Literature DB >> 7590437

Flow cytometric analysis of DNA synthetic phase fraction of the normal appearing colonic mucosa in patients with colorectal neoplasms.

S Nakamura1, J Goto, Y Kitayama, J P Sheffield, I C Talbot.   

Abstract

DNA synthetic (S) phase fractions of normal appearing colonic mucosa in Japanese and British patients with colorectal neoplasms were compared with those in patients without colonic neoplasms. Normal crypts were isolated from fresh surgical specimens of the large intestine by the use of EDTA. After fixation with 70% ethanol, isolated crypts were digested with pepsin into single nuclei suspensions. These were stained with propidium iodide and examined by flow cytometry. S phase fraction was calculated from the flow cytometry DNA histogram using Baisch's method. S phase fractions of normal appearing crypts in Japanese and British patients with colorectal tumours were not significantly different and analysed together. S phase fraction of normal appearing colonic crypts in 14 patients with familial adenomatous polyposis (FAP) was 10.23 (2.59%) (mean SD)) ranging from 5.8 to 18.8. S phase fraction of background normal mucosal in patients with large adenomas (over 2 cm) and adenocarcinomas were 9.74 (3.76%) (range, 2.7-16.1) and 8.93 (3.54%) (range, 2.9-18.9) respectively. In normal mucosa of patients without any colorectal neoplasms, S phase fraction was 8.99 (3.94)% (range, 3.9-17.7). There was no statistically significant difference in S phase fractions of normal mucosa in the four groups. Our results show that an increase in proliferative activity of background colonic crypts is not necessary for tumour development.

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Year:  1995        PMID: 7590437      PMCID: PMC1382822          DOI: 10.1136/gut.37.3.398

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


  22 in total

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Authors:  H Baisch; W Göhde; W A Linden
Journal:  Radiat Environ Biophys       Date:  1975-06-13       Impact factor: 1.925

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Journal:  Cancer       Date:  1974-09       Impact factor: 6.860

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

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Authors:  E E Deschner; M Lipkin
Journal:  Cancer       Date:  1975-02       Impact factor: 6.860

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Authors:  S Nakamura; I Kino; S Baba
Journal:  Gut       Date:  1993-09       Impact factor: 23.059

6.  Proliferating cell nuclear antigen expression in normal, preneoplastic, and neoplastic colonic epithelium of the rat.

Authors:  K Yamada; K Yoshitake; M Sato; D J Ahnen
Journal:  Gastroenterology       Date:  1992-07       Impact factor: 22.682

7.  Single-parameter DNA flow cytometric analysis of normal-appearing colonic mucosa does not predict the presence of colonic neoplasia.

Authors:  E Nsien; W M Steinberg; D S Wilkinson; J G Rhame; J P Henry
Journal:  Am J Gastroenterol       Date:  1991-10       Impact factor: 10.864

8.  Rectal cell proliferation and colorectal cancer risk level in patients with nonfamilial adenomatous polyps of the large bowel.

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Journal:  Cancer       Date:  1991-12-01       Impact factor: 6.860

9.  Application of the crypt-isolation technique to flow-cytometric analysis of DNA content in colorectal neoplasms.

Authors:  S Nakamura; J Goto; M Kitayama; I Kino
Journal:  Gastroenterology       Date:  1994-01       Impact factor: 22.682

10.  Proliferation in human gastrointestinal epithelium using bromodeoxyuridine in vivo: data for different sites, proximity to a tumour, and polyposis coli.

Authors:  C S Potten; M Kellett; D A Rew; S A Roberts
Journal:  Gut       Date:  1992-04       Impact factor: 23.059

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  2 in total

1.  APC mutation and the crypt cycle in murine and human intestine.

Authors:  M Bjerknes; H Cheng; K Hay; S Gallinger
Journal:  Am J Pathol       Date:  1997-03       Impact factor: 4.307

2.  Immunohistochemical estimation of cell cycle phase in laryngeal neoplasia.

Authors:  P Chatrath; I S Scott; L S Morris; R J Davies; K Bird; S L Vowler; N Coleman
Journal:  Br J Cancer       Date:  2006-07-11       Impact factor: 7.640

  2 in total

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