Key result
A newly developed thallium flux assay in T84 cells successfully screened 1352 compounds, identifying 8 novel KCa3.1 inhibitors with IC50 values ranging from 0.14 to 6.57 µM.
Why the study?
Inhibition of the KCa3.1 channel has therapeutic potential, but KCa3.1 inhibitors with high therapeutic promise are currently not available.
A newly developed thallium flux assay in T84 cells successfully identified 8 novel KCa3.1 inhibitors from a library of 1352 natural product-derived compounds.
New assay enables KCa3.1 inhibitor screening; leaves open therapeutic relevance in cardiovascular disease.
Inhibition of the K Ca 3.1 potassium channel has therapeutic potential in a variety of human diseases, including inflammation-associated disorders and cancers. However, K Ca 3.1 inhibitors with high therapeutic promise are currently not available. This study aimed to establish a screening assay for identifying inhibitors of K Ca 3.1 in native cells and from library compounds derived from natural products in Thailand. The screening platform was successfully developed based on a thallium flux assay in intestinal epithelial (T84) cells with a Z′ factor of 0.52. The screening of 1352 compounds and functional validation using electrophysiological analyses identified 8 compounds as novel K Ca 3.1 inhibitors with IC 50 values ranging from 0.14 to 6.57 µM. These results indicate that the assay developed is of excellent quality for high-throughput screening and capable of identifying K Ca 3.1 inhibitors. This assay may be useful in identifying novel K Ca 3.1 inhibitors that may have therapeutic potential for inflammation-associated disorders and cancers.
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Jakakul et al. (2020) studied Inflammation-associated disorders and cancers. Cell-based screening assay for KCa3.1 inhibitors was evaluated on Identification of novel KCa3.1 inhibitors. A newly developed thallium flux assay in T84 cells successfully screened 1352 compounds, identifying 8 novel KCa3.1 inhibitors with IC50 values ranging from 0.14 to 6.57 µM.
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