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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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Literature Corpus work
d7fcb485-b97c-56ee-9675-4140e2656f11
DOI
10.1101/2023.11.29.568817
Open publication

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Identification of a targetable ST2-expressing fibroblast subset driving Peutz-Jeghers syndrome polyposisDOI 10.1101/2023.11.29.568817
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