» Articles » PMID: 33445713

The WNT/ROR Pathway in Cancer: From Signaling to Therapeutic Intervention

Overview
Journal Cells
Publisher MDPI
Date 2021 Jan 15
PMID 33445713
Citations 56
Authors
Affiliations
Soon will be listed here.
Abstract

The WNT pathway is one of the major signaling cascades frequently deregulated in human cancer. While research had initially focused on signal transduction centered on β-catenin as a key effector activating a pro-tumorigenic transcriptional response, nowadays it is known that WNT ligands can also induce a multitude of β-catenin-independent cellular pathways. Traditionally, these comprise WNT/planar cell polarity (PCP) and WNT/Ca signaling. In addition, signaling via the receptor tyrosine kinase-like orphan receptors (RORs) has gained increasing attention in cancer research due to their overexpression in a multitude of tumor entities. Active WNT/ROR signaling has been linked to processes driving tumor development and progression, such as cell proliferation, survival, invasion, or therapy resistance. In adult tissue, the RORs are largely absent, which has spiked the interest in them for targeted cancer therapy. Promising results in preclinical and initial clinical studies are beginning to unravel the great potential of such treatment approaches. In this review, we summarize seminal findings on the structure and expression of the RORs in cancer, their downstream signaling, and its output in regard to tumor cell function. Furthermore, we present the current clinical anti-ROR treatment strategies and discuss the state-of-the-art, as well as the challenges of the different approaches.

Citing Articles

Wnt Pathway-Targeted Therapy in Gastrointestinal Cancers: Integrating Benchside Insights with Bedside Applications.

Nayak A, Streiff H, Gonzalez I, Adekoya O, Silva I, Shenoy A Cells. 2025; 14(3).

PMID: 39936971 PMC: 11816596. DOI: 10.3390/cells14030178.


Targeting ROR2 homooligomerization disrupts ROR2-dependent signaling and suppresses stem-like cell properties of human breast adenocarcinoma.

Leng F, Huang J, Wu L, Zhang J, Lin X, Deng R iScience. 2025; 28(1):111589.

PMID: 39829682 PMC: 11742321. DOI: 10.1016/j.isci.2024.111589.


Hitting the target: cell signaling pathways modulation by extracellular vesicles.

Cerrotti G, Buratta S, Latella R, Calzoni E, Cusumano G, Bertoldi A Extracell Vesicles Circ Nucl Acids. 2024; 5(3):527-552.

PMID: 39697631 PMC: 11648414. DOI: 10.20517/evcna.2024.16.


Therapeutic advances in the targeting of ROR1 in hematological cancers.

Tigu A, Munteanu R, Moldovan C, Rares D, Kegyes D, Tomai R Cell Death Discov. 2024; 10(1):471.

PMID: 39551787 PMC: 11570672. DOI: 10.1038/s41420-024-02239-1.


Therapeutic advances of targeting receptor tyrosine kinases in cancer.

Tomuleasa C, Tigu A, Munteanu R, Moldovan C, Kegyes D, Onaciu A Signal Transduct Target Ther. 2024; 9(1):201.

PMID: 39138146 PMC: 11323831. DOI: 10.1038/s41392-024-01899-w.


References
1.
Faiao-Flores F, Emmons M, Durante M, Kinose F, Saha B, Fang B . HDAC Inhibition Enhances the Efficacy of MEK Inhibitor Therapy in Uveal Melanoma. Clin Cancer Res. 2019; 25(18):5686-5701. PMC: 6744978. DOI: 10.1158/1078-0432.CCR-18-3382. View

2.
Xu Y, Ma Y, Pang Y, Zhao Z, Lu J, Mao H . Ectopic repression of receptor tyrosine kinase-like orphan receptor 2 inhibits malignant transformation of ovarian cancer cells by reversing epithelial-mesenchymal transition. Tumour Biol. 2017; 39(5):1010428317701627. DOI: 10.1177/1010428317701627. View

3.
Matsuda T, Nomi M, Ikeya M, Kani S, Oishi I, Terashima T . Expression of the receptor tyrosine kinase genes, Ror1 and Ror2, during mouse development. Mech Dev. 2001; 105(1-2):153-6. DOI: 10.1016/s0925-4773(01)00383-5. View

4.
Hasan M, Widhopf 2nd G, Zhang S, Lam S, Shen Z, Briggs S . Wnt5a induces ROR1 to recruit cortactin to promote breast-cancer migration and metastasis. NPJ Breast Cancer. 2019; 5:35. PMC: 6814774. DOI: 10.1038/s41523-019-0131-9. View

5.
Villarroel A, Del Valle-Perez B, Fuertes G, Curto J, Ontiveros N, Garcia de Herreros A . Src and Fyn define a new signaling cascade activated by canonical and non-canonical Wnt ligands and required for gene transcription and cell invasion. Cell Mol Life Sci. 2019; 77(5):919-935. PMC: 11104847. DOI: 10.1007/s00018-019-03221-2. View