Abstract
Reacquiring the target: A proteomic profiling approach has been used to show that aldehyde dehydrogenase 1 may be an additional or alternative target of duocarmycin. Selective inhibition of this enzyme in lung cancer cells explains the antitumor activity of duocarmycin analogues (see scheme).
Original language | English |
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Pages (from-to) | 2874-2877 |
Number of pages | 4 |
Journal | Angewandte Chemie International Edition in English |
Volume | 51 |
Issue number | 12 |
DOIs | |
State | Published - 19 Mar 2012 |
Keywords
- antitumor agents
- cancer
- duocarmycin
- natural products
- proteomics