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  • Top
  • Abstract
  • Divergent functions for Dickkopf-1
  • CKAP4 is a DKK-1 receptor that activates AKT signaling
  • Targeting DKK-1/CKAP4 interactions in cancer
  • Conclusions and future directions
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Commentary Free access | 10.1172/JCI88620

CKAP4 is identified as a receptor for Dickkopf in cancer cells

Dheeraj Bhavanasi,1 Kelsey F. Speer,2 and Peter S. Klein1,2

1Department of Medicine, (Hematology-Oncology), and

2Cell and Molecular Biology Graduate Group, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Address correspondence to: Peter S. Klein, 9-103 SCTR, 3400 Civic Center Blvd., Philadelphia, Pennsylvania 19104, USA. Phone: 215.898.2179; E-mail: pklein@upenn.edu.

Authorship note: D. Bhavanasi and K.F. Speer contributed equally to this work.

Find articles by Bhavanasi, D. in: PubMed | Google Scholar |

1Department of Medicine, (Hematology-Oncology), and

2Cell and Molecular Biology Graduate Group, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Address correspondence to: Peter S. Klein, 9-103 SCTR, 3400 Civic Center Blvd., Philadelphia, Pennsylvania 19104, USA. Phone: 215.898.2179; E-mail: pklein@upenn.edu.

Authorship note: D. Bhavanasi and K.F. Speer contributed equally to this work.

Find articles by Speer, K. in: PubMed | Google Scholar

1Department of Medicine, (Hematology-Oncology), and

2Cell and Molecular Biology Graduate Group, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Address correspondence to: Peter S. Klein, 9-103 SCTR, 3400 Civic Center Blvd., Philadelphia, Pennsylvania 19104, USA. Phone: 215.898.2179; E-mail: pklein@upenn.edu.

Authorship note: D. Bhavanasi and K.F. Speer contributed equally to this work.

Find articles by Klein, P. in: PubMed | Google Scholar

Authorship note: D. Bhavanasi and K.F. Speer contributed equally to this work.

Published June 20, 2016 - More info

Published in Volume 126, Issue 7 on July 1, 2016
J Clin Invest. 2016;126(7):2419–2421. https://doi.org/10.1172/JCI88620.
Copyright © 2016, American Society for Clinical Investigation
Published June 20, 2016 - Version history
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Related article:

CKAP4 is a Dickkopf1 receptor and is involved in tumor progression
Hirokazu Kimura, … , Eiichi Morii, Akira Kikuchi
Hirokazu Kimura, … , Eiichi Morii, Akira Kikuchi
Research Article Cell biology Oncology

CKAP4 is a Dickkopf1 receptor and is involved in tumor progression

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Abstract

Dickkopf1 (DKK1) is a secretory protein that antagonizes oncogenic Wnt signaling by binding to the Wnt coreceptor low-density lipoprotein receptor–related protein 6 (LRP6). DKK1 may also regulate its own signaling to promote cancer cell proliferation, but the mechanism is not understood. Here, we identified cytoskeleton-associated protein 4 (CKAP4) as a DKK1 receptor and evaluated CKAP4-mediated DKK1 signaling in cancer cell proliferation. We determined that DKK1 binds CKAP4 and LRP6 with similar affinity but interacts with these 2 receptors with different cysteine-rich domains. DKK1 induced internalization of CKAP4 in a clathrin-dependent manner, further supporting CKAP4 as a receptor for DKK1. DKK1/CKAP4 signaling activated AKT by forming a complex between the proline-rich domain of CKAP4 and the Src homology 3 domain of PI3K, resulting in proliferation of normal cells and cancer cells. Expression of DKK1 and CKAP4 was frequent in tumor lesions of human pancreatic and lung cancers, and simultaneous expression of both proteins in patient tumors was negatively correlated with prognosis and relapse-free survival. An anti-CKAP4 antibody blocked the binding of DKK1 to CKAP4, suppressed AKT activity in a human cancer cell line, and attenuated xenograft tumor formation in immunodeficient mice. Together, our results suggest that CKAP4 is a potential therapeutic target for cancers that express both DKK1 and CKAP4.

Authors

Hirokazu Kimura, Katsumi Fumoto, Kensaku Shojima, Satoshi Nojima, Yoshihito Osugi, Hideo Tomihara, Hidetoshi Eguchi, Yasushi Shintani, Hiroko Endo, Masahiro Inoue, Yuichiro Doki, Meinoshin Okumura, Eiichi Morii, Akira Kikuchi

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Abstract

The secretory protein Dickkopf-1 (DKK-1) is a known Wnt antagonist and has been shown to suppress tumorigenesis in some cancer cells; however, it is also upregulated in many types of cancer and associated with poor prognosis. Wnt-independent mechanisms by which DKK-1 promotes cancer cell proliferation are not well understood. In this issue of the JCI, Kimura and colleagues demonstrate that DKK-1 interacts with cytoskeleton-associated protein 4 (CKAP4) to promote activation of AKT. They show that both DKK-1 and CKAP4 are frequently upregulated in pancreatic and lung cancers. Importantly, targeting this interaction with an anti-CKAP4 antibody prevented tumor formation in murine xenograft models. These results identify a previously unrecognized DKK-1–mediated pathway and suggest CKAP4 as a potential therapeutic target for certain cancers.

Divergent functions for Dickkopf-1

Dickkopf-1 (DKK-1) was first identified in Xenopus as an extracellular antagonist of canonical Wnt signaling (1), a fundamental pathway that controls cell fate, survival, and proliferation. Aberrant activation of Wnt signaling also drives tumorigenesis in colon, breast, hepatocellular, and many other cancers (2–4). As a Wnt signaling inhibitor, DKK-1 suppresses tumorigenesis in some cancer cells, including renal cell carcinoma (5), breast carcinoma (6), and colon cancer cells (7–9). However, DKK-1 is often elevated in cancers, is associated with aggressive disease, and promotes proliferation in multiple cell types (10, 11), suggesting that DKK-1 also functions independently of Wnt inhibition.

In this issue, Kimura and colleagues investigate the molecular events that lead to DKK-1–induced cancer cell proliferation (12). Their work has identified a Wnt-independent signaling role for DKK-1 through interaction with the type-II transmembrane protein cytoskeleton-associated protein 4 (CKAP4; also known as p63, ERGIC-63, or CLIMP-63). These findings also indicate that the DKK-1/CKAP4 interaction represents a promising therapeutic target for cancer.

CKAP4 is a DKK-1 receptor that activates AKT signaling

DKK family proteins contain two cysteine-rich domains (CRDs). The C-terminal CRD (CRD-2) of DKK-1 inhibits Wnt signaling by directly binding to the Wnt coreceptors LRP5/6 (LDL-related proteins 5 and 6), thereby preventing interaction with Wnts, and by binding to the transmembrane protein KREMEN to promote LRP5/6 internalization (11, 13–15). Kimura et al. have now demonstrated that CRD-1 of DKK-1 binds to CKAP4 at the apical surface of epithelial cells (Figure 1 and ref. 12). Furthermore, DKK-1 binds to CKAP4 with high affinity that is comparable to but independent of its interaction with LRP5/6. Upon DKK-1 binding, CKAP4 recruits phosphatidylinositol-3 kinase (PI3K) to its cytoplasmic domain through interaction with the SH3 domain of the p85α subunit of PI3K. Through this mechanism, DKK-1 activates AKT and promotes proliferation. These findings substantially expand our understanding of DKK-1 signaling mechanisms and define a previously unrecognized input to the PI3K/AKT pathway.

DKK-1 stimulates proliferation by binding to CKAP4 and activating AKT.Figure 1

DKK-1 stimulates proliferation by binding to CKAP4 and activating AKT. DKK-1 is secreted from epithelial cells and binds to the extracellular domain of CKAP4 at the apical surface of the cell. The CRD-1 of DKK-1 and the leucine zipper (LZ) domain of CKAP4 are required for this interaction (although a direct interaction between the two has not yet been shown). Upon DKK-1 binding, CKAP4 binds to the p85α subunit of PI3K to activate PI3K/AKT signaling and stimulate cancer cell proliferation. This signaling motif is in contrast to the well-established role for DKK-1 as a canonical Wnt antagonist, in which CRD-2 of DKK-1 binds to the Wnt coreceptor LRP5/6 (preventing interaction with Wnts) and to Kremen (driving internalization of LRP5/6).

The findings of Kimura et al. also raise questions about the potential functions of other DKK family members (12). The DKK family comprises four conserved proteins, DKK-1 through -4 (and DKK-like 1, which lacks the CRDs). DKK-1 antagonizes Wnt/β-catenin signaling, activates AKT (as shown here), and may also activate JNK signaling (16); however, the functions of other DKK family members are less well characterized. DKK-2 and -4 antagonize Wnt signaling, similar to DKK-1, but DKK-2 can also activate canonical Wnt signaling depending on the cellular context (11, 17). In contrast, DKK-3 positively regulates Wnt signaling (18) and binds to integrin α6b to induce myogenesis in zebrafish (19). As Kimura and colleagues point out (12), CRD-1 is highly conserved among the four Dkk genes, raising the possibility that DKK-2, -3, and -4 could also interact with CKAP4. In support of this proposal, DKK-3 protects cells from proapoptotic stimuli (18). While the mechanism of this DKK-3–mediated effect has not been characterized, the prosurvival function of DKK-3 could be mediated by interaction with CKAP4 and subsequent AKT activation.

Targeting DKK-1/CKAP4 interactions in cancer

DKK1 is a Wnt target gene and functions in a negative feedback loop that may in some cases suppress tumorigenesis. Consistent with a tumor suppressor function, DKK family genes are silenced by hypermethylation in colon cancer, renal cell carcinoma, and melanoma. However, DKK-1 expression is increased in many other cancers, including multiple myeloma, hepatocellular carcinoma, and ovarian adenocarcinoma and is associated with more aggressive behavior (11). In these cases, the findings of Kimura et al. suggest a second, potentially counteracting effect of DKK-1 to stimulate proliferation through an AKT-dependent, Wnt-independent mechanism (12).

Thus, the DKK-1/CKAP4 interaction could be a promising therapeutic target for some cancers. Kimura and colleagues found that approximately 70% of pancreatic ductal adenocarcinomas, lung adenocarcinomas, and lung squamous cell carcinomas express high levels of DKK-1 and CKAP4 compared with adjacent, nontransformed tissue and that expression of both proteins correlates with lower relapse-free survival (12). Kimura et al. also demonstrated that DKK-1–expressing cancer cells require CKAP4 expression for tumor growth in mouse xenograft models. Furthermore, an antibody targeting the extracellular domain of CKAP4 suppressed tumorigenesis in DKK-1–expressing cell lines and in a mouse xenograft model. These findings are consistent with published data showing that anti–DKK-1 antibodies impair growth of engrafted human cancers, such as multiple myeloma, in mice (10, 20, 21). However, given that DKK-1 may also suppress tumors by inhibiting Wnt signaling, an antibody to CKAP4 may have more specific, antiproliferative effects that spare the potential tumor suppressor function of DKK-1. Therefore, this CKAP4-targeting antibody may be a valuable therapeutic agent for DKK-1/CKAP4–positive cancers.

Conclusions and future directions

This study by Kimura and colleagues reveals a previously unknown signaling pathway in which DKK-1 binds to CKAP4, resulting in activation of AKT through PI3K to enhance Wnt-independent cellular proliferation (12). The thorough signaling data presented by Kimura et al. provide an explanation for the proliferative effects of DKK-1 and the strong correlation between elevated DKK-1 and aggressive tumor behavior. This work also provides intriguing preclinical data to support the use of anti-CKAP4 antibodies in DKK-1/CKAP4–positive tumors.

DKK-1 is often used experimentally to test whether a biological process is mediated by canonical Wnt signaling. The findings of Kimura et al., along with other studies supporting non-Wnt functions for DKK-1 (11, 16, 19, 22), underscore the limitations of this approach by showing that DKK-1 is not a specific inhibitor of canonical Wnt signaling. Kimura et al. also raise questions for further study. It will be important to determine whether DKK-1 binds directly to CKAP4 or through an intermediate binding partner. Additionally, interaction of CKAP4 with DKK-2 through -4, which contain the highly conserved CRD-1, also remains to be investigated. Other questions to be addressed include whether expression of CKAP4 and DKK-1 will play a role in diagnosis or staging of pancreatic or lung cancers and whether these observations will extend to other cancers. Finally, the comprehensive mechanistic experiments in this study focused on cell lines and xenograft models, leaving open the question of whether the DKK-1/CKAP4 interaction plays a role in primary tumor proliferation or in the proliferation of nontransformed cells. Kimura and colleagues did not observe any obvious effect on normal tissues in their mouse model after 4 weeks of anti-CKAP4 antibody treatment, which is reassuring that inhibiting DKK-1 does not have short-term deleterious effects on normal proliferative tissues; however, the longer-term effects of this strategy are not yet known. Nevertheless, the identification of a signaling mechanism for DKK-1 and the strong preclinical observations presented here are sure to lead to exciting work in the future.

Acknowledgments

This work is supported by grants from the NIH (5R01MH100923 and 7R01GM107435), the Institute for Translational Medicine and Applied Therapeutics, the Institute for Regenerative Medicine, and the Orphan Disease Center at the University of Pennsylvania School of Medicine.

Address correspondence to: Peter S. Klein, 9-103 SCTR, 3400 Civic Center Blvd., Philadelphia, Pennsylvania 19104, USA. Phone: 215.898.2179; E-mail: pklein@upenn.edu.

Footnotes

Conflict of interest: The authors have declared that no conflict of interest exists.

Reference information: J Clin Invest. 2016;126(7):2419–2421. doi:10.1172/JCI88620.

See the related article at CKAP4 is a Dickkopf1 receptor and is involved in tumor progression.

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  • Top
  • Abstract
  • Divergent functions for Dickkopf-1
  • CKAP4 is a DKK-1 receptor that activates AKT signaling
  • Targeting DKK-1/CKAP4 interactions in cancer
  • Conclusions and future directions
  • Acknowledgments
  • Footnotes
  • References
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