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Department of Cancer Biology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas
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ABSTRACT |
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 Top ABSTRACT INTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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and -ß on their surfaces. The percentage of positive endothelial cells and the intensity of receptor expression directly correlated with proximity to bone tissue. Oral administration of PKI166 inhibited the phosphorylation of EGF-R but not PDGF-R, whereas oral administration of STI571 inhibited the phosphorylation of PDGF-R but not EGF-R. Combination therapy using oral PKI166 and STI571 with i.p. injections of paclitaxel induced a high level of apoptosis in tumor vascular endothelial cells and tumor cells in parallel with inhibition of tumor growth in the bone, preservation of bone structure, and reduction of lymph node metastasis. Collectively, these data demonstrate that blockade of phosphorylation of EGF-R and PDGF-R coupled with administration of paclitaxel significantly suppresses experimental human prostate cancer bone metastasis. |
INTRODUCTION |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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24% of patients have metastatic lesions at initial diagnosis, and in an additional 30% of the patients, metastases are discovered during surgical staging. A significant number of patients with clinically localized disease who are treated with radical prostatectomy may also develop metastasis (5, 6, 7, 8)
. Clearly then, the development of new treatment modalities for metastatic prostate cancer is important to the many men who will have metastatic prostate cancer. Developing such a treatment requires an understanding of the progression of prostate cancer. To produce metastasis in the bone, prostate cancer cells must complete a series of sequential and highly selective steps (5 , 9 , 10) . We recently confirmed the "seed and soil" hypothesis of Stephen Paget (11) that certain tumor cells have a specific affinity for the milieu of certain organs. Specifically, we reported that the expression of various cytokines, growth factors, and their receptors on prostate cancer cells and endothelial cells differ in different organ microenvironments (12 , 13) . Moreover, cell response to protein tyrosine kinase receptor inhibitors, such as epidermal growth factor receptor (EGF-R; Ref. 12 ) and platelet-derived growth factor receptor (PDGF-R; Ref. 13 ), depends on the host organ microenvironment. EGF and EGF-R pathways have been reported to be related to cell proliferation (14 , 15) , activation of antiapoptotic effects (16) , and disease progression (17, 18, 19, 20, 21) . The PDGF and PDGF-R pathways are involved in cell division (22, 23, 24) , cell migration (25) , angiogenesis (26) , and cell survival (27) .
In our animal model, endothelial cells in tumors growing in the bone expressed phosphorylated EGF-R or PDGF-R on their surfaces, whereas endothelial cells in tumors growing in the muscle or endothelial cells in unaffected tissues did not (12 , 13) . Oral administration of the protein tyrosine kinase inhibitors PKI166 (28) or STI571 (29 , 30) has been found to inhibit phosphorylation of EGF-R and PDGF-R, respectively, and when each was combined with i.p. injection of paclitaxel, these inhibitors significantly inhibited tumor growth (12 , 13) . Because human prostate cancer cells growing adjacent to bone tissue express both EGF and PDGF and both tumor cells and tumor-associated endothelial cells express phosphorylated EGF-R and PDGF-R, we hypothesized that simultaneous targeting of both receptors combined with systemic injections of paclitaxel would produce additive therapeutic results. We report here the therapeutic effects of combining PKI166 with STI571 and paclitaxel on experimental human prostate cancer bone metastases in the tibias of nude mice.
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MATERIALS AND METHODS |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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Animals.
Male athymic nude mice (NCI-nu) were purchased from the Animal Production Area of the National Cancer Institute-Frederick Cancer Research Facility (Frederick, MD). The mice were housed and maintained in specific pathogen-free conditions. The facilities were approved by the American Association for Accreditation of Laboratory Animal Care and met all current regulations and standards of the United States Department of Agriculture, United States Department of Health and Human Services, and the NIH. The mice were used in accordance with institutional guidelines when they were 6 to 8 weeks of age.
Intratibial Injection of Tumor Cells.
To produce bone tumors, PC-3MM2 cells were harvested from subconfluent cultures by brief exposure to 0.25% trypsin and 0.02% EDTA. Trypsinization was stopped with medium containing 10% fetal bovine serum, and the cells were washed once in serum-free medium and resuspended in Ca2+- and Mg2+-free HBSS. Cell viability was determined by trypan blue exclusion, and only single-cell suspensions with >95% viability were used to produce tumors in the tibias of mice.
Nude mice were anesthetized with Nembutal (0.5 mg/g of body weight; Abbott Laboratories, Chicago, IL). A percutaneous intraosseal injection was made by drilling a 27-gauge needle into the tibia immediately proximal to the tuberositas tibia. After penetration of the cortical bone, the needle was inserted into the shaft of the tibia, and 20 µl of the cell suspension (2 x 105 cells) were deposited in the bone cortex by use of a calibrated, push-button-controlled dispensing device (Hamilton Syringe Co., Reno, NV). To prevent leakage of cells into the surrounding muscles, a cotton swab was held for 1 min over the site of injection. The animals tolerated the surgical procedure well, and no anesthesia-related deaths occurred.
Therapy for Human Prostate Cancer Cells Growing in the Tibias of Athymic Nude Mice.
PKI166 (4-phenethylamino-6-[hydroxyl]phenyl-7H-pyrrolo[2.3-d]-pyrimidine), a novel EGF-R tyrosine kinase inhibitor, was synthesized and provided by Novartis Pharma (Basel, Switzerland). For oral administration (three times per week), PKI166 was dissolved in DMSO–0.5% Tween 80 and then diluted 1:20 in water (12)
. The PDGF-R tyrosine kinase inhibitor STI571 (imatinib meslate, Gleevec), synthesized and provided by Novartis Pharma (Basel, Switzerland), was dissolved in distilled water at 6.25 mg/ml for daily oral administration (13)
. Paclitaxel (Taxol) purchased from Bristol-Myers Squibb (Princeton, NJ) was diluted in water for once per week i.p. injection.
Three days after the implantation of tumor cells into the tibias, five mice were killed, and the presence of actively growing cancer cells was confirmed by histology. The remaining mice were randomized into eight treatment groups (n = 10) as follows: (a) control mice receiving daily administration of distilled water and one i.p. injection per week of distilled water (n = 5) or oral administration three times per week of water diluted 1:20 with DMSO–0.5% Tween 80 and a once-per-week i.p. injection of distilled water (n = 5); (b) once-per-week i.p. injection of paclitaxel at 8 mg/kg and daily oral administration of distilled water (n = 5) or oral administration three times per week of water diluted 1:20 with DMSO–0.5% Tween 80 (n = 5); (c) oral administration three times per week of 100 mg/kg PKI166 and once per week i.p. injection of distilled water; (d) daily administration of 50 mg/kg STI571 and once per week i.p. injection of distilled water; (e) oral administration three times per week of 100 mg/kg PKI166, a daily oral administration of STI571 at 50 mg/kg, and once per week i.p. injection of distilled water; (f) oral administration three times per week of 100 mg/kg PKI166 and once per week i.p. injection of paclitaxel at 8 mg/kg; (g) a daily oral administration of STI571 at 50 mg/kg and once per week i.p. injection of paclitaxel at 8 mg/kg; and (h) oral administration three times per week of 100 mg/kg PKI166, daily oral administrations of STI571 at 50 mg/kg, and once per week i.p. injection of paclitaxel at 8 mg/kg. All mice were treated for 5 weeks. Tumor size and status of injected bone (lysis) were evaluated by gross observation and digital radiography as described below.
Digital Radiography and Harvest of Tumors.
After 3 and 4 weeks of treatment, three mice selected randomly from each of the different treatment groups were anesthetized with Nembutal (0.5 mg/g body weight) and placed in a prone position. Digital radiography was carried out with a Faxitron (Faxitron X-Ray Corporation, Wheeling, IL). On week 6 of the study (5 weeks of treatment), all mice were euthanized by injection of Nembutal (1.0 mg/g) and weighed. Digital radiography was carried out on the hind limbs of each mouse, and tumor incidence and size were recorded. The tumor-bearing leg and the tumor-free contralateral leg of each mouse were resected at the head of the femur and weighed. The net tumor weight was calculated by subtraction. Macroscopically enlarged lymph nodes were harvested and prepared for histological examination to determine the presence of metastasis.
Reagents for Immunohistochemistry and Terminal Deoxynucleotidyltransferase-Mediated Nick End Labeling (TUNEL) Assay.
All antibodies for immunohistochemistry were purchased as follows: rabbit anti-EGF-R (Santa Cruz Biotechnology, Santa Cruz, CA); rabbit anti-phospho-EGF-R (activated EGF-R, Tyr845; Cell Signaling Technology, Inc., Beverly, MA); rabbit anti-PDGF-R and -ß (Santa Cruz Biotechnology); goat polyclonal anti-phospho-PDGF-Rß (activated PDGF-Rß; Santa Cruz Biotechnology); rat antimouse CD31-PECAM-1 (PharMingen, San Diego, CA); mouse anti-proliferative cellular nuclear antigen (PCNA) clone PC-10 (DAKO A/S, Copenhagen, Denmark); peroxidase-conjugated goat antirabbit IgG, peroxidase-conjugated goat antirat IgG, Texas Red-conjugated goat antirat IgG, and FITC-conjugated goat antirabbit IgG (Jackson Research Laboratories, West Grove, CA); peroxidase-conjugated rat antimouse IgG2a (Serotec; Harlan Bioproducts for Science, Inc., Indianapolis, IN); and Alexa Fluor 594-conjugated goat antirabbit IgG and Alexa Fluor 594-conjugated rabbit antigoat IgG (Molecular Probes, Eugene, OR). Stable 3,3'-diaminobenzidine (Research Genetics, Huntsville, AL) and Gill’s hematoxylin (Sigma, St. Louis, MO) were used for visualization of immunohistochemical (IHC) reaction and counterstaining, respectively. TUNEL was assayed with a commercial apoptosis detection kit (Promega Corp., Madison, WI).
Preparation of Tissues.
The tibias and surrounding muscles were fixed in 10% buffered formalin for 24 h at room temperature, washed with PBS for 30 min, decalcified with 10% EDTA (pH 7.4) for 7–10 days at 4°C, sectioned, and embedded in paraffin. The method described by Morris et al. (32)
was used for preparation of frozen sections with the following modifications: The tibias and surrounding muscles were fixed in 4% paraformaldehyde containing 0.075 M lysine and 0.01 M sodium periodate solution for 24 h, washed with PBS for 30 min, decalcified with 10% EDTA (pH 7.4) for 7–10 days, and washed three times, once with PBS containing 10% sucrose for 4 h, once with PBS containing 15% sucrose for 4 h, and once with PBS containing 20% sucrose for 16 h. All procedures were carried out at 4°C. The tissues were then embedded in OCT compound (Miles, Inc., Elkhart, IN), rapidly frozen in liquid nitrogen, and stored at –70°C.
IHC Determination of EGF-R, Activated EGF-R, PDGF-R, Activated PDGF-R, PCNA, and CD31/PECAM-1.
Paraffin-embedded tissues were sectioned (4- to 6-µm thick) and used to detect expression of EGF-R, activated EGF-R, PDGF-R and -ß, activated PDGF-Rß, and PCNA. Sections were mounted on positively charged Superfrost slides (Fisher Scientific Co., Houston, TX) and dried overnight on a hot (65°C) plate. Sections were deparaffinized in xylene, dehydrated with a graded series of alcohol [100, 95, and 80% (v/v) ethanol in doubly distilled H2O], and then rehydrated in PBS (pH 7.5). Sections analyzed for PCNA were microwaved for 5 min to improve "antigen retrieval." Periodate-lysine-paraformaldehyde-fixed frozen tissues used for CD31/PECAM-1 were sectioned (8–10 µm), mounted on positively charged Plus slides (Fisher Scientific), and air-dried for 30 min. Frozen sections were washed three times with PBS. IHC procedures were performed as described previously (12
, 13)
. Control samples exposed to secondary antibody alone showed no specific staining. Dilutions of primary antibodies were as follows: EGF-R (1:50), phosphorylated EGF-R (1:50), PDGF-R and -ß (1:100), phosphorylated PDGF-Rß (1:100), PCNA (1:100), and CD31/PECAM-1 (1:400). The samples for EGF-R, activated EGF-R, PDGF-R and -ß, CD31/PECAM-1, and PCNA were incubated with protein-blocking solution containing 5% normal horse serum and 1% normal goat serum for 20 min, and the sample for activated PDGF-Rß was incubated with protein-blocking solution containing 4% fish gel (Cold Water Fish Skin Gelatin, 40%, Aurion; Electron Microscopy Science, Fort Washington, PA) in PBS for 20 min.
We used stable 3,3'-diaminobenzidine (Research Genetics) and Gill’s hematoxylin (Sigma) for visualization of the IHC reaction with EGF-R or PDGF-R, PDGF-Rß, PCNA, and CD31/PECAM-1 and counterstaining or Alexa Fluor 594-conjugated secondary antibody for immunohistochemistry of EGF-R, PDGF-R, phosphorylated EGF-R, and phosphorylated PDGF-Rß. The sections stained with immunofluorescence-tagged secondary antibody were rinsed with distilled water and mounted with Vectashield (mounting medium with 4',6-diamidino-2-phenylindole; Vector Laboratories, Inc., Burlingame, CA), which gave blue fluorescence nuclear staining. Immunofluorescence microscopy was performed with an x20 or x40 objective on an epifluorescence microscope equipped with narrow band-pass excitation filters mounted on a filter wheel (Ludl Electronic Products, Hawthorne, NY).
Distance from bone fragments was marked, and cells were counted in x100 fields (x10 objective and x10 ocular; 0.14 mm2/field) to calculate the percentage of cells stained positively for EGF-R or PDGF-R and -ß (% positive cells = number of positive cells in 0.14 mm2/total number of cells in 0.14 mm2 x 100%). The intensity of staining was measured in the same fields where positivity of cells was calculated by use of ImageQuant analyzer and Optima software program (Bioscan, Edmonds, WA). Cell counting and intensity measurements were performed in six fields of each slide and analyzed statistically.
Immunofluorescence Double Staining for CD31/PECAM-1 (Endothelial Cells) and EGF-R, PDGF-R, or TUNEL.
Pyridoxal phosphate-fixed tissues were sectioned (8–10 µm), mounted on positively charged slides, and air-dried for 30 min. The samples were washed three times with PBS, incubated with protein-blocking solution containing 5% normal horse serum and 1% normal goat serum in PBS for 20 min at room temperature, and then incubated with a 1:400 dilution of rat monoclonal antimouse CD31 antibody (human cross-reactive) over 18 h at 4°C. After the samples were rinsed four times with PBS for 3 min each, the slides were incubated with a 1:200 dilution of secondary goat antirat antibody conjugated to Texas Red for 1 h at room temperature in the dark. Samples were then washed twice with PBS containing 0.1% Brij and once with PBS for 5 min. EGF-R, PDGF-R, and PDGF-Rß immunostaining was performed after CD31 staining. Samples were incubated with protein-blocking solution for 5 min at room temperature and incubated with a 1:50 dilution of anti-EGF-R antibody or 1:100 dilution of anti-PDGF-R or -PDGF-Rß antibody for 18 h at 4°C. The samples were then rinsed four times with PBS for 3 min each, and the slides were incubated with a 1:200 dilution of secondary goat antirabbit antibody conjugated to FITC for 1 h at room temperature. Samples were washed twice with PBS containing 0.1% Brij and once with PBS for 5 min and mounted with Vectashield. Endothelial cells were identified by red fluorescence, and EGF-R, PDGF-R, and PDGF-Rß were identified by green fluorescence. Colocalization of endothelial cells/EGF-R or endothelial cells/PDGF-R, PDGF-Rß (endothelial cells, red + EGF-R, PDGF-R, or PDGF-Rß green = yellow) was obtained by superimposing two images. We measured the distance of endothelial cells expressing EGF-R or PDGF-R and -ß (yellow) from the cells expressing EGF-R or PDGF-R and -ß (green) with the Euclidian distance map (33
, 34)
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TUNEL was performed using an apoptosis detection kit with the following modification: samples were fixed with 4% paraformaldehyde (methanol free) for 10 min at room temperature, washed twice with PBS for 5 min, and then incubated with 0.2% Triton X-100 for 15 min at room temperature. After being washed twice with PBS for 5 min, the samples were incubated with equilibration buffer (from the kit) for 10 min at room temperature. The equilibrium buffer was drained, and reaction buffer containing equilibration buffer, nucleotide mixture, and terminal deoxynucleotidyl transferase enzyme was added to the tissue sections. The sections were incubated in a humidified atmosphere at 37°C for 1 h in the dark. The reaction was terminated by immersing the samples in 2x SSC for 15 min, and samples were washed three times for 5 min to remove unincorporated fluorescein-dUTP.
For quantification of endothelial cells, the samples were incubated with 300 µg/ml Hoechst stain for 10 min at room temperature. Fluorescence bleaching was minimized by treating the slides with an enhancing reagent (Prolong Solution, Prolong Anifade Kit; Molecular Probes). Immunofluorescence microscopy was performed with a x40 objective on a Zeiss epifluorescence microscope equipped with narrow band-pass excitation filters mounted on a filter wheel (Ludl Electronic Products) to individually select for green, red, and blue fluorescence. Images were captured by use of a Sony 3-chip camera (Sony Corporation of America, Montvale, NJ) mounted on a Zeiss universal microscope (Carl Zeiss, Thornwood, NY) and Optimas Image Analysis software (Bioscan, Edmond, WA) installed on a Compaq computer with Pentium chip, a frame grabber, an optical disk storage system, and a Sony Mavigraph UP-D7000 digital color printer (Tokyo, Japan). To produce prints, images were further processed by use of Adobe PhotoShop software (Adobe Systems, Mountain View, CA). Endothelial cells were identified by red fluorescence, and DNA fragmentation was detected by localized green and yellow fluorescence within the nuclei of apoptotic cells. Apoptosis in endothelial cells was expressed as an average of the ratio of apoptotic endothelial cells to total number of endothelial cells in 5–10 random 0.011-mm2 fields at x400 magnification.
Quantification of Mean Vessel Density and PCNA.
For quantification of microvessel density, 10 random 0.159-mm2 fields in the bone at x100 magnification were captured for each tumor, and the vessel fields were counted according to the method described previously (35)
. Cells positively stained with anti-PCNA antibody were counted in the same fields.
Statistical Analysis.
Tumor incidence (
2 test), weight, positivity and intensity of EGF-R and PDGF-R (Mann–Whitney U test), incidence of lymph node metastasis (2 test), and PCNA-positive cells, mean vessel density (CD31/PECAM-1), and ratio of CD31/PECAM-1/TUNEL colocalized cells (unpaired Student’s t test) were compared.
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RESULTS |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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. All control mice had large tumors in the tibias and surrounding muscles (median weight, 4.0 g; range, 2.5–6.4 g) with 100% incidence of lymph node metastasis. All mice receiving only paclitaxel also developed large tumors (median weight, 3.4 g; range, 1.2–5.0 g) with 100% incidence of lymph node metastasis. Similar to our previous reports (12
, 13)
, oral administrations of PKI166 (three times per week) significantly (P < 0.05) decreased tumor incidence, tumor size, and lymph node metastasis. The daily oral administration of STI571 also significantly (P < 0.05) decreased tumor incidence, tumor size, and lymph node metastasis. Tumor incidence, size of tumor, and lymph node metastasis were decreased even more (P < 0.01) in mice receiving the combination of PKI166 and paclitaxel. Similarly, therapy with STI571 and paclitaxel significantly decreased (P < 0.01) tumor incidence, median tumor weight, and lymph node metastasis. Combination treatment with PKI166 and STI571 did not produce any additive effects over either PKI166 or STI571 administered as single agents; however, combination therapy with PKI166, STI571, and paclitaxel produced the greatest improvement (P < 0.001). Specifically, tumor incidence, median tumor weight, and incidence of lymph node metastasis were all further reduced.
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. Control mice and mice treated with paclitaxel alone had severe lysis of the tibia. In mice given oral PKI166 or STI571, lysis of the bone was less pronounced. In mice treated with oral PKI166 and STI571, the lysis of bone was reduced. Mice treated with oral PKI166 and injectable Taxol and mice treated with oral STI571 and injectable Taxol exhibited a significant decrease in bone lysis. In mice given the combination of PKI166, STI571, and paclitaxel, the bone structure was remarkably preserved (Fig. 1)
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. The percentage of cells positive for EGF-R decreased with distance from the nearest bone tissue, from 84 ± 10% (mean ± SD) in tumors within 0.5 mm from the nearest bone fragment to 4% ± 2% in tumors 2.0–2.5 mm from nearest bone fragment (P < 0.001, Mann–Whitney U test; Table 2
). The intensity of staining for EGF-R was significantly decreased in cells growing more than 1.0 mm away from the nearest bone fragment (P < 0.001, Mann-Whitney U test). The percentage of positive cells stained with PDGF-R also correlated with distance from nearest bone fragment-tissue (Table 3)
. The percentage of positive tumor cells growing more than 2 mm away from the nearest bone tissue was significantly decreased (P < 0.001, Mann-Whitney U test). Staining intensity also inversely correlated with distance from the bone tissue (Table 3)
.
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, and PDGF-Rß on endothelial cell surfaces correlated with expression on tumor cells. Endothelial cells expressing EGF-R on their surfaces were mostly located within 20 µm (19.6 ± 8.0 µm) of tumor cells expressing EGF-R on their surfaces (Fig. 3)
. Endothelial cells expressing PDGF-R or PDGF-Rß were located within 36–37 µm (36.6 ± 11.4 and 37.4 ± 10.6 µm, respectively) of tumor cells positive for this receptor.
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, PKI166 and STI571 treatments were specific for cells that expressed the corresponding receptor. Control treatments did not inhibit phosphorylation (activation) of EGF-R or PDGF-Rß. Treatment with PKI166 inhibited phosphorylation only of EGF-R, treatment with STI571 inhibited phosphorylation only of PDGF-Rß, and the combination of PKI166 and STI571 inhibited phosphorylation of both EGF-R and PDGF-Rß (Fig. 4)
. Similar data were obtained with PDGF-R (data not shown).
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. Tumors from control mice had 130 ± 21 PCNA+ cells. Mice in all other treatment groups had significant reductions in the number of PCNA+ cells, with the combination of all three agents producing the greatest reduction (32 ± 12; P < 0.001).
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). The largest increase occurred with the combination of all three agents (83 ± 20 TUNEL+ cells; P < 0.001).
Mean Vessel Density.
In the next set of IHC studies, we determined the mean vessel density in the bone tumors as indicated by the number of CD31+ cells (Table 4)
. There were 55 ± 14 CD31+ endothelial cells in control mice. All of the various treatments produced significant reductions, with the largest decrease (to 12 ± 6) in CD31+ cells occurring in mice given a combination of all three agents (P < 0.001).
Immunofluorescence Double Staining for CD31/PECAM-1 (Endothelial Cells) and TUNEL (Apoptotic Cells).
Using the results of our previous study, we determined whether the combination of all three agents would significantly increase apoptosis in endothelial cells. The CD31/TUNEL fluorescent double-labeling technique (colocalization) revealed a median percentage of apoptotic endothelial cells in control mice of 2% (range, 0–7%). Mice in the treatment groups had median percentages of 7% (range, 0–15%) to 19% (range, 5–26%) apoptotic endothelial cells (Table 4)
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DISCUSSION |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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In the first set of experiments, we determined the relationship of tumor cell phenotype to specific organ microenvironment. By detailed IHC analysis, we demonstrated that the expression of EGF-R and PDGF-R on the surface of human prostate cancer cells directly correlates with their proximity to bone tissue. Tumor cells that proliferate in bone tissue induce inflammatory changes. Inflammation or damage to bone tissue is associated with expression of transforming growth factor-ß, which in turn induces expression of EGF (38, 39, 40)
and PDGF (41
, 42) in osteoblasts and osteoclasts. The production of EGF and PDGF can up-regulate (and activate) the expression of their respective receptors in an autocrine (tumor cells) and paracrine manner (tumor-associated endothelial cells). Indeed, our present study demonstrates that endothelial cells expressing EGF-R on their surface are located within 20 µm of tumor cells expressing EGF/EGF-R. Endothelial cells expressing PDGF-R or -ß are located within 36–37 µm of tumor cells expressing PDGF/PDGF-R. These slight differences may well be due to either the concentration of the ligands or to differences in their diffusion coefficients within solid tissues.
The expression of EGF or PDGF and their receptors has been shown to correlate with progressive growth of human carcinomas of the prostate (43 , 44) , ovary (45 , 46) , lung (47 , 48) , colon (49 , 50) , stomach (51 , 52) , and esophagus (53 , 54) , breast (55 , 56) as well as gliomas (57 , 58) and melanomas (59 , 60) ; therefore, blockade of their signaling pathways has been developed as a new therapeutic strategy (61, 62, 63, 64, 65) . Specifically, blockade of EGF-R signaling has been shown to produce arrest at the G1 restriction point (66 , 67) and to increase apoptosis (68 , 69) . Administration of STI571, which inhibits phosphorylation of PDGF-R, has been shown to inhibit depolymerization of microtubules (70 , 71) .
Whether protein tyrosine kinase inhibitors have specific, restricted activity has been controversial (61) . Our present data directly addressed this question. We report that the systemic administration of PKI166 inhibited phosphorylation of EGF-R but not PDGF-R in tumor cells and endothelial cells, whereas systemic administration of STI571 inhibited phosphorylation of PDGF-R but not EGF-R in tumor cells and endothelial cells. Systemic administration of both agents blocked the phosphorylation of both receptors.
Blockade of EGF-R or PDGF-R can alter phosphatidylinositol 3'-kinase activity, leading to a change in interstitial fluid homeostasis, which results in a reduction of interstitial hypertension with an increase in transcapillary transport (72, 73, 74) . The roles of EGF and PDGF in angiogenesis have been reported for several human tumors (75, 76, 77, 78) , and destruction of the vasculature within neoplasms can produce necrosis of actively growing tumors (79 , 80) . The induction of apoptosis in tumor-associated endothelial cells suggests that this regimen of therapy is directed against tumor vasculature.
Activation of the PDGF-R has been shown to increase expression of Bcl2 and P13K/Akt and to decrease the level of caspase in cells, i.e., increase resistance to apoptosis (81) . Because treatment of cells with STI571 increases their sensitivity to an anticycling drug, e.g., Taxol, the results support the hypothesis that PDGF could be a survival factor for tumor cells and endothelial cells. The proliferation rate of endothelial cells within the vasculature of normal organs is <0.01%, whereas 2–9% of endothelial cells in tumor-associated vessels divide daily (82) . Because the activation of the PDGF-R on tumor-associated endothelial cells can enhance their resistance to anticycling drugs (36) , the administration of protein tyrosine kinase inhibitors such as STI571 can inhibit the resistance of dividing endothelial cells to anticycling drugs, such as paclitaxel. Indeed, the oral administration of PKI166 and STI571 without Taxol completely blocked the phosphorylation of EGF-R and PDGF-R but did not produce therapeutic effects, whereas the combination of PKI166, STI571, and paclitaxel produced the best therapeutic outcome. These results support the rationale that a heterogeneous disease such as cancer should be treated with combined modalities that target both tumor cells and host microenvironment factors, such as unique vasculature and thus support the rationale that cancer (5) should be treated by combination therapy targeting both tumor cells and factors of the host microenvironment, such as the tumor vasculature.
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ACKNOWLEDGMENTS |
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FOOTNOTES |
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The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.
Requests for reprints: Isaiah J. Fidler, Department of Cancer Biology, Unit 173, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030. Phone: (713) 792-8577; Fax: (713) 792-8747; E-mail: ifidler{at}mdanderson.org
Received 12/ 2/03. Revised 3/10/04. Accepted 4/ 9/04.
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Y. Kitadai, T. Sasaki, T. Kuwai, T. Nakamura, C. D. Bucana, and I. J. Fidler Targeting the Expression of Platelet-Derived Growth Factor Receptor by Reactive Stroma Inhibits Growth and Metastasis of Human Colon Carcinoma Am. J. Pathol., December 1, 2006; 169(6): 2054 - 2065. [Abstract] [Full Text] [PDF]
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 S.-J. Kim, H. Uehara, S. Yazici, J. E. Busby, T. Nakamura, J. He, M. Maya, C. Logothetis, P. Mathew, X. Wang, et al. Targeting platelet-derived growth factor receptor on endothelial cells of multidrug-resistant prostate cancer. J Natl Cancer Inst, June 7, 2006; 98(11): 783 - 793. [Abstract] [Full Text] [PDF]
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B. Spankuch, S. Heim, E. Kurunci-Csacsko, C. Lindenau, J. Yuan, M. Kaufmann, and K. Strebhardt Down-regulation of Polo-like Kinase 1 Elevates Drug Sensitivity of Breast Cancer Cells In vitro and In vivo Cancer Res., June 1, 2006; 66(11): 5836 - 5846. [Abstract] [Full Text] [PDF]
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E. Naumova, P. Ubezio, A. Garofalo, P. Borsotti, L. Cassis, E. Riccardi, E. Scanziani, S. A. Eccles, M. R. Bani, and R. Giavazzi The Vascular Targeting Property of Paclitaxel Is Enhanced by SU6668, a Receptor Tyrosine Kinase Inhibitor, Causing Apoptosis of Endothelial Cells and Inhibition of Angiogenesis. Clin. Cancer Res., March 15, 2006; 12(6): 1839 - 1849. [Abstract] [Full Text] [PDF]
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 P. Sun, H. Xiong, T. H. Kim, B. Ren, and Z. Zhang Positive Inter-Regulation between beta-Catenin/T Cell Factor-4 Signaling and Endothelin-1 Signaling Potentiates Proliferation and Survival of Prostate Cancer Cells Mol. Pharmacol., February 1, 2006; 69(2): 520 - 531. [Abstract] [Full Text] [PDF]
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 M. Mimeault and S. K. Batra Recent advances on multiple tumorigenic cascades involved in prostatic cancer progression and targeting therapies Carcinogenesis, January 1, 2006; 27(1): 1 - 22. [Abstract] [Full Text] [PDF]
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T. Zhang, H.-C. Sun, Y. Xu, K.-Z. Zhang, L. Wang, L.-X. Qin, W.-Z. Wu, Y.-K. Liu, S.-L. Ye, and Z.-Y. Tang Overexpression of Platelet-Derived Growth Factor Receptor {alpha} in Endothelial Cells of Hepatocellular Carcinoma Associated with High Metastatic Potential Clin. Cancer Res., December 15, 2005; 11(24): 8557 - 8563. [Abstract] [Full Text] [PDF]
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 S. M. Pulukuri, C. S. Gondi, S. S. Lakka, A. Jutla, N. Estes, M. Gujrati, and J. S. Rao RNA Interference-directed Knockdown of Urokinase Plasminogen Activator and Urokinase Plasminogen Activator Receptor Inhibits Prostate Cancer Cell Invasion, Survival, and Tumorigenicity in Vivo J. Biol. Chem., October 28, 2005; 280(43): 36529 - 36540. [Abstract] [Full Text] [PDF]
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 C. V. Ustach and H.-R. C. Kim Platelet-Derived Growth Factor D Is Activated by Urokinase Plasminogen Activator in Prostate Carcinoma Cells Mol. Cell. Biol., July 15, 2005; 25(14): 6279 - 6288. [Abstract] [Full Text] [PDF]
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M. N. Younes, O. G. Yigitbasi, Y. W. Park, S.-J. Kim, S. A. Jasser, V. S. Hawthorne, Y. D. Yazici, M. Mandal, B. N. Bekele, C. D. Bucana, et al. Antivascular Therapy of Human Follicular Thyroid Cancer Experimental Bone Metastasis by Blockade of Epidermal Growth Factor Receptor and Vascular Growth Factor Receptor Phosphorylation Cancer Res., June 1, 2005; 65(11): 4716 - 4727. [Abstract] [Full Text] [PDF]
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G. J. Kelloff, J. M. Hoffman, B. Johnson, H. I. Scher, B. A. Siegel, E. Y. Cheng, B. D. Cheson, J. O'Shaughnessy, K. Z. Guyton, D. A. Mankoff, et al. Progress and Promise of FDG-PET Imaging for Cancer Patient Management and Oncologic Drug Development Clin. Cancer Res., April 15, 2005; 11(8): 2785 - 2808. [Abstract] [Full Text] [PDF]
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 R. K. Jain Normalization of Tumor Vasculature: An Emerging Concept in Antiangiogenic Therapy Science, January 7, 2005; 307(5706): 58 - 62. [Abstract] [Full Text] [PDF]
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