Independent variation in susceptibilities of six different mouse strains to induction of pepsinogen-altered pyloric glands and gastric tumor intestinalization by N-methyl-N-nitrosourea

Cancer Lett. 2002 May 28;179(2):121-32. doi: 10.1016/s0304-3835(02)00013-7.

Abstract

Strain differences in susceptibility regarding stomach carcinogenesis due to N-methyl-N-nitrosourea were examined in males of six strains of mice: BALB/cA (BALB), C57BL/6N (C57BL6), CBA/JN (CBA), C3H/HeN (C3H), DBA/2N (DBA/2), and CD-1 (ICR). The frequency of pepsinogen-altered pyloric glands (PAPGs), putative precancerous lesions, was highest (19.6+/-9.9%) in the BALB and lowest in the ICR (12.3+/-5.7%) mice (P<0.05). Incidences of adenocarcinomas at week 52 were 59.3% (16 of 27) and 18.5% (5 of 27), respectively (P<0.005). Invasion also tended to be deepest in BALB compared with the other strains. Intestinal alkaline phosphatase-positive intestinal type cells were observed heterogeneously in some hyperplasias, adenomas and adenocarcinomas consisting of gastric type cells. Thus, intestinalization appeared to occur at random in both non-neoplastic and monoclonal neoplastic lesions, making it unlikely that IAP-positive cells could be precursors of gastric tumors. In contrast, the data suggest a direct histogenetic role for the PAPG, a useful preneoplastic marker lesion in mouse strains.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / chemically induced
  • Adenocarcinoma / mortality
  • Adenocarcinoma / pathology
  • Adenoma / chemically induced
  • Adenoma / mortality
  • Adenoma / pathology
  • Alkaline Phosphatase / metabolism
  • Animals
  • Disease Susceptibility
  • Immunohistochemistry
  • Intestinal Mucosa / chemistry
  • Intestinal Mucosa / drug effects
  • Intestinal Mucosa / pathology*
  • Male
  • Methylnitronitrosoguanidine / toxicity*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C3H
  • Mice, Inbred C57BL
  • Mice, Inbred CBA
  • Mice, Inbred DBA
  • Mice, Inbred ICR
  • Pepsinogen A / metabolism*
  • Precancerous Conditions / metabolism
  • Precancerous Conditions / mortality
  • Precancerous Conditions / pathology
  • Pylorus / metabolism
  • Pylorus / pathology
  • Species Specificity
  • Stomach / chemistry
  • Stomach / drug effects
  • Stomach / pathology
  • Stomach Neoplasms / chemically induced
  • Stomach Neoplasms / mortality
  • Stomach Neoplasms / pathology*
  • Survival Rate

Substances

  • Methylnitronitrosoguanidine
  • Pepsinogen A
  • Alkaline Phosphatase