Article
Identification of a targetable ST2-expressing fibroblast subset driving Peutz-Jeghers syndrome polyposis
2023-11-30
Abstract excerpt
Peutz-Jeghers syndrome (PJS) is associated with early-onset and recurring gastrointestinal hamartomatous polyposis caused by hereditary inactivating mutations in the tumor suppressor gene LKB1 (STK11). Due to lack of efficient prophylactic therapies PJS patients require regular surgical interventions and have an increased risk of cancer. LKB1-deficient fibroblasts have been identified as drivers of polyposis, but...
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Identifiers and source
- Literature Corpus work
- d7fcb485-b97c-56ee-9675-4140e2656f11
- DOI
- 10.1101/2023.11.29.568817
