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Tumor Biology |
Cancer Metastasis Laboratory, University of Queensland and the Queensland Institute of Medical Research, Brisbane, Queensland, 4029 [A. P. B., J. A. R., T. M. A.]; Department of Surgery, Princess Alexandra Hospital, Woolloongabba, Queensland, 4102 [A. P. B., J. F., D. C. G.]; and Department of Pathology, University of Queensland, Brisbane, Queensland, 4029 [M. D. W.] Australia
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ABSTRACT |
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INTRODUCTION |
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Here we have tested the functional role of the full-length CD44v2-10 isoform in tumor growth and metastasis. We developed a novel model of spontaneous metastasis using SKHep1 cells, a human hepatocellular cancer cell line that constitutively expresses only CD44s and not CD44 variant isoforms. The results show, for the first time, that the full-length CD44 splice variant can confer a metastatic phenotype on a human cancer and that the v3 HS attachment site is critical for this metastatic phenotype.
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MATERIALS AND METHODS |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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HS stub") 3G10 were obtained from Seikagaku America.
Cell Culture.
SKHep1 (American Type Culture Collection; HTB52) is a human hepatocellular carcinoma cell line, and HTM29 is a metastatic derivative of HT29 cells (American Type Culture Collection; HTB38) that was obtained from Dr. Elise Kohn, NIH, Bethesda, MD. Cell lines were maintained in RPMI 1640 supplemented with 10% FCS, 2 mM glutamate, 25 mM HEPES, 60 mg/ml penicillin G, 100 mg/ml streptomycin sulfate, and 1 mM sodium pyruvate in a 5% CO2 and 95% air atmosphere at 37°C. Cell viability was determined by trypan blue dye exclusion.
DNA Constructs.
A neomycin-resistant eukaryotic expression plasmid containing the human EF-1
promoter (pEFDNA3) was generated by inserting a 1.2-kb blunt-ended HindIII DNA fragment encoding the EF-1 promoter from pEFBOS-H3 (derived from Ref. 13
) into the blunt-ended HindIII/NruI restriction enzyme site of pcDNA3 (Invitrogen), thereby replacing the existing cytomegalovirus and T7 promoter regions. The 2270-bp cDNA encoding CD44v2-10 was isolated from a human HT29 cDNA library in pCDM8 and cloned into the EcoRV site of pEFDNA3. This construct was designated pcDNA3/CD44v2-10.
The CD44 signal peptide (encoded by exon 1) was replaced with the CD33 signal peptide, which has been shown previously to improve the efficiency of CD44v-Rg expression and is cleaved after secretion (14) . To replace the CD44 signal sequence (exon 1) with the CD33 signal sequence, a 391-bp DNA fragment encoding the CD33 signal sequence was amplified by PCR from pCD44v3–10-Ig (14) . The forward amplification primer was CD33F: 5'-TAGGTACCTAGAATTCATAAGCTTATCCATTGTGCTCTAAAGC-3', which contains the restriction enzyme sites KpnI, EcoRI, and HindIII (italicized). The reverse amplification primer was CD44BamR: 5'-GGTGGATCCGGGGAATCACCACATGCCCTTC-3', containing a BamHI restriction enzyme site. PCR was performed using PfuTurbo DNA Polymerase (Stratagene, La Jolla, CA), and the reaction was incubated at 96°C for 1 min, 94°C for 1 min, 60°C for 1 min, and 72°C for 1 min, cycled 30 times. The amplified DNA was cloned into the KpnI/BamHI site of pCD44v2-10/cDNA3 generating pCD44v2-10/EFDNA3.
The CD44v2-10HSM was generated by in vitro site-directed mutagenesis using the QuickChange Site-Directed Mutagenesis kit (Stratagene), according to the manufacturer’s instructions. T
G mutations at nucleotides 862 and 868 were introduced, altering the Ser-Gly-Ser-Gly HS attachment motif in CD44v3 to Ala-Gly-Ala-Gly. The synthesized oligonucleotides used were 7FHSM: 5'-CCTCAGTTTTGCTGGAGCAGGCATTGATG and 7RHSM: 5'-CATCAATGCCTGCTCCAGCAAAACTGAGG (mutant nucleotides are italicized).
PCR reactions were carried out following the manufacturer’s instructions, and the resultant mutant clones were verified by DNA sequence analysis.
Generation of Stable Transfectants.
SKHep1 cells (2 x 106) in log phase were combined with 20 µg of purified pCD44v2-10/EFDNA3, pCD44v2-10HSM/EFDNA3, or pEFDNA3 vector alone, and electroporated at 250 mV and 960 µF. Clones resistant to 0.8 mg/ml G418 (Life Technologies, Inc., Gaithersburg, MD) were isolated and analyzed for CD44s and CD44v expression by FACS analyses. Two independent lines demonstrating the highest levels of CD44v surface expression were selected for additional experiments.
Reverse Transcription-PCR.
First-strand cDNA synthesis was performed using 1 µg DNase-free total RNA from SKHep1 cells in the presence of 0.5 µl (2 mg) oligo(dT)12–18 and 4 µl of 5x reverse transcriptase buffer [50 mm Tris-HCl (pH 8.3), 10 mm MgCl2, and 2 µl DTT (0.1 m)], 1 µl deoxynucleoside triphosphates (10 mm), 0.5 µl RNasin (40 units/µl), and 1 µl (200 units) Moloney murine leukemia virus RNase H- reverse transcriptase. PCR amplification of the cDNA was performed in a total volume of 50 µl containing 1 µl of the first-strand cDNA synthesis reaction, 5 µl of 10x Taq polymerase buffer [25 mM TAPS (tris-hydroxymethyl-methyl-amino-propane-sulfonic acid), sodium salt (pH 9.3), and 50 mM KCl], 1 µl deoxynucleoside triphosphates (10 mM), 4 µl MgCl2 (25 mM), 2 µl (20 pmol) of forward and reverse primers, and 0.5 µl (2.5 units) Amplitaq Gold Taq polymerase. The primers used were: 3F 5'-TCCCAGTATGACACATATTGC-3' and 17R 5'-CCAAGATGATCAGCCATTCTGG-3'. The PCR amplification conditions were: 94°C for 30 s, 45°C for 1 min, 72°C for 2 min, cycled 4 times; then 94°C for 30 s, 55°C for 30 s, 72°C for 2 min, cycled 30 times; with a final extension time of 7 min.
FACS Analysis.
Cells were deattached and then washed in cold IF Buffer (0.5% BSA, BSA, and 0.1% NaN3 in PBS). The cells were then incubated with the primary antibody (2–20 µg/ml) in 50 µl of IF Buffer for 30 min to 16 h at 4°C, washed, and incubated with the secondary antibody (1:100 dilution in 50 µl of IF Buffer) for 30 min at 4°C. Where biotinylated secondary antibodies were used, the cells were subsequently incubated with SP-FITC 18 µg/ml in 50 µl of IF Buffer and washed three times in IF Buffer. The cells were analyzed by using a FACScan (Becton Dickinson, Franklin Lakes, NJ). For growth factor binding, cells were incubated with the recombinant HS-binding growth factors (as indicated) for 1 h at 4°C before incubation with antibody and analysis by FACS.
Western Blot Analysis.
For detection of HS attachment to CD44v3, cells (2 x 106) were incubated in the presence or absence of 25 milliunits of heparitinase (Seikagaku, Tokyo, Japan) in PBS at 37°C for 3 h. Cells were solubilized in ice-cold lysis buffer containing 50 mM Tris (pH 7.4), 150 mM NaCl, 1 mM EDTA, 1 mM EGTA, 0.2% Triton X-100, 0.3% NP40, 0.1% deoxycholate, 10 µg/ml leupeptin, 10 µg/ml aprotinin (Roche Diagnostics, Mannheim, Germany), and 1 mM 4-(2-aminoethyl) benzenesulfonylfluoride (Calbiochem, Los Angeles, CA). Insoluble material was removed by centrifugation at 1 x 104 x g at 4°C for 20 min, and the supernatants diluted in Laemmli sample buffer, boiled for 5 min, and subjected to SDS-PAGE. Blots were stained with mAb 3G10 followed by horseradish peroxidase-linked rabbit antimouse immunoglobulin (Amersham Life Science, Little Chalfont, Buckinghamshire, United Kingdom), detected by enhanced chemiluminescence (Amersham Life Science), according to the manufacturer’s instructions.
Cellular Adhesion to Immobilized Hyaluronan and bFGF.
Flat-bottomed 96-well tissue culture plates (Costar, Corning, NY) were coated with potassium hyaluronate (5 mg/ml), and SKHep1 cell adhesion was determined as described previously (8)
. For experiments where potassium hyaluronan was used to compete for adhesion, the cells were preincubated with potassium hyaluronan at the concentrations indicated for 30 min at room temperature. Nontissue culture-treated polyvinylchloride 96-well plates were coated with 50 µl of bFGF 313 ng/ml as described (15)
. Eighty µl (2 x 105) of cells were added to each well and the 96-well plate incubated at 37°C for 60 min. The bound cells were stained with crystal violet, lysed, and the absorbance at 570 nm measured (Microtiter Plate Reader Model 3550; Bio-Rad, Hercules, CA).
In Vitro Cell Proliferation Assays.
Cells were seeded into 96-well tissue culture plates (Costar) in triplicate at a density of 2 x 103 cells/well, and proliferation monitored daily over a period of 3 days. Proliferation by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay was performed as described previously (8)
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In Vivo Metastasis Assay.
Five-week-old severe combined immune deficient mice (C.B-17-scid) were obtained from the Australian Resource Centre, Perth, Western Australia, Australia. Mice were anesthetized by i.p. injection of 7 µg of fentanyl and 125 µg of midazolam in 100 µl of sterile water. One x 106 viable cells (SKHep1, SKHep1/NEO, SKHep1/CD44v2-10 clone#7, SKHep1/CD44v2-10 clone #13, SKHep1/CD44v2-10HSM clone #7, and SKHep1/CD44v2-10HSM clone #9) suspended in 0.05 ml of PBS were injected s.c. into the left flank of each mouse. All of the cell lines were tested in the same experiment. The mice were sacrificed after 10 weeks or sooner if moribund. Flank tumors were excised and measured in three dimensions with digital calipers. Representative samples from the liver and lung (inflated with 1 ml of Bouin’s Fixative), and the flank sites were preserved for histological examination by fixation in 10% buffered formalin followed by paraffin embedding. These studies were performed according to the Australian Code of Practice for the care and use of animals for scientific purposes. The procedures were approved through the Bancroft Centre Research Ethics Committee (approval number A960302012).
Immunohistochemistry.
Immunohistochemical staining was performed on formalin-fixed, paraffin-embedded sections of tumor tissues by the avidin-biotin complex method, with the following exceptions. Sections of tumor tissues on glass slides were dried, deparaffinized, and stained using antihuman CD44s, CD44v3, CD44v6, or CD44v9 mAbs. Nonspecific antibody binding was inhibited using the Vector M.O.M. Immunodetection kit (Vector Laboratories, Burlingame, CA).
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RESULTS |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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promoter. The CD44 signal peptide in exon 1 was replaced with the CD33 signal peptide to increase efficiency of membrane expression (14)
. The resulting construct (pCD44v2-10/EFDNA3) is schematically represented in Fig. 1A
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. Amplification of cDNA prepared from SKHep1 cells using an exon 3 forward primer and an exon 17 reverse primer showed a single band of 
648 bp (Fig. 1B
, Lane 1), demonstrating the presence of CD44s only. This contrasts with the 2322-bp band detected in SKHep1CD44v2-10, representing the full-length CD44 variant isoform (Fig. 1B
, Lane 2). SKHep1/CD44v2-10 and control SKHep1 cell lines were analyzed for CD44v cell surface expression by FACS analysis, and two high-expressing cell lines (clones #7 and #13) were selected. SKHep1 and SKHep1/NEO showed similar patterns of expression with an antibody directed to the core domain of CD44, with no detectable expression of variant domains corresponding to v3, v6, or v9. In contrast, HTM29, a colorectal cancer cell line, expressed substantial levels of variant isoforms containing v3, v6, or v9. SKHep1/CD44v2-10 showed abundant expression of v3, v6, and v9, confirming cell surface expression of the CD44v2-10 protein by the SKHep1/CD44v2-10 transfectants (data not shown).
Expression of CD44v2-10 by SKHep1 Cells Confers a Metastatic Phenotype in Vivo.
To test the metastatic propensity of the CDv2–10 isoform in vivo, a mouse model of spontaneous metastasis was established. The human HCC cell-line SKHep1 forms tumors after s.c. inoculation in SCID mice but does not form spontaneous lung metastases. Groups of 8–9 mice were s.c. inoculated with 1 x 106 SKHep1 cells expressing CD44v2-10 (clones #7 and #13), SKHep1/NEO cells, or parental SKHep1 cells. Primary tumor development was observed at the s.c. sites 2–3 weeks after injection, and all of the mice developed primary tumors during the 10-week course of the experiment. The mice were sacrificed when the majority of the primary tumors in the control group were 1 cm3.
There was no significant difference in primary tumor size between mice inoculated with the control SKHep1 cell lines and those expressing CD44v2-10 (Table 1)
. In contrast, histological examination of the lungs of the mice revealed the presence of pulmonary metastases of SKHep1 cells expressing CD44v2-10 (7 of 17), whereas the lungs of animals injected s.c. with SKHep1/NEO and parental SKHep1 cells were free of tumor (0 of 16; P < 0.01). These results demonstrate that expression of CD44v2-10 promotes the metastasis of SKHep1 cells in vivo.
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. In addition to the absence of CD44v3, these sections were negative for CD44v6 and CD44v9 (data not shown). Primary tumors formed by SKHep1/CD44v2-10 cell lines (and SKHep1/CD44v2-10HSM cell lines, see below) displayed strong membrane staining for core CD44 and CD44v3 (Fig. 2, G–L)
, as well as for CD44v6 and CD44v9 (data not shown). Pulmonary metastases from mice inoculated with SKHep1/CD44v2-10 maintained strong membrane staining for core CD44 and CD44v3 protein expression (Fig. 2, M–O)
, as well as for CD44v6 and CD44v9 (data not shown).
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and was not seen in control cell lines. This band was not seen in SKHep1/CD44HSM cell lysates. These data show that CD44v2-10 is modified by HS at the CD44v3-HS attachment site, when expressed in SKHep1 cells.
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). An identical mutation has been shown by others to eliminate the attachment of HSy to CD44v3 isoforms, preventing the binding of bFGF to fusion proteins containing CD44v3 (16)
. The mutant construct (pCD44v2-10HSM/EFDNA3) was transfected into SKHep1 cells, and stable cell lines were selected. Two cell lines with high cell surface CD44v2-10 expression were selected by FACS. Both cell lines showed substantial expression of core CD44, v3, v6, and v9 at levels similar to SKHep1/CD44v2-10 (data not shown). Analysis of CD44s expression in each of the parental SKHep1, SKHep1/NEO, SKHep1/CD44v2-10, and SKHep1/v2-10HSM cell lines by Western blot analysis using an antibody specifically directed to the core CD44 domain showed similar levels of the Mr 90,000 CD44s isoform (data not shown).
Two SKHep1/CD44v2-10HSM-expressing cell lines were inoculated s.c. into SCID mice. Primary tumors developed within 10 weeks at a similar rate to that observed for SKHep1/CD44v2-10 cells, SKHep1/NEO cells, and parental SKHep1 cells. There was no significant difference in primary tumor size between the CD44v2-10HSM and the other cell-lines (Table 1)
. In contrast, histological examination of the lungs revealed the absence of pulmonary metastases in mice inoculated with SKHep1 cells expressing CD44v2-10HSM (0 of 16), compared with mice bearing CD44v2-10-expressing tumors (7 of 17; P < 0.01). These results demonstrate that HS modification of v3 is required for metastasis of CD44v2-10-expressing SKHep1 cells in vivo.
CD44v2-10-expressing SKHep1 Cells Bind Heparin-binding Growth Factors in Vitro: Requirement for CD44v3.
To investigate the binding of heparin-binding growth factors to SKHep1/CD44v2-10 cells, quantitative ligand-binding analyses were performed. HGF/SF and VEGF binding to the cells was measured by FACS using anti-HGF/SF and anti-VEGF mAbs. bFGF binding was determined by measuring the adhesion of the cells to bFGF-coated PVC plates. Parental SKHep1 and SKHep1NEO control cell lines displayed low levels of binding with bFGF, HGF/SF, and VEGF (Fig. 3, B–D)
. In contrast, SKHep1 cells expressing CD44v2-10 displayed 14-fold, 10-fold, and 13-fold higher levels of binding for HGF/SF, VEGF, and bFGF heparin-binding growth factors, respectively (Fig. 3, B–D)
. SKHep1/CD44v2-10HSM cells, in which the HS attachment site was mutated, displayed heparin-binding growth factor binding similar to that of the control cell-lines (Fig. 3, B–D)
. SKHep1/CD44v2-10 growth factor binding was competitively inhibited by excess heparin or treatment with heparitinase (data not shown). These data demonstrate that growth factor binding is dependent on a functional CD44v3 isoform and additionally show that HS modification of CD44v3 is required for growth factor binding.
CD44v2-10 Expression Does Not Change in Vitro Tumor Cell Proliferation, Cell Migration, Invasion, or Motility.
To investigate whether expression of CD44v2-10 by SKHep1 cells may initiate an autocrine loop to enhance growth factor binding, and hence, the proliferation of SKHep1 cells in vitro, cell growth was monitored over a period of 3 days in the absence and presence of added HB-EGF (10 pM to 10 nM), bFGF (10 pM to 10 nM), and HGF/SF (10 pM to 10 nM). No differences were found between the proliferation rates of SKHep1/CD44v2-10, SKHep1/CD44v2-10HSM, SKHep1/NEO, or parental SKHep1 cells in the absence or presence of added growth factors (data not shown). These results suggest that CD44v2-10-mediated metastasis is not dependent on increased proliferation of SKHep1cells. Increased cell migration and invasion are key phenotypic advantages of malignant cells favoring metastasis. To determine whether expression of CD44v2-10 by SKHep1 cells promotes increased cell migration, SKHep1 parental, SKHep1/NEO controls, SKHep1/CD44v2-10, and SKHep1/CD44v2-10HSM cells were subjected to in vitro monolayer wounding in wells (on coverslips) with and without HA coating. No difference in cell migration was seen between any of the cell lines. The same studies were repeated in the presence of exogenous growth factors bFGF and HGF/SF, with no differences observed. Cell invasion was studied in Matrigel-coated transwells. In separate studies, BSA and BSA with bFGF were used as attractants. Additional studies used cells pretreated with PMA in serum-free medium. In none of the studies did cells migrate or invade Matrigel. Transwell migration studies were performed with and without HGF as an attractant, and in the presence and absence of HA and Matrigel. None of the cell lines migrated through the Matrigel, and no differences in cell migration were observed between any of the clones.
These studies did not demonstrate in vitro phenotypic differences between parental SKHep1 cells and NEO controls, and SKHep1/CD44v2-10 and SKHep1/CD44v2-10HSM cells in migration or invasion.
Expression of CD44v2-10 Decreases SKHep1 Cell Adhesion to Hyaluronan.
The effect of CD44v2-10 expression by SKHep1 cells on hyaluronan binding was examined by adhesion assays on immobilized hyaluronan. Parental SKHep1 and SKHep1/NEO cell lines displayed high levels of binding to immobilized hyaluronan, which was effectively competed out by preincubation with soluble hyaluronan (Fig. 3E)
. In contrast, SKHep1/CD44v2-10 cells showed an 3-fold reduced affinity for hyaluronan. SKHep1/CD44v2-10HSM cells demonstrated a level of binding similar to that of the control cell lines. These data show that HS modification of CD44v3 interferes with CD44-hyaluronan interactions, a result in agreement with Bennett et al. (17)
. Thus, CD44v2-10 expression by SKHep1 cells has a dominant-negative effect on hyaluronan binding, leading to a less adhesive phenotype.
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DISCUSSION |
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Although CD44 variant isoforms have been implicated in the metastatic process in a number of clinical and experimental studies, the precise mechanisms by which tumor cells exploit CD44v are not well understood. CD44v3 is a domain that can be modified by HS attachment (16) . We found that an intact HS attachment site in CD44v3 was essential for CD44v2-10-mediated metastasis in the SKHep1 experimental tumor model. Moreover, SKHep1 cells expressing HS-modified CD44v2-10 displayed an enhanced ability to bind the heparin-binding growth factors HGF/SF, bFGF, and VEGF compared with cells expressing a HS-deficient mutant CD44v2-10 (CD44v2-10HSM) and SKHep1 control cell lines. This finding is consistent with those of other authors (9 , 12) who have shown that the HS-modified CD44v3 HS binding domain binds heparin-binding growth factors in vitro. It is believed that HSPGs, such as CD44v3-HSPG, act as high-capacity, low-affinity receptors that increase the concentration of heparin-binding growth factors at the cell surface, thereby potentially enhancing high-affinity growth factor receptor binding and activation. The effect of HSPGs is most apparent at submaximal concentrations of growth factor, enhancing the effects of the locally available growth factors (18) . Because CD44v3-HSPG can promote c-Met activation (12) , we addressed the possibility that SKHep1 cells expressing CD44v2-10 are able to sequester and present heparin-binding growth factors in an autocrine loop, promoting tumor cell activation in vivo proliferation and motility. However, CD44v2-10-expressing cells did not display increased cell proliferation in vitro, even after incubation with exogenous HGF/SF, bFGF, HB-EGF, or VEGF compared with control cell lines. Furthermore, primary tumors derived from s.c. inoculation of SKHep1/CD44v2-10 cells in the mouse did not grow more rapidly and were not larger than those derived from control cell lines. These results suggest that the mechanism of CD44v2-10-mediated metastasis in SKHep1 cells is unlikely to be that of enhanced (autocrine) cell proliferation.
Other properties considered important in the metastatic cascade include increased cellular motility and invasion, which can be mediated by certain heparin-binding growth factors including HGF/SF. SKHep1/CD44v2-10 cells did not demonstrate enhanced migration or invasion in vitro, even after incubation with exogenous HGF/SF. Moreover, immunoprecipitated h-met from SKHep1/CD44v2-10 cells did not demonstrate enhanced tyrosine phosphorylation of h-met with HGF stimulation (data not shown). These experiments are at variance with previous findings in Namalwa cells double-transfected with CD44v3-10 and c-met under HGF stimulation, where enhanced tyrosine phosphorylation of c-met was demonstrated (12) . However, this Namalwa experimental system is not spontaneously metastatic in vivo and, hence, may not be directly relevant to tumor metastasis.
There are other possible mechanisms for CD44v2-10-mediated metastasis in SKHep1 cells. Cell surface CD44v3-HSPG cannot only efficiently stimulate bFGF-mediated proliferation in a cell-line transfected with fibroblast growth factor receptor-1, but macrophage CD44v3-HSPG can present bFGF to adjacent cells in inflamed synovial tissue (19) . Such findings suggest that SKHep1 cells expressing CD44v3-HSPG may use similar paracrine regulation of growth factor function. This would allow tumor cells to modify their microenvironment, such as establishing chemotactic gradients for endothelial cells and stromal fibroblasts. Such a two-way paracrine exchange of growth factors between tumor cells and vascular endothelial cells has been demonstrated clearly by Fukumura et al. (20) . The potential relationship between CD44v3-HSPG-expressing tumor cells, microvascular endothelial cells, and host stromal cells warrants additional study.
An alternative mechanism for the observed metastatic behavior might be through signal transduction. There is accumulating evidence that, in general, adhesion molecules participate not only in mediating cell adhesion, but also in signal transduction (21 , 22) . CD44 has been implicated in signal transduction involving Src kinases, including Lck, Fyn, Lyn, and Hck in lipid rafts (23) , and the Rho family of proteins through association with ERM proteins. It is conceivable that on growth factor binding by CD44v3, outside-in signaling may influence pathways associated with metastatic behavior.
Several studies have shown that metastatic behavior is dependent on CD44-HA interactions (24) , whereas others have demonstrated that CD44 variant isoforms confer a metastatic phenotype independent of HA binding (25) . The data presented here demonstrate that CD44v2-10 expression in SKHep1 cells conferred reduced HA binding and a metastatic phenotype, which may indicate that reduced HA binding is important for metastasis in this experimental model. HS-modified CD44v3-containing isoforms have been shown to have a reduced affinity for HA that is restored by removal of HS side chains by heparitinase (17) . Consistent with these findings, CD44v2-10HSM expression in SKHep1 cells did not alter HA binding nor promote metastasis compared with control SKHep1 cell lines in this model, suggesting that either HA binding is not important or that metastasis requires both reduced HA binding and an intact CD44v3 domain. Additional experiments will be required to clarify the role of HA binding in metastasis in this model.
This is the first study demonstrating that HS-modified CD44v2-10 confers a metastatic phenotype on human cancer cells in vivo but that the mechanism is unlikely to be through an autocrine enhancement of tumor cell proliferation or migration. These findings suggest that strategies directed against CD44v3-HS attachment could provide realistic antimetastasis therapies.
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ACKNOWLEDGMENTS |
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FOOTNOTES |
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1 Supported by grants from the National Health and Medical Research Council of Australia and the Australian Research Council of Australia. A. P. B. was supported by a Medical and Dental Postgraduate Research Scholarship from the National Health and Medical Research Council of Australia, the Royal Australasian College of Surgeons, and the Research and Development Foundation of the Princess Alexandra Hospital. 
2 These authors contributed equally to this work and should be considered joint senior authors.
3 To whom requests for reprints should be addressed, at Queensland Institute of Medical Research, Post Office Royal Brisbane Hospital, Brisbane, 4029, Queensland, Australia. Phone: 61-7-3362-0312; Fax: 61-7-3362-0107; E-mail: d.gotley{at}mailbox.uq.edu.au
4 The abbreviations used are: HA, hyaluronic acid; FACS, fluorescence-activated cell sorting; bFGF, basic fibroblast growth factor; HB-EGF, heparin-binding epidermal growth factor; HGF/SF, hepatocyte growth factor/scatter factor; HS, heparan sulfate; HSM, heparan sulfate mutant; HSPG, heparan sulfate proteoglycan; VEGF, vascular endothelial growth factor; mAb, monoclonal antibody; SP, streptavidin; EF-1, elongation factor-1; IF, immunofluorescence.
Received 8/ 3/01. Accepted 12/16/02.
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and 
represent core and variably spliced exons, respectively. The CD33 signal peptide, replacing CD44 exon 1, is represented by 
. The sequence of the mutation in CD44v2-10HSM is as indicated. The positions of the oligonucleotide primers used in PCR analyses relative to the variant exons are as shown. B, reverse transcription-PCR analysis of CD44 variant expression in parental SKHep1 (Lane 1) and SKHep1/CD44v2-10 (Lane 2) using PCR primers 3F and 17R. The predicted size after amplification of CD44s is 648 bp, and the predicted size for CD44v2-10 is 1791 bp.
