| 2011 |
FZD7 knockdown in TNBC cells suppresses canonical Wnt signaling, evidenced by loss of nuclear β-catenin accumulation and decreased TCF7 transcriptional activity, establishing FZD7 as a required receptor for canonical Wnt/β-catenin pathway activation in triple-negative breast cancer. |
shRNA knockdown, β-catenin nuclear localization assay, TCF7 reporter assay, xenograft tumor model |
Oncogene |
High |
21532620
|
| 2011 |
Wnt7a binds Fzd7 and directly activates the Akt/mTOR anabolic growth pathway in differentiated myofibers through a complex containing Gαs and PI(3)K, independent of IGF-receptor activation, demonstrating a non-canonical Wnt7a-Fzd7 signaling axis distinct from its planar cell polarity role in satellite stem cells. |
Co-immunoprecipitation (Fzd7 complex with Gαs and PI(3)K), Wnt7a treatment of myotubes, PI3K inhibitor, KO/KD with Akt/mTOR readout |
Nature cell biology |
High |
22179044
|
| 2014 |
ΔNp63 transcription factor promotes mammary stem cell activity and basal breast cancer tumor-initiating ability by directly enhancing Fzd7 expression, thereby increasing Wnt signaling. |
Gain/loss-of-function of ΔNp63, Fzd7 expression analysis, mammary stem cell activity assays, tumor-initiating cell assays |
Nature cell biology |
High |
25241036
|
| 2014 |
FZD7 is required for maintenance of the pluripotent state in human embryonic stem cells; a FZD7-specific Fab antibody blocks Wnt3a signaling by downregulating FZD7 protein levels, and shRNA-mediated knockdown disrupts the pluripotent state, demonstrating that hESCs require endogenous WNT/β-catenin signaling through FZD7. |
shRNA knockdown, FZD7-specific Fab antibody blocking, Wnt3a treatment, pluripotency marker analysis |
Proceedings of the National Academy of Sciences of the United States of America |
High |
24474766
|
| 2008 |
FZD7 is highly expressed in human embryonic stem cells, and shRNA-mediated knockdown induces colony morphology changes and rapid loss of OCT4 expression, identifying FZD7 as a component of hESC self-renewal signaling. |
shRNA knockdown, quantitative RT-PCR, flow cytometry, morphological analysis |
Biological chemistry |
Medium |
18681827
|
| 2014 |
FZD7 knockdown in Stem-A ovarian cancer cells causes actin cytoskeletal rearrangement via reciprocal regulation of RhoA and Rac1 (reduced RhoA activity, increased Rac1 activity), changes in phospho-myosin light chain distribution, and increased TopFlash reporter activity, establishing FZD7 involvement in the non-canonical Wnt/PCP pathway through casein kinase 1ε. |
siRNA knockdown, RhoA/Rac1 activity assays, phospho-MLC immunofluorescence, TopFlash reporter assay |
Cell death & disease |
Medium |
25032869
|
| 2016 |
Fzd7 expressed by endothelial cells controls postnatal angiogenesis via activation of Dvl/β-catenin signaling, acting upstream of Notch signaling to regulate Dll4 and Jagged1 expression; endothelial-specific deletion of fzd7 (fzd7ECKO) delays retinal plexus formation due to impaired tip cell phenotype and decreased stalk cell proliferation, rescued by LiCl treatment. |
Conditional endothelial KO (fzd7ECKO mice), retinal vascular imaging, LiCl pharmacological rescue, Dvl1/3 double KO comparison |
Arteriosclerosis, thrombosis, and vascular biology |
High |
27758766
|
| 2017 |
RSPO2 physically interacts with Fzd7 and promotes ZNRF3-mediated ubiquitination and degradation of cell-surface Fzd7, suppressing downstream PKC/ERK signaling; Wnt5a prevents Fzd7 degradation, and RSPO2 antagonizes Wnt5a-driven noncanonical Wnt signaling by blocking Wnt5a binding to Fzd7. |
Co-immunoprecipitation, ubiquitination assay, ZNRF3 involvement, PKC/ERK signaling readout, Wnt5a competitive binding |
Cancer letters |
High |
28600110
|
| 2020 |
YTHDF1 promotes translation of FZD7 mRNA in an m6A-dependent manner, leading to hyperactivation of the Wnt/β-catenin pathway; mutated YTHDF1 further enhances FZD7 expression and gastric carcinogenesis. |
YTHDF1 knockdown/overexpression, m6A methylation analysis, FZD7 protein translation assay, Wnt/β-catenin pathway readout, in vitro and in vivo tumor models |
Cancer research |
High |
32788173
|
| 2021 |
circACTN4 recruits Y-box binding protein 1 (YBX1) to stimulate FZD7 transcription in intrahepatic cholangiocarcinoma, identified via RNA pulldown, mass spectrometry, ChIP, RIP, EMSA, and luciferase reporter assays. |
RNA pulldown, mass spectrometry, chromatin immunoprecipitation (ChIP), RNA-binding protein immunoprecipitation (RIP), EMSA, luciferase reporter assay |
Journal of hepatology |
High |
34509526
|
| 2020 |
WNT11-FZD7-DAAM1 signaling activates Rho-ROCK1/2-Myosin II and plays a crucial role in amoeboid melanoma invasion, tumor-initiating potential, and distant metastasis formation. |
KD of WNT11/FZD7/DAAM1, Rho-ROCK-Myosin II pathway readout, invasion assays, in vivo metastasis models |
Nature communications |
High |
33082334
|
| 2020 |
Fzd7 in breast cancer cells interacts with Wnt5a/b to modulate phosphorylated STAT3, Smad3, and YAP1; Fzd7-Wnt5b signaling upregulates Col6a1, which mediates Fzd7-Wnt5b-induced mesenchymal-like stemness, establishing a non-canonical Wnt pathway role for Fzd7 in EMT and stemness. |
Co-IP (Fzd7 with Wnt5a/b), KD of Fzd7/Wnt5b/Col6a1, immunofluorescence, mammosphere formation, xenograft, lung metastasis assay |
Cell communication and signaling : CCS |
Medium |
32894152
|
| 2022 |
GIPC2 directly binds the WNT co-receptor Fzd7 through its PDZ domain, enabling activation of WNT-β-catenin cascades and stimulating prostate cancer metastasis. |
Co-immunoprecipitation, PDZ domain binding assay, GIPC2 KD with WNT-β-catenin readout, in vitro and in vivo metastasis assays |
Oncogene |
Medium |
35347223
|
| 2019 |
FZD7 regulates TWIST1 expression through epigenetic modifications of H3K4me3 and H3K27ac at the TWIST1 proximal promoter; the FZD7-TWIST1 axis controls BCL2 expression to confer anoikis resistance in ovarian cancer cells. |
FZD7 KD, chromatin histone modification analysis (H3K4me3/H3K27ac at TWIST1 promoter), TWIST1 overexpression rescue, BCL2 expression assay, anoikis resistance assays |
Molecular oncology |
Medium |
30548372
|
| 2016 |
Notch3, but not Notch1, 2, or 4, uniquely regulates FZD7 expression in human breast epithelial cells through a non-canonical (CSL-independent) Notch signaling mechanism. |
Gain and loss-of-function of NOTCH1-4, FZD7 expression analysis, CSL-independence assay |
Stem cells and development |
Medium |
26847503
|
| 2018 |
GCM1 transcription factor promotes trophoblast cell migration through transcriptional activation of WNT10B; WNT10B then signals through FZD7 as its cognate receptor to upregulate Rac1-mediated cytoskeletal remodeling and cell migration; SFRP3 from decidual cells blocks WNT10B-FZD7 interaction to suppress migration. |
GCM1 target gene identification, WNT10B-FZD7 interaction (co-immunoprecipitation/functional blocking), Rac1 activity assay, SFRP3 competitive binding, trophoblast migration assays |
FASEB journal |
Medium |
29979633
|
| 2020 |
Selective engagement of FZD7 and LRP6 by engineered bispecific antibody F7L6 is sufficient to potently activate WNT/β-catenin signaling and drive mesendodermal differentiation of human pluripotent stem cells, demonstrating that FZD7 specifically can transduce canonical Wnt signals. |
Engineered FZD7-specific scFv bispecific agonist (F7L6), WNT/β-catenin reporter assay, transcriptional profiling of hPS cell differentiation, comparison to Wnt3a |
eLife |
High |
33331818
|
| 2020 |
CDDO-Me inhibits Wnt/β-catenin signaling by inducing ubiquitination and lysosomal degradation of the LRP6/FZD7 receptor complex; the ectodomain of LRP6 is required for CDDO-Me-induced FZD7 degradation, revealing LRP6-dependent regulation of FZD7 protein stability. |
Ubiquitination assay, lysosomal pathway inhibitor, LRP6 ectodomain deletion constructs, FZD7 and LRP6 protein stability assays, Wnt target gene readout |
The Journal of pharmacology and experimental therapeutics |
Medium |
32015160
|
| 2023 |
BCL6 directly binds and transcriptionally represses FZD7, reducing Wnt/β-catenin signaling and promoting ferroptosis via the FZD7/β-catenin/TP63/GPX4 pathway in gastric cancer. |
ChIP assay (BCL6 binding to FZD7 promoter), dual luciferase reporter assay, rescue experiments, ferroptosis markers (lipid peroxidation, MDA, Fe2+), GPX4 expression |
Cell & bioscience |
Medium |
37060074
|
| 2024 |
Cryo-EM structures of Clostridioides difficile toxin B (TcdB) alone and in complex with full-length FZD7 reveal that large structural rearrangements of the combined repetitive polypeptide (CROPs) domain are required for FZD7 binding; bezlotoxumab (FDA-approved antibody) favors the apo-TcdB conformation and disrupts FZD7 binding. |
Cryo-EM structure determination of TcdB-FZD7 complex, live-cell binding assay, bezlotoxumab competition assay |
Cell reports |
High |
38308843
|
| 2023 |
Vangl1 and Fzd7 form a complex at the leading edge of migrating GBM cells, promoting actin cytoskeletal rearrangements, Rho GTPase engagement, and tumor cell proliferation, migration, and invasiveness via non-canonical Wnt/PCP signaling. |
Co-immunoprecipitation (Vangl1/Fzd7 complex), KD of FZD7 and Vangl1, Rho GTPase assays, actin dynamics imaging, intracranial xenograft model |
Cancer letters |
Medium |
37336284
|
| 2023 |
Structure-based ligand discovery targeting the transmembrane domain (TMD) of FZD7 identified compound F7H as an antagonist (IC50 = 1.25 μM); molecular docking, MD simulation, and FEP calculations defined the binding pocket and key residue interactions. |
Virtual screening, molecular docking, molecular dynamics simulation, free energy perturbation, functional Wnt antagonism assay |
Journal of medicinal chemistry |
Medium |
37669317
|
| 2024 |
SIRT7 promotes FZD7 expression via transcription factor PU.1 upregulation, and FZD7 is essential for SIRT7-mediated β-catenin stabilization (preventing its association with the destruction complex) and activation of canonical Wnt signaling in hepatocellular carcinoma. |
SIRT7/PU.1/FZD7 KD, nuclear cytosol fractionation, β-catenin ubiquitination/stability assay, TopFlash reporter, ChIP-PCR for PU.1 at FZD7 promoter |
Life sciences |
Medium |
39542206
|
| 2025 |
FZD7 and FZD2 activate β-catenin signaling with different kinetics in hPSCs; FZD7 activation promotes both paraxial and lateral mesoderm differentiation while FZD2 favors only paraxial mesoderm, demonstrating non-redundant roles of these closely related FZD receptors in mesoderm specification. |
Selective FZD7- and FZD2-specific antibody-based agonists, β-catenin signaling kinetics measurement, directed differentiation of hPSCs, transcriptional profiling of mesoderm subtypes |
Stem cell reports |
Medium |
39824186
|
| 2024 |
WNT7A activates FZD7 to stimulate the JAK1/STAT3 signaling pathway (not the canonical Wnt-β-catenin pathway) in head and neck squamous cell carcinoma, promoting cell proliferation, self-renewal, and resistance to apoptosis. |
WNT7A overexpression, β-catenin pathway reporter (negative), FZD7/JAK1/STAT3 pathway analysis, PDX tumor model |
International journal of oral science |
Medium |
38246919
|
| 2022 |
FZD7 silencing in pancreatic cancer attenuates TGF-β1-induced EMT and reduces stemness markers (ABCG2, CD24, CD44), demonstrating that FZD7 participates in both canonical Wnt and TGF-β/SMAD3 signaling to drive EMT and cancer stem cell properties. |
shRNA FZD7 silencing, TGF-β1 stimulation, EMT marker Western blot, sphere formation, flow cytometry for CD24/CD44, β-catenin activation assay |
Molecular medicine (Cambridge, Mass.) |
Medium |
35854234
|
| 2020 |
Wnt5a upregulates ABCG2 expression through FZD7 in pancreatic cancer cells, and FZD7 silencing or inhibition abolishes Wnt5a-induced ABCG2 upregulation and gemcitabine resistance, placing FZD7 as the essential receptor for Wnt5a-driven drug resistance. |
Recombinant Wnt5a treatment, siRNA FZD7 silencing, FZD7 inhibitor, ABCG2 expression assay, gemcitabine resistance assay |
Molecular medicine reports |
Medium |
33200805
|
| 2019 |
Fibronectin promotes limbal epithelial stem cell self-renewal by facilitating Wnt11-Fzd7 interaction and activating the non-canonical Wnt11/Fzd7/ROCK pathway to modulate cell cycle regulators. |
Fibronectin treatment, Wnt11/Fzd7 co-expression and interaction analysis, ROCK1/2 activity assay, cell cycle analysis, stemness assays |
Experimental eye research |
Low |
31150636
|
| 2016 |
FZD7 overexpression in glioma activates TAZ (transcriptional coactivator with PDZ-binding motif), and TAZ is required for FZD7-driven glioma cell proliferation, placing TAZ as a downstream effector of FZD7 signaling. |
FZD7 overexpression/KD, TAZ activity assay, TAZ KD rescue experiment, xenograft proliferation assay |
Oncotarget |
Medium |
27852064
|
| 2025 |
KIAA1429 phosphorylation by BRAF drives its cytoplasmic accumulation, where it binds and stabilizes FZD7, leading to WNT pathway activation, enhanced cancer stemness and oxaliplatin resistance in colorectal cancer. |
Co-immunoprecipitation (KIAA1429-FZD7), IP-MS, immunofluorescence (nuclear/cytoplasmic distribution), FZD7 stability assay, in vitro and in vivo drug resistance experiments |
Journal of experimental & clinical cancer research : CR |
Medium |
40611274
|