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Radioligand therapy target profile

EDNRB as a Radioligand Therapy Target

endothelin receptor type B · Ensembl ENSG00000136160 · Data updated 2026-08-01

EDNRB, endothelin receptor type B, is a cell-surface protein (GPCR). In Human Protein Atlas immunohistochemistry, EDNRB staining is highest in breast cancer (100% of samples positive), ovarian cancer (83% of samples positive) and pancreatic cancer (60% of samples positive). Evidence on whether EDNRB internalizes is mixed. Clinical status: Clinical-stage (up to phase 3, any modality).

LocalizationCell-Surface
Top cancer (IHC)Breast Cancer
InternalizationUncertain
Clinical stageClinical-stage (up to phase 3, any modality)
Active trialsSee ClinicalTrials.gov
Cancer association (Open Targets)0.30

Is EDNRB a good radioligand therapy target?

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

EDNRB expression in cancer

Protein expression of EDNRB 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
Breast Cancer0.69High100%
Ovarian Cancer0.50Medium83%
Pancreatic Cancer0.27Medium60%
Gastric Cancer0.22Medium56%
Cervical Cancer0.19Low33%
Kidney Cancer0.17Low33%
Colorectal Cancer0.14Low33%
Endometrial Cancer0.14Low33%
Bladder Cancer0.14Low25%
Liver Cancer0.14Low25%
Lung Cancer0.11Low22%
Thyroid Cancer0.08Low25%
Testicular Cancer0.04Low11%
Melanoma0.03Low10%

Not detected by IHC in: skin cancer, head and neck cancer, lymphoma, neuroendocrine tumors, prostate cancer, glioma.

Is EDNRB internalized?

Uncertain. Insufficient literature found.

EDNRB clinical trials

Clinical-stage (up to phase 3, any modality). Nuclens hasn't indexed trials for EDNRB yet. Search ClinicalTrials.gov for EDNRB trials.

EDNRB 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 EDNRB in the Human Protein Atlas tissue atlas, and read how normal-tissue expression predicts radioligand dosimetry risk.

EDNRB gene essentiality (DepMap)

CRISPR knockout effect across 1252 cancer cell lines: 0.04 (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 breast cancer radioligand targets

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

See all radioligand therapy targets in breast 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.