Preventive effects of Juzen-taiho-to on N-methyl-N-nitrosourea and estradiol-17beta-induced endometrial carcinogenesis in mice

Carcinogenesis. 2001 Apr;22(4):587-91. doi: 10.1093/carcin/22.4.587.

Abstract

Two experiments were conducted to determine effects of Juzen-taiho-to on endometrial carcinogenesis in mice. In the first experiment, Juzen-taiho-to treatment (2 weeks) decreased the levels of estradiol-17beta (E(2))-stimulated expression of c-fos/jun mRNA and their oncoproteins, determined by reverse transcription-polymerase chain reaction and Southern blot analysis, and the immunohistochemical method, in the uteri of ovarectomized mice. For the second experiment, 93 female ICR mice were given N-methyl-N-nitrosourea (MNU) solution (1 mg/100 g body weight) and normal saline (as controls) into their left and right uterine corpora, respectively, and were divided into four groups. Group 1 was given a diet containing 0.2% Juzen-taiho-to and 5 p.p.m. E(2). Group 2 was given a diet containing 5 p.p.m. E(2) alone. Group 3 was given a diet containing 0.2% Juzen-taiho-to alone. Group 4 was kept on the basal diet alone and treated as a control. Juzen-taiho-to treatment significantly decreased incidences of the uterine endometrial atypical (P<0.01), complex (P<0.05) and simple hyperplasias (P<0.01), under estrogenic stimulation. It is suggested that Juzen-taiho-to has an inhibitory effect on E2-related endometrial carcinogenesis in mice, relevantly through suppression of estrogen-induced c-fos/jun-expression.

MeSH terms

  • Animals
  • Anticarcinogenic Agents / therapeutic use*
  • Blotting, Southern
  • Body Weight / drug effects
  • Carcinogens*
  • Drugs, Chinese Herbal / therapeutic use*
  • Endometrial Neoplasms / chemically induced*
  • Endometrial Neoplasms / prevention & control*
  • Estradiol / metabolism*
  • Female
  • Immunohistochemistry
  • Methylnitrosourea*
  • Mice
  • Mice, Inbred ICR
  • Proto-Oncogene Proteins c-fos / metabolism
  • Proto-Oncogene Proteins c-jun / metabolism
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Time Factors
  • Uterus / metabolism

Substances

  • Anticarcinogenic Agents
  • Carcinogens
  • Drugs, Chinese Herbal
  • Proto-Oncogene Proteins c-fos
  • Proto-Oncogene Proteins c-jun
  • RNA, Messenger
  • juzentaihoto
  • Estradiol
  • Methylnitrosourea