Literature DB >> 7828986

Rectal mucosal ornithine decarboxylase activity in familial adenomatous polyposis after ileorectal anastomosis.

S E Patchett1, E M Alstead, L Trzeciak, T Wocial, R K Phillips, M J Farthing.   

Abstract

Resection of the colon in patients with familial adenomatous polyposis frequently results in the regression of polyps in the remaining rectum, suggesting a reduction of cellular proliferation. These patients remain at risk of developing rectal cancer but whether this risk increases with time is uncertain. Since ornithine decarboxylase activity is associated with cellular proliferation, mucosal ornithine decarboxylase was measured in rectal biopsy specimens from patients with familial adenomatous polyposis after ileorectal anastomosis (n = 36) and from normal controls (n = 30). The relationship between ornithine decarboxylase activity, age, and time from surgery was also examined. Median ornithine decarboxylase activity in familial adenomatous polyposis patients after ileorectal anastomosis (186, interquartile range (IQR) 107-534 pmol/mg protein/h) was not different from that in control subjects (227, IQR 123-374, p = 0.6). When patients were divided into three equal groups according to age, however, younger patients (< 25 years) had significantly higher activity than both older age groups (p < 0.02). Similarly, when patients were stratified according to the time elapsed since surgery, those who had had surgery less than six years previously had a significantly higher ornithine decarboxylase activity than those in whom a longer time interval had elapsed since surgery (p = 0.02). These results indicate that after colon resection, ornithine decarboxylase activity in patients with familial adenomatous polyposis is similar to that in normal controls but seems to fall over time. This may explain the regression of rectal polyps after colonic resection in this disorder.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 7828986      PMCID: PMC1375625          DOI: 10.1136/gut.35.11.1624

Source DB:  PubMed          Journal:  Gut        ISSN: 0017-5749            Impact factor:   23.059


  17 in total

1.  Ileorectal anastomosis--familial adenomatous polyposis.

Authors:  D G Jagelman
Journal:  Hepatogastroenterology       Date:  1991-12

2.  Epithelial cell kinetics in the crypts of familial polyposis of colon.

Authors:  T Iwama; J Utzunomiya; J Sasaki
Journal:  Jpn J Surg       Date:  1977-12

Review 3.  Subtotal colectomy for familial polyposis. A clinical series and review of the literature.

Authors:  M A Skinner; D Tyler; G D Branum; G Cucchiaro; M A Branum; W C Meyers
Journal:  Arch Surg       Date:  1990-05

Review 4.  Familial colorectal cancer and familial adenomatous polyposis.

Authors:  J M Northover; V Murday
Journal:  Baillieres Clin Gastroenterol       Date:  1989-07

Review 5.  Genetics of gastrointestinal polyposis.

Authors:  H J Bussey; A M Veale; B C Morson
Journal:  Gastroenterology       Date:  1978-06       Impact factor: 22.682

6.  Ornithine decarboxylase activity is critical for cell transformation.

Authors:  M Auvinen; A Paasinen; L C Andersson; E Hölttä
Journal:  Nature       Date:  1992-11-26       Impact factor: 49.962

7.  Biliary bile acid profiles in familial adenomatous polyposis.

Authors:  A D Spigelman; R W Owen; M J Hill; R K Phillips
Journal:  Br J Surg       Date:  1991-03       Impact factor: 6.939

8.  Fecal and stomal bile acid composition after ileostomy or ileoanal anastomosis in patients with chronic ulcerative colitis and adenomatosis coli.

Authors:  H Natori; J Utsunomiya; T Yamamura; Y Benno; K Uchida
Journal:  Gastroenterology       Date:  1992-04       Impact factor: 22.682

9.  Changes in rectal epithelial cell proliferation and intestinal bile acids after subtotal colectomy in familial adenomatous polyposis.

Authors:  A Cats; J H Kleibeuker; F Kuipers; M J Hardonk; R C Verschueren; W Boersma; R J Vonk; W J Sluiter; N H Mulder; B G Wolthers
Journal:  Cancer Res       Date:  1992-07-01       Impact factor: 12.701

10.  Ornithine decarboxylase is important in intestinal mucosal maturation and recovery from injury in rats.

Authors:  G D Lux; L J Marton; S B Baylin
Journal:  Science       Date:  1980-10-10       Impact factor: 47.728

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.