SLC12A2 as a Radioligand Therapy Target
SLC12A2, solute carrier family 12 member 2, is a cell-surface protein. In Human Protein Atlas immunohistochemistry, SLC12A2 staining is highest in colorectal cancer (100% of samples positive), head and neck cancer (100% of samples positive) and endometrial cancer (100% of samples positive). Clinical status: Discovery-stage (no clinical drug program).
Is SLC12A2 a good radioligand therapy target?
Scored against the six criteria that decide whether a protein can become a radioligand therapy:
- ✅ Cell-surface accessibility: Localized to the cell surface, so a radioligand can reach it from circulation.
- ✅ Tumor expression: High IHC staining in colorectal cancer, 100% of samples positive.
- ❔ Internalization: Not yet assessed.
- ⚠️ Clinical precedent: Discovery-stage (no clinical drug program)
- ❔ Shedding: Not yet assessed.
- ❔ Normal-tissue dosimetry: Check kidney, liver, bone marrow and salivary expression in the Human Protein Atlas tissue atlas.
SLC12A2 expression in cancer
Protein expression of SLC12A2 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 type | IHC score | Level | % positive |
|---|---|---|---|
| Colorectal Cancer | 1.00 | High | 100% |
| Head and Neck Cancer | 0.89 | High | 100% |
| Endometrial Cancer | 0.83 | High | 100% |
| Pancreatic Cancer | 0.78 | High | 100% |
| Thyroid Cancer | 0.75 | High | 100% |
| Prostate Cancer | 0.75 | High | 100% |
| Gastric Cancer | 0.73 | High | 91% |
| Liver Cancer | 0.69 | High | 100% |
| Glioma | 0.67 | High | 100% |
| Breast Cancer | 0.64 | High | 100% |
| Ovarian Cancer | 0.58 | High | 83% |
| Lung Cancer | 0.58 | High | 73% |
| Neuroendocrine Tumors | 0.50 | Medium | 75% |
| Cervical Cancer | 0.47 | Medium | 83% |
| Bladder Cancer | 0.33 | Medium | 75% |
| Melanoma | 0.27 | Medium | 55% |
| Kidney Cancer | 0.25 | Medium | 50% |
| Skin Cancer | 0.22 | Medium | 50% |
| Testicular Cancer | 0.18 | Low | 36% |
| Lymphoma | 0.17 | Low | 25% |
Is SLC12A2 internalized?
Nuclens has not yet extracted internalization evidence for SLC12A2. Internalization matters for radioligands because an internalizing receptor traps the radionuclide inside the tumor cell. Run a full analysis to pull the latest literature.
SLC12A2 clinical trials
Discovery-stage (no clinical drug program). Nuclens hasn't indexed trials for SLC12A2 yet. Search ClinicalTrials.gov for SLC12A2 trials.
SLC12A2 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 SLC12A2 in the Human Protein Atlas tissue atlas, and read how normal-tissue expression predicts radioligand dosimetry risk.
SLC12A2 gene essentiality (DepMap)
CRISPR knockout effect across 1258 cancer cell lines: 0.06 (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 colorectal cancer radioligand targets
c-MET (MET) · HER3 (ERBB3) · FAP · EGFR · CEA (CEACAM5) · EPCAM · SSTR2 · STEAP2
See all radioligand therapy targets in colorectal cancer.
See how SLC12A2 ranks against 15,000 targets for your indication.
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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.