Mapping cellular targets of covalent cancer drugs in the entire mammalian body

As our understanding of biological systems reaches single-cell and high spatial resolutions, it becomes imperative that pharmacological approaches match this precision to understand drug actions. This need is particularly urgent for the targeted covalent inhibitors that are currently re-entering the stage for cancer treatments. By leveraging the unique kinetics of click reactions, we developed volumetric clearing-assisted tissue click chemistry (vCATCH) to enable deep and homogeneous click labeling across the three-dimensional (3D) mammalian body. With simple and passive incubation steps, vCATCH offers cellular-resolution drug imaging in the entire adult mouse. We combined vCATCH with hydrogel-based reinforcement of three-dimensional imaging solvent-cleared organs (HYBRiD) imaging and virtual reality to visualize and quantify in vivo targets of two clinical cancer drugs, afatinib and ibrutinib, which recapitulated their known pharmacological distribution and revealed previously unreported tissue and cell-type engagement potentially linked to off-target effects. vCATCH provides a body-wide, unbiased platform to map covalent drug engagements at unprecedented scale and precision.

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Publication Details

Journal
Cell
Published
2025-12-22
DOI
https://doi.org/10.1016/j.cell.2025.11.030
Citations
1
Primary Topic
Click Chemistry and Applications
Type
article
Field-Weighted Citation Impact
0.94
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article

Mapping cellular targets of covalent cancer drugs in the entire mammalian body

Ahmadreza Attarpour, Zhengyuan Pang, Verina H. Leung, Javid J. Moslehi et al.
1 citations
Cell
Click Chemistry and Applications
0.94
article

Mapping cellular targets of covalent cancer drugs in the entire mammalian body

Ahmadreza Attarpour, Zhengyuan Pang, Verina H. Leung, Javid J. Moslehi, Hanbing Shen, Jonathan Z. Long, Cailynn C. Wang, Anthony Rinaldi, Maged Goubran, Senhan Xu, Li Ye, Alexandra Selke, Melaina Yender, Benjamin F. Cravatt, Claire Rammel, Logan H. Sigua, Peng Wu, Christopher Glynn, Maria Dolores Moya-Garzon
article en
1 citations

Abstract

As our understanding of biological systems reaches single-cell and high spatial resolutions, it becomes imperative that pharmacological approaches match this precision to understand drug actions. This need is particularly urgent for the targeted covalent inhibitors that are currently re-entering the stage for cancer treatments. By leveraging the unique kinetics of click reactions, we developed volumetric clearing-assisted tissue click chemistry (vCATCH) to enable deep and homogeneous click labeling across the three-dimensional (3D) mammalian body. With simple and passive incubation steps, vCATCH offers cellular-resolution drug imaging in the entire adult mouse. We combined vCATCH with hydrogel-based reinforcement of three-dimensional imaging solvent-cleared organs (HYBRiD) imaging and virtual reality to visualize and quantify in vivo targets of two clinical cancer drugs, afatinib and ibrutinib, which recapitulated their known pharmacological distribution and revealed previously unreported tissue and cell-type engagement potentially linked to off-target effects. vCATCH provides a body-wide, unbiased platform to map covalent drug engagements at unprecedented scale and precision.

CellVol. 189(3)
Scripps Research Institute (US), Sunnybrook Health Science Centre (CA), Howard Hughes Medical Institute (US), University of California, San Francisco (US), Stanford Medicine (US), Sunnybrook Research Institute, Stanford University (US)
Good health and well-being
Openalex Percentile: Top 19%
Click Chemistry and Applications
0.94
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