Advances in TRP channel drug discovery: from target validation to clinical studies.
Advances in TRP channel drug discovery: from target validation to clinical studies.
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DOI:
10.1038/s41573-021-00268-4
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发表时间:
2022-01
期刊:
影响因子:
--
通讯作者:
Szallasi A
中科院分区:
文献类型:
--
作者:
Koivisto AP;Belvisi MG;Gaudet R;Szallasi A
Transient receptor potential (TRP) channels are multifunctional signalling molecules with many roles in sensory perception and cellular physiology. Therefore, it is not surprising that TRP channels have been implicated in numerous diseases, including hereditary disorders caused by defects in genes encoding TRP channels (TRP channelopathies). Most TRP channels are located at the cell surface, which makes them generally accessible drug targets. Early drug discovery efforts to target TRP channels focused on pain, but as our knowledge of TRP channels and their role in health and disease has grown, these efforts have expanded into new clinical indications, ranging from respiratory disorders through neurological and psychiatric diseases to diabetes and cancer. In this Review, we discuss recent findings in TRP channel structural biology that can affect both drug development and clinical indications. We also discuss the clinical promise of novel TRP channel modulators, aimed at both established and emerging targets. Last, we address the challenges that these compounds may face in clinical practice, including the need for carefully targeted approaches to minimize potential side-effects due to the multifunctional roles of TRP channels. This Review discusses recent findings in transient receptor potential (TRP) channel structural biology and the impact of these findings in drug development and clinical indications. It also addresses the challenges of modulating TRP channels and the need for targeted approaches to minimize potential side-effects due to the multifunctional roles of TRP channels.
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影响因子:
5.8
作者:
Baker K;Raemdonck K;Dekkak B;Snelgrove RJ;Ford J;Shala F;Belvisi MG;Birrell MA
通讯作者:
Birrell MA
影响因子:
15.9
作者:
Bessac, Bret F.;Sivula, Michael;Jordt, Sven-Eric
通讯作者:
Jordt, Sven-Eric
DOI:
10.1152/physiol.00026.2008
发表时间:
2008-12
期刊:
Physiology (Bethesda, Md.)
影响因子:
--
作者:
Bessac BF;Jordt SE
通讯作者:
Jordt SE
影响因子:
--
作者:
Rasmus KC;O'Neill CE;Bachtell RK;Cooper DC
通讯作者:
Cooper DC
影响因子:
6.5
作者:
Asakawa, Makoto;Yoshioka, Takeshi;Sakata, Tsuneaki
通讯作者:
Sakata, Tsuneaki