Abstract
Most human tumors accumulate a multitude of genetic changes due to defects in the DNA damage response. Recently, small-molecule inhibitors have been developed that target cells with specific DNA repair defects, providing hope for precision treatment of such tumors. Here we discuss the rationale behind these therapies and how an important bottleneck-patient selection-can be approached.
| Original language | Undefined/Unknown |
|---|---|
| Pages (from-to) | 2145-2148 |
| Number of pages | 4 |
| Journal | Molecular Biology of the Cell |
| Volume | 27 |
| Issue number | 14 |
| DOIs | |
| Publication status | Published - 2016 |
Research programs
- EMC MGC-01-12-03