DNAJB6 Induces Degradation of β-Catenin and Causes Partial Reversal of Mesenchymal Phenotype*

We showed that expression of MRJ (DNAJB6) protein is lost in invasive ductal carcinoma, and restoration of MRJ(L) restricts malignant behavior of breast cancer and melanoma cells. However, the signaling pathways influenced by MRJ(L) are largely unknown. Our observations revealed that MRJ(L) expression causes changes in cell morphology concomitant with down-regulation of several mesenchymal markers, viz. vimentin, N-cadherin, Twist, and Slug, and up-regulation of epithelial marker keratin 18. Importantly, MRJ(L) expression led to reduced levels of β-catenin, an epithelial mesenchymal transition marker, and a critical player in the Wnt pathway. We found that MRJ(L) up-regulates expression of DKK1, a well known Wnt/β-catenin signaling inhibitor, that causes degradation of β-catenin. Re-expression of DNAJB6 alters the Wnt/β-catenin signaling in cancer cells, leading to partial reversal of the mesenchymal phenotype. Thus, MRJ(L) may play a role in maintaining an epithelial phenotype, and inhibition of the Wnt/β-catenin pathway may be one of the potential mechanisms contributing to the restriction of malignant behavior by MRJ(L).

The Hsp40/DnaJ family of proteins is known to be a specific client protein provider for the Hsp70/DnaK family of chaperones (1). The important role of the Hsp40 family in a variety of aspects of tumor biology is being described only very recently (2-6). DNAJB6 is a member of the class II Hsp40/DnaJ family of proteins comprising two differentially spliced variants (7). MRJ(S), the shorter variant of DNAJB6, has been widely studied and has been reported to regulate keratin8/k18 organization, assist in NFATc3-mediated transcriptional repression, and play a critical role in Huntington disease (8 -10). On the contrary, the role of the long variant, MRJ(L), in various pathophysiologies has still to be revealed with the exception of a potential role in the nuclear import of human immunodeficiency virus type-2 vpx (11). We and others have reported loss of DNAJB6 in advanced breast cancer patients (7,12). A detailed functional characterization of DNAJB6 performed by us revealed that MRJ(L) can act as a nuclear protein by virtue of its nuclear localization signal and can considerably reduce the expression of several secreted proteins that promote invasion, migration, and metastasis of cancer cells. Functionally, MRJ(L) was found to reduce tumorigenicity and metastasis of melanoma and breast cancer cells (7). But the mechanistic clues to the downstream signaling regulated by MRJ(L) are still largely unknown.
In the course of our studies, we observed distinct morphological changes in the cells that were restored for MRJ(L) expression. The cells were more epithelial like in appearance. In this study, we describe the role of MRJ(L) in causing partial reversal of epithelial mesenchymal transition (EMT). 3 Our studies show that MRJ(L) inhibits Wnt/␤-catenin signaling by up-regulating DKK1, a secreted inhibitor of Wnt signaling, and reverts certain aspects of EMT. We also demonstrate that this inhibition of Wnt/␤-catenin signaling is responsible, in part, for the ability of MRJ(L) to restrict malignant behavior.
MDA-MB-435 has now been confirmed to be of melanoma origin (13)(14)(15). However., there still are convincing arguments about the lineage infidelity of this cell line (16). However, the work presented here uses this cell line as a model system for signaling studies.
SUM159 cells were cultured in Ham's F-12 with 5% fetal bovine serum supplemented with insulin (5 mg/ml) and hydrocortisone (1 mg/ml). The cell line SUM1315 was cultured in Ham's F-12 with 5% fetal bovine serum supplemented with insulin (5 mg/ml) and epidermal growth factor (10 ng/ml). Both SUM lines were bought from Asterand plc, Detroit, MI.
RNA Isolation and Real Time Quantitative RT-PCR-TRIzol reagent (Invitrogen) was used to isolate total RNA from cultured cells. RNA was treated with DNase I (Promega, Madison, WI). cDNA synthesis was carried out using a cDNA synthesis kit (Applied Biosystems Inc., Foster City, CA) with 1 g of total RNA as the template and random primers. Real time quantitative RT-PCR (QRT-PCR) analysis was performed on the experimental mRNAs. The PCR primers and probes for Dickkopf1 (DKK1), DNAJB6 (MRJ(L)), c-myc, E-cadherin, and keratin 18 and normalization control gene glyceraldehyde-3-phosphate dehydrogenase were purchased from Applied Biosystems Inc. QRT-PCR was performed on an ABI 7500 HT instrument (Applied Biosystems). The gene expression ⌬Ct values of mRNAs from each sample were calculated by normalizing with normalization control, glyceraldehyde-3-phosphate dehydrogenase, and relative quantitation values were plotted using GraphPad Prism (La Jolla, CA). QRT-PCR analysis was performed on the experimental mRNAs in triplicate, and the experiment was repeated once from an independent passage to confirm the findings.
Plasmids and Constructs-pDKK-707, a luciferase construct encompassing Ϫ707 to ϩ43 bp of human DKK1 promoter was a gift from the Varmus laboratory (21). M50 TOPFlash luciferase construct was a generous gift from Dr. Randall Moon (22).
shRNA Knockdown-Oligo Design Tool TM (Oligoengine, Seattle, WA) was used to design two shRNAs, NM_807 and NM_808, predicted to silence the expression of MRJ(L). The heteroduplexes supplied as asymmetric oligomers were annealed following the manufacturer's instructions and cloned into pSUPERIOR.neoϩGFP (Oligoengine) at the BglII and HindIII sites. Recombinants were analyzed by restriction diges-tion using EcoRI and HindIII (Promega), and recombinant DNA was prepared using the QIA Maxiprep kit (Qiagen, Valencia, CA).
MCF10A cells were transfected with shRNA targeting MRJ(L) (NM_ 808) or a control nontargeting shRNA using Lipofectamine 2000 according to the manufacturer's instructions. The extent of knockdown was assessed using QRT-PCR, using RNA isolated 32 h after transfection.
siRNA Knockdown-Cells were transiently transfected with SMARTpool siRNA (Dharmacon, Chicago) designed to target DKK1 or nontargeting siRNA control using Dharmafect1 (Dharmacon) following the manufacturer's protocol. Conditioned serum-free medium and lysates were collected from both control and DKK1-siRNA-treated cells 38 h post-transfection. The extent of knockdown was assessed using Western blot analysis.
Immunocytochemistry-Cells cultured on coverslips were fixed in 4% paraformaldehyde in PBS for 20 min at room temperature and then permeabilized in PBS containing 0.1% Triton X-100 and 3% bovine serum albumin. F-actin was stained with phalloidin-TRITC (1:100, Molecular Probes) for 1 h at room temperature and observed after mounting the coverslip in VECTASHIELD (Vector Laboratories, Burlingame, CA). Cells were viewed using a Zeiss Axiovert 200 M microscope equipped with an Axiocam camera and Axiovision software (Carl Zeiss, Inc., Thornwood, NY).
Luciferase Assay-Cells were transfected using Lipofectamine 2000 (Invitrogen) as per the manufacturer's instructions. Total protein was harvested and luciferase activity measured using a Turner 20/20 luminometer (Turner Biosystems, Sunnyvale, CA). The luciferase reading was normalized to the total protein concentration. Data are expressed as relative luciferase activity, where control is 100%.
Western Blot-The cell monolayer was washed twice with calcium-and magnesium-free PBS and lysed with cold lysis buffer (150 mM NaCl, 50 mM Tris, 1% Nonidet P-40, and protease and phosphatase inhibitors). The lysates were kept on ice for 1 h and centrifuged at 10,000 rpm for 30 min at 4°C. Protein concentration was measured using Bradford reagent (Bio-Rad). Proteins were subjected to SDS-PAGE and transferred to polyvinylidene difluoride membranes (0.2 m). The membranes were blocked with 5% skimmed milk in TBST (1 M Tris, pH 7.5, 9% NaCl, 0.5% Tween 20) and incubated with primary antibodies overnight at 4°C. The membranes were then washed three times with TBST, incubated with respective secondary antibodies for 1 h at room temperature, and then developed using SuperSignal TM (Pierce) following washes for 1 h with three changes of TBST.
Colony Formation Assay-MDA-MB-435 cells stably expressing MRJ(L) were plated in 6-well plates and transfected with DKK1 siRNA and control siRNA using Lipofectamine 2000 (Invitrogen) as per the manufacturer's instructions. After 24 h of transfection, the cells were plated into three 10-cm plates in selection medium and were allowed to grow for 12 days. Crystal violet staining was used for visualization of foci. Six different fields were counted for the number of foci, and data are represented as average Ϯ S.E.
Soft Agar Colonization Assay-MDA-MB-435 cells (2 ϫ 10 3 ) treated with DKK1siRNA or control siRNA suspended in 0.35% agar were plated onto a layer of 0.75% BactoAgar in DMEM/ F-12 (10% fetal bovine serum) in 6-well tissue culture dishes. Visible colonies (Ͼ50 cells) were counted after 15 days with the aid of a dissecting microscope.
Wound Healing Assay-Cells were cultured to confluence on 6-well plates, which were previously externally marked with parallel lines to use as guides for the subsequent photography. The cells were transfected with DKK1 siRNA and control siRNA using Lipofectamine 2000 (Invitrogen) as per the manufacturer's instructions. After 24 h of transfection, a central linear wound (perpendicular to the guide lines) was made with a 200-l sterile pipette tip. Media were changed gently to remove any floating cells. Phase micrographs of the wound cultures were taken at 0 and 16 h (average doubling time is about 20 h). The photographs were analyzed by measuring the distance from the wound edge of the cell sheet at the end of 16 h to the original wound site. Wound healing activity was calculated as the mean distance between edges in 12 independent fields per well. Each test group was assayed in triplicate, and the results are expressed relative to vector control cell migration.
Migration Assay-Migration assays were conducted using 8-m polyethylene terephthalate filters (BD Pharmingen), as described previously (23). Cells (treated with DKK1siRNA or control siRNA), which migrated to the lower sides of the transwell, were stained using 0.05% crystal violet, and the cell number was counted. Each test group was assayed in triplicate. Four different fields of each insert were photographed at 10ϫ magnification using a Zeiss Axiocam 200 M microscope (Zeiss Axiocam, Carl Zeiss Microimaging Inc.). Each field was divided into quadrants, and cells in diagonally opposite quadrants were counted.

MRJ(L) Expression Leads to Change in Cell
Shape-We compared the morphology of the cells that were engineered to constitutively express MRJ(L) to the corresponding vector control. As seen in Fig. 1, A and B, MRJ(L) stable transfectants of MDA-  MB-435 and MCF7 cells show a well spread/pavement-like appearance and a differential actin staining when compared with the respective controls that look elongated and spindleshaped. The discrete morphological difference is highlighted by the extended filopodia very distinctly present on the surface of MRJ(L) expressors (Fig. 1, A  Loss of ␤-catenin and gain of keratin 18 were consistent in all three cell lines (Fig. 2).
Degradation of ␤-Catenin by MRJ(L) Is Proteasome-dependent-Stabilized ␤-catenin characteristically represents activated Wnt/␤-catenin signaling. MRJ(L) expressors showed distinctly reduced levels of ␤-catenin protein. We saw no sig-nificant change in the steady state mRNA levels for ␤-catenin (data not shown); hence, we tested if this reduction was due to enhanced degradation of ␤-catenin. As seen in Fig. 3, A and B 1 We observed greater than 85% reduction in the TOPFlash activity in all the cell lines, indicating a significant inhibition of the Wnt/␤-catenin signaling (Fig. 4, A-C). MRJ(L) Up-regulates DKK1-DKK1 is a secreted inhibitor of Wnt/␤-catenin signaling that blocks Wnt signaling by binding to the Wnt co-receptor Lrp5/6. QRT-PCR analysis of different breast cancer cell lines showed that all of them express lower levels of DKK1 mRNA as compared with nontumorigenic MCF10A cells. SUM1315, SUM159, and MCF10.DCIS.com express very low levels of DKK1, whereas MCF7 and MDA-MB-231 cells seem to express slightly higher levels. The levels of DKK1 in MCF10CA1d.cl.1 cells were intermediate (Fig. 5A). We have also evaluated DKK1 mRNA levels in MDA-MB-435 and found it to be very low. Hence, we examined the MRJ(L) expressors for expression of DKK1. As seen in Fig. 5B, we observed a substantial increase in the levels of secreted DKK1 in serum-free conditioned medium from 435-MRJ(L) and MCF10CA1d.cl.1-MRJ(L) cells. These results corroborate with the increased DKK1 transcript by QRT-PCR (supplemental Fig. 1).
To determine whether the increase in DKK1 is at a transcriptional level, we assessed the activity of the luciferase reporter construct pDKK1-707 in MCF10CA1d.cl Silencing of DKK1 from MRJ(L) Expressors Leads to Restoration of ␤-Catenin-DKK1 binding to the Lrp5/6 receptors directs ␤-catenin to phosphorylation and subsequent proteosome-mediated degradation. If the degradation of ␤-catenin in MRJ(L) expressing cells is due to the elevated DKK1 levels,  6A). MCF10CA1d.cl.1 MRJ(L) expressors also show comparable restoration of ␤-catenin levels upon DKK1 silencing (Fig. 6B). For reasons not known to us, we always noticed a slight elevation of ␤-catenin in the control siRNA transfectants of MCF10CA1d.cl.1MRJ(L). Because most of the elevated mesenchymal markers observed by us in Fig. 2 are downstream targets of ␤-catenin transcription, we hypothesized that DKK1 silencing will increase the ␤-catenin protein levels and result in changes in the transcript levels of the mesenchymal markers. We explored the effect of DKK1 silencing, in MDA-MB-435-MRJ(L), on the EMT markers (supplemental Fig. 2). We observed that there was a noticeable up-regulation of mesen-   Silencing of DKK1 from MRJ(L) Expressors Increases Their Malignant Activity-We had previously reported that MRJ(L) expression reduced malignant activity of cancer cell lines as measured by in vitro assays. Cells ectopically expressing MRJ(L) showed reduced invasion through Matrigel TM and reduced migration using modified Boyden chamber assay, decreased scratch motility (wound healing) assay, and less anchorage independence as measured by soft agar colony formation. If the reduced malignant behavior of MRJ(L) expressor cells was due to the inhibition of the Wnt/␤-catenin signaling by the elevated DKK1 levels, silencing DKK1 expression will revert their phenotype and make them more malignant. As observed from the data in Fig. 7, silencing of DKK1 from 435-MRJ(L) increased the foci formation ability by about 3-fold (Fig. 7A), its motility (wound healing ability) by about 2-fold (Fig. 7B), and anchorage-independent growth as measured by soft agar colony formation by about 2.5-fold (Fig. 7C).
Abrogating of MRJ(L) from MCF10A Leads to Activation of Wnt/␤-Catenin Signaling-MCF10A (immortalized breast epithelial line), expresses noticeably high levels of MRJ(L) as compared with breast cancer cell lines (7). Based on our observations described thus far, we hypothesized that knockdown of MRJ(L) from MCF10A would activate Wnt/␤-catenin signaling. As seen in Fig. 8A, knockdown of MRJ(L) using shRNA NM_808 increases the ␤-catenin levels. We independently tested the activity of Wnt/␤-catenin signaling in the MCF10A-MRJ(L) knockdown cells using M50-TOPFlash reporter assays. We saw a significant and reproducible activation of the reporter in the MRJ(L) knockdown cells, indicative of active Wnt/␤catenin signaling (Fig. 8A). We tested the effect of MRJ(L) knockdown on invasion and motility. We saw a significant (p Ͻ 0.05) 1.5 times increase in number of cells migrated. The invasion ability of the knockdown cells was doubled. These observations indicated a shift toward a malignant phenotype. To test if the MCF10A cells, which show a mostly epithelial phenotype, will show a shift toward a mesenchymal phenotype, we evaluated the changes in transcript levels of some key epithelial markers upon MRJ(L) knockdown from MCF10A cells. As seen in Fig. 8C, we observed that the shRNA knockdown of MRJ(L) was accompanied by a concomitant reduction in DKK1 transcript and down-regulation of CDH1 (E-cadherin) transcript indicating loss of epithelial phenotype. c-Myc is a key oncogenic target of the Wnt/␤-catenin signaling. We observed that MRJ(L) knockdown increased c-Myc transcript in MCF10A by 2.5-fold, suggesting activation of Wnt/␤-catenin signaling. However, we did not see any change in the levels of KRT18 (keratin 18), an epithelial marker that gets up-regulated at protein levels upon MRJ(L) overexpression.

DISCUSSION
Heat shock proteins (HSPs) are a group of proteins whose expression is increased when cells are exposed to stress; however, HSPs are also present in cells under normal conditions (26 -28). They are popularly called "chaperones" and are implicated in protein folding and destruction. However, they also have roles in immunological processes, cell cycle regulation, transcriptional activation, and signal transduction (29 -31). Heat shock proteins are overexpressed in a wide range of human cancers, conferring resistance to cytotoxic therapies (29,31). HSP90 and HSP70 are widely studied for their involvement in molecular signaling events that have direct bearing on understanding cancer biology (32)(33)(34)(35)(36). However, the role of HSP40 family members is only recently described (2, 3, 37-42). DNAJB6 is an HSP40 family member whose involvement in cancer has been recently realized (2, 7, 12). Expression of this protein is lost in aggressive breast cancer. The large spliced variant of DNAJB6, MRJ(L) shows reduced expression in aggressive cancer cells. Restoration of MRJ(L) in aggressive breast cancer cells reduces tumorigenicity and metastasis (7). However, the signaling pathways impacted by MRJ(L) were not known.
We observed that MRJ(L) expressors have a distinct epithelial-like appearance and increased expression of filopodia on the surface (Fig. 1). Recent studies have indicated that distinctive filopodia differing in length, positioning, and dynamics are seen in different cells (43). Filopodia can act as sensors of the environment and change to lamellipodia when the cell decides to migrate (44). Besides their role in cell migration, filopodia also have been reported to play a role in formation of adherens junctions between epithelial cells (45). MRJ(L)-expressing cells show numerous filopodia indicative of epithelial transformation that may be a prerequisite for the cells to search for an adjacent cell with extended filopodia leading to interdigitation of filopodia and formation of adherens junctions. Based on known phenotypes, MCF7 is more epithelial-like and MCF10CA1d.cl.1 is much more mesenchyme-like than MCF7, but MDA-MB-435 is the most mesenchyme-like. At the molecular level, we observed that protein levels of mesenchymal markers like CTNNB1 (␤-catenin), Vim (vimentin), CDH2 (N-cadherin), Twist1, and Slug (SNAI2) were down-regulated in MRJ(L) expressors, whereas the epithelial marker, KRT18 (keratin 18) was up-regulated (Fig. 2). We did not see any noticeable changes in E-cadherin levels (tested in MCF7 and MCF10CA1d.cl.1), but interestingly, MCF10A cells did show a loss of E-cadherin transcript (CDH1) upon MRJ(L) knockdown (Fig. 8). N-cadherin expression has been reported to increase motility of breast cancer cells regardless of their E-cadherin status (46). Vimentin is an important cytoskeletal protein that controls the formation of focal adhesions for efficient migration and invasion (47,48). Buhler and Schaller (49) have shown that forced expression of keratin 18 in aggressive breast cancer cells reduces vimentin expression, alters cell shape, and reduces invasion. Thus, down-regulation of vimentin, N-cadherin levels, and up-regulation of keratin 18 in MRJ(L) cells suggests a shift toward a less malignant phenotype. Taken together, MRJ(L) is capable of down-regulating mesenchymal markers and upregulating the expression of epithelial marker keratin 18. MRJ(L) overexpression led to increased expression of keratin 18 consistently in three different cell lines as observed in Fig. 2. However, this change may be independent of DKK1; when we silenced DKK1 from MDA-MB-435-MRJ(L) cells, we did not see an effect on keratin 18 (data not shown). This could mean that keratin 18 up-regulation by MRJ(L) may be independent of the suppression of the Wnt/␤-catenin pathway. Also, we did not see keratin 18 transcript levels down concomitant with MRJ(L) knockdown from MCF10A (Fig. 8C). We think that keratin 18, an epithelial marker, may be under multiple checks and controls, and merely silencing MRJ(L) may not be changing its levels. miR-200 family and Zeb1/2 have a critical role in regulating EMT through Slug and Twist levels (50 -53). To see if these signaling pathways affecting mesenchymal phenotype may also be altered by MRJ(L), we tested miR-200 and Zeb1/2 levels in MDA-MB-435-MRJ(L) and found a 10-fold up-regulation of miR-200b and a several fold (C t value Ͼ40, practically not detected) reduction in Zeb2 levels (supplemental Fig. 4). Zeb1 levels were unaltered. Effectively, expression of MRJ(L) appears to be necessary, in part, to maintain the epithelial phenotype. It is tempting to speculate that loss of MRJ(L) may be one of the triggers in tipping cells toward the metastable phenotype (54,55).
EMT is one of the important series of molecular changes in cancer progression, which may affect prognosis of cancers such as breast cancer (56 -58). Several signaling pathways have been implicated to play a role in EMT of cancer cells, and Wnt/␤catenin is one of the important ones (59,60). Of all the EMTrelated signaling changes that accompanied MRJ(L) overexpression, reduced levels of ␤-catenin protein were most consistent across the different cell types examined by us. This reduction led to significant inhibition of the Wnt/␤-catenin signaling in the MRJ(L) expressors (Fig. 4). ␤-Catenin is a major player in the Wnt signaling pathway, as well as an important was transiently transfected using NM_808 cloned in pSuperior.neo ϩ GFP. Total protein (35 g) was immunoblotted and analyzed for the levels of MRJ(L) and ␤-catenin. ␤-Tubulin was used to verify equal loading. Activity of TCF/Lef reporter, TOPFlash (50 g), evaluated in MCF10A was transiently transfected using NM_808 compared with their corresponding scrambled shRNA controls. The experiment was performed in triplicate and repeated two times. The error bars represent means Ϯ S.E. Statistical significance was determined if it reached 95% confidence. * indicates p Ͻ 0.05. B, knockdown of MRJ(L) from MCF10A shows increased malignant activity as measured by invasion through Matrigel TM and migration using modified Boyden chamber assay. The experiments were performed in triplicate and repeated one time. The error bars represent means Ϯ S.E. Statistical significance was determined if it reached 95% confidence. * indicates p Ͻ 0.05. C, quantitative RT-PCR analysis was performed to measure transcript levels of epithelial markers E-cadherin and keratin 18 using RNA from MCF10A transiently transfected using NM_808 and compared with the corresponding scrambled (scr) shRNA control. The knockdown of MRJ(L) and simultaneous down-regulation of DKK1 was also monitored as a control. c-Myc levels were evaluated as an indicator of Wnt/␤-catenin pathway activity. Analysis was performed on the experimental mRNAs in triplicate, and the experiment was repeated once. Statistical significance was determined if it reached 95% confidence. E-cadherin, MRJ(L) and DKK1 had significant changes compared with the scrambled shRNA control p Ͻ 0.05. regulator of EMT in cancer cells and possibly in maintaining a metastable phenotype (54,61,62). It is important to note that ␤-catenin is a molecule that has multiple functions based on its location and partners. At the cell membrane, it binds to ␣-catenin and E-cadherin contributing to the formation of cadherincatenin junctions. These junctions are contributors to cell polarity and the epithelial phenotype, whereas nuclear ␤-catenin binds to Tcf/Lef transcription factors and promotes transcription of target genes that among other phenotypes are responsible for regulating mesenchymal markers (63). Our observations indicate that MRJ(L) expression promotes the degradation of ␤-catenin in a proteasome-dependent manner (Fig. 3). The known pathways that drive the degradation of ␤-catenin are initiated by inhibition of Wnt ligands or their receptors by their inhibitors like sFRPs, DKKs, etc. (64,65). We observed that breast cancer cells show relatively lower mRNA levels of DKK1 as compared with nontumorigenic MCF10A cells (Fig. 5A); moreover, the expression profiles of DKK1 paralleled that of MRJ(L) (supplemental Fig. 3). Analysis of MRJ(L) overexpressors showed increased levels of secreted DKK1, due to the transcriptional up-regulation of DKK1 (Fig. 5C), which possibly caused reduced ␤-catenin protein levels (Fig. 5B). Knockdown of up-regulated endogenous DKK1 by treatment of 435-MRJ(L) with DKK1-siRNA restored ␤-catenin levels in MRJ(L). This confirmed the role of MRJ(L) up-regulated DKK1 in degrading ␤-catenin (Fig. 6). Enhancement in motility, increased foci formation, as well as increased soft agar colonization were seen in DKK1-silenced MDA-MB-435 cells indicating that the MRJ(L) up-regulated DKK1 contributed to the reduction of malignant activity. Importance of MRJ(L) and DKK1 is also evident in Fig. 8B and supplemental Fig. 5 as silencing the expression of either of these genes leads to increased invasion and motility in MCF10A cells. DKK1 loss has been correlated with aggressive breast cancer and is reported to be frequently inactivated by epigenetic inactivation (66). DKK1 is implicated as a player in inhibiting malignant behavior of breast cancer (67)(68)(69)(70)(71). Stable expression of DKK1 in breast cancer cells has been reported to increase expression of keratin 18 levels concomitantly with a decrease in ␤-catenin levels (72). Recently, interesting studies by DiMeo et al. (70) showed that silencing LRP6, a Wnt co-receptor that is blocked by DKK1, reduced the capacity of cancer cells to selfrenew and seed tumors in vivo and also resulted in the re-expression of breast epithelial differentiation markers and repression of EMT transcription factors Slug and Twist.
The Wnt signaling pathway has been reported to be associated with the invasive ductal carcinoma of the breast (73). Stabilized ␤-catenin induces hyperplasia and mammary tumors in mice (74). Activation of Wnt/␤-catenin signaling components in mammary epithelium induces trans-differentiation (75). In melanoma as well, Wnt signaling has been shown to be involved in inhibition of metastasis suppressors and activation of EMT (76). Our observations demonstrate a role for MRJ(L) in up-regulating DKK1, leading to inhibition of the Wnt/␤-catenin signaling pathway. This inhibition could be one of the ways by which MRJ(L) reduces tumorigenicity and metastasis of aggressive cancer cells.