Skip to main content
Top
Published in: Discover Oncology 1/2021

Open Access 01-12-2021 | Prostate Cancer | Review

Wnt/β-catenin signal transduction pathway in prostate cancer and associated drug resistance

Authors: Chunyang Wang, Qi Chen, Huachao Xu

Published in: Discover Oncology | Issue 1/2021

Login to get access

Abstract

Globally, prostate cancer ranks second in cancer burden of the men. It occurs more frequently in black men compared to white or Asian men. Usually, high rates exist for men aged 60 and above. In this review, we focus on the Wnt/β-catenin signal transduction pathway in prostate cancer since many studies have reported that β-catenin can function as an oncogene and is important in Wnt signaling. We also relate its expression to the androgen receptor and MMP-7 protein, both critical to prostate cancer pathogenesis. Some mutations in the androgen receptor also impact the androgen-β-catenin axis and hence, lead to the progression of prostate cancer. We have also reviewed MiRNAs that modulate this pathway in prostate cancer. Finally, we have summarized the impact of Wnt/β-catenin pathway proteins in the drug resistance of prostate cancer as it is a challenging facet of therapy development due to the complexity of signaling pathways interaction and cross-talk.
Literature
2.
go back to reference Sharma RP, Chopra VL. Effect of the wingless (wg1) mutation on wing and haltere development in Drosophila melanogaster. Dev Biol. 1976;48(2):461–5.PubMedCrossRef Sharma RP, Chopra VL. Effect of the wingless (wg1) mutation on wing and haltere development in Drosophila melanogaster. Dev Biol. 1976;48(2):461–5.PubMedCrossRef
3.
go back to reference Nusse R, et al. Mode of proviral activation of a putative mammary oncogene (int-1) on mouse chromosome 15. Nature. 1984;307(5947):131–6.PubMedCrossRef Nusse R, et al. Mode of proviral activation of a putative mammary oncogene (int-1) on mouse chromosome 15. Nature. 1984;307(5947):131–6.PubMedCrossRef
4.
go back to reference De A. Wnt/Ca2+ signaling pathway: a brief overview. Acta Biochim Biophys Sin. 2011;43(10):745–56.PubMedCrossRef De A. Wnt/Ca2+ signaling pathway: a brief overview. Acta Biochim Biophys Sin. 2011;43(10):745–56.PubMedCrossRef
5.
go back to reference Klaus A, Birchmeier W. Wnt signalling and its impact on development and cancer. Nat Rev Cancer. 2008;8(5):387–98.PubMedCrossRef Klaus A, Birchmeier W. Wnt signalling and its impact on development and cancer. Nat Rev Cancer. 2008;8(5):387–98.PubMedCrossRef
7.
go back to reference van Es JH, Barker N, Clevers H. You Wnt some, you lose some: oncogenes in the Wnt signaling pathway. Curr Opin Genet Dev. 2003;13(1):28–33.PubMedCrossRef van Es JH, Barker N, Clevers H. You Wnt some, you lose some: oncogenes in the Wnt signaling pathway. Curr Opin Genet Dev. 2003;13(1):28–33.PubMedCrossRef
8.
go back to reference Grumolato L, et al. Canonical and noncanonical Wnts use a common mechanism to activate completely unrelated coreceptors. Genes Dev. 2010;24(22):2517–30.PubMedPubMedCentralCrossRef Grumolato L, et al. Canonical and noncanonical Wnts use a common mechanism to activate completely unrelated coreceptors. Genes Dev. 2010;24(22):2517–30.PubMedPubMedCentralCrossRef
9.
go back to reference Ho HY, et al. Wnt5a-Ror-dishevelled signaling constitutes a core developmental pathway that controls tissue morphogenesis. Proc Natl Acad Sci USA. 2012;109(11):4044–51.PubMedPubMedCentralCrossRef Ho HY, et al. Wnt5a-Ror-dishevelled signaling constitutes a core developmental pathway that controls tissue morphogenesis. Proc Natl Acad Sci USA. 2012;109(11):4044–51.PubMedPubMedCentralCrossRef
10.
go back to reference Schlesinger A, et al. Wnt pathway components orient a mitotic spindle in the early Caenorhabditis elegans embryo without requiring gene transcription in the responding cell. Genes Dev. 1999;13(15):2028–38.PubMedPubMedCentralCrossRef Schlesinger A, et al. Wnt pathway components orient a mitotic spindle in the early Caenorhabditis elegans embryo without requiring gene transcription in the responding cell. Genes Dev. 1999;13(15):2028–38.PubMedPubMedCentralCrossRef
11.
go back to reference Walston T, et al. Multiple Wnt signaling pathways converge to orient the mitotic spindle in early C. elegans embryos. Dev Cell. 2004;7(6):831–41.PubMedCrossRef Walston T, et al. Multiple Wnt signaling pathways converge to orient the mitotic spindle in early C. elegans embryos. Dev Cell. 2004;7(6):831–41.PubMedCrossRef
12.
go back to reference Schlessinger K, Hall A, Tolwinski N. Wnt signaling pathways meet Rho GTPases. Genes Dev. 2009;23(3):265–77.PubMedCrossRef Schlessinger K, Hall A, Tolwinski N. Wnt signaling pathways meet Rho GTPases. Genes Dev. 2009;23(3):265–77.PubMedCrossRef
13.
go back to reference Qiu W, Chen L, Kassem M. Activation of non-canonical Wnt/JNK pathway by Wnt3a is associated with differentiation fate determination of human bone marrow stromal (mesenchymal) stem cells. Biochem Biophys Res Commun. 2011;413(1):98–104.PubMedCrossRef Qiu W, Chen L, Kassem M. Activation of non-canonical Wnt/JNK pathway by Wnt3a is associated with differentiation fate determination of human bone marrow stromal (mesenchymal) stem cells. Biochem Biophys Res Commun. 2011;413(1):98–104.PubMedCrossRef
14.
go back to reference Heinonen KM, et al. Wnt4 enhances murine hematopoietic progenitor cell expansion through a planar cell polarity-like pathway. PLoS ONE. 2011;6(4): e19279.PubMedPubMedCentralCrossRef Heinonen KM, et al. Wnt4 enhances murine hematopoietic progenitor cell expansion through a planar cell polarity-like pathway. PLoS ONE. 2011;6(4): e19279.PubMedPubMedCentralCrossRef
15.
go back to reference Jeays-Ward K, et al. Endothelial and steroidogenic cell migration are regulated by WNT4 in the developing mammalian gonad. Development. 2003;130(16):3663–70.PubMedCrossRef Jeays-Ward K, et al. Endothelial and steroidogenic cell migration are regulated by WNT4 in the developing mammalian gonad. Development. 2003;130(16):3663–70.PubMedCrossRef
16.
go back to reference Zhao L, et al. E6-induced selective translation of WNT4 and JIP2 promotes the progression of cervical cancer via a noncanonical WNT signaling pathway. Signal Transduct Target Ther. 2019;4:32.PubMedPubMedCentralCrossRef Zhao L, et al. E6-induced selective translation of WNT4 and JIP2 promotes the progression of cervical cancer via a noncanonical WNT signaling pathway. Signal Transduct Target Ther. 2019;4:32.PubMedPubMedCentralCrossRef
17.
go back to reference Hardy KM, et al. Non-canonical Wnt signaling through Wnt5a/b and a novel Wnt11 gene, Wnt11b, regulates cell migration during avian gastrulation. Dev Biol. 2008;320(2):391–401.PubMedPubMedCentralCrossRef Hardy KM, et al. Non-canonical Wnt signaling through Wnt5a/b and a novel Wnt11 gene, Wnt11b, regulates cell migration during avian gastrulation. Dev Biol. 2008;320(2):391–401.PubMedPubMedCentralCrossRef
18.
go back to reference Humphries AC, Mlodzik M. From instruction to output: Wnt/PCP signaling in development and cancer. Curr Opin Cell Biol. 2018;51:110–6.PubMedCrossRef Humphries AC, Mlodzik M. From instruction to output: Wnt/PCP signaling in development and cancer. Curr Opin Cell Biol. 2018;51:110–6.PubMedCrossRef
19.
go back to reference Li R, et al. WNT6 promotes the migration and differentiation of human dental pulp cells partly through c-Jun N-terminal kinase signaling pathway. J Endod. 2014;40(7):943–8.PubMedCrossRef Li R, et al. WNT6 promotes the migration and differentiation of human dental pulp cells partly through c-Jun N-terminal kinase signaling pathway. J Endod. 2014;40(7):943–8.PubMedCrossRef
20.
go back to reference Wang, Q., et al., A novel role for Wnt/Ca2+ signaling in actin cytoskeleton remodeling and cell motility in prostate cancer. PLoS One, 2010. 5(5): p. e10456. Wang, Q., et al., A novel role for Wnt/Ca2+ signaling in actin cytoskeleton remodeling and cell motility in prostate cancer. PLoS One, 2010. 5(5): p. e10456.
21.
go back to reference Katoh M, Katoh M. Molecular genetics and targeted therapy of WNT-related human diseases (review). Int J Mol Med. 2017;40(3):587–606.PubMedPubMedCentral Katoh M, Katoh M. Molecular genetics and targeted therapy of WNT-related human diseases (review). Int J Mol Med. 2017;40(3):587–606.PubMedPubMedCentral
22.
25.
go back to reference Bello JO, et al. Regulation of the Wnt/beta-catenin signaling pathway by human papillomavirus E6 and E7 oncoproteins. Viruses. 2015;7(8):4734–55.PubMedCrossRef Bello JO, et al. Regulation of the Wnt/beta-catenin signaling pathway by human papillomavirus E6 and E7 oncoproteins. Viruses. 2015;7(8):4734–55.PubMedCrossRef
26.
go back to reference Maye P, et al. Multiple mechanisms for Wnt11-mediated repression of the canonical Wnt signaling pathway. J Biol Chem. 2004;279(23):24659–65.PubMedCrossRef Maye P, et al. Multiple mechanisms for Wnt11-mediated repression of the canonical Wnt signaling pathway. J Biol Chem. 2004;279(23):24659–65.PubMedCrossRef
27.
28.
go back to reference Medrek C, et al. Wnt-5a-CKI{alpha} signaling promotes {beta}-catenin/E-cadherin complex formation and intercellular adhesion in human breast epithelial cells. J Biol Chem. 2009;284(16):10968–79.PubMedPubMedCentralCrossRef Medrek C, et al. Wnt-5a-CKI{alpha} signaling promotes {beta}-catenin/E-cadherin complex formation and intercellular adhesion in human breast epithelial cells. J Biol Chem. 2009;284(16):10968–79.PubMedPubMedCentralCrossRef
29.
go back to reference Kypta RM, Waxman J. Wnt/beta-catenin signalling in prostate cancer. Nat Rev Urol. 2012;9(8):418–28.PubMedCrossRef Kypta RM, Waxman J. Wnt/beta-catenin signalling in prostate cancer. Nat Rev Urol. 2012;9(8):418–28.PubMedCrossRef
31.
go back to reference Arend RC, et al. The Wnt/beta-catenin pathway in ovarian cancer: a review. Gynecol Oncol. 2013;131(3):772–9.PubMedCrossRef Arend RC, et al. The Wnt/beta-catenin pathway in ovarian cancer: a review. Gynecol Oncol. 2013;131(3):772–9.PubMedCrossRef
32.
35.
go back to reference Yun EJ, et al. Wnt/beta-catenin signaling pathway induces autophagy-mediated temozolomide-resistance in human glioblastoma. Cell Death Dis. 2020;11(9):771.PubMedPubMedCentralCrossRef Yun EJ, et al. Wnt/beta-catenin signaling pathway induces autophagy-mediated temozolomide-resistance in human glioblastoma. Cell Death Dis. 2020;11(9):771.PubMedPubMedCentralCrossRef
36.
go back to reference Yu X, et al. Wnt/beta-catenin activation promotes prostate tumor progression in a mouse model. Oncogene. 2011;30(16):1868–79.PubMedCrossRef Yu X, et al. Wnt/beta-catenin activation promotes prostate tumor progression in a mouse model. Oncogene. 2011;30(16):1868–79.PubMedCrossRef
37.
go back to reference Moparthi L, Pizzolato G, Koch S. Wnt activator FOXB2 drives the neuroendocrine differentiation of prostate cancer. Proc Natl Acad Sci USA. 2019;116(44):22189–95.PubMedPubMedCentralCrossRef Moparthi L, Pizzolato G, Koch S. Wnt activator FOXB2 drives the neuroendocrine differentiation of prostate cancer. Proc Natl Acad Sci USA. 2019;116(44):22189–95.PubMedPubMedCentralCrossRef
38.
go back to reference Voeller HJ, Truica CI, Gelmann EP. Beta-catenin mutations in human prostate cancer. Cancer Res. 1998;58(12):2520–3.PubMed Voeller HJ, Truica CI, Gelmann EP. Beta-catenin mutations in human prostate cancer. Cancer Res. 1998;58(12):2520–3.PubMed
39.
go back to reference Chen G, et al. Up-regulation of Wnt-1 and beta-catenin production in patients with advanced metastatic prostate carcinoma: potential pathogenetic and prognostic implications. Cancer. 2004;101(6):1345–56.PubMedCrossRef Chen G, et al. Up-regulation of Wnt-1 and beta-catenin production in patients with advanced metastatic prostate carcinoma: potential pathogenetic and prognostic implications. Cancer. 2004;101(6):1345–56.PubMedCrossRef
40.
go back to reference de la Taille A, et al. Beta-catenin-related anomalies in apoptosis-resistant and hormone-refractory prostate cancer cells. Clin Cancer Res. 2003;9(5):1801–7.PubMed de la Taille A, et al. Beta-catenin-related anomalies in apoptosis-resistant and hormone-refractory prostate cancer cells. Clin Cancer Res. 2003;9(5):1801–7.PubMed
41.
go back to reference Schweizer L, et al. The androgen receptor can signal through Wnt/beta-catenin in prostate cancer cells as an adaptation mechanism to castration levels of androgens. BMC Cell Biol. 2008;9:4.PubMedPubMedCentralCrossRef Schweizer L, et al. The androgen receptor can signal through Wnt/beta-catenin in prostate cancer cells as an adaptation mechanism to castration levels of androgens. BMC Cell Biol. 2008;9:4.PubMedPubMedCentralCrossRef
42.
go back to reference Thiele S, et al. Expression profile of WNT molecules in prostate cancer and its regulation by aminobisphosphonates. J Cell Biochem. 2011;112(6):1593–600.PubMedCrossRef Thiele S, et al. Expression profile of WNT molecules in prostate cancer and its regulation by aminobisphosphonates. J Cell Biochem. 2011;112(6):1593–600.PubMedCrossRef
43.
go back to reference Katoh M. Frequent up-regulation of WNT2 in primary gastric cancer and colorectal cancer. Int J Oncol. 2001;19(5):1003–7.PubMed Katoh M. Frequent up-regulation of WNT2 in primary gastric cancer and colorectal cancer. Int J Oncol. 2001;19(5):1003–7.PubMed
44.
go back to reference Hall CL, et al. Prostate cancer cells promote osteoblastic bone metastases through Wnts. Cancer Res. 2005;65(17):7554–60.PubMedCrossRef Hall CL, et al. Prostate cancer cells promote osteoblastic bone metastases through Wnts. Cancer Res. 2005;65(17):7554–60.PubMedCrossRef
45.
go back to reference Verras M, et al. Wnt3a growth factor induces androgen receptor-mediated transcription and enhances cell growth in human prostate cancer cells. Cancer Res. 2004;64(24):8860–6.PubMedCrossRef Verras M, et al. Wnt3a growth factor induces androgen receptor-mediated transcription and enhances cell growth in human prostate cancer cells. Cancer Res. 2004;64(24):8860–6.PubMedCrossRef
46.
go back to reference Ayub SG, Kaul D, Ayub T. Microdissecting the role of microRNAs in the pathogenesis of prostate cancer. Cancer Genet. 2015;208(6):289–302.PubMedCrossRef Ayub SG, Kaul D, Ayub T. Microdissecting the role of microRNAs in the pathogenesis of prostate cancer. Cancer Genet. 2015;208(6):289–302.PubMedCrossRef
47.
go back to reference Zhao S, et al. MiR-26a inhibits prostate cancer progression by repression of Wnt5a. Tumour Biol. 2014;35(10):9725–33.PubMedCrossRef Zhao S, et al. MiR-26a inhibits prostate cancer progression by repression of Wnt5a. Tumour Biol. 2014;35(10):9725–33.PubMedCrossRef
48.
go back to reference Yokoyama NN, et al. Wnt signaling in castration-resistant prostate cancer: implications for therapy. Am J Clin Exp Urol. 2014;2(1):27–44.PubMedPubMedCentral Yokoyama NN, et al. Wnt signaling in castration-resistant prostate cancer: implications for therapy. Am J Clin Exp Urol. 2014;2(1):27–44.PubMedPubMedCentral
49.
go back to reference Yamamoto H, et al. Wnt5a signaling is involved in the aggressiveness of prostate cancer and expression of metalloproteinase. Oncogene. 2010;29(14):2036–46.PubMedCrossRef Yamamoto H, et al. Wnt5a signaling is involved in the aggressiveness of prostate cancer and expression of metalloproteinase. Oncogene. 2010;29(14):2036–46.PubMedCrossRef
50.
go back to reference Sandsmark E, et al. A novel non-canonical Wnt signature for prostate cancer aggressiveness. Oncotarget. 2017;8(6):9572–86.PubMedCrossRef Sandsmark E, et al. A novel non-canonical Wnt signature for prostate cancer aggressiveness. Oncotarget. 2017;8(6):9572–86.PubMedCrossRef
52.
go back to reference Zhu H, et al. Analysis of Wnt gene expression in prostate cancer: mutual inhibition by WNT11 and the androgen receptor. Cancer Res. 2004;64(21):7918–26.PubMedCrossRef Zhu H, et al. Analysis of Wnt gene expression in prostate cancer: mutual inhibition by WNT11 and the androgen receptor. Cancer Res. 2004;64(21):7918–26.PubMedCrossRef
53.
go back to reference Kirikoshi H, Katoh M. Expression of WNT7A in human normal tissues and cancer, and regulation of WNT7A and WNT7B in human cancer. Int J Oncol. 2002;21(4):895–900.PubMed Kirikoshi H, Katoh M. Expression of WNT7A in human normal tissues and cancer, and regulation of WNT7A and WNT7B in human cancer. Int J Oncol. 2002;21(4):895–900.PubMed
54.
go back to reference Kirikoshi H, Sekihara H, Katoh M. Molecular cloning and characterization of human WNT7B. Int J Oncol. 2001;19(4):779–83.PubMed Kirikoshi H, Sekihara H, Katoh M. Molecular cloning and characterization of human WNT7B. Int J Oncol. 2001;19(4):779–83.PubMed
55.
go back to reference Katoh M, et al. Cloning, expression and chromosomal localization of Wnt-13, a novel member of the Wnt gene family. Oncogene. 1996;13(4):873–6.PubMed Katoh M, et al. Cloning, expression and chromosomal localization of Wnt-13, a novel member of the Wnt gene family. Oncogene. 1996;13(4):873–6.PubMed
56.
go back to reference Madueke I. The roles of canonical Wnt2 and Wnt10b in prostate gland development and prostate cancer progression. Doctoral dissertation, University of Illinois at Chicago. 2015. Madueke I. The roles of canonical Wnt2 and Wnt10b in prostate gland development and prostate cancer progression. Doctoral dissertation, University of Illinois at Chicago. 2015.
57.
go back to reference Schneider JA, Logan SK. Revisiting the role of Wnt/beta-catenin signaling in prostate cancer. Mol Cell Endocrinol. 2018;462(Pt A):3–8.PubMedCrossRef Schneider JA, Logan SK. Revisiting the role of Wnt/beta-catenin signaling in prostate cancer. Mol Cell Endocrinol. 2018;462(Pt A):3–8.PubMedCrossRef
58.
go back to reference Fujita K, Nonomura N. Role of androgen receptor in prostate cancer: a review. World J Mens Health. 2019;37(3):288–95.PubMedCrossRef Fujita K, Nonomura N. Role of androgen receptor in prostate cancer: a review. World J Mens Health. 2019;37(3):288–95.PubMedCrossRef
59.
go back to reference Chen SY, et al. Activation of beta-catenin signaling in prostate cancer by peptidyl-prolyl isomerase Pin1-mediated abrogation of the androgen receptor-beta-catenin interaction. Mol Cell Biol. 2006;26(3):929–39.PubMedPubMedCentralCrossRef Chen SY, et al. Activation of beta-catenin signaling in prostate cancer by peptidyl-prolyl isomerase Pin1-mediated abrogation of the androgen receptor-beta-catenin interaction. Mol Cell Biol. 2006;26(3):929–39.PubMedPubMedCentralCrossRef
60.
go back to reference Seo WI, et al. Wnt signaling promotes androgen-independent prostate cancer cell proliferation through up-regulation of the hippo pathway effector YAP. Biochem Biophys Res Commun. 2017;486(4):1034–9.PubMedCrossRef Seo WI, et al. Wnt signaling promotes androgen-independent prostate cancer cell proliferation through up-regulation of the hippo pathway effector YAP. Biochem Biophys Res Commun. 2017;486(4):1034–9.PubMedCrossRef
62.
go back to reference Taplin ME, et al. Mutation of the androgen-receptor gene in metastatic androgen-independent prostate cancer. N Engl J Med. 1995;332(21):1393–8.PubMedCrossRef Taplin ME, et al. Mutation of the androgen-receptor gene in metastatic androgen-independent prostate cancer. N Engl J Med. 1995;332(21):1393–8.PubMedCrossRef
63.
go back to reference Marcelli M, et al. Androgen receptor mutations in prostate cancer. Cancer Res. 2000;60(4):944–9.PubMed Marcelli M, et al. Androgen receptor mutations in prostate cancer. Cancer Res. 2000;60(4):944–9.PubMed
64.
go back to reference Shi XB, et al. Functional analysis of 44 mutant androgen receptors from human prostate cancer. Cancer Res. 2002;62(5):1496–502.PubMed Shi XB, et al. Functional analysis of 44 mutant androgen receptors from human prostate cancer. Cancer Res. 2002;62(5):1496–502.PubMed
65.
go back to reference Schoenberg MP, et al. Microsatellite mutation (CAG24–>18) in the androgen receptor gene in human prostate cancer. Biochem Biophys Res Commun. 1994;198(1):74–80.PubMedCrossRef Schoenberg MP, et al. Microsatellite mutation (CAG24–>18) in the androgen receptor gene in human prostate cancer. Biochem Biophys Res Commun. 1994;198(1):74–80.PubMedCrossRef
66.
go back to reference Watanabe M, et al. Genetic alterations of androgen receptor gene in Japanese human prostate cancer. Jpn J Clin Oncol. 1997;27(6):389–93.PubMedCrossRef Watanabe M, et al. Genetic alterations of androgen receptor gene in Japanese human prostate cancer. Jpn J Clin Oncol. 1997;27(6):389–93.PubMedCrossRef
67.
go back to reference Steinkamp MP, et al. Treatment-dependent androgen receptor mutations in prostate cancer exploit multiple mechanisms to evade therapy. Cancer Res. 2009;69(10):4434–42.PubMedPubMedCentralCrossRef Steinkamp MP, et al. Treatment-dependent androgen receptor mutations in prostate cancer exploit multiple mechanisms to evade therapy. Cancer Res. 2009;69(10):4434–42.PubMedPubMedCentralCrossRef
68.
go back to reference Takahashi H, et al. Prevalence of androgen receptor gene mutations in latent prostatic carcinomas from Japanese men. Cancer Res. 1995;55(8):1621–4.PubMed Takahashi H, et al. Prevalence of androgen receptor gene mutations in latent prostatic carcinomas from Japanese men. Cancer Res. 1995;55(8):1621–4.PubMed
69.
go back to reference Sanchez D, et al. Androgen receptor mutations are associated with Gleason score in localized prostate cancer. BJU Int. 2006;98(6):1320–5.PubMedCrossRef Sanchez D, et al. Androgen receptor mutations are associated with Gleason score in localized prostate cancer. BJU Int. 2006;98(6):1320–5.PubMedCrossRef
70.
go back to reference Yang F, et al. Linking beta-catenin to androgen-signaling pathway. J Biol Chem. 2002;277(13):11336–44.PubMedCrossRef Yang F, et al. Linking beta-catenin to androgen-signaling pathway. J Biol Chem. 2002;277(13):11336–44.PubMedCrossRef
71.
go back to reference Verras M, Sun Z. Roles and regulation of Wnt signaling and beta-catenin in prostate cancer. Cancer Lett. 2006;237(1):22–32.PubMedCrossRef Verras M, Sun Z. Roles and regulation of Wnt signaling and beta-catenin in prostate cancer. Cancer Lett. 2006;237(1):22–32.PubMedCrossRef
72.
go back to reference Jung SJ, et al. Clinical significance of Wnt/beta-catenin signalling and androgen receptor expression in prostate cancer. World J Mens Health. 2013;31(1):36–46.PubMedPubMedCentralCrossRef Jung SJ, et al. Clinical significance of Wnt/beta-catenin signalling and androgen receptor expression in prostate cancer. World J Mens Health. 2013;31(1):36–46.PubMedPubMedCentralCrossRef
73.
go back to reference Grindel BJ, et al. Matrilysin/matrix metalloproteinase-7(MMP7) cleavage of perlecan/HSPG2 creates a molecular switch to alter prostate cancer cell behavior. Matrix Biol. 2014;36:64–76.PubMedPubMedCentralCrossRef Grindel BJ, et al. Matrilysin/matrix metalloproteinase-7(MMP7) cleavage of perlecan/HSPG2 creates a molecular switch to alter prostate cancer cell behavior. Matrix Biol. 2014;36:64–76.PubMedPubMedCentralCrossRef
74.
go back to reference Reid JC, et al. Pericellular regulation of prostate cancer expressed kallikrein-related peptidases and matrix metalloproteinases by cell surface serine proteases. Am J Cancer Res. 2017;7(11):2257–74.PubMedPubMedCentral Reid JC, et al. Pericellular regulation of prostate cancer expressed kallikrein-related peptidases and matrix metalloproteinases by cell surface serine proteases. Am J Cancer Res. 2017;7(11):2257–74.PubMedPubMedCentral
75.
go back to reference Hashimoto K, et al. Expression of matrix metalloproteinase-7 and tissue inhibitor of metalloproteinase-1 in human prostate. J Urol. 1998;160(5):1872–6.PubMedCrossRef Hashimoto K, et al. Expression of matrix metalloproteinase-7 and tissue inhibitor of metalloproteinase-1 in human prostate. J Urol. 1998;160(5):1872–6.PubMedCrossRef
76.
go back to reference Zhang Q, et al. Interleukin-17 promotes prostate cancer via MMP7-induced epithelial-to-mesenchymal transition. Oncogene. 2017;36(5):687–99.PubMedCrossRef Zhang Q, et al. Interleukin-17 promotes prostate cancer via MMP7-induced epithelial-to-mesenchymal transition. Oncogene. 2017;36(5):687–99.PubMedCrossRef
77.
go back to reference Santiago L, et al. Wnt signaling pathway protein LEF1 in cancer, as a biomarker for prognosis and a target for treatment. Am J Cancer Res. 2017;7(6):1389–406.PubMedPubMedCentral Santiago L, et al. Wnt signaling pathway protein LEF1 in cancer, as a biomarker for prognosis and a target for treatment. Am J Cancer Res. 2017;7(6):1389–406.PubMedPubMedCentral
78.
go back to reference Gravdal K, et al. A switch from E-cadherin to N-cadherin expression indicates epithelial to mesenchymal transition and is of strong and independent importance for the progress of prostate cancer. Clin Cancer Res. 2007;13(23):7003–11.PubMedCrossRef Gravdal K, et al. A switch from E-cadherin to N-cadherin expression indicates epithelial to mesenchymal transition and is of strong and independent importance for the progress of prostate cancer. Clin Cancer Res. 2007;13(23):7003–11.PubMedCrossRef
79.
go back to reference Ghali F, et al. Characterization of Wnt signaling pathway (WSP) aberrations in advanced prostate cancer. J Clin Oncol. 2020;38:203.CrossRef Ghali F, et al. Characterization of Wnt signaling pathway (WSP) aberrations in advanced prostate cancer. J Clin Oncol. 2020;38:203.CrossRef
81.
82.
go back to reference Liu Y, et al. Cripto-1 promotes epithelial-mesenchymal transition in prostate cancer via Wnt/beta-catenin signaling. Oncol Rep. 2017;37(3):1521–8.PubMedCrossRef Liu Y, et al. Cripto-1 promotes epithelial-mesenchymal transition in prostate cancer via Wnt/beta-catenin signaling. Oncol Rep. 2017;37(3):1521–8.PubMedCrossRef
83.
go back to reference Cheng S, et al. The expression of YAP1 is increased in high-grade prostatic adenocarcinoma but is reduced in neuroendocrine prostate cancer. Prostate Cancer Prostatic Dis. 2020;23(4):661–9.PubMedPubMedCentralCrossRef Cheng S, et al. The expression of YAP1 is increased in high-grade prostatic adenocarcinoma but is reduced in neuroendocrine prostate cancer. Prostate Cancer Prostatic Dis. 2020;23(4):661–9.PubMedPubMedCentralCrossRef
86.
go back to reference Cui Y, et al. miR-15a-3p suppresses prostate cancer cell proliferation and invasion by targeting SLC39A7 Via downregulating Wnt/beta-catenin signaling pathway. Cancer Biother Radiopharm. 2019;34(7):472–9.PubMedCrossRef Cui Y, et al. miR-15a-3p suppresses prostate cancer cell proliferation and invasion by targeting SLC39A7 Via downregulating Wnt/beta-catenin signaling pathway. Cancer Biother Radiopharm. 2019;34(7):472–9.PubMedCrossRef
87.
go back to reference Pashaei E, et al. Meta-analysis of miRNA expression profiles for prostate cancer recurrence following radical prostatectomy. PLoS ONE. 2017;12(6): e0179543.PubMedPubMedCentralCrossRef Pashaei E, et al. Meta-analysis of miRNA expression profiles for prostate cancer recurrence following radical prostatectomy. PLoS ONE. 2017;12(6): e0179543.PubMedPubMedCentralCrossRef
88.
go back to reference Hsieh IS, et al. MicroRNA-320 suppresses the stem cell-like characteristics of prostate cancer cells by downregulating the Wnt/beta-catenin signaling pathway. Carcinogenesis. 2013;34(3):530–8.PubMedCrossRef Hsieh IS, et al. MicroRNA-320 suppresses the stem cell-like characteristics of prostate cancer cells by downregulating the Wnt/beta-catenin signaling pathway. Carcinogenesis. 2013;34(3):530–8.PubMedCrossRef
89.
go back to reference Yu Z, et al. miR138 modulates prostate cancer cell invasion and migration via Wnt/betacatenin pathway. Mol Med Rep. 2018;17(2):3140–5.PubMed Yu Z, et al. miR138 modulates prostate cancer cell invasion and migration via Wnt/betacatenin pathway. Mol Med Rep. 2018;17(2):3140–5.PubMed
90.
go back to reference Situ J, et al. MicroRNA-939 directly targets HDGF to inhibit the aggressiveness of prostate cancer via deactivation of the WNT/beta-catenin pathway. Onco Targets Ther. 2020;13:4257–70.PubMedPubMedCentralCrossRef Situ J, et al. MicroRNA-939 directly targets HDGF to inhibit the aggressiveness of prostate cancer via deactivation of the WNT/beta-catenin pathway. Onco Targets Ther. 2020;13:4257–70.PubMedPubMedCentralCrossRef
91.
go back to reference Guan H, et al. MicroRNA-744 promotes prostate cancer progression through aberrantly activating Wnt/beta-catenin signaling. Oncotarget. 2017;8(9):14693–707.PubMedPubMedCentralCrossRef Guan H, et al. MicroRNA-744 promotes prostate cancer progression through aberrantly activating Wnt/beta-catenin signaling. Oncotarget. 2017;8(9):14693–707.PubMedPubMedCentralCrossRef
92.
go back to reference Wang D, et al. MiR-182 promotes prostate cancer progression through activating Wnt/beta-catenin signal pathway. Biomed Pharmacother. 2018;99:334–9.PubMedCrossRef Wang D, et al. MiR-182 promotes prostate cancer progression through activating Wnt/beta-catenin signal pathway. Biomed Pharmacother. 2018;99:334–9.PubMedCrossRef
94.
go back to reference Liang X, et al. MicroRNA-1297 inhibits prostate cancer cell proliferation and invasion by targeting the AEG-1/Wnt signaling pathway. Biochem Biophys Res Commun. 2016;480(2):208–14.PubMedCrossRef Liang X, et al. MicroRNA-1297 inhibits prostate cancer cell proliferation and invasion by targeting the AEG-1/Wnt signaling pathway. Biochem Biophys Res Commun. 2016;480(2):208–14.PubMedCrossRef
95.
go back to reference Liu B, et al. miR-1303 promotes the proliferation, migration and invasion of prostate cancer cells through regulating the Wnt/beta-catenin pathway by targeting DKK3. Exp Ther Med. 2019;18(6):4747–57.PubMedPubMedCentral Liu B, et al. miR-1303 promotes the proliferation, migration and invasion of prostate cancer cells through regulating the Wnt/beta-catenin pathway by targeting DKK3. Exp Ther Med. 2019;18(6):4747–57.PubMedPubMedCentral
96.
go back to reference Dong B, et al. MiR-34a affects G2 arrest in prostate cancer PC3 cells via Wnt pathway and inhibits cell growth and migration. Eur Rev Med Pharmacol Sci. 2020;24(16):8349–58.PubMed Dong B, et al. MiR-34a affects G2 arrest in prostate cancer PC3 cells via Wnt pathway and inhibits cell growth and migration. Eur Rev Med Pharmacol Sci. 2020;24(16):8349–58.PubMed
97.
go back to reference Nadiminty N, et al. MicroRNA let-7c suppresses androgen receptor expression and activity via regulation of Myc expression in prostate cancer cells. J Biol Chem. 2012;287(2):1527–37.PubMedCrossRef Nadiminty N, et al. MicroRNA let-7c suppresses androgen receptor expression and activity via regulation of Myc expression in prostate cancer cells. J Biol Chem. 2012;287(2):1527–37.PubMedCrossRef
98.
go back to reference Wan X, et al. Androgen-induced miR-27A acted as a tumor suppressor by targeting MAP2K4 and mediated prostate cancer progression. Int J Biochem Cell Biol. 2016;79:249–60.PubMedCrossRef Wan X, et al. Androgen-induced miR-27A acted as a tumor suppressor by targeting MAP2K4 and mediated prostate cancer progression. Int J Biochem Cell Biol. 2016;79:249–60.PubMedCrossRef
99.
go back to reference Shiina M, et al. Differential expression of miR-34b and androgen receptor pathway regulate prostate cancer aggressiveness between African-Americans and Caucasians. Oncotarget. 2017;8(5):8356–68.PubMedCrossRef Shiina M, et al. Differential expression of miR-34b and androgen receptor pathway regulate prostate cancer aggressiveness between African-Americans and Caucasians. Oncotarget. 2017;8(5):8356–68.PubMedCrossRef
100.
go back to reference Kroiss A, et al. Androgen-regulated microRNA-135a decreases prostate cancer cell migration and invasion through downregulating ROCK1 and ROCK2. Oncogene. 2015;34(22):2846–55.PubMedCrossRef Kroiss A, et al. Androgen-regulated microRNA-135a decreases prostate cancer cell migration and invasion through downregulating ROCK1 and ROCK2. Oncogene. 2015;34(22):2846–55.PubMedCrossRef
101.
go back to reference Larne O, et al. miR-145 suppress the androgen receptor in prostate cancer cells and correlates to prostate cancer prognosis. Carcinogenesis. 2015;36(8):858–66.PubMedCrossRef Larne O, et al. miR-145 suppress the androgen receptor in prostate cancer cells and correlates to prostate cancer prognosis. Carcinogenesis. 2015;36(8):858–66.PubMedCrossRef
103.
104.
go back to reference Sun T, et al. MiR-221 promotes the development of androgen independence in prostate cancer cells via downregulation of HECTD2 and RAB1A. Oncogene. 2014;33(21):2790–800.PubMedCrossRef Sun T, et al. MiR-221 promotes the development of androgen independence in prostate cancer cells via downregulation of HECTD2 and RAB1A. Oncogene. 2014;33(21):2790–800.PubMedCrossRef
105.
go back to reference Epis MR, et al. miR-331-3p regulates expression of neuropilin-2 in glioblastoma. J Neurooncol. 2014;116(1):67–75.PubMedCrossRef Epis MR, et al. miR-331-3p regulates expression of neuropilin-2 in glioblastoma. J Neurooncol. 2014;116(1):67–75.PubMedCrossRef
106.
go back to reference Meng D, et al. A transcriptional target of androgen receptor, miR-421 regulates proliferation and metabolism of prostate cancer cells. Int J Biochem Cell Biol. 2016;73:30–40.PubMedCrossRef Meng D, et al. A transcriptional target of androgen receptor, miR-421 regulates proliferation and metabolism of prostate cancer cells. Int J Biochem Cell Biol. 2016;73:30–40.PubMedCrossRef
107.
go back to reference Yeh Y, et al. Wnt/beta-catenin signaling and prostate cancer therapy resistance. Adv Exp Med Biol. 2019;1210:351–78.PubMedCrossRef Yeh Y, et al. Wnt/beta-catenin signaling and prostate cancer therapy resistance. Adv Exp Med Biol. 2019;1210:351–78.PubMedCrossRef
108.
109.
go back to reference Seruga B, Ocana A, Tannock IF. Drug resistance in metastatic castration-resistant prostate cancer. Nat Rev Clin Oncol. 2011;8(1):12–23.PubMedCrossRef Seruga B, Ocana A, Tannock IF. Drug resistance in metastatic castration-resistant prostate cancer. Nat Rev Clin Oncol. 2011;8(1):12–23.PubMedCrossRef
111.
go back to reference Armstrong CM, Gao AC. Drug resistance in castration resistant prostate cancer: resistance mechanisms and emerging treatment strategies. Am J Clin Exp Urol. 2015;3(2):64–76.PubMedPubMedCentral Armstrong CM, Gao AC. Drug resistance in castration resistant prostate cancer: resistance mechanisms and emerging treatment strategies. Am J Clin Exp Urol. 2015;3(2):64–76.PubMedPubMedCentral
112.
113.
go back to reference Zhong Z, Virshup DM. Wnt signaling and drug resistance in cancer. Mol Pharmacol. 2020;97(2):72–89.PubMedCrossRef Zhong Z, Virshup DM. Wnt signaling and drug resistance in cancer. Mol Pharmacol. 2020;97(2):72–89.PubMedCrossRef
114.
go back to reference Zhang Z, et al. Inhibition of the Wnt/beta-catenin pathway overcomes resistance to enzalutamide in castration-resistant prostate cancer. Cancer Res. 2018;78(12):3147–62.PubMedPubMedCentralCrossRef Zhang Z, et al. Inhibition of the Wnt/beta-catenin pathway overcomes resistance to enzalutamide in castration-resistant prostate cancer. Cancer Res. 2018;78(12):3147–62.PubMedPubMedCentralCrossRef
115.
116.
go back to reference Cristobal I, et al. Cross talk between Wnt/beta-catenin and CIP2A/Plk1 signaling in prostate cancer: promising therapeutic implications. Mol Cell Biol. 2016;36(12):1734–9.PubMedPubMedCentralCrossRef Cristobal I, et al. Cross talk between Wnt/beta-catenin and CIP2A/Plk1 signaling in prostate cancer: promising therapeutic implications. Mol Cell Biol. 2016;36(12):1734–9.PubMedPubMedCentralCrossRef
117.
go back to reference Chen WS, et al. Genomic drivers of poor prognosis and enzalutamide resistance in metastatic castration-resistant prostate cancer. Eur Urol. 2019;76(5):562–71.PubMedPubMedCentralCrossRef Chen WS, et al. Genomic drivers of poor prognosis and enzalutamide resistance in metastatic castration-resistant prostate cancer. Eur Urol. 2019;76(5):562–71.PubMedPubMedCentralCrossRef
118.
go back to reference Kohli M, et al. Association of Wnt pathway activation with prechemotherapy abiraterone acetate resistance in metastatic castration-resistant prostate cancer (mCRPC) by genome-wide analysis of metastases. J Clin Oncol. 2017;35:175.CrossRef Kohli M, et al. Association of Wnt pathway activation with prechemotherapy abiraterone acetate resistance in metastatic castration-resistant prostate cancer (mCRPC) by genome-wide analysis of metastases. J Clin Oncol. 2017;35:175.CrossRef
119.
go back to reference Vesel M, et al. ABCB1 and ABCG2 drug transporters are differentially expressed in non-small cell lung cancers (NSCLC) and expression is modified by cisplatin treatment via altered Wnt signaling. Respir Res. 2017;18(1):52.PubMedPubMedCentralCrossRef Vesel M, et al. ABCB1 and ABCG2 drug transporters are differentially expressed in non-small cell lung cancers (NSCLC) and expression is modified by cisplatin treatment via altered Wnt signaling. Respir Res. 2017;18(1):52.PubMedPubMedCentralCrossRef
120.
121.
go back to reference Zhu M, et al. Capsaicin suppressed activity of prostate cancer stem cells by inhibition of Wnt/beta-catenin pathway. Phytother Res. 2020;34(4):817–24.PubMedCrossRef Zhu M, et al. Capsaicin suppressed activity of prostate cancer stem cells by inhibition of Wnt/beta-catenin pathway. Phytother Res. 2020;34(4):817–24.PubMedCrossRef
122.
go back to reference Bian P, et al. Activated Wnt/beta-Catenin signaling contributes to E3 ubiquitin ligase EDD-conferred docetaxel resistance in prostate cancer. Life Sci. 2020;254: 116816.PubMedCrossRef Bian P, et al. Activated Wnt/beta-Catenin signaling contributes to E3 ubiquitin ligase EDD-conferred docetaxel resistance in prostate cancer. Life Sci. 2020;254: 116816.PubMedCrossRef
123.
go back to reference Cojoc M, et al. Aldehyde dehydrogenase is regulated by beta-catenin/TCF and promotes radioresistance in prostate cancer progenitor cells. Cancer Res. 2015;75(7):1482–94.PubMedCrossRef Cojoc M, et al. Aldehyde dehydrogenase is regulated by beta-catenin/TCF and promotes radioresistance in prostate cancer progenitor cells. Cancer Res. 2015;75(7):1482–94.PubMedCrossRef
Metadata
Title
Wnt/β-catenin signal transduction pathway in prostate cancer and associated drug resistance
Authors
Chunyang Wang
Qi Chen
Huachao Xu
Publication date
01-12-2021
Publisher
Springer US
Published in
Discover Oncology / Issue 1/2021
Print ISSN: 1868-8497
Electronic ISSN: 2730-6011
DOI
https://doi.org/10.1007/s12672-021-00433-6

Other articles of this Issue 1/2021

Discover Oncology 1/2021 Go to the issue
Live Webinar | 27-06-2024 | 18:00 (CEST)

Keynote webinar | Spotlight on medication adherence

Live: Thursday 27th June 2024, 18:00-19:30 (CEST)

WHO estimates that half of all patients worldwide are non-adherent to their prescribed medication. The consequences of poor adherence can be catastrophic, on both the individual and population level.

Join our expert panel to discover why you need to understand the drivers of non-adherence in your patients, and how you can optimize medication adherence in your clinics to drastically improve patient outcomes.

Prof. Kevin Dolgin
Prof. Florian Limbourg
Prof. Anoop Chauhan
Developed by: Springer Medicine
Obesity Clinical Trial Summary

At a glance: The STEP trials

A round-up of the STEP phase 3 clinical trials evaluating semaglutide for weight loss in people with overweight or obesity.

Developed by: Springer Medicine