Met-Independent Hepatocyte Growth Factor-mediated regulation of cell adhesion in human prostate cancer cells
© Tate et al. 2006
Received: 21 April 2006
Accepted: 25 July 2006
Published: 25 July 2006
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© Tate et al. 2006
Received: 21 April 2006
Accepted: 25 July 2006
Published: 25 July 2006
Prostate cancer cells communicate reciprocally with the stromal cells surrounding them, inside the prostate, and after metastasis, within the bone. Each tissue secretes factors for interpretation by the other. One stromally-derived factor, Hepatocyte Growth Factor (HGF), was found twenty years ago to regulate invasion and growth of carcinoma cells. Working with the LNCaP prostate cancer progression model, we found that these cells could respond to HGF stimulation, even in the absence of Met, the only known HGF receptor. The new HGF binding partner we find on the cell surface may help to clarify conflicts in the past literature about Met expression and HGF response in cancer cells.
We searched for Met or any HGF binding partner on the cells of the PC3 and LNCaP prostate cancer cell models, using HGF immobilized on agarose beads. By using mass spectrometry analyses and sequencing we have identified nucleolin protein as a novel HGF binding partner. Antibodies against nucleolin (or HGF) were able to ameliorate the stimulatory effects of HGF on met-negative prostate cancer cells. Western blots, RT-PCR, and immunohistochemistry were used to assess nucleolin levels during prostate cancer progression in both LNCaP and PC3 models.
We have identified HGF as a major signaling component of prostate stromal-conditioned media (SCM) and have implicated the protein nucleolin in HGF signal reception by the LNCaP model prostate cancer cells. Antibodies that silence either HGF (in SCM) or nucleolin (on the cell surfaces) eliminate the adhesion-stimulatory effects of the SCM. Likewise, addition of purified HGF to control media mimics the action of SCM. C4-2, an LNCaP lineage-derived, androgen-independent human prostate cancer cell line, responds to HGF in a concentration-dependent manner by increasing its adhesion and reducing its migration on laminin substratum. These HGF effects are not due to shifts in the expression levels of laminin-binding integrins, nor can they be linked to expression of the known HGF receptor Met, as neither LNCaP nor clonally-derived C4-2 sub-line contain any detectable Met protein. Even in the absence of Met, small GTPases are activated, linking HGF stimulation to membrane protrusion and integrin activation. Membrane-localized nucelolin levels increase during cancer progression, as modeled by both the PC3 and LNCaP prostate cancer progression cell lines.
We propose that cell surface localized nucleolin protein may function in these cells as a novel HGF receptor. Membrane localized nucleolin binds heparin-bound growth factors (including HGF) and appears upregulated during prostate cancer progression. Antibodies against nucleolin are able to ameliorate the stimulatory effects of HGF on met-negative prostate cancer cells. HGF-nucleolin interactions could be partially responsible for the complexity of HGF responses and met expression reported in the literature.
In the prostate, cell-matrix adhesion, cell motility and invasive behaviors are regulated by an interplay of signals between the epithelial cells and surrounding stromal cells [1–6]. Signal reciprocity allows prostate stromal fibroblasts to control epithelial cell proliferation , while epithelial cells control such processes as stromal smooth muscle maturation . When signal reception or intercellular signal interpretation alter adhesion-based behaviors, tumor formation and cancer progression can result. Cancer cells are known to optimize their stromal growth environments [6, 9, 10]. Indeed, the list of factors involved in bi-directional epithelial-stromal cell interactions is long, with representatives from many growth factor families, and includes Hepatocyte Growth Factor (HGF) , a subject of this study.
HGF regulates cell behaviors in organ development, tissue regeneration and cancer [12–15]. HGF's source, reception by, and effects on prostate cancer cells are discussed in many review articles, as is the Met protein, the only known cell surface receptor for HGF [16–21]. Once secreted, it is likely that most HGF is immobilized within the extracellular matrix of the stromal cells by binding heparan sulfate proteoglycans [22–26]. HGF encounters the Met receptor in the basal cells of the prostatic ducts and acini, and in low numbers on the luminal cells of the prostatic ducts and stromal smooth muscle cells [27–29]. During puberty, developing branches within the prostate show high concentrations of Met in ductal tips and respond to stromal stimulation [30, 31], a hallmark for HGF/Met-mediated activity. Met signaling is also critical for ductal system formation in kidney, mammary gland, liver, pancreas and lung [32–35]. High levels of Met expression correlate with increased cell movement, and indeed metastasis is linked to the uncontrolled branching seen at earlier stages of prostate disease [36, 37]. Furthermore, dysfunctional and high Met expression is found in a variety of human cancers [38–41, 21, 42, 43] and correlates with some metastasis in animals [44, 45].
Met expression levels during cancer progression remain somewhat confusing, and conflicting reports are common in the published literature. Met expression does appear to increase during prostate disease progression, but the correlation of Met expression with Gleason grade has been tenuous. Approximately 50% of localized cancers (and even more metastatic cancers) express Met [28, 29, 43, 46]. In one study, Met elevations were found in 84% of localized prostate cancers , but Humphry et al.  reported that 45% of 108 cases show no correlation between disease progression and Met expression; further, the receptors in this study were localized by staining to both the cell surface and the cytoplasm. There are two other reports [43, 46] of a clear increase in Met expression correlating with higher grades of adenocarcinomas (with metastases expressing more Met in bone than lymph node ), but no correlation between Met expression and disease progression, in a 5-year follow up period . Not only are Met expression profiles not consistently linked to disease outcome [21, 42, 43], but Met expression is also confounding in the commonly-studied in vitro model systems. Met expression is higher in some metastatic prostate cancer samples compared to less-progressed cells [47–49]; for example, met RNA and protein levels are elevated in the androgen-independent cell lines DU145, PC3 and PC3M, compared to androgen-dependent LNCaP cells [27, 28, 43, 50–54]. But, this correlation does not hold within the LNCaP-derived cell lines themselves, since neither parental LNCaP nor its lineage-derived, androgen-independent variant C4-2 actually express the HGF receptor Met. Thus, although both HGF and Met are arguably very important for prostate cancer progression, the details of their functions remain far from clear.
HGF likely acts through multiple isoforms, receptors and/or signaling cascades to bring about a variety of cell responses. Also called Scatter Factor (SF), HGF stimulates motility in both endothelial and metastatic epithelial cancers [53, 55, 64, 65], similar to the invasion-promoting factor plasminogen [19, 66, 67]. Not surprisingly, HGF levels affect the function of prostate integrins [53, 55], molecules involved in cell adhesion and motility. In this study, we have focused upon HGF's regulation of cell adhesive behaviors in a collection of human prostate cancer cell lines, including cell lines that do not express the Met receptor for HGF, but nonetheless exhibit distinct, concentration-dependent responses to the growth factor and to stromal-conditioned media (SCM). We previously reported that SCM increased cell spreading in the metastatic prostate cancer cell line C4-2, while having little effect on attachment of the lineage-related, non-metastatic LNCaP cell line . We have now extended this work, further identifying HGF as responsible for the effects of SCM and describing HGF dose-dependent effects on the adhesive behaviors of these cell lines. In addition, we have especially searched for the responsible HGF receptors in these cells, as we and others have found both cell lines to lack the met protein, the one known HGF receptor ( and this study). Here, we introduce the protein nucleolin as a novel HGF binding partner in prostate cancer cells. Nucleolin, an abundant nuclear protein [69, 70], is also found on the cell surface, where it has been shown to interact with heparin-bound growth factors [71–73], and where it functions as a cell surface receptor and a shuttle protein for nuclear import [72, 74–76]. Significantly, nucleolin is also currently the focus of a phase II clinical trial as a cancer therapy target [77, 78].
Prostate epithelial and stromal cell lines were maintained in T-media with 5% fetal bovine serum, at 37°C with 5% CO2. Primary cultures of prostate stromal cells were derived from the tissue surrounding prostatic adenocarcinomas, as described by Ozen et al. . Conditioned media were prepared by adding fresh media without serum when cells reached 80% confluence and removing it 48 h later. For signaling assays, cells were starved in RPMI-1640 phenol red-free medium (Life Technologies, Inc.) un-supplemented with serum. Laminin-1 (a kind gift of Roy Ogle at the University of Virginia) was purified from Engelbreth-Holme-Swarm (EHS) tumors according to the method of Davis et al., based on the protocol of Kleinman et al. [80, 81]. Hepatocyte Growth Factor (HGF) and all other chemicals were purchased from Sigma (St. Louis, MO). Anti-FAK and HGF antibodies were from Sigma (St. Louis, MO) and Santa Cruz Biotechnology (Santa Cruz, CA). Antibodies to nucleolin were purchased from Santa Cruz Biotechnology or received as a gift from Dr. Deng at Pittsburgh Medical Center. Met antibodies, as well as cdc-42 and Rac immuno-precipitation reagent were purchased from both UpState Biotechnology (Lake Placid, NY) and Transduction Laboratories (Lexington, KY). Phospho-tyrosine antibodies were from Transduction Laboratories (Lexington, KY). Phospho-Akt (Ser 473) antibody and Akt antibody were purchased from Cell Signaling Technology Inc. (Beverly, MA). Anti-β actin antibody was from Abcam Inc. (Cambridge, MA). All secondary-conjugated antibodies were from Jackson Immunochemicals (West Grove, PA).
Total cellular RNA was isolated with RNA-STAT (BioTec-X, Houston, TX). 5 μg of RNA was reverse transcribed using the OmniScript RT Kit (Qiagen, Inc., Valencia, CA). The primers used for met amplification were as follow: F-met 5'-GGTTGCTGATTTTGGTCAT-3' and B-met 5'-TTCGGGTTGTGGAGTCTT-3'.
Cells were allowed to grow to 80% confluency and then serum starved for 48 hours. Plates were rinsed twice in ice-cold phosphate buffered saline (PBS) and solubilized in lysis buffer (1% NP-40, 50 mM Tris-HCl, 150 mM NaCl, 2 mM EDTA, 50 mg/ml leupeptin, 0.5% aprotinin, 1 mM sodium orthovanadate, 1 mM PMSF). Insoluble material was removed by centrifugation for 30 min at 10,000 × g at 4°C. Protein concentration was determined by BRC assay (BioRad, Hercules, CA). 1–2 mg of protein was used for each immunoprecipitation condition. Antibodies were incubated with the cell lysate for 2 hrs at 4°C, and an additional 30 min with Protein A/G-sepharose beads (Sigma). The beads were washed three times with lysis buffer and resuspended in SDS-PAGE loading buffer. Samples were resolved on gradient (4–12%) or 10% polyacrylamide gels (Novex) and electro-blotted. After transfer, the filters were blocked in BSA (5%) overnight at 4°C. Filters were incubated with primary antibodies for 1 hr at room temperature. Membranes were then probed for 1 hr with peroxidase-conjugated secondary antibody (diluted 1:5000; Jackson Immunoresearch Labs, Bar Harbor, ME) and the proteins were detected with Enhanced Chemi-Luminescence (ECL)(Amersham Biosciences, Little Chalfont, England).
Attachment assays were performed as previously described in Edlund et al., and Vafa et al., [68, 82]. Cell lines were grown to confluence, trypsinized, and re-plated (1:8) on tissue culture dishes, where they were allowed to grow for another two days before being lifted after a brief treatment with 10 mM EDTA, 20 mM Hepes buffer in T-media. After neutralizing the EDTA with CaCl2 and MgSO4, the cells were washed with T-media containing 0.1% BSA. Cells were placed on laminin1-coated dishes, allowed to adhere for 30 to 90 min with or without addition of either HGF or function blocking integrin antibodies, and then fixed in para-formaldehyde (3.8%). The percentage of spread cells was scored for each cell line, based on cell membrane protrusion (lamellipodia and/or filopodia), and all values were normalized to control cells treated identically except for being subjected to conditioned media or growth factors. This normalization step was necessary because of the differences in speed of attachment between the cell lines. Cell growth was quantified using MTT [83, 84].
ELISAs were performed as suggested in Pharmigen Research Products Catalog, 1999. Briefly, rabbit anti-human HGF antibodies were diluted to a concentration of 1 μg/ml in 0.1 M Na2HPO4 and 0.1 M NaH2PO, pH 9.0. Wells of a 96 well ELISA plate (Costar) were filled with 50 μl, sealed with parafilm, and incubated overnight at 4°C. Plates were then brought to room temperature and antibodies captured and removed. 200 μl of blocking buffer (10% FBS in PBS) was added to each well and the plate incubated at room temperature for 2 hours. The plate was washed three times with PBS/Tween 20 (0.05%) (Sigma). 100 μl of standard or sample diluted in blocking buffer/Tween 20 (0.05%) was added to each plate, which was then sealed with parafilm and incubated at 4°C overnight. The following day, the plate was washed four times with PBS/Tween. 100 ul of the detection antibody, Goat anti-human HGF antibody (Sigma), diluted to a concentration of 0.01 μg/ml in blocking buffer/Tween 20, was added to each well. After one hour incubation at room temperature, and 4 washes with PBS/Tween 20, 100 μl of avidin-horseradish peroxidase conjugated mouse anti-goat IgG (Jackson ImmunoReseach) diluted 1:1000 in blocking buffer/Tween 20 was added to each well. After 30 minutes incubation at room temperature and five washes with PBS/Tween 20, 200 μl of Sigma Fast OPD solution (Sigma) was added to each well. After 20 minutes, the plate was read at a wavelength of 405 nm using a microplate reader (Molecular Devices, Sunnyvale, CA). Data were analyzed using the Molecular Devices SOFTmax program.
Cell migration assays were preformed according to product instructions (CSM Inc. Phoenix, AZ). Chilled cell manifolds were placed on Teflon-printed, precoated microscope slides, subdivided into 10 wells, and filled with ice-cold media. One μl of cell suspension (2500 cells) was added to each chamber and allowed to precipitate by gravity and adhere to the coverslip. After two hours, the manifold was moved to a cell incubator (37°C under 5% CO2) and allowed to reach growth temperature for 4 hours, at which point the cell sedimentation manifold was removed and the coverslip submerged in media, to which HGF was added. The area covered by cells was recorded at 2 hrs and subsequently every 24 hours. The 2 hr area was used as a reference point for all succeeding measurements. Results are presented as increases relative to this area.
The HGF and major co-immunoprecipitated product from C4-2 cell lysates were excised from the gel and transferred to a siliconized tube, washed and destained in 50% methanol overnight. The gel pieces were dehydrated in aceto-nitrile, rehydrated in 10 mM dithiothreitol (DTT) in 0.1 M ammonium bicarbonate, and reduced at room temperature for 30 minutes. The DTT solution was removed and the samples alkylated in 50 mM iodoacetamide, in 0.1 M ammonium bicarbonate, for 30 minutes at room temperature. Samples were then dehydrated again in aceto-nitrile, rehydrated in 0.1 M ammonium bicarbonate, dehydrated in aceto-nitrile and completely dried by vacuum centrifugation. Finally, samples were rehydrated for 10 minutes in 20 ng/ml trypsin in 50 mM ammonium bicarbonate on ice. Any excess trypsin solution was removed, and 50 mM ammonium bicarbonate added. Samples were digested overnight at 37°C and the sequences of generated peptides were identified by mass specectrometry.
All cells were lysed in ice-cold lysis buffer (20 mMTris PH7.4, 40 mM NaCl, 20 mM beta-glycerophosphate, 2 mM EGTA, 1 mM sodium orthovanadate, 2 mM DTT, 2 mM PMSF, 1μg/ml aprotinin, and 1μg/ml aprotinin). The Map kinase assay was done with an assay kit (Upstate, Lake Placid, NY). The kinase reaction was started by addition of kinase reaction buffer that contains 2 mg/ml dephosphorylated myelin basic protein for each substrate, 20 mM MOPS (pH 7.2), 25 mM beta-Glycerophosphate, 5 mM EGTA, 0.4 mM MnCl2, 1 mM sodium orthovanadate, 1 mM dithiothreitol, 75 mM MgCl2, and 500 μM ATP. To prevent effects from other unknown kinases in the lysate, 20 μM PKC inhibitor peptide, 2 μM PKA inhibitor peptide, and 20 mM R24571 compound were added to the kinase reaction buffer. The reaction was incubated for 20 min at 30°C, terminated by the addition of the LDS sample buffer and loaded as aliquots for SDS-PAGE and immunoblot analyses. Membrane enriched fractions were purified as previously described .
After centrifugation for 15 min at 15000 rpm in 4°C, the lysate supernatant was collected. Protein concentration was determined by BRC assay (BioRad, Hercules, CA). Immunoblotting was performed using the NOVEX (Invitrogen, Carlsbad, CA) system. Briefly, 7.5 μg of cell extracts and Erk kinase assay products were separated on 4–12% Tris glycine PAGE gels and transferred onto a PVDF membrane (Immoblin-P, Millipore, Billerica, MA). The membrane was blocked 1 h at room temperature with TBST blocking buffer [50 mM Tris-HCl (pH 8.0), 150 mM NaCl, 0.05% Tween 20, and 5% nonfat milk]. The membrane was incubated for 1 hr at room temperature with primary anti-phosph MBP polyclonal antibody, anti-Erk 1,2 antibody, anti-PKB antibody, and anti-phosph PKB antibody (Ser 473) in PBSN blocking buffer. A secondary antibody (horseradish peroxidase-anti-rabbit or mouse antibody) (Amersham Bioscience, Inc., Piscataway, NJ) at a 1:5000 dilution was used in PBSN blocking buffer and incubated for 1 hr at room temperature. ECL plus (Amersham Bioscience, Inc.) reagent was used for detection.
Results were analyzed for statistical significance using the nonparametric Mann-Whitney U test, with significance at P < 0.05.
ELISA measurements of HGF concentrations in stromal-conditioned media from normal prostate stromal cells after 24 hr. culture
Using RT-PCR, we assess met expression levels in prostate cancer cell lines of different metastatic potential (LNCaP, C4-2, PC3 and DU145). Met receptor transcript (262 bp) was present in DU145, PC3, PC3M and HeLa cells, but absent or at very low levels in both LNCaP and C4-2 cells (Figure 4A). These results were further confirmed by Western blot analyses. Doublets of c-Met were observed, with similar results for both the N-terminal and C-terminal Met antibodies, used to check for possible Met isoforms differing in their cytoplasmic tails (Figure 4B and 4C).
24 peptides were sequenced from cell lysates, based on co-immunoprecipitation with purified HGF protein. All peptides showed 100% sequence homology to previously cloned nucleolin (NCBI#4885511). Numbers within the Table refer to the peptide's location within the published nucleolin sequence.
We have used prostate cancer cell lines and stromal-conditioned media to study the regulatory interplay between prostate epithelial and stromal cells during prostate cancer progression, and have now begun to tease apart the relationships between stromally-derived HGF signal, Met signal reception, integrin-based cell adhesive responses, and a new HGF binding partner, the nucleolin protein. We report here: 1) that it is the HGF in stromal-conditioned media that affects C4-2 metastatic prostate cancer cell adhesive behavior, 2) that this action is through the integrins, and 3) that the dose-dependent response of Met-negative C4-2 cells to HGF treatment can be abolished through the addition of antibodies against the nucleolin protein.
A Met-independent pathway acting in the absence of Met and/or alongside Met could increase the variety of possible cell responses to HGF. Classically, the binding of HGF to Met induces receptor dimerization and phosphorylation of two conserved tyrosine sites; when these sites are mutated, mice show similar phenotypes to those with HGF or Met knockouts . But C4-2 cells, which lack this signaling pair, could be revealing spreading behaviors due to low-affinity HGF sites that allow response to higher levels of HGF (compared to Met-expressing PC3 cells; Figure 2). Past research on HGF affinity has identified some binding sites in hepatocytes with 10-fold lower affinity . HGF interactions with proteoglycans and CD44 is linked to enhanced Met signaling and possible Met autophosphorylation [91, 92]. Pollack et al.  suggest that in Madin Darby canine kidney (MDCK) cells, low-affinity binding of HGF in the presence of the Met receptor may alter downstream responses. Thus, we are certainly not the first to suggest either additional HGF receptors, or HGF binding to heparin and oligosaccharide signaling systems [94, 95]. Our study is unique, however, in our identification of the HGF binding partner nucleolin.
Nucleolin, originally called C23 , was first characterized as an abundant nuclear protein with a role in ribosome biogenesis [69, 70]. Because nucleolin synthesis correlates positively with cell growth, the especially high expression of nucleolin in tumor cells is not surprising . Nucleolin is further a major regulatory and phosphorylation target following androgen treatment [98, 99]. Nucleolin's in vivo localization to the cell surface in aggressive tumor cells [77, 78, 99, 100] agrees with our in vitro finding of membrane localization in both LNCaP and PC3 progression model cell lines (Figure 7). This membrane localization has recently generated interest in the use of nucleolin as a tumor marker and therapeutic target. A nucleolin functional inhibitor called AGRO100 (a guanine-rich oligonucletide) has been successful in Phase I clinical trials, and Phase II trials are underway [77, 78, 101]. Further evidence of nucleolin's role in cancer progression comes from our unrelated, in vivo bio-panning study. While bio-panning with a 12-mer peptide phage-display library, a peptide (designated L13) was found to bind with high specificity to murine bone marrow. When human bone marrow endothelial cell lysates were passed across an L13 column, the major species eluted was found to be nucleolin ( and unpublished observations). Indeed, a tumor homing peptide, F3, that binds specifically to tumor endothelial cells was described by Christian et al.  as interacting directly with nucleolin. Together, there is now clear evidence of nucleolin's involvement in cancer cell behavior and response to HGF, although this protein's direct and/or indirect functions remain to be discovered.
Nucleolin is named for the fact that it makes up as much as 10% of the total nucleolar protein , but it also functions as a shuttle protein between the cytoplasm and the nucleus, is found in clusters associated with the actin cytoskeleton [104–106], and is sensitive to cytochalasin D . Nucleolin is present on the cell surfaces of a variety of cell types [71, 107, 108], and surface-expressed nucleolin appears to interact with an array of other proteins, including viral proteins during infections [109, 110], βFGF and Midkine , and laminin-1 [112, 113].
A three-way interaction between nucleolin, HGF, and integrins is suggested by our ability, in short-term assays, to inhibit HGF's cell spreading effects using anti-nucleolin antibodies (Figure 6D); Nucleolin inhibition, alone, however, in the absence of HGF stimulation, does not alter C4-2 laminin adhesion (data not shown). Also, nucleolin by itself is not able to sustain laminin adhesion, as we were able to completely block cell spreading under stimulated and un-stimulated conditions, using function-blocking antibodies to either β1 or α6 integrin (data not shown). Yu et al.  studied the cellular distribution of nucleolin after stimulation with ECM proteins, and report that, following laminin stimulation, nucleolin translocates from the cytoplasm to the nucleus and stimulates cell proliferation. Following HGF stimulation, we do not detect changes in laminin-binding integrin expression profiles (data not shown), but we have previously seen changes in integrin function (not expression) in these same prostate cells . Also possible is the movement of additional nucleolin protein to the cell surface, providing direct increase in laminin adhesion [72, 112, 114]. Nucleolin may function as a generic GF-HS binding receptor, linking HGF and integrin function. Like syndecan, nucleolin has been found to bind HGF's heparin-binding domain, thereby sequestering HGF on the cell surface. In our studies, nucleolin does not co-immunoprecipitate with other heparin-binding growth factors (data not shown), but HGF-Nucleolin interactions do respond to heparin competition (data not shown). We are currently searching for other components in nucleolin-HGF interactions using BIAcore. The findings we report here, together with the nucleolin-focused independent clinical trial underway [77, 78], introduce nucleolin as an attractive target for therapeutic regulation of prostate cancer, although the details of its position in cancer cell HGF signaling remain to be found.
We sought to begin placing nucleolin in or beside well-described HGF-met signaling pathways affecting integrin-based cell behaviors. Cell spreading and membrane ruffling behaviors seen in C4-2's met-independent HGF cell responses led us to look first at small GTPases (Figure 5). We found that Rac is activated by HGF treatment of met-negative C4-2 cells (Figure 5D,E). Rho, Rac and cdc42 are part of the Ras small GTPase superfamily, and play key roles in regulating cell shape, contraction, adhesion, motility, and proliferation [115–117]. Members of this GTPase superfamily are also known molecular triggers to response cascades following growth factor stimulation ( and references within). Rac, in particular is a regulator of the superoxide generating NADPH oxidase in phagocytes . The production of reactive oxygen species (ROS) mediates activation of NF-κB-dependent gene expression, essential for tumorigenesis and metastasis.
We have found evidence that HGF secreted by prostate stromal cells regulates prostate cancer cell adhesive behaviors, even in cells that lack Met, the one known HGF receptor. Further, we report that the nucleolin protein expressed on the surfaces of these prostate cancer cells (in increasing levels during disease progression) is involved in the HGF regulatory interplay between stromal and epithelial cells within the prostate, and possibly also at sites of metastasis. A family of drugs targeting the nucleolin protein are being developed for cancer therapy; these AGRO100 drugs (named for G uanine- R ich O ligonucleotides) reportedly acted against cultured cell lines from several different cancers and successfully stabilized disease in six of nine patients in phase I clinical trials. They are now in phase II trials [77, 78]. We have independently identified nucleolin protein as having a role in cancer progression, and have now linked nucleolin's function to prostate cancer cell reception of Hepatocyte Growth Factor (HGF) and integrin-based cell adhesive behaviors.
Abbreviations are defined in the text
This work was supported by grants to ME from the Georgia Cancer Coalition and NIH CA098912 and CA120001. Also grants to LWK from NIH grant CA-76620, and the Kluge and CaPCURE Foundations
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