| 2011 |
FZD7 knockdown in triple-negative breast cancer cells (MDA-MB-231, BT-20) suppresses cell proliferation, invasiveness, and colony formation through silencing of canonical Wnt signaling, as evidenced by loss of nuclear β-catenin accumulation and decreased TCF7 transcriptional activity; in vivo xenograft studies confirmed reduced tumor formation. |
shRNA knockdown, β-catenin nuclear localization assay, TCF7 reporter assay, xenograft mouse model |
Oncogene |
Medium |
21532620
|
| 2011 |
In differentiated myofibres, Wnt7a binding to Fzd7 directly activates the Akt/mTOR anabolic growth pathway via a receptor complex associated with Gαs and PI(3)K, independently of IGF-receptor activation, thereby inducing myofibre hypertrophy. |
Wnt7a ligand treatment, co-immunoprecipitation of Fzd7 with Gαs and PI3K, Akt/mTOR pathway readouts, IGF-receptor independence experiments |
Nature cell biology |
High |
22179044
|
| 2014 |
ΔNp63 transcription factor promotes mammary stem cell activity and basal breast cancer tumor-initiating activity by increasing FZD7 expression, thereby enhancing Wnt signaling; FZD7-dependent Wnt signaling governed tumor-initiating activity of basal breast cancer. |
Gain- and loss-of-function of ΔNp63 and FZD7, mammary stem cell and tumor-initiating cell assays |
Nature cell biology |
Medium |
25241036
|
| 2014 |
FZD7 is required for maintenance of the pluripotent state of human embryonic stem cells (hESCs); shRNA-mediated knockdown or blockade with a FZD7-specific Fab fragment disrupts pluripotency. The FZD7-specific Fab blocks Wnt3a signaling by down-regulating FZD7 protein levels, indicating that FZD7 transduces Wnt/β-catenin signals in hESCs. |
shRNA knockdown, FZD7-specific Fab antibody treatment, Wnt3a signaling assay, FZD7 protein level measurement |
Proceedings of the National Academy of Sciences of the United States of America |
Medium |
24474766
|
| 2014 |
FZD7 knockdown in Stem-A ovarian cancer cells reduces proliferation, induces epithelial-like morphology, increases cadherin-based cell-cell adhesion, rearranges actin cytoskeleton, decreases RhoA activity, and increases Rac1 activity; increased TopFlash activity and PCP pathway gene regulation suggest FZD7 drives aggressiveness via the non-canonical Wnt/PCP pathway through casein kinase 1ε. |
siRNA knockdown, cell proliferation and morphology assays, immunofluorescence, RhoA/Rac1 activity assays, TopFlash reporter assay, PCP gene expression profiling |
Cell death & disease |
Medium |
25032869
|
| 2008 |
FZD7 is expressed at up to 200-fold higher levels in human embryonic stem cells versus differentiated cell types; shRNA-mediated knockdown in hESCs induces changes in colony morphology, perturbation of germ layer marker gene expression, and rapid loss of OCT4 expression, establishing FZD7 as required for ES cell self-renewal capacity. |
Quantitative RT-PCR, flow cytometry, shRNA knockdown, OCT4 expression analysis |
Biological chemistry |
Medium |
18681827
|
| 2016 |
Fzd7 expressed by endothelial cells is required for postnatal retinal vascular formation; endothelial cell-specific deletion of Fzd7 delays retinal plexus formation by impairing tip cell phenotype and stalk cell proliferation. Fzd7 acts via Dvl/β-catenin activation upstream of Notch signaling to control Dll4 and Jagged1 expression; LiCl treatment rescued the vascular phenotype of Fzd7 mutants. |
Conditional endothelial knockout mouse, retinal vascular phenotype analysis, Dvl3 depletion in dvl1-/- mice, LiCl pharmacological rescue, Notch target gene expression |
Arteriosclerosis, thrombosis, and vascular biology |
High |
27758766
|
| 2017 |
RSPO2 physically interacts with Fzd7 and increases degradation of cell-surface Fzd7 via ZNRF3-mediated ubiquitination, suppressing downstream PKC/ERK signaling and CRC cell migration; Wnt5a prevents Fzd7 degradation and promotes CRC cell migration, while RSPO2 antagonizes Wnt5a/Fzd7 signaling by blocking Wnt5a binding to FZD7. |
Co-immunoprecipitation, ubiquitination assay, PKC/ERK signaling readouts, migration/invasion assays, ligand competition experiments |
Cancer letters |
High |
28600110
|
| 2020 |
YTHDF1 promotes translation of FZD7 mRNA in an m6A-dependent manner in gastric cancer; mutated YTHDF1 enhances FZD7 expression, leading to hyperactivation of Wnt/β-catenin pathway. |
m6A-seq, YTHDF1 knockdown/overexpression, polysome profiling or translation assay, in vitro and in vivo gastric cancer models |
Cancer research |
Medium |
32788173
|
| 2020 |
WNT11-FZD7-DAAM1 signaling activates the Rho-ROCK1/2-Myosin II pathway to regulate tumour-initiating potential, amoeboid invasion, local invasion, and distant metastasis in melanoma. |
KD/KO of WNT11, FZD7, DAAM1 in melanoma cells; Rho-ROCK-Myosin II signaling readouts; in vivo metastasis assays; human melanoma tissue analysis |
Nature communications |
High |
33082334
|
| 2019 |
FZD7 regulates TWIST1 expression through epigenetic modifications (H3K4me3 and H3K27ac) at the TWIST1 proximal promoter; the FZD7-TWIST1 axis then regulates BCL2 expression to confer anoikis resistance in ovarian cancer. Overexpression of TWIST1 partially rescued phenotypes abolished by FZD7 knockdown. |
FZD7 knockdown/overexpression, TWIST1 overexpression rescue, chromatin immunoprecipitation for H3K4me3/H3K27ac, BCL2 expression analysis, anoikis and spheroid assays |
Molecular oncology |
Medium |
30548372
|
| 2020 |
Non-canonical Fzd7 signaling in breast cancer cells involves Fzd7 binding to Wnt5a/b, and modulates phospho-STAT3, Smad3, YAP1, and Col6a1 expression; Fzd7-Wnt5b regulates Col6a1 to mediate mesenchymal-like stemness and EMT. |
Fzd7 knockdown/overexpression, co-immunoprecipitation of Fzd7 with Wnt5a/b, pathway protein western blots, Col6a1 knockdown epistasis, xenograft and metastasis assays |
Cell communication and signaling : CCS |
Medium |
32894152
|
| 2022 |
GIPC2 directly binds to FZD7 through its PDZ domain, enabling activation of WNT-β-catenin cascades and stimulating prostate cancer metastasis. |
Co-immunoprecipitation, PDZ domain interaction mapping, β-catenin signaling assays, in vitro and in vivo metastasis assays |
Oncogene |
Medium |
35347223
|
| 2020 |
Selective engagement of FZD7 (and not other FZD proteins) by the engineered bispecific protein F7L6, which bridges FZD7 and LRP6, potently activates WNT/β-catenin signaling and is sufficient to initiate mesendodermal differentiation programs in human pluripotent stem cells, mimicking primitive streak formation. |
Engineered FZD7-selective/LRP6-bridging agonist (F7L6), WNT/β-catenin reporter assays, transcriptome profiling of hPS cells, comparison with Wnt3a and other FZD-selective agonists |
eLife |
High |
33331818
|
| 2024 |
CryoEM structures of TcdB alone and in complex with full-length FZD7 reveal that large structural rearrangements of the combined repetitive polypeptide (CROPs) domain of TcdB are required for FZD7 interaction; bezlotoxumab (FDA-approved antibody) favors the apo-TcdB conformation and disrupts FZD7 binding. Dynamic transition between TcdB conformations also governs stability of the pore-forming region. |
CryoEM structure determination, live-cell affinity assay, bezlotoxumab competition binding assay |
Cell reports |
High |
38308843
|
| 2023 |
Structure-based ligand discovery targeting the transmembrane domain (TMD) of FZD7 identified compound F7H as an FZD7 antagonist (IC50 = 1.25 μM); molecular docking, MD simulation, and free energy perturbation calculations defined key binding-pocket residues in the TMD. |
Structure-based virtual screening, compound synthesis, Wnt/β-catenin reporter antagonism assay, molecular docking/MD/FEP calculations |
Journal of medicinal chemistry |
Medium |
37669317
|
| 2020 |
CDDO-Me inhibits Wnt/β-catenin signaling by inducing ubiquitination and lysosomal degradation of the LRP6/FZD7 receptor complex; degradation of FZD7 is dependent on the LRP6 ectodomain, and CDDO-Me reduces phospho-DVL2 and active β-catenin levels in breast cancer cells. |
LRP6 and FZD7 protein degradation assays, ubiquitination assay, lysosomal pathway inhibitors, LRP6 ectodomain deletion constructs, DVL2 and β-catenin western blots, xenograft model |
The Journal of pharmacology and experimental therapeutics |
Medium |
32015160
|
| 2016 |
NOTCH3, but not NOTCH1, 2, or 4, regulates FZD7 expression in human breast epithelial cells through a non-canonical (CSL-independent) Notch signaling mechanism; gain- and loss-of-function experiments showed this regulation is unique and non-redundant. |
Constitutively active NOTCH1-4 overexpression, NOTCH loss-of-function, CSL-independent signaling assay, FZD7 expression analysis |
Stem cells and development |
Medium |
26847503
|
| 2018 |
GCM1 transcription factor promotes trophoblast cell migration by activating WNT10B expression; WNT10B signals through FZD7 (identified as its cognate receptor) to upregulate cell migration via Rac1-mediated cytoskeletal remodeling. SFRP3 from decidual cells blocks WNT10B-FZD7 interaction to decrease trophoblast migration. |
FZD7 receptor identification for WNT10B, cell migration assays, Rac1 activity assays, SFRP3 competition binding, trophoblast-decidual co-culture |
FASEB journal |
Medium |
29979633
|
| 2023 |
Vangl1 forms a novel complex with Fzd7 at the leading edge of migrating GBM cells; this Vangl1/Fzd7 complex drives cellular proliferation, migration, and invasiveness by engaging Rho GTPases to promote cytoskeletal rearrangements and actin dynamics. |
Co-immunoprecipitation, co-localization at leading edge, Rho GTPase activity assays, FZD7 depletion in intracranial xenograft model, KD functional assays |
Cancer letters |
Medium |
37336284
|
| 2024 |
SIRT7 promotes FZD7 expression by upregulating the transcription factor PU.1, which then drives FZD7 transcription; FZD7 is required for SIRT7-mediated stabilization of β-catenin and its nuclear localization in hepatocellular carcinoma cells. FZD7 knockdown reversed SIRT7-overexpression-mediated β-catenin stabilization. |
SIRT7 knockdown/overexpression, FZD7 knockdown rescue, PU.1 manipulation, nuclear/cytoplasmic fractionation, β-catenin ubiquitination and stability assays, Top-Flash reporter, immunofluorescence |
Life sciences |
Medium |
39542206
|
| 2023 |
BCL6 transcription repressor directly binds the FZD7 promoter and transcriptionally represses FZD7 to inhibit gastric cancer cell proliferation and metastasis; BCL6 also promotes ferroptosis through the FZD7/β-catenin/TP63/GPX4 pathway. |
ChIP assay, dual luciferase reporter assay, FZD7 rescue experiments, ferroptosis readouts (lipid peroxidation, MDA, Fe2+), rescue experiments |
Cell & bioscience |
Medium |
37060074
|
| 2022 |
Wnt5a regulates ABCG2 expression in pancreatic cancer cells through FZD7; siRNA silencing or pharmacological inhibition of FZD7 blocked Wnt5a-induced ABCG2 upregulation and attenuated gemcitabine resistance. |
siRNA knockdown of FZD7, FZD7 inhibitors, recombinant Wnt5a treatment, ABCG2 expression analysis, gemcitabine resistance assay |
Molecular medicine reports |
Medium |
33200805
|
| 2025 |
FZD7 activation (via selective agonist) triggers β-catenin signaling with distinct kinetics from FZD2, enabling both paraxial and lateral mesoderm differentiation of hPSCs, whereas FZD2 activation favors only paraxial mesoderm; FZD7 shows more rapid dampening of β-catenin signaling than FZD2, permitting lateral mesoderm induction. |
FZD2- and FZD7-selective antibody-based agonists, hPSC directed differentiation assays, β-catenin signaling kinetics measurement, mesoderm subtype marker analysis |
Stem cell reports |
Medium |
39824186
|
| 2025 |
YTHDF1 binds to m6A-modified FZD7 mRNA in cisplatin-resistant ovarian cancer cells, enhancing its stability and translation, thereby sustaining Wnt/β-catenin signaling activation; YTHDF1 silencing reduces FZD7 expression, inhibits Wnt/β-catenin signaling, and restores cisplatin sensitivity in vitro and in xenograft models. |
YTHDF1 knockdown/overexpression, m6A-IP, mRNA stability assay, FZD7 expression analysis, Wnt/β-catenin pathway readouts, xenograft mouse model |
Apoptosis |
Medium |
40281310
|
| 2022 |
FZD7 knockdown in pancreatic cancer cells reduces EMT marker expression, reduces mesenchymal phenotype, decreases cancer stem cell proportions (CD24+CD44+, ABCG2), and attenuates TGF-β1-induced EMT; FZD7 acts through both canonical Wnt/β-catenin and TGF-β/SMAD3 signaling pathways. |
lentiviral shRNA knockdown, FZD7 overexpression, TGF-β1 stimulation assays, EMT marker western blots, CSC flow cytometry, sphere formation assays |
Molecular medicine (Cambridge, Mass.) |
Medium |
35854234
|
| 2024 |
WNT7A activates the FZD7/JAK1/STAT3 signaling pathway in head and neck squamous cell carcinoma, leading to enhanced cell proliferation, self-renewal, and resistance to apoptosis, without activating canonical Wnt/β-catenin signaling. |
WNT7A overexpression, FZD7/JAK1/STAT3 pathway analysis, β-catenin reporter (negative result), patient-derived xenograft model |
International journal of oral science |
Medium |
38246919
|
| 2025 |
Cytoplasmic KIAA1429, phosphorylated by BRAF, stabilizes FZD7 protein in colorectal cancer cells by direct binding, thereby activating the WNT pathway and promoting cancer stemness and oxaliplatin resistance. |
Co-immunoprecipitation, immunofluorescence, RNA-seq, in vitro and in vivo oxaliplatin resistance assays, FZD7 stabilization experiments |
Journal of experimental & clinical cancer research |
Medium |
40611274
|
| 2019 |
Fibronectin promotes non-canonical Wnt signaling through Wnt11-Fzd7 interaction in limbal epithelial stem cells, and modulates cell cycle regulators via upregulation of ROCK1 and ROCK2 to enhance stem cell self-renewal and proliferation. |
Wnt11 and Fzd7 co-expression/interaction analysis, ROCK inhibition, proliferation and stemness assays under fibronectin conditions |
Experimental eye research |
Low |
31150636
|
| 2019 |
FZD7 knockdown reduces expression of Lgr5 (a WNT target) and is required for intestinal stem cell function in mice, but gastric Lgr5+ stem cells do not require Fzd7 for epithelial homeostasis, establishing tissue-specific differential requirement for FZD7 in Wnt-dependent stem cell maintenance. |
Conditional Fzd7 deletion in gastric Lgr5+ cells, intestinal comparison, homeostasis and regeneration assays |
Biomedicines |
Medium |
31288403
|