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Published in: Journal of Translational Medicine 1/2019

Open Access 01-12-2019 | Prostate Cancer | Research

RSPO3 is a prognostic biomarker and mediator of invasiveness in prostate cancer

Authors: Aruz Mesci, Fabrice Lucien, Xiaoyong Huang, Eric H. Wang, David Shin, Michelle Meringer, Christianne Hoey, Jessica Ray, Paul C. Boutros, Hon S. Leong, Stanley K. Liu

Published in: Journal of Translational Medicine | Issue 1/2019

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Abstract

Background

While prostate cancer can often manifest as an indolent disease, the development of locally-advanced or metastatic disease can cause significant morbidity or mortality. Elucidation of molecular mechanisms contributing to disease progression is crucial for more accurate prognostication and effective treatments. R-Spondin 3 (RSPO3) is a protein previously implicated in the progression of colorectal and lung cancers. However, a role for RSPO3 in prostate cancer prognosis and behaviour has not been explored.

Methods

We compare the relative levels of RSPO3 expression between normal prostate tissue and prostate cancer in two independent patient cohorts (Taylor and GSE70768—Cambridge). We also examine the association of biochemical relapse with RSPO3 levels in these cohorts. For elucidation of the biological effect of RSPO3, we use siRNA technology to reduce the levels of RSPO3 in established prostate cancer cell lines, and perform in vitro proliferation, invasion, western blotting for EMT markers and clonogenic survival assays for radiation resistance. Furthermore, we show consequences of RSPO3 knockdown in an established chick chorioallantoic membrane (CAM) assay model of metastasis.

Results

RSPO3 levels are lower in prostate cancer than normal prostate, with a tendency for further loss in metastatic disease. Patients with lower RSPO3 expression have lower rates of biochemical relapse-free survival. SiRNA-mediated loss of RSPO3 results in no change to clonogenic survival and a lower proliferative rate, but increased invasiveness in vitro with induction of epithelial–mesenchymal transition (EMT) markers. Consistent with these results, lower RSPO3 expression translates to greater metastatic capacity in the CAM assay. Together, our preclinical findings identify a role of RSPO3 downregulation in prostate cancer invasiveness, and provide a potential explanation for how RSPO3 functions as a positive prognostic marker in prostate cancer.
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Literature
2.
go back to reference Murillo-Garzón V, Kypta R. WNT signalling in prostate cancer. Nat Rev Urol. 2017;14:683–96.CrossRef Murillo-Garzón V, Kypta R. WNT signalling in prostate cancer. Nat Rev Urol. 2017;14:683–96.CrossRef
3.
go back to reference Schneider JA, Logan SK. Revisiting the role of Wnt/β-catenin signaling in prostate cancer. Mol Cell Endocrinol. 2018;46:3–8.CrossRef Schneider JA, Logan SK. Revisiting the role of Wnt/β-catenin signaling in prostate cancer. Mol Cell Endocrinol. 2018;46:3–8.CrossRef
4.
go back to reference Chesire DR, Isaacs WB. Ligand-dependent inhibition of b-catenin/TCF signaling by androgen receptor. Oncogene. 2002;21:8453–69.CrossRef Chesire DR, Isaacs WB. Ligand-dependent inhibition of b-catenin/TCF signaling by androgen receptor. Oncogene. 2002;21:8453–69.CrossRef
5.
go back to reference Schweizer L, et al. The androgen receptor can signal through Wnt/β-Catenin in prostate cancer cells as an adaptation mechanism to castration levels of androgens. BMC Cell Biol. 2008;9:4.CrossRef Schweizer L, et al. The androgen receptor can signal through Wnt/β-Catenin in prostate cancer cells as an adaptation mechanism to castration levels of androgens. BMC Cell Biol. 2008;9:4.CrossRef
6.
go back to reference Thiele S, et al. WNT5A has anti-prostate cancer effects in vitro and reduces tumor growth in the skeleton in vivo. J Bone Miner Res. 2015;30(3):471–80.CrossRef Thiele S, et al. WNT5A has anti-prostate cancer effects in vitro and reduces tumor growth in the skeleton in vivo. J Bone Miner Res. 2015;30(3):471–80.CrossRef
7.
go back to reference Khaja AS, et al. Elevated level of wnt5a protein in localized prostate cancer tissue is associated with better outcome. PLoS ONE. 2011;6(10):e26539.CrossRef Khaja AS, et al. Elevated level of wnt5a protein in localized prostate cancer tissue is associated with better outcome. PLoS ONE. 2011;6(10):e26539.CrossRef
8.
go back to reference Khaja ASS, et al. Emphasizing the role of Wnt5a protein expression to predict favorable outcome after radical prostatectomy in patients with low-grade prostate cancer. Cancer Med. 2013;1(1):96–104.CrossRef Khaja ASS, et al. Emphasizing the role of Wnt5a protein expression to predict favorable outcome after radical prostatectomy in patients with low-grade prostate cancer. Cancer Med. 2013;1(1):96–104.CrossRef
9.
go back to reference Sandsmark E, et al. A novel non-canonical Wnt signature for prostate cancer aggressiveness. Oncotarget. 2017;8(6):9572–86.CrossRef Sandsmark E, et al. A novel non-canonical Wnt signature for prostate cancer aggressiveness. Oncotarget. 2017;8(6):9572–86.CrossRef
10.
go back to reference Volante M, et al. Androgen deprivation modulates gene expression profile along prostate cancer progression. Hum Pathol. 2016;56:81–8.CrossRef Volante M, et al. Androgen deprivation modulates gene expression profile along prostate cancer progression. Hum Pathol. 2016;56:81–8.CrossRef
11.
go back to reference Uysal-Onganer P, et al. Wnt-11 promotes neuroendocrine-like differentiation, survival and migration of prostate cancer cells. Mol Cancer. 2010;9:55.CrossRef Uysal-Onganer P, et al. Wnt-11 promotes neuroendocrine-like differentiation, survival and migration of prostate cancer cells. Mol Cancer. 2010;9:55.CrossRef
12.
go back to reference Fujiwara M, et al. C-mannosylation of R-spondin3 regulates its secretion and activity of Wnt/β-catenin signaling in cells. FEBS Lett. 2016;590:2639–49.CrossRef Fujiwara M, et al. C-mannosylation of R-spondin3 regulates its secretion and activity of Wnt/β-catenin signaling in cells. FEBS Lett. 2016;590:2639–49.CrossRef
13.
go back to reference Chen JZ, et al. Cloning and identification of a cDNA that encodes a novel human protein with thrombospondin type I repeat domain, hPWTSR. Mol Biol Rep. 2002;29:287–92.CrossRef Chen JZ, et al. Cloning and identification of a cDNA that encodes a novel human protein with thrombospondin type I repeat domain, hPWTSR. Mol Biol Rep. 2002;29:287–92.CrossRef
14.
go back to reference Jin YR, Yoon JK. The R-spondin family of proteins: emerging regulators of WNT signaling. Int J Biochem Cell Biol. 2012;44:2278–87.CrossRef Jin YR, Yoon JK. The R-spondin family of proteins: emerging regulators of WNT signaling. Int J Biochem Cell Biol. 2012;44:2278–87.CrossRef
15.
go back to reference Glinka A, et al. LGR4 and LGR5 are R-spondin receptors mediating Wnt/β-catenin and Wnt/PCP signalling. EMBO Rep. 2011;12:1055–61.CrossRef Glinka A, et al. LGR4 and LGR5 are R-spondin receptors mediating Wnt/β-catenin and Wnt/PCP signalling. EMBO Rep. 2011;12:1055–61.CrossRef
16.
go back to reference Ohkawara B, Glinka A, Niehrs C. Rspo3 binds syndecan 4 and induces Wnt/PCP signaling via clathrin-mediated endocytosis to promote morphogenesis. Dev Cell. 2011;20:303–14.CrossRef Ohkawara B, Glinka A, Niehrs C. Rspo3 binds syndecan 4 and induces Wnt/PCP signaling via clathrin-mediated endocytosis to promote morphogenesis. Dev Cell. 2011;20:303–14.CrossRef
17.
go back to reference Kazanskaya O, et al. The Wnt signaling regulator R-spondin 3 promotes angioblast and vascular development. Development. 2008;135:3655–64.CrossRef Kazanskaya O, et al. The Wnt signaling regulator R-spondin 3 promotes angioblast and vascular development. Development. 2008;135:3655–64.CrossRef
18.
go back to reference Cambier L, Plate M, Sucov HM, Pashmforoush M. Nkx2-5 regulates cardiac growth through modulation of Wnt signaling by R-spondin3. Development. 2014;141:2959–71.CrossRef Cambier L, Plate M, Sucov HM, Pashmforoush M. Nkx2-5 regulates cardiac growth through modulation of Wnt signaling by R-spondin3. Development. 2014;141:2959–71.CrossRef
19.
go back to reference Han XH, Jin YR, Seto M, Yoon JK. A WNT/β-catenin signaling activator, R-spondin, plays positive regulatory roles during skeletal myogenesis. J Biol Chem. 2011;12:10649–59.CrossRef Han XH, Jin YR, Seto M, Yoon JK. A WNT/β-catenin signaling activator, R-spondin, plays positive regulatory roles during skeletal myogenesis. J Biol Chem. 2011;12:10649–59.CrossRef
20.
go back to reference Neufeld S, et al. A conditional allele of Rspo3 reveals redundant function of R-spondins during mouse limb development. Genesis. 2012;50:741–9.CrossRef Neufeld S, et al. A conditional allele of Rspo3 reveals redundant function of R-spondins during mouse limb development. Genesis. 2012;50:741–9.CrossRef
21.
go back to reference Heid IM, et al. Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nat Genet. 2010;42(11):949–60.CrossRef Heid IM, et al. Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nat Genet. 2010;42(11):949–60.CrossRef
22.
go back to reference Duncan EL, et al. Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. PLoS Genet. 2011;7(4):e1001372.CrossRef Duncan EL, et al. Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. PLoS Genet. 2011;7(4):e1001372.CrossRef
23.
go back to reference Theodorou V, et al. MMTV insertional mutagenesis identifies genes, gene families and pathways involved in mammary cancer. Nat Genet. 2007;39(6):759–69.CrossRef Theodorou V, et al. MMTV insertional mutagenesis identifies genes, gene families and pathways involved in mammary cancer. Nat Genet. 2007;39(6):759–69.CrossRef
24.
go back to reference Recouvreux MS, et al. RUNX1 and FOXP3 interplay regulates expression of breast cancer related genes. 2016;7(6):6552–65. Recouvreux MS, et al. RUNX1 and FOXP3 interplay regulates expression of breast cancer related genes. 2016;7(6):6552–65.
25.
go back to reference Coussy F, et al. Clinical value of R-spondins in triple-negative and metaplastic breast cancers. Br J Cancer. 2017;116:1595–603.CrossRef Coussy F, et al. Clinical value of R-spondins in triple-negative and metaplastic breast cancers. Br J Cancer. 2017;116:1595–603.CrossRef
26.
go back to reference Seshagiri S, et al. Recurrent R-spondin fusions in colon cancer. Nature. 2012;488:660–7.CrossRef Seshagiri S, et al. Recurrent R-spondin fusions in colon cancer. Nature. 2012;488:660–7.CrossRef
27.
go back to reference Storm EE, et al. Targeting PTPRK-RSPO3 colon tumours promotes differentiation and loss of stem-cell function. Nature. 2016;529:97–101.CrossRef Storm EE, et al. Targeting PTPRK-RSPO3 colon tumours promotes differentiation and loss of stem-cell function. Nature. 2016;529:97–101.CrossRef
28.
go back to reference Han T, et al. R-Spondin chromosome rearrangements drive Wnt-dependent tumour initiation and maintenance in the intestine. Nat Commun. 2017;8:15945.CrossRef Han T, et al. R-Spondin chromosome rearrangements drive Wnt-dependent tumour initiation and maintenance in the intestine. Nat Commun. 2017;8:15945.CrossRef
29.
go back to reference Hilkens J, et al. RSPO3 expands intestinal stem cell and niche compartments and drives tumorigenesis. Gut. 2017;66:1095–105.CrossRef Hilkens J, et al. RSPO3 expands intestinal stem cell and niche compartments and drives tumorigenesis. Gut. 2017;66:1095–105.CrossRef
30.
go back to reference Boone JD, et al. Targeting the Wnt/β-catenin pathway in primary ovarian cancer with the porcupine inhibitor WNT974. Lab Invest. 2016;96:249–59.CrossRef Boone JD, et al. Targeting the Wnt/β-catenin pathway in primary ovarian cancer with the porcupine inhibitor WNT974. Lab Invest. 2016;96:249–59.CrossRef
31.
go back to reference Gong X, et al. Aberrant RSPO3-LGR4 signaling in Keap1-deficient lung adenocarcinomas promotes tumor aggressiveness. Oncogene. 2015;34(36):4692–701.CrossRef Gong X, et al. Aberrant RSPO3-LGR4 signaling in Keap1-deficient lung adenocarcinomas promotes tumor aggressiveness. Oncogene. 2015;34(36):4692–701.CrossRef
32.
go back to reference Zhang Y, et al. Comprehensive analysis of the long noncoding RNA HOXA11-AS gene interaction regulatory network in NSCLC cells. Cancer Cell Int. 2016;16:89.CrossRef Zhang Y, et al. Comprehensive analysis of the long noncoding RNA HOXA11-AS gene interaction regulatory network in NSCLC cells. Cancer Cell Int. 2016;16:89.CrossRef
33.
go back to reference Liu SK, et al. miRNA-95 Mediates radioresistance in tumors by targeting the sphingolipid phosphatase SGPP1. Cancer Res. 2013;23:6972–86. Liu SK, et al. miRNA-95 Mediates radioresistance in tumors by targeting the sphingolipid phosphatase SGPP1. Cancer Res. 2013;23:6972–86.
34.
go back to reference Kim Y, et al. Quantification of cancer cell extravasation in vivo. Nat Protoc. 2016;11(5):937–48.CrossRef Kim Y, et al. Quantification of cancer cell extravasation in vivo. Nat Protoc. 2016;11(5):937–48.CrossRef
35.
go back to reference Taylor BS, et al. Integrative genomic profiling of human prostate cancer. Cancer Cell. 2010;18:11–22.CrossRef Taylor BS, et al. Integrative genomic profiling of human prostate cancer. Cancer Cell. 2010;18:11–22.CrossRef
36.
go back to reference Goswami CP, Nakshatri H. PROGgeneV2: enhancements on the existing database. BMC Cancer. 2014;14:970.CrossRef Goswami CP, Nakshatri H. PROGgeneV2: enhancements on the existing database. BMC Cancer. 2014;14:970.CrossRef
37.
go back to reference Ross-Adams H, et al. Integration of copy number and transcriptomics provides risk stratification in prostate cancer: a discovery and validation cohort study. EBioMedicine. 2015;2:1133–44.CrossRef Ross-Adams H, et al. Integration of copy number and transcriptomics provides risk stratification in prostate cancer: a discovery and validation cohort study. EBioMedicine. 2015;2:1133–44.CrossRef
38.
go back to reference Montanari M, et al. Epithelial-mesenchymal transition in prostate cancer: an overview. Oncotarget. 2017;8(21):35376–89.CrossRef Montanari M, et al. Epithelial-mesenchymal transition in prostate cancer: an overview. Oncotarget. 2017;8(21):35376–89.CrossRef
39.
go back to reference Odero-Marah Valerie and Hawsawi, O. a. H. V. a. S. J., in Cell & molecular biology of prostate cancer: updates, insights and new frontiers. Schatten H, editor. Cham: Springer International Publishing; 2018. p. 101–10. Odero-Marah Valerie and Hawsawi, O. a. H. V. a. S. J., in Cell & molecular biology of prostate cancer: updates, insights and new frontiers. Schatten H, editor. Cham: Springer International Publishing; 2018. p. 101–10.
40.
go back to reference Lebensohn AM, Rohatgi R. R-spondins can potentiate WNT signaling without LGRs. eLife. 2018;7:e33126.CrossRef Lebensohn AM, Rohatgi R. R-spondins can potentiate WNT signaling without LGRs. eLife. 2018;7:e33126.CrossRef
Metadata
Title
RSPO3 is a prognostic biomarker and mediator of invasiveness in prostate cancer
Authors
Aruz Mesci
Fabrice Lucien
Xiaoyong Huang
Eric H. Wang
David Shin
Michelle Meringer
Christianne Hoey
Jessica Ray
Paul C. Boutros
Hon S. Leong
Stanley K. Liu
Publication date
01-12-2019
Publisher
BioMed Central
Published in
Journal of Translational Medicine / Issue 1/2019
Electronic ISSN: 1479-5876
DOI
https://doi.org/10.1186/s12967-019-1878-3

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