Abstract
In this issue of Cell Chemical Biology, Palve et al. (2022) identified PARP16 as a non-canonical therapeutic target of the PARP1 inhibitor talazoparib, which synergizes with the WEE1 inhibitor adavosertib to enhance its efficacy. The dual targeting of PARP1 and PARP16 may explain the greater efficacy of talazoparib in some cancers.
Original language | English (US) |
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Pages (from-to) | 171-173 |
Number of pages | 3 |
Journal | Cell Chemical Biology |
Volume | 29 |
Issue number | 2 |
DOIs |
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State | Published - Feb 17 2022 |
ASJC Scopus subject areas
- Biochemistry
- Molecular Medicine
- Molecular Biology
- Pharmacology
- Drug Discovery
- Clinical Biochemistry