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Radioligand therapy target profile

HCAR2 as a Radioligand Therapy Target

hydroxycarboxylic acid receptor 2 · Ensembl ENSG00000182782 · Data updated 2026-08-01

HCAR2, hydroxycarboxylic acid receptor 2, is a cell-surface protein (GPCR). In Human Protein Atlas immunohistochemistry, HCAR2 staining is highest in head and neck cancer (67% of samples positive), bladder cancer (73% of samples positive) and gastric cancer (50% of samples positive). Evidence on whether HCAR2 internalizes is mixed. Clinical status: Clinical-stage (up to phase 2, any modality).

LocalizationCell-Surface
Top cancer (IHC)Head and Neck Cancer
InternalizationUncertain
Clinical stageClinical-stage (up to phase 2, any modality)
Active trialsSee ClinicalTrials.gov
Cancer association (Open Targets)0.25

Is HCAR2 a good radioligand therapy target?

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

HCAR2 expression in cancer

Protein expression of HCAR2 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
Head and Neck Cancer0.33Medium67%
Bladder Cancer0.30Medium73%
Gastric Cancer0.19Low50%
Pancreatic Cancer0.15Low46%
Kidney Cancer0.12Low36%
Breast Cancer0.12Low27%
Lung Cancer0.12Low27%
Liver Cancer0.11Low33%
Testicular Cancer0.08Low25%
Ovarian Cancer0.06Low18%
Colorectal Cancer0.06Low17%
Cervical Cancer0.06Low17%
Prostate Cancer0.06Low17%
Endometrial Cancer0.06Low17%
Skin Cancer0.03Low8%
Lymphoma0.03Low8%

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

Is HCAR2 internalized?

Uncertain. Insufficient literature found.

HCAR2 clinical trials

Clinical-stage (up to phase 2, any modality). Nuclens hasn't indexed trials for HCAR2 yet. Search ClinicalTrials.gov for HCAR2 trials.

HCAR2 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 HCAR2 in the Human Protein Atlas tissue atlas, and read how normal-tissue expression predicts radioligand dosimetry risk.

HCAR2 gene essentiality (DepMap)

CRISPR knockout effect across 1252 cancer cell lines: 0.09 (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 head and neck cancer radioligand targets

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

See all radioligand therapy targets in head and neck 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.