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Radioligand therapy target profile

FZD5 as a Radioligand Therapy Target

frizzled class receptor 5 · Ensembl ENSG00000163251 · Data updated 2026-08-01

FZD5, frizzled class receptor 5, is a cell-surface protein (GPCR). In Human Protein Atlas immunohistochemistry, FZD5 staining is highest in liver cancer (67% of samples positive), prostate cancer (64% of samples positive) and endometrial cancer (40% of samples positive). Evidence on whether FZD5 internalizes is mixed. Clinical status: Clinical-stage (up to phase 1, any modality).

LocalizationCell-Surface
Top cancer (IHC)Liver Cancer
InternalizationUncertain
Clinical stageClinical-stage (up to phase 1, any modality)
Active trialsSee ClinicalTrials.gov
Cancer association (Open Targets)0.29

Is FZD5 a good radioligand therapy target?

Scored against the six criteria that decide whether a protein can become a radioligand therapy:

FZD5 expression in cancer

Protein expression of FZD5 across 20 cancer types from Human Protein Atlas immunohistochemistry. The score is a weighted staining intensity from 0 to 1; "% positive" is the share of patient samples with detectable staining.

Cancer typeIHC scoreLevel% positive
Liver Cancer0.28Medium67%
Prostate Cancer0.24Medium64%
Endometrial Cancer0.20Medium40%
Gastric Cancer0.17Low33%
Colorectal Cancer0.15Low46%
Pancreatic Cancer0.14Low33%
Head and Neck Cancer0.11Low33%
Breast Cancer0.11Low33%
Lung Cancer0.11Low22%
Melanoma0.10Low30%
Bladder Cancer0.09Low18%
Ovarian Cancer0.06Low18%
Cervical Cancer0.06Low18%
Testicular Cancer0.06Low18%
Lymphoma0.06Low8%

Not detected by IHC in: skin cancer, kidney cancer, thyroid cancer, neuroendocrine tumors, glioma.

Is FZD5 internalized?

Uncertain. Insufficient literature found.

FZD5 clinical trials

Clinical-stage (up to phase 1, any modality). Nuclens hasn't indexed trials for FZD5 yet. Search ClinicalTrials.gov for FZD5 trials.

FZD5 normal tissue expression

Normal-tissue expression in dose-limiting organs (kidney, liver, bone marrow, salivary glands) drives radioligand dosimetry risk. Nuclens is re-validating its normal-tissue values, so they are not shown here yet. See FZD5 in the Human Protein Atlas tissue atlas, and read how normal-tissue expression predicts radioligand dosimetry risk.

FZD5 gene essentiality (DepMap)

CRISPR knockout effect across 1258 cancer cell lines: -0.13 (not essential). Radioligands kill by radiation, not by blocking the target, so essentiality matters less than for inhibitors. A non-essential target can still be an excellent radioligand target.

Related liver cancer radioligand targets

EGFR · c-MET (MET) · HER3 (ERBB3) · SSTR2 · STEAP2 · HER2 (ERBB2) · Mesothelin (MSLN) · B7-H3 (CD276)

See all radioligand therapy targets in liver cancer.

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Data sources

Subcellular localization: UniProt via Open Targets (CC BY 4.0 / CC0). Tumor immunohistochemistry: Human Protein Atlas (CC BY-SA 4.0). Clinical trials: ClinicalTrials.gov (public domain). Gene essentiality: DepMap (CC BY 4.0). Internalization and shedding: AI-extracted from PubMed abstracts, so verify against the cited papers before relying on them. Nuclens is a first-pass triage layer, not a substitute for wet-lab validation or clinical dosimetry. Derived expression data on this page is shared under CC BY-SA 4.0.