Development and distribution of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP)-induced aberrant crypt foci in the rat large intestine

Tetsuya Tsukamoto, Ken Ichi Kozaki, Yoko Nishikawa, Masami Yamamoto, Hiroko Fukami, Manami Inoue, Keiji Wakabayashi, Masae Tatematsu

Research output: Contribution to journalArticle

20 Citations (Scopus)

Abstract

Aberrant crypt foci (ACF) are generally considered to be preneoplastic lesions for colon cancer. To assess their induction by 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP), a colon carcinogen, we performed a sequential study of ACF morphology and localization. F344 male rats were given PhIP, and methylene blue-stained colon epithelium and isolated crypts were analyzed at weeks 12, 25, 50, and 75. Each crypt was classified into 2 groups, 'single' with round bottoms and 'bifurcating' displaying V-shaped clefts (indicating proliferation). In combination with the number of crypts in an ACF, this classification was a good indicator for the generation of ACF in line with the fission mechanism of growth. Increasing numbers of crypts in ACF through weeks 12 to 75 and decreased percentages of ACF with bifurcating crypts at the late time points indicated that proliferation of crypts occurs predominantly during the early stages. The distribution pattern showed a significant shift (P <0.000005) from the distal to the proximal part of the large intestine between weeks 25 and 50. Adenocarcinomas were first found to develop at week 50 in the ascending colon and cecum where bifurcating crypts were generally lacking at weeks 12 and 25. These data suggest the existence of (1) proliferating ACF which contains bifurcating crypt(s) and (2) quiescent or senescent ACF which consists of only single crypts.

Original languageEnglish
Pages (from-to)720-725
Number of pages6
JournalJapanese Journal of Cancer Research
Volume90
Issue number7
Publication statusPublished - Jul 1999
Externally publishedYes

Fingerprint

Aberrant Crypt Foci
Large Intestine
Colon
Ascending Colon
Cecum
2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine
Methylene Blue
Inbred F344 Rats
Carcinogens
Colonic Neoplasms
Adenocarcinoma
Epithelium

Keywords

  • Aberrant crypt foci
  • Bifurcating crypts
  • Crypt isolation technique
  • PhIP

ASJC Scopus subject areas

  • Cancer Research
  • Oncology

Cite this

Tsukamoto, T., Kozaki, K. I., Nishikawa, Y., Yamamoto, M., Fukami, H., Inoue, M., ... Tatematsu, M. (1999). Development and distribution of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP)-induced aberrant crypt foci in the rat large intestine. Japanese Journal of Cancer Research, 90(7), 720-725.

Development and distribution of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP)-induced aberrant crypt foci in the rat large intestine. / Tsukamoto, Tetsuya; Kozaki, Ken Ichi; Nishikawa, Yoko; Yamamoto, Masami; Fukami, Hiroko; Inoue, Manami; Wakabayashi, Keiji; Tatematsu, Masae.

In: Japanese Journal of Cancer Research, Vol. 90, No. 7, 07.1999, p. 720-725.

Research output: Contribution to journalArticle

Tsukamoto, T, Kozaki, KI, Nishikawa, Y, Yamamoto, M, Fukami, H, Inoue, M, Wakabayashi, K & Tatematsu, M 1999, 'Development and distribution of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP)-induced aberrant crypt foci in the rat large intestine', Japanese Journal of Cancer Research, vol. 90, no. 7, pp. 720-725.
Tsukamoto, Tetsuya ; Kozaki, Ken Ichi ; Nishikawa, Yoko ; Yamamoto, Masami ; Fukami, Hiroko ; Inoue, Manami ; Wakabayashi, Keiji ; Tatematsu, Masae. / Development and distribution of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP)-induced aberrant crypt foci in the rat large intestine. In: Japanese Journal of Cancer Research. 1999 ; Vol. 90, No. 7. pp. 720-725.
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abstract = "Aberrant crypt foci (ACF) are generally considered to be preneoplastic lesions for colon cancer. To assess their induction by 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP), a colon carcinogen, we performed a sequential study of ACF morphology and localization. F344 male rats were given PhIP, and methylene blue-stained colon epithelium and isolated crypts were analyzed at weeks 12, 25, 50, and 75. Each crypt was classified into 2 groups, 'single' with round bottoms and 'bifurcating' displaying V-shaped clefts (indicating proliferation). In combination with the number of crypts in an ACF, this classification was a good indicator for the generation of ACF in line with the fission mechanism of growth. Increasing numbers of crypts in ACF through weeks 12 to 75 and decreased percentages of ACF with bifurcating crypts at the late time points indicated that proliferation of crypts occurs predominantly during the early stages. The distribution pattern showed a significant shift (P <0.000005) from the distal to the proximal part of the large intestine between weeks 25 and 50. Adenocarcinomas were first found to develop at week 50 in the ascending colon and cecum where bifurcating crypts were generally lacking at weeks 12 and 25. These data suggest the existence of (1) proliferating ACF which contains bifurcating crypt(s) and (2) quiescent or senescent ACF which consists of only single crypts.",
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