The hard-to-close window of T-type calcium channels

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Visa Pretel, Anna
Shaikh, Soni
Alza, LíaAlza, Lía - ORCID ID
Herreros Danés, JuditHerreros Danés, Judit - ORCID ID
Cantí Nicolás, CarlesCantí Nicolás, Carles - ORCID ID
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cc-by-nc-nd (c) Elsevier, 2019
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Volume Title
T-Type calcium channels (TTCCs) are key regulators of membrane excitability, which is the reason why TTCC pharmacology is subject to intensive research in the neurological and cardiovascular fields. TTCCs also play a role in cancer physiology, and pharmacological blockers such as tetralols and dihydroquinazolines (DHQs) reduce the viability of cancer cells in vitro and slow tumor growth in murine xenografts. However, the available compounds are better suited to blocking TTCCs in excitable membranes rather than TTCCs contributing window currents at steady potentials. Consistently, tetralols and dihydroquinazolines exhibit cytostatic/cytotoxic activities at higher concentrations than those required for TTCC blockade, which may involve off-target effects. Gene silencing experiments highlight the targetability of TTCCs, but further pharmacological research is required for TTCC blockade to become a chemotherapeutic option.
Journal or Serie
Trends in Molecular Medicine, 2019, vol. 25, núm. 7, p. 571-584