Literature DB >> 28843957

Association of Aneuploidy and Flat Dysplasia With Development of High-Grade Dysplasia or Colorectal Cancer in Patients With Inflammatory Bowel Disease.

Jia-Huei Tsai1, Peter S Rabinovitch2, Danning Huang3, Thomas Small2, Aras N Mattis4, Sanjay Kakar4, Won-Tak Choi5.   

Abstract

There is controversy over how to best manage patients with inflammatory bowel disease and flat low-grade dysplasia (fLGD) in the colon. We performed a retrospective analysis of formalin-fixed paraffin-embedded colon tissues with fLGD from 37 patients undergoing surveillance colonoscopy for inflammatory bowel disease from 1990 to 2015 at the University of California at San Francisco Medical Center, to determine whether detection of aneuploidy is associated with later development of high-grade dysplasia (HGD) or colorectal cancer. Medical data were collected from the patients for a mean follow-up time of 37 months. Using flow cytometry analysis of paraffin-embedded colon tissue, we detected aneuploidy in 15 of 37 samples with fLGD (40.5%). By comparison, aneuploidy was detected in 14 of 15 samples with flat HGD (93.3%) and 2 of 45 samples that were negative for dysplasia (4.4%). The univariate hazard ratio for subsequent detection of HGD or colorectal cancer in patients with fLGD and aneuploidy was 5.3 (95% CI, 1.542-24.121) within a mean follow-up time of 37 months. The presence of aneuploidy therefore identifies patients with fLGD in colon tissue who have an increased risk for HGD or colorectal cancer and may provide supportive evidence to a morphologic impression or suspicion of flat HGD.
Copyright © 2017 AGA Institute. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Colon Cancer Risk Factor; Early Detection; IBD; Marker

Mesh:

Year:  2017        PMID: 28843957     DOI: 10.1053/j.gastro.2017.08.031

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   22.682


  12 in total

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4.  Utility of DNA flow cytometry in distinguishing between malignant and benign intrahepatic biliary lesions.

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5.  Dynamics of Genome Alterations in Crohn's Disease-Associated Colorectal Carcinogenesis.

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6.  Unique evolutionary trajectories of breast cancers with distinct genomic and spatial heterogeneity.

Authors:  Tanya N Phung; Timothy H Webster; Elizabeth Lenkiewicz; Smriti Malasi; Mariacarla Andreozzi; Ann E McCullough; Karen S Anderson; Barbara A Pockaj; Melissa A Wilson; Michael T Barrett
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Review 8.  From Colitis to Cancer: An Evolutionary Trajectory That Merges Maths and Biology.

Authors:  Ibrahim Al Bakir; Kit Curtius; Trevor A Graham
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10.  Inflammation-Associated Microsatellite Alterations Caused by MSH3 Dysfunction Are Prevalent in Ulcerative Colitis and Increase With Neoplastic Advancement.

Authors:  Koji Munakata; Minoru Koi; Takahito Kitajima; Stephanie Tseng-Rogenski; Mamoru Uemura; Hiroshi Matsuno; Kenji Kawai; Yuki Sekido; Tsunekazu Mizushima; Yuji Toiyama; Takuya Yamada; Masayuki Mano; Eiji Mita; Masato Kusunoki; Masaki Mori; John M Carethers
Journal:  Clin Transl Gastroenterol       Date:  2019-12       Impact factor: 4.488

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