» Articles » PMID: 33126517

Wnt Pathway: An Integral Hub for Developmental and Oncogenic Signaling Networks

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2020 Oct 31
PMID 33126517
Citations 20
Authors
Affiliations
Soon will be listed here.
Abstract

The Wnt pathway is an integral cell-to-cell signaling hub which regulates crucial development processes and maintenance of tissue homeostasis by coordinating cell proliferation, differentiation, cell polarity, cell movement, and stem cell renewal. When dysregulated, it is associated with various developmental diseases, fibrosis, and tumorigenesis. We now better appreciate the complexity and crosstalk of the Wnt pathway with other signaling cascades. Emerging roles of the Wnt signaling in the cancer stem cell niche and drug resistance have led to development of therapeutics specifically targeting various Wnt components, with some agents currently in clinical trials. This review highlights historical and recent findings on key mediators of Wnt signaling and how they impact antitumor immunity and maintenance of cancer stem cells. This review also examines current therapeutics being developed that modulate Wnt signaling in cancer and discusses potential shortcomings associated with available therapeutics.

Citing Articles

Non-canonical Wnt signaling pathway activated NFATC3 promotes GDF15 expression in MASH: prospective analyses of UK biobank proteomic data.

Wang H, Xu X, Shi L, Huang C, Sun Y, You H Hepatol Int. 2025; .

PMID: 39836348 DOI: 10.1007/s12072-024-10775-2.


SP140 represses specific loci by recruiting polycomb repressive complex 2 and NuRD complex.

Tamburri S, Zucchelli C, Matafora V, Zapparoli E, Jevtic Z, Farris F Nucleic Acids Res. 2024; 53(4).

PMID: 39718989 PMC: 11879014. DOI: 10.1093/nar/gkae1215.


Signaling pathways activated and regulated by stem cell-derived exosome therapy.

Li D, Li D, Wang Z, Li J, Shahzad K, Wang Y Cell Biosci. 2024; 14(1):105.

PMID: 39164778 PMC: 11334359. DOI: 10.1186/s13578-024-01277-7.


Stress granules in cancer: Adaptive dynamics and therapeutic implications.

Jia Y, Jia R, Dai Z, Zhou J, Ruan J, Chng W iScience. 2024; 27(8):110359.

PMID: 39100690 PMC: 11295550. DOI: 10.1016/j.isci.2024.110359.


A Comparison of Common Quantum Dot Alternatives to Cadmium-Based Quantum Dots on the Basis of Liver Cytotoxicity.

Harris S, Kim K Nanomaterials (Basel). 2024; 14(13).

PMID: 38998690 PMC: 11243397. DOI: 10.3390/nano14131086.


References
1.
Lijam N, Paylor R, McDonald M, Crawley J, Deng C, Herrup K . Social interaction and sensorimotor gating abnormalities in mice lacking Dvl1. Cell. 1997; 90(5):895-905. DOI: 10.1016/s0092-8674(00)80354-2. View

2.
Koo B, van Es J, van den Born M, Clevers H . Porcupine inhibitor suppresses paracrine Wnt-driven growth of Rnf43;Znrf3-mutant neoplasia. Proc Natl Acad Sci U S A. 2015; 112(24):7548-50. PMC: 4475934. DOI: 10.1073/pnas.1508113112. View

3.
Korvala J, Juppner H, Makitie O, Sochett E, Schnabel D, Mora S . Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity. BMC Med Genet. 2012; 13:26. PMC: 3374890. DOI: 10.1186/1471-2350-13-26. View

4.
Gonsalves F, Klein K, Carson B, Katz S, Ekas L, Evans S . An RNAi-based chemical genetic screen identifies three small-molecule inhibitors of the Wnt/wingless signaling pathway. Proc Natl Acad Sci U S A. 2011; 108(15):5954-63. PMC: 3076864. DOI: 10.1073/pnas.1017496108. View

5.
Yang A, Fan F, Camp E, Van Buren G, Liu W, Somcio R . Chronic oxaliplatin resistance induces epithelial-to-mesenchymal transition in colorectal cancer cell lines. Clin Cancer Res. 2006; 12(14 Pt 1):4147-53. DOI: 10.1158/1078-0432.CCR-06-0038. View