Literature DB >> 16361578

Prediction of colorectal neoplasia by quantitative methylation analysis of estrogen receptor gene in nonneoplastic epithelium from patients with ulcerative colitis.

Keiichi Tominaga1, Shigehiko Fujii, Kenichiroh Mukawa, Mikio Fujita, Kazuhito Ichikawa, Shigeki Tomita, Yasuo Imai, Kazunari Kanke, Yuko Ono, Akira Terano, Hideyuki Hiraishi, Takahiro Fujimori.   

Abstract

PURPOSE: The incidence of colorectal neoplasia has increased among patients with longstanding and extensive ulcerative colitis (UC). Therefore, surveillance colonoscopy has been widely recommended. However, there is controversy about the impact of cancer surveillance, and ways to improve its effectiveness are being sought. The estrogen receptor (ER) gene shows age-related methylation in the colorectal epithelium and is frequently methylated in colorectal neoplasia, suggesting that ER methylation occurs early in the process of colorectal tumorigenesis. EXPERIMENTAL
DESIGN: To clarify whether methylation analysis of the ER gene in nonneoplastic epithelium can help predict an increased risk for UC-associated neoplasia, a total of 105 nonneoplastic colorectal epithelia from 18 patients with longstanding and extensive UC, including 8 patients with neoplasia and 10 patients without neoplasia, were analyzed. In all patients, multiple samples were taken from six regions of the colorectum. The combined bisulfite restriction analysis method was used to determine the methylation status of the ER gene.
RESULTS: The mean methylation level of the ER gene was 25.4% in the nonneoplastic epithelia from UC patients with neoplasia, whereas it was only 4.0% in those without neoplasia (P<0.001). The methylation level of the ER gene in UC patients with neoplasia was significantly higher than in UC patients without neoplasia throughout the colorectum except for the cecum. In UC patients with neoplasia, the mean ER methylation level in the distal colon (36.1%) was significantly higher than in the proximal colon (14.6%; P<0.001).
CONCLUSIONS: These results suggest that the analysis of ER gene methylation in nonneoplastic colorectal epithelium could have the potential to be a useful adjunct for identifying individuals with longstanding and extensive UC who are at increased risk of neoplasia and contribute to more effective cancer surveillance.

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Year:  2005        PMID: 16361578     DOI: 10.1158/1078-0432.CCR-05-1309

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  17 in total

Review 1.  DNA Methylation Dynamics During Differentiation, Proliferation, and Tumorigenesis in the Intestinal Tract.

Authors:  Can-Ze Huang; Tao Yu; Qi-Kui Chen
Journal:  Stem Cells Dev       Date:  2015-10-20       Impact factor: 3.272

Review 2.  DNA methylation patterns as noninvasive biomarkers and targets of epigenetic therapies in colorectal cancer.

Authors:  Yutaka Hashimoto; Timothy J Zumwalt; Ajay Goel
Journal:  Epigenomics       Date:  2016-04-22       Impact factor: 4.778

Review 3.  [Pathogenesis of colitis-associated neoplasms].

Authors:  M Vieth; H Neumann
Journal:  Pathologe       Date:  2012-11       Impact factor: 1.011

4.  Patterns of DNA methylation in the normal colon vary by anatomical location, gender, and age.

Authors:  Andrew M Kaz; Chao-Jen Wong; Slavomir Dzieciatkowski; Yanxin Luo; Robert E Schoen; William M Grady
Journal:  Epigenetics       Date:  2014-01-10       Impact factor: 4.528

5.  A Panel of Methylated MicroRNA Biomarkers for Identifying High-Risk Patients With Ulcerative Colitis-Associated Colorectal Cancer.

Authors:  Yuji Toiyama; Yoshinaga Okugawa; Koji Tanaka; Toshimitsu Araki; Keiichi Uchida; Asahi Hishida; Motoi Uchino; Hiroki Ikeuchi; Seiichi Hirota; Masato Kusunoki; C Richard Boland; Ajay Goel
Journal:  Gastroenterology       Date:  2017-08-25       Impact factor: 22.682

6.  Effect of ageing on colonic mucosal regeneration.

Authors:  Ferenc Sipos; Katalin Leiszter; Zsolt Tulassay
Journal:  World J Gastroenterol       Date:  2011-07-07       Impact factor: 5.742

7.  Enhanced induction of mucin-depleted foci in estrogen receptor {beta} knockout mice.

Authors:  Diana Saleiro; Genoveva Murillo; Dennis B Lubahn; Levy Kopelovich; Kenneth S Korach; Rajendra G Mehta
Journal:  Cancer Prev Res (Phila)       Date:  2010-08-17

8.  Promoter methylation of protease-activated receptor (PAR2) is associated with severe clinical phenotypes of ulcerative colitis (UC).

Authors:  Tomomitsu Tahara; Tomoyuki Shibata; Masakatsu Nakamura; Hiromi Yamashita; Daisuke Yoshioka; Masaaki Okubo; Naoko Maruyama; Toshiaki Kamano; Yoshio Kamiya; Hiroshi Fujita; Yoshihito Nakagawa; Mitsuo Nagasaka; Masami Iwata; Kazuya Takahama; Makoto Watanabe; Hiroshi Nakano; Ichiro Hirata; Tomiyasu Arisawa
Journal:  Clin Exp Med       Date:  2009-01-30       Impact factor: 3.984

9.  Estrogen receptor α or β loss in the colon of Min/+ mice promotes crypt expansion and impairs TGFβ and HNF3β signaling.

Authors:  Rian M Hasson; Alexandra Briggs; Adelaide M Carothers; Jennifer S Davids; Jiping Wang; Sara H Javid; Nancy L Cho; Monica M Bertagnolli
Journal:  Carcinogenesis       Date:  2013-10-08       Impact factor: 4.944

Review 10.  Ulcerative colitis: from inflammation to cancer. Do estrogen receptors have a role?

Authors:  Mariabeatrice Principi; Michele Barone; Maria Pricci; Nicola De Tullio; Giuseppe Losurdo; Enzo Ierardi; Alfredo Di Leo
Journal:  World J Gastroenterol       Date:  2014-09-07       Impact factor: 5.742

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