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Updated: May 29, 2026

Quantifying Antibody-Dependent Cellular Cytotoxicity in a Tumor Spheroid Model: Application for Drug Discovery
Published on: April 26, 2024
Tumor cell-selective apoptosis induction through targeting of K(V)10.1 via bifunctional TRAIL antibody
Franziska Hartung1, Walter Stühmer, Luis A Pardo
1Max-Planck-Institut für Experimentelle Medizin, Hermann-Rein-Str, 3, 37075 Göttingen, Germany.
Background:
The search for strategies to target ion channels for therapeutic applications has become of increasing interest. Especially, the potassium channel K(V)10.1 (Ether-á-go-go) is attractive as target since this surface protein is virtually not detected in normal tissue outside the central nervous system, but is expressed in approximately 70% of tumors from different origins.
Methods:
We designed a single-chain antibody against an extracellular region of K(V)10.1 (scFv62) and fused it to the human soluble TRAIL. The K(V)10.1-specific scFv62 antibody -TRAIL fusion protein was expressed in CHO-K1 cells, purified by chromatography and tested for biological activity.
Results:
Prostate cancer cells, either positive or negative for K(V)10.1 were treated with the purified construct. After sensitization with cytotoxic drugs, scFv62-TRAIL induced apoptosis only in K(V)10.1-positive cancer cells, but not in non-tumor cells, nor in tumor cells lacking K(V)10.1 expression. In co-cultures with K(V)10.1-positive cancer cells the fusion protein also induced apoptosis in bystander K(V)10.1-negative cancer cells, while normal prostate epithelial cells were not affected when present as bystander.
Conclusions:
K(V)10.1 represents a novel therapeutic target for cancer. We could design a strategy that selectively kills tumor cells based on a K(V)10.1-specific antibody.
Insights
Researchers developed a novel antibody-TRAIL fusion protein targeting the K(V)10.1 ion channel. This strategy selectively induces apoptosis in K(V)10.1-positive cancer cells, sparing normal tissues and offering a promising new cancer therapy.
Area of Science:
- Oncology
- Molecular Biology
- Immunotherapy
Background:
- The K(V)10.1 ion channel is a potential therapeutic target due to its restricted expression in normal tissues but high prevalence in various cancers.
- Targeting ion channels offers a promising avenue for novel cancer therapies.
Purpose of the Study:
- To develop and evaluate a novel therapeutic strategy targeting the K(V)10.1 ion channel for cancer treatment.
- To assess the selective killing of K(V)10.1-expressing tumor cells using a targeted fusion protein.
Main Methods:
- A single-chain antibody (scFv62) targeting an extracellular K(V)10.1 region was engineered.
- The antibody was fused to human soluble TRAIL (scFv62-TRAIL) and expressed in CHO-K1 cells.
- The purified fusion protein's biological activity was tested on cancer cells and normal cells.
Main Results:
- The scFv62-TRAIL fusion protein selectively induced apoptosis in K(V)10.1-positive cancer cells, including bystander cells.
- No significant toxicity was observed in non-tumor cells or K(V)10.1-negative tumor cells.
- Normal prostate epithelial cells were unaffected when present as bystanders.
Conclusions:
- K(V)10.1 is a viable and novel therapeutic target for various cancers.
- A K(V)10.1-specific antibody-based strategy can effectively and selectively eliminate tumor cells.
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