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Research Articles: Therapeutics, Targets, and Development
Wnt3/RhoA/ROCK signaling pathway is involved in adhesion-mediated drug resistance of multiple myeloma in an autocrine mechanism
1 Fourth Department of Internal Medicine and 2 Department of Molecular Medicine, Sapporo Medical University School of Medicine, Sapporo, Japan
Requests for reprints: Yoshiro Niitsu, Fourth Department of Internal Medicine, Sapporo Medical University, Chuo-ku S1, W17, Sapporo, 060-8556, Japan. Phone: 81-11-611-2111, ext. 3254; Fax: 81-11-612-7987. E-mail: niitsu{at}sapmed.ac.jp
Abstract
Adhesion of myeloma cells to bone marrow stromal cells is now considered to play a critical role in chemoresistance. However, little is known about the molecular mechanism governing cell adhesion–mediated drug resistance (CAM-DR) of myeloma cells. In this study, we focused our interests on the implication of the Wnt signal in CAM-DR. We first screened the expression of Wnt family in myeloma cell lines and found that Wnt3 was overexpressed in all the myeloma cells examined. KMS-5 and ARH77, which highly expressed Wnt3 protein, tightly adhered to human bone marrow stromal cells, and accumulation of ß-catenin and GTP-bounded RhoA was observed in these myeloma cell lines. Conversely, RPMI8226 and MM1S, which modestly expressed Wnt3 protein, rather weakly adhered to human bone marrow stromal. We then examined the relevance of Wnt3 expression to adhesive property to stromal cells and to CAM-DR of myeloma cells. KMS-5 and ARH-77 exhibited apparent CAM-DR against doxorubicin. This CAM-DR was significantly reduced by anti-integrin ß1 antibody, anti-integrin 
6 antibody and a Wnt-receptor competitor, secreted Frizzled-related protein-1, and Rho kinase inhibitor Y27632, but not by the specific inhibitor of canonical signaling (Dickkopf-1), indicating that Wnt-mediated CAM-DR that is dependent on integrin 6/ß1 (VLA-6)–mediated attachment to stromal cells is induced by the Wnt/RhoA/Rho kinase pathway signal. This CAM-DR was also significantly reduced by Wnt3 small interfering RNA transfer to KMS-5. These results indicate that Wnt3 contributes to VLA-6–mediated CAM-DR via the Wnt/RhoA/ROCK pathway of myeloma cells in an autocrine manner. Thus, the Wnt3 signaling pathway could be a promising molecular target to overcome CAM-DR of myeloma cells. [Mol Cancer Ther 2007;6(6):1774–82]
Introduction
Multiple myeloma is an end-stage B-cell neoplasia characterized by localization of malignant plasma cells in the bone marrow and not in other locations. Despite tremendous efforts in developing effective treatment modalities such as autologous stem cell transplantation, exploring new molecular targeting drugs, etc., the disease still remains incurable, mainly due to the ultimate acquisition of drug resistance (1–7).
One of the main mechanisms underlying the drug resistance has been ascribed to the adhesive property of myeloma cells to the extracellular matrix or stromal cells in bone marrow (8–11). We and others have reported that in various hematologic malignancies, including multiple myeloma, molecules responsible for the adhesive nature of tumor cells were integrins such as VLA-4 and VLA-5 (12–14). Through the interaction of integrins with their ligands, up-regulation of antiapoptotic bcl-2 family members and/or overexpression of multidrug resistant gene 1 are induced, thereby causing tumor cells to become unresponsive to anticancer drugs (12, 13, 15). This cell adhesion–mediated drug resistance (CAM-DR) has been overcome in vitro and in vivo by a combination of chemotherapy with anti-integrin antibodies or inhibitors to drug resistance–related intracellular signal pathways (16). Furthermore, recent studies have revealed that various humoral factors from tumor cells and/or stromal cells were implicated in the adhesion and motility of myeloma plasma cells by their autocrine or paracrine action (17–21). Among the humoral factors, Wnt family members, which play a crucial role in differentiation and proliferation of normal and malignant cells in addition to the motility or adhesion mentioned above, are often activated in both bone marrow stromal cells and B-cell neoplasia including multiple myeloma (4, 22–26). On the basis of these notions, in the present study, we elucidated if any Wnt family members are involved in CAM-DR of multiple myeloma.
Materials and Methods
Cell Lines and Human Stromal Cells
Human myeloma cell lines RPMI8226, EBV-transformed ARH-77 (27, 28), MM1S, and KMS-5 (29, 30); lymphoma cell lines Ramos, PEER, and Molt-4; and leukemia cell lines KG-1, HL-60, and U937 were cultured in RPMI 1640 containing 10% heat-inactivated FCS (Life Technologies), 2 mmol/L L-glutamine, 0.1% penicillin (100 units/mL), and streptomycin (100 mg/mL). hTERT gene–transduced human stromal cells (hTERT-stromal cells) were generated as previously described (31, 32) and were cultured in long-term culture medium containing MEM-, 12.5% horse serum (Life Technologies), 12.5% FCS, 1 x 10–6 mol/L hydrocortisone (Sigma), 1 x 10–4 mol/L ß-mercaptoethanol (Sigma), 2 mmol/L L-glutamine, 0.1% penicillin (100 units/mL), and streptomycin (100 mg/mL).
Antibodies, Wnt Antagonists, and Chemical Reagents
The specific antibody for ß-catenin (clone 14) was purchased from BD. The specific antibodies for Wnt3 (sc-5212), RhoA (sc-418), and Cdc42 (sc-8401) were from Santa Cruz Biotechnology. The specific antibody for Rac (clone 23A8) was from Upstate, and the specific antibody for Wnt5a was purchased from R&D Systems. Function-blocking anti-integrin ß1 antibody 4B4, anti-integrin 4 antibody HP2/1, and anti-integrin 5 antibody SAM1 were obtained from Coulter, and anti-integrin 
AMF7, anti-integrin 2 Gi9, anti-integrin 3 C3, and anti-integrin 6 GoH3 (33) were obtained from Immunotech. Isotype control mouse IgG1 antibody MOPC21 (Sigma) and rat IgG2a antibody DD13 (Chemicon) was used in the control experiments. Recombinant secreted Frizzled-related protein-1 (sFRP-1) and Dickkopf-1 (DKK-1) were obtained from R&D Systems. Rho kinase (ROCK) inhibitor Y-27632 and GRGDS (H-Gly-Arg-Gly-Asp-Ser-OH) peptide were purchased from Calbiochem. Doxorubicin was obtained from Sigma and dissolved in sterile double-distilled water before use.
Reverse Transcription-PCR
One microgram of total RNA was reverse transcribed by SuperScript II (Invitrogen) and amplified using TaKaRa Ex Taq (TAKARA BIO, Inc.), with the primers described below. All PCR reactions were done using a PTC-200 Peltier Thermal Cycler (MJ Japan). PCR amplification using specific primers for Wnt1 (5-GCTCCTGCTCAGAAGGTTCCAT-3, 5-GTCCGCTGTACGTGCAGAAGTT-3), Wnt2B (5-GTAGCCAGGGTGAACTGAGTGT-3, 5-CTAGGGAACCTGCAGCCTTGT-3), Wnt3 (5-ATCATAAGGGGCCGCCTGGCGAA-3, 5-CTTGCAGGTGTGCACGTCGTAGA-3), Wnt3A (5-CTGGACAAAGCTACCAGGGAGT-3, 5-GTGGGCACCTTGAAGTAGGTGT-3), Wnt5A (5-CAAGGTGGGTGATGCCCTGAA-3, 5-GCACGGTCTTGAACTGGTCGTA-3), Wnt7A (5-CCTGGACGAGTGTCAGTTTCAG-3, 5-GGCCTCGTTGTACTTGTCCTTG-3), Wnt10B (5-GCAAGAGTTTCCCCCACTCTCT-3, 5-GTCTCGCTCACAGAAGTCAGGA-3), Wnt11 (5-CTCTGCGCGCCTCTCTGGAAA-3, 5-GTGGGAGCCCACCTTCTCATT-3), or glyceraldehyde phosphate dehydrogenase (5-ACATCAAGAAGGTGGTGAAGCAGG-3, 5-CTCTTCCTCTTGTGCTCTTTGCTGG-3) was done under the following conditions: one cycle of 98°C for 30 s; 35 cycles (33 cycles for Wnt3) of 98°C for 10 s, 62°C for 20 s, 72°C for 60 s; and one cycle of 72°C for 10 min. The PCR products were electrophoresed on an agarose gel and visualized by ethidium bromide staining.
Transfection of Small Interfering RNA
Dicer substrate RNA duplexes for use in RNA interference against Wnt3 (NM_ 030753) were obtained from iGENE Therapeutics. The sequences of dsRNA synthesized newly were as follows: sense, 5'-ACGGAGAAGCGGAAGGAAAAAUGCCAG-3'; antisense, 5'-UAUGCCUCUUCGCCUUCCUUUUUACGG-3'. The non-silencing control small interfering RNA (siRNA) for human was purchased from iGENE Therapeutics.
RNA duplexes specific for the human Wnt3 were transfected into KMS-5 or ARH-77 cells using the DeliverX transfection kit (Panomics) according to provided protocols. Briefly, 5 µmol/L working stocks of siRNA were diluted with Buffer-1, and siRNA Transfection Reagent was diluted with Buffer-2. Both solutions were mixed well and incubated at 37°C for 20 min to form working siRNA/siRNA transfection reagent complex. Cells were pelleted in a microtube (Falcon) by spinning for 5 min at 400 x g. Cells were washed thrice by PBS and pelleted again at 400 x g for 5 min. After aspiration of the PBS, cells were resuspended with 300 µL of working siRNA/siRNA transfection reagent complex and incubated at room temperature for 5 min. After adding 300 µL of Opti-MEM (Invitrogen) to the microtubes, 600 µL of cells/transfection complex were transferred into one well of a six-well plate. Final concentration of Wnt3 siRNA in the sample well was 30 nmol/L. Cells/transfection complex was incubated for 4 h at 37°C and 5% CO2. Subsequently, 1 mL of complete growth media was added and incubated overnight. Next day, after cells were washed once, and cells were washed to remove transfection complex and cultured in complete growth media at 37°C and 5% CO2 before use.
Plasmid Vectors, Gene Transduction, and Wnt3 Conditioned Medium
The CA promoter (chicken ß-actin promoter with cytomegalovirus enhancer)–based plasmid vector pCAcc was employed in this study. Human Wnt3 cDNA containing plasmid, pCR®2.1-hWnt3, was previously described (34). To construct pCAcc-hWnt3, pCR®2.1-hWnt3 was digested with EcoRI and ligated in pCAcc. The integrity of the pCAcc-Wnt3 was confirmed by restriction endonuclease digestion and DNA sequencing. pCAcc-Wnt3 and pcDNA3-neo were cotransfected into L cells (American Type Culture Collection) using LipofectAMINE 2000 (Invitrogen) according to manufacturer's instructions. G418-resistant colonies were cultured using 600 µg/mL G418 for 2 weeks, and stably transfected clones that revealed ß-catenin stabilizing activity were selected. Wnt3 conditioned medium (CM) or control CM was prepared from Wnt3-producing L cells (L-Wnt3) or control L cells grown to confluency in DMEM containing 10% FCS, 72 h after which culture supernatants were collected and designated Wnt3 CM and control CM, respectively.
Contact and Non-Contact Culture System
Stromal contact culture systems were constructed using BD Falcon Cell Culture Inserts and Companion Plates (BD; pore size: 0.4 µm, pore density: 1 x 108/cm2, 12 wells) to avoid contamination of stromal cells as reported previously (13, 35). Briefly, 1 x 104 or 5 x 104 hTERT-stromal cells were plated on the back side of the insert membrane. After obtaining a confluent stromal layer, stromal cells were washed twice and were cultured in companion plates for 2 days. For the adhesion assay, myeloma cells were washed once and resuspended in RPMI 1640 supplemented with 10% FCS, and 2 x 105 cells were added to each culture insert. In some experiments, 30 µg/mL of function-blocking anti-integrin antibodies were added to each culture insert at the time of cell seeding. Following 24 h of incubation at 37°C and 5%CO2, suspended cells were collected, and attached cells were harvested by three trypsin-EDTA treatments. The percentage of adhesion was calculated by the ratio between the number of attached cells and the total number of collected cells. In non-contact culture, 5 x 104 hTERT-stromal cells were plated on companion plates; thereby, myeloma cells were physically separated from the stromal layer by a membrane of culture insert.
Immunofluorescent Staining for Assessment of Cell Morphology
Myeloma cells were serum starved for 12 h and incubated with control or Wnt3 CM with or without DKK-1 or sFRP-1 for 6 h. After two washings with PBS, the cells were fixed in 4% paraformaldehyde in PBS for 30 min. The fixed cells were permeabilized with PBS containing 0.2% Triton X-100 for 15 min. After the cells were soaked in 10% goat serum (Life Technologies) with PBS for 30 min, they were treated with the anti-vinculin antibody (clone hVIN-1; Sigma) in 10% goat serum with PBS for 2 h. The cells were then washed with PBS thrice followed by incubation with Alexa Fluor 488 (Molecular Probes) in 10% goat serum with PBS for 30 min. For the detection of actin filaments, Texas Red phalloidin (Molecular Probe) was mixed with the second antibody solution. After the cells were washed with PBS thrice, they were covered with an anti-fade medium containing the nuclear stain 4',6-diamidino-2-phenylindole (VECTASHIELD DAPI, Vector Laboratories). Subsequently, they were examined using an R2100AG2 confocal laser scanning microscope (Bio-Rad, Laboratories).
Drug Cytotoxicity Assay
For drug cytotoxicity assays, myeloma cells were washed once and resuspended in RPMI 1640 containing 10% FCS, and 1 x 105 cells were added to each culture insert and cultured in the presence or absence of function-blocking anti-integrin antibodies or the Wnt inhibitors sFRP-1 or DKK-1. After 24 h, 0.03 to 3.0 µmol/L doxorubicin or vehicle control was added to each well and incubated for 1 h, then medium containing doxorubicin was removed and replaced by drug-free medium with or without the blocking antibodies, or the Wnt inhibitors sFRP-1 or DKK-1. After 24 h of incubation, suspended and attached myeloma cells were collected by three treatments of trypsin-EDTA, and cells was pelleted at 400 x g for 5 min, resuspended by 200 µL of complete culture medium, and placed into 96-well palates. The survival cells were assessed by Annexin V-FITC Apoptosis Detection kit (Medical & Biological Laboratories) and Premix WST-1 assay Cell Proliferation Assay System (Takara). The WST-1 assay is based on mitochondrial conversion of WST-1 to yellowish formazan, being indicative of the number of viable cells. The number of viable cells was evaluated by absorbance A450 nm using Model 680 microplate reader (Bio-Rad Laboratories).
Western Blotting
For immunoblot analysis of Wnts, total protein lysates from myeloma cells were extracted with lysis buffer containing 50 mmol/L Tris, 150 mmol/L NaCl, 1.0% NP40, 0.5% sodium deoxycholic acid, and 0.1% SDS and inhibitor cocktails (Roche). Alternatively, for immunoblot analysis of ß-catenin, cells were serum starved for 12 h with or without 10 µg/mL sFRP-1 or 1 µg/mL DKK-1. Subsequently, the cytosolic proteins of the cells were prepared with the Subcellular Proteome Extraction kit (Calbiochem) according to provided protocols. After protein contents were determined using a protein assay kit (Bio-Rad), protein lysates were separated on 4% to 20% SDS-polyacrylamide gradient gel and transferred to a polyvinylidene fluoride membrane using a semidry transfer apparatus (Bio-Rad). Immunoblots were probed with primary antibodies then with horseradish peroxidase–conjugated anti-IgG (Zymed) as a secondary antibody and visualized using the enhanced chemiluminescence method (ECL plus, Amersham Pharmacia Biotech) according to the supplier's instructions.
Rho Family GTPase Activity Assay
Activity of Rho, Rac, and Cdc42 was examined with a pull-down assay using a Rho Activation Assay kit and Rac Activation Assay kit (Upstate). Briefly, cells were serum starved for 12 h with or without 10 µg/mL sFRP-1 or 1 µg/mL DKK-1. The cells were washed and lysed, and lysates were incubated with glutathione S-transferase–tagged Rhotekin Rho-binding domain or glutathione S-transferase p21-binding domain bound to glutathione-agarose for 1 h at 4°C in a rotary shaker. The beads were pelleted and washed. Protein recovered was analyzed for immunoblotting with anti-RhoA, anti-Rac, or anti-Cdc42 antibodies as described above. Whole-cell lysates were similarly immunoblotted for comparison.
Statistical Analysis
Each data set was first evaluated for normality of distribution by the Komolgorov-Smirnov test to decide whether a nonparametric rank-based analysis or a parametric analysis should be used. Two groups were compared by either the Wilcoxon signed-rank test or the Student's t test (two-tailed test). P < 0.05 was considered statistically significant.
Results
Relevance of Adhesive Property of Myeloma Cells onto Stromal Cells to CAM-DR
To gain insight into the relationship between the adhesive property and drug resistance of multiple myeloma, we first examined the adhesive potential of four myeloma cell lines, including ARH-77, KMS-5, RPMI8226, and MM1S, to hTERT-stromal cells. As shown in Fig. 1A
, ARH-77, KMS-5 showed high adhesive potential onto hTERT-stroma cells, and RPMI8226 showed moderate adhesive potential, whereas MM1S exhibited relatively low adhesive potential (Fig. 1A). Next, we assessed the drug resistance of these myeloma cell lines in both contact and non-contact culture systems with hTERT-stromal cells. High adhesive cell lines ARH-77 and KMS-5, moderate adhesive cell line RPMI8226, and low adhesive cell line MM1S were used in WST-1 assay (Fig. 1B) and Annexin V-propidium iodide assay (Fig. 1C). In adhesive cell lines, sensitivity for doxorubicin in contact culture condition was significantly lower than that seen in non-contact culture condition or stroma-free culture (Fig. 1B and C). However, no significant difference of doxorubicin sensitivity among stroma-free culture, non-contact culture, and contact culture was observed in low adhesive MM1S (Fig. 1B and C). These results suggest that direct adhesive interaction between myeloma cells and human stromal cells are relevant to induce drug resistance.
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4, 5, 6, or ß1 were commonly expressed on both high adhesive KMS-5 and ARH-77 (Fig. 2A and B
). Hence, we next investigated whether the adhesion of myeloma cells to hTERT-stromal cells could be inhibited by antibodies for integrins 4, 5, 6, or ß1. However, these antibodies did not affect the adhesion rates of ARH-77, KMS-5, or RPMI8226 onto stromal cells (Fig. 2C), although GRGDS peptide partially inhibited adhesion between myeloma cells and stromal cells, suggesting that the adhesive property of these myeloma cell lines to stromal cells is determined not only by 4, 5, 6, or ß1 integrins but also by other unknown adhesion molecules (15, 17). We further assessed whether CAM-DR of multiple myeloma was inhibited by these anti-integrin antibodies. As shown in Fig. 3A
, CAM-DR of KMS-5 and ARH-77 were substantially reduced by neutralizing anti-integrin ß1 4B4 in a dose-dependent manner (Fig. 3A). However, the reduction level did not reach that seen in the stroma free condition, and it leveled out at concentrations of 10 to 30 µg/mL of the 4B4 antibody (Fig. 3A and B). The reduction rate of CAM-DR in the presence of anti-integrin 4 HP2/1 was not significantly different from that in the absence of the neutralizing antibody, although a similar tendency as that seen in the anti-integrin ß1 antibody was observed (P = 0.10; Supplementary Fig. S1A).3 In addition, anti-integrin 5 SAM1 did not affect CAM-DR (Supplementary Fig. S1B).3 Interestingly, CAM-DR of KMS-5 and ARH-77 were significantly reduced by neutralizing anti-integrin 6 GoH3 (ref. 33; Fig. 3C and D; Supplementary Fig. S2).3 Collectively, substantial inhibition of CAM-DR was observed by blocking the integrin ß1/integrin 6 molecule (VLA-6) without changing the adhesive property of myeloma cells to stromal cells. These findings are consistent with previous reports showing that integrin ß1 was a key molecule of CAM-DR. (12, 36) However, these results also suggested that some additional but minor molecular mechanisms should be involved in CAM-DR because the inhibitory effect of neutralizing anti-integrin ß1 on CAM-DR was not complete.
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Reduction of CAM-DR of Multiple Myeloma by Inhibition of Wnt/RhoA Pathway
We next investigated whether the Wnt signal pathway is involved in induction of CAM-DR of multiple myeloma (43, 44). To evaluate this possibility, we did a cytotoxic assay using a stroma-free or stromal contact culture system in the presence or absence of Wnt inhibitors. As the results show in Fig. 4C and D, sFRP-1 significantly inhibited drug resistance evoked by contact culture with hTERT-stromal cells and KMS-5 or ARH-77 myeloma cell lines, whereas DKK-1 did not (Supplementary Fig. S3),3 indicating that RhoA signaling is the main pathway in modulation of CAM-DR of multiple myeloma. To examine whether Wnt3 produced by myeloma cells directly induced CAM-DR, we conducted knockdown study by using Wnt3 siRNA. As shown in Fig. 5A
, dicer substrate Wnt3 siRNA could decrease expression of Wnt3 protein (Fig. 5A). Furthermore, CAM-DR elicited by coculture with hTERT-stroma cells and KMS-5 or ARH-77 cells was significantly reduced by transfer of Wnt3 siRNA into these myeloma cells (Fig. 5B). These results suggested that Wnt3 was involved in CAM-DR in autocrine manner. However, the degree of reduction of CAM-DR by sFRP-1 or Wnt3 siRNA was not complete. On the contrary, complete reduction of CAM-DR to a stroma-free level was attained by addition of Y27632, which is an inhibitor of Rho kinase, downstream of RhoA (Fig. 5C). Collectively, in multiple myeloma, activation of RhoA signaling is responsible for generation of CAM-DR, and the main stimulant of this pathway (Wnt3), secreted from tumor cells through some other minor, non-Wnt stimulants to RhoA, is involved in induction of CAM-DR (45).
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Discussion
In the present study, we first confirmed a linkage of refractoriness to doxorubicin with adhesiveness to stromal cells using four different cell lines of multiple myeloma; three adhesive cell lines (ARH-77, KMS-5, and RPMI8226) showed CAM-DR, whereas the non-adhesive cell line (MM1S) was sensitive to doxorubicin. When the effect of anti-integrin antibodies on CAM-DR of the adhesive cell lines (KMS-5 and ARH-77) was examined, the anti-integrin ß1 and the anti-integrin 6, but neither anti-integrin 4 nor anti-integrin 5 antibody, largely restored sensitivity to doxorubicin (Fig. 3; Supplementary Fig. S1).3 Our findings and the previous reports that the laminin receptor VLA6 was expressed on most myeloma cell lines (27, 37, 38) suggest a pertinence of strategy to use anti-VLA6 antibody to overcome CAM-DR of multiple myeloma. However, this notion is not commonly valid for all multiple myeloma cell types but contradicts previous reports showing involvement of VLA-4 (47) or VLA-4 plus LFA-1 (45) in CAM-DR of myeloma cell lines NCI-H929 and 5TGM1. The discrepancy may be due to the difference in myeloma cell lines and the epitope of the anti-integrin 4 monoclonal antibody (27) in each experiment because extracellular matrix on stromal cells consists of quite heterogeneous molecules, and each myeloma cell line could express diverse adhesive molecule(s) relevant to CAM-DR (45, 48). Likewise, the observation that none of the antibodies against integrin ß1, 4, 5, or 6 effectively detached myeloma cells from stroma (Fig. 2C) may be rationalized by heterogeneous constituents of stromal extracellular matrix, each of which imparts some adhesive nature of stromal cells to myeloma cells. In other words, adhesion of myeloma cells to stroma via interaction of certain adhesive molecules, such as integrin ß1 or VLA-6 with extracellular matrix, is necessary to bring about CAM-DR because adhesion and CAM-DR were closely related (Fig. 2B), but the molecule(s) relevant to CAM-DR alone may not be sufficient to cause tight adhesion. Nevertheless, the fact that integrin ß1 irrespective of its counterpart subunits (integrin 4, 5, or 6) is commonly involved in CAM-DR of various multiple myeloma cells is indicative of future use of anti-integrin ß1 in combination with anticancer drug for treatment of multiple myeloma.
Having confirmed the close linkage of CAM-DR to adhesiveness of multiple myeloma cell lines, we then extended our exploration to examine the implication of Wnt(s), a large family of secreted glycoproteins involved in cell proliferation, differentiation, and oncogenesis, of which certain family members, such as Wnt1 and Wnt3a, have been shown to stimulate migration and invasion of multiple myeloma cells (22). We chose Wnt1, Wnt2b, Wnt3, Wnt3a, Wnt5a, Wnt7a, Wnt10b, and Wnt11 in the present study to analyze because we and others have previously found these proteins were highly expressed in human bone marrow cells (24, 40). The results of reverse transcription-PCR and Western blotting revealed prominent expression of Wnt3 with a concomitantly increased level of ß-catenin and GTP-RhoA in CAM-DR relevant cells (ARH-77, KMS-5, and RPMI8226) but not in CAM-DR non-relevant cells (MM1S; Fig. 4A and B), suggesting on autocrine signaling of a canonical and a non-canonical pathway by Wnt3. To directly prove the autocrine activation of the Wnt signaling pathway in the CAM-DR relevant cell line (KMS-5 and ARH-77), sFRP-1, which binds a wide variety Wnt family member, including Wnt3, significantly inhibits both canonical and non-canonical pathways. Furthermore, sFRP-1 significantly inhibited CAM-DR of KMS-5 and ARH-77, whereas DKK-1, which binds to the co-receptor for the ß-catenin canonical signal, did not inhibit CAM-DR. Collectively, Wnt, secreted from KMS-5 or ARH-77, is considered to be indeed involved in induction of CAM-DR by autocrine manner through the Wnt/RhoA pathway. As to the Wnt(s) that is actually functioning in the culture medium of KMS-5 and ARH-77, Wnt3 was speculated to be one of the most plausible candidates because the close correlation of Wnt3 expression with the increase of ß-catenin and the GTP-RhoA in CAM-DR relevant cells was observed (Fig. 4A and B). To support the notion that Wnt3 indeed potently augments CAM-DR, we then conducted Wnt3 siRNA transfer into CAM-DR relevant cell lines and found significant reduction of CAM-DR (Fig. 5B). Moreover, when we added Wnt3 CM to KMS-5 and ARH-77 cells, there was a significant increase in CAM-DR of KMS-5 and ARH-77 (Fig. 6A; Supplementary Fig. S4).3 Regarding the incompleteness of inhibition by sFRP-1, there may be two possibilities: (a) stromal cell–derived Wnt5a (24), which is not interfered with by sFRP-1 (49, 50), transduced the Wnt/RhoA signal to evoke CAM-DR in a paracrine manner; (b) stromal cell–derived factor-1 and/or insulin-like growth factor-1, which are both secreted from stromal cells and potently activate the RhoA, participated in paracrine induction of CAM-DR in addition to the Wnt effect (17–21). The possibility that signals other than the RhoA pathway is responsible for the Wnt unrelated CAM-DR of ARH-77 is not likely because the inhibitor of Rho kinase almost completely negated the CAM-DR (Fig. 5C). Thus, the activation of RhoA is considered to play a crucial role in induction of CAM-DR, and molecular targeting to this signal pathway may be an option in overcoming CAM-DR in multiple myeloma. With respect to the molecular mechanism by which CAM-DR is induced by the Wnt/RhoA signal, although direct evidence was not elucidated in the present investigation, it is conceivable that activated RhoA stimulates integrin clustering, thereby inducing CAM-DR, because a Wnt3 CM actually caused morphologic change with a concomitant rearrangement of the actin filament and accumulation of vinculin in the present study (Fig. 6C), which is known to associate with the ß subunit of integrin in the adhesion plaques (51, 52), and activation of RhoA has been reportedly proven to stimulate integrin-mediated adhesion in peripheral T cells and thymocytes (53). Thus, in our cell lines, Wnt3 was considered to stimulate RhoA signal to bring inactive cells into a primed state for subsequent activation by integrin-mediated interaction.
In conclusion, the present study disclosed that Wnt3, which myeloma cells themselves produce, stimulate the Wnt/RhoA signal, thereby bringing cells into a primed state by which cells adhere to extracellular matrix of stromal cells, resulting in the induction of CAM-DR. Hence, targeting the RhoA signal would be a promising strategy to overcome CAM-DR.
Acknowledgments
We thank K. Litton (Bachelor of Arts in English from The University of Massachusetts, Amherst, MA) for editorial assistance.
Footnotes
Grant support: Ministry of Education, Culture, Sports, Science and Technology of Japan (H. Hamada) and Ministry of Health, Labour and Welfare of Japan (M. Kobune).
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.
Note: M. Kobune and H. Chiba contributed equally to this work.
3 Supplementary material for this article are available at Molecular Cancer Therapeutics Online (http://mct.aacrjournals.org/). 
Received 11/ 7/06; revised 3/23/07; accepted 5/ 1/07.
References
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, stroma-free culture; 
, non-contact culture; 
, stromal contact culture. a, KMS-5 (LD50: stroma-free, 0.305 µmol/L; non-contact, 0.360 µmol/L; contact, 1.439 µmol/L); b, ARH77 (LD50: stroma-free, 0.053 µmol/L; non-contact, 0.052 µmol/L; contact, 0.265 µmol/L); c, RPMI8226 (LD50: stroma-free, 0.106 µmol/L; non-contact, 0.139 µmol/L; contact, 0.265 µmol/L); d, MM1S (LD50: stroma-free, 0.096 µmol/L; non-contact, 0.099 µmol/L; contact, 0.139 µmol/L). Represent three independent experiments, each done in quadruplicate. *, P < 0.05, non-contact culture versus contact culture; **, P < 0.01, non-contact culture versus contact culture (Student's t test). C, annexin assay of myeloma cell lines. Y-axis, propidium iodide (PI). KMS-5 myeloma cells were analyzed 24 h after exposure of 0.3 µmol/L doxorubicin, and other myeloma cells were analyzed 24 h after exposure of 0.1 µmol/L doxorubicin. One representative experiment of five showing similar results. The propidium iodide–positive KMS-5, ARH77, RPMI8226, or MM1S myeloma cells before doxorubicin exposure were 0.47 ± 0.10%, 0.29 ± 0.09%, 0.74 ± 0.12%, or 0.04 ± 0.02% in non-contact culture and 0.37 ± 0.12%, 0.12 ± 0.09%, 1.82 ± 0.59%, or 0.10 ± 0.09% in contact culture, respectively.
, P < 0.01, contact culture with isotype control versus contact culture with neutralizing antibody (Student's t test; A and C). *, P < 0.05, non-contact culture versus contact culture (B and D). Represent three independent experiments, each done in quadruplicate. Columns/points, absorbance A450 nm; bars, SD.
, P < 0.05, contact culture without inhibitor versus contact culture with inhibitor; 
