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Radioligand therapy target profile

CA2: IHC Expression in Cancer and Radioligand Target Profile

carbonic anhydrase 2 · Ensembl ENSG00000104267 · Data updated 2026-11-01

CA2, carbonic anhydrase 2, is a cell-surface protein. In Human Protein Atlas immunohistochemistry, CA2 staining is highest in liver cancer (30% of samples positive), gastric cancer (20% of samples positive) and pancreatic cancer (25% of samples positive). Clinical status: FDA-approved drug (any modality).

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LocalizationCell-Surface
Top cancer (IHC)Liver Cancer
InternalizationNot assessed
Clinical stageFDA-approved drug (any modality)
Active trialsSee ClinicalTrials.gov
Cancer association (Open Targets)0.32

Is CA2 a good radioligand therapy target?

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

CA2 IHC staining by cancer type

Protein expression of CA2 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 Cancer0.20Medium30%
Gastric Cancer0.20Medium20%
Pancreatic Cancer0.17Low25%
Ovarian Cancer0.12Low36%
Breast Cancer0.11Low17%
Cervical Cancer0.11Low17%
Glioma0.08Low8%
Endometrial Cancer0.06Low9%
Skin Cancer0.03Low9%

Not detected by IHC in: colorectal cancer, head and neck cancer, lymphoma, melanoma, kidney cancer, thyroid cancer, bladder cancer, neuroendocrine tumors, lung cancer, prostate cancer, testicular cancer.

Is CA2 internalized?

Nuclens has not yet extracted internalization evidence for CA2. Internalization matters for radioligands because an internalizing receptor traps the radionuclide inside the tumor cell. Run a free analysis to pull the latest literature.

CA2 clinical trials

FDA-approved drug (any modality). Nuclens hasn't indexed trials for CA2 yet. Search ClinicalTrials.gov for CA2 trials.

CA2 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 CA2 in the Human Protein Atlas tissue atlas, and read how normal-tissue expression predicts radioligand dosimetry risk.

CA2 gene essentiality (DepMap)

CRISPR knockout effect across 1254 cancer cell lines: 0.03 (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.

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