Abstract
Although somatic KRAS mutations are common in human tumors, no inhibitor of mutant KRAS was clinically available until recently. Canon and colleagues describe the ability of a clinically available KRASG12C inhibitor to drive immunogenic cancer cell death, thus constituting a promising combinatorial partner for immune checkpoint blockers.
| Original language | English |
|---|---|
| Pages (from-to) | 1-3 |
| Number of pages | 3 |
| Journal | Trends in Pharmacological Sciences |
| Volume | 41 |
| Issue number | 1 |
| DOIs | |
| State | Published - Jan 2020 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Antineoplastic Agents/therapeutic use
- Humans
- Immunogenic Cell Death
- Lung Neoplasms/drug therapy
- Mutation
- Proto-Oncogene Proteins p21(ras)/genetics
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