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AGPAT1 as a Novel Colonic Biomarker for Discriminating Between Ulcerative Colitis With and Without Primary Sclerosing Cholangitis

Vessby, Johan, 1972- (författare)
Uppsala universitet,Gastroenterologi/hepatologi
Wisniewski, Jacek R. (författare)
Max Planck Inst Biochem, Dept Prote & Signal Transduct, Biochem Prote Grp, Martinsried, Germany.
Lindskog, Cecilia (författare)
Uppsala universitet,Klinisk och experimentell patologi
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Eriksson, Niclas, 1978- (författare)
Uppsala universitet,Uppsala kliniska forskningscentrum (UCR)
Gabrysch, Katja (författare)
Uppsala universitet,Uppsala kliniska forskningscentrum (UCR)
Zettl, Katharina (författare)
Max Planck Inst Biochem, Dept Prote & Signal Transduct, Biochem Prote Grp, Martinsried, Germany.
Wanders, Alkwin (författare)
Aalborg Univ Hosp, Dept Pathol, Aalborg, Denmark.
Carlson, Marie, 1957- (författare)
Uppsala universitet,Gastroenterologi/hepatologi,Uppsala Univ, Gastroenterol Res Grp, Dept Med Sci, Uppsala, Sweden.
Rorsman, Fredrik, Docent, 1960- (författare)
Uppsala universitet,Gastroenterologi/hepatologi,Uppsala Univ, Gastroenterol Res Grp, Dept Med Sci, Uppsala, Sweden.
Åberg, Mikael (författare)
Uppsala universitet,Science for Life Laboratory, SciLifeLab,Klinisk kemi
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 (creator_code:org_t)
2022-05
2022
Engelska.
Ingår i: Clinical and Translational Gastroenterology. - : Ovid Technologies (Wolters Kluwer Health). - 2155-384X. ; 13:5
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • INTRODUCTION: Ulcerative colitis (UC) associated with primary sclerosing cholangitis (PSC-UC) is considered a unique inflammatory bowel disease (IBD) entity. PSC diagnosis in an IBD individual entails a significantly higher risk of gastrointestinal cancer; however, biomarkers for identifying patients with UC at risk for PSC are lacking. We, therefore, performed a thorough PSC-UC biomarker study, starting from archived colonic tissue.METHODS: Proteins were extracted out of formalin-fixed paraffin-embedded proximal colon samples from PSC-UC (n = 9), UC (n = 7), and healthy controls (n = 7). Patients with IBD were in clinical and histological remission, and all patients with UC had a history of pancolitis. Samples were processed by the multienzyme digestion FASP and subsequently analyzed by liquid chromatography-tandem mass spectrometry. Candidate proteins were replicated in an independent cohort (n: PSC-UC = 16 and UC = 21) and further validated by immunohistochemistry.RESULTS: In the discovery step, 7,279 unique proteins were detected. The top 5 most differentiating proteins (PSC-UC vs UC) based on linear regression analysis were selected for replication. Of these, 1-acetylglycerol-3-phosphate O-acyltransferase 1 (AGPAT1) was verified as higher in PSC-UC than UC (P = 0.009) in the replication cohort. A difference on the group level was also confirmed by immunohistochemistry, showing more intense AGPAT1 staining in patients with PSC-UC compared with UC.DISCUSSION: We present AGPAT1 as a potential colonic biomarker for differentiating PSC-UC from UC. Our findings have possible implication for future PSC-IBD diagnostics and surveillance.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Gastroenterologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Gastroenterology and Hepatology (hsv//eng)

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