoid of TGF-ß1 (
/4, where l is length, h is height, and w is width of the tumor. A, tumor volume. Results are expressed as percentage of sham control and are the means ± SE from three separate experiments in which tumor volume was determined 28 days after injection of 2 x 106 COLO-357 cells/site (two sites/mouse). Error bars for the control groups are not shown because they were exceedingly small. B, time course. Data are the means ± SE from three mice that received injections with sham-transfected cells and six mice that received injections with COLO-357 clones expressing pMHsTßRII (6 x 105 cells/site). However, two mice that received injections with sham-transfected cells were sacrificed after 35 days because of tumor size. Therefore, data from day 56 for sham-derived tumors are the means ± SD. One site that received injections with clone 1 did not yield a tumor, and this site was excluded from the volume calculations. *, P < 0.04; **, P < 0.001 when compared with the sham control.
