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Intervention of nicotine on MNU-induced bladder cancer in rats.

Abstract
This study examined the effect of nicotine on the expression of mutant p53 (mt-p53) in bladder cancer rats. The rat models of bladder cancer were established by infusing N-methyl-nitroso-urea (MNU, 10 mg/kg every 2 weeks for 8 weeks) into the bladder. Pathological examination on the bladder was conducted to confirm the establishment of the model. All the bladder cancer rats were randomly divided into an MNU group and 3 nicotine groups. In the nicotine groups, the rats were intragastrically administered nicotine at different concentrations (25, 15, 5 mg/kg respectively) 3 times per week for 8 weeks. The mt-p53 expression was detected by the immunohistochemical method. The results showed that rat bladder cancer models developed histopathological changes of bladder transitional cell carcinoma. The positive rate of mt-p53 expression in the 3 nicotine groups (25, 15, 5 mg/kg) was 75.00%, 58.33% and 41.67% by the 14th week, respectively, significantly higher than that in the MNU group (33.33%) (all P<0.05). The mt-p53 expression rate was positively correlated with the medication dose and time (P<0.05). It is concluded that nicotine may play an important role in the development of bladder cancer partially by increasing the expression of mt-p53.
AuthorsDi Liu, Feng Pan, Bing Li, Xiaomin Han, Wencheng Li, Ying Shi, Zili Pang, Qijun Zhang
JournalJournal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban (J Huazhong Univ Sci Technolog Med Sci) Vol. 31 Issue 1 Pg. 103-106 (Feb 2011) ISSN: 1672-0733 [Print] China
PMID21336733 (Publication Type: Journal Article)
Chemical References
  • Carcinogens
  • Tumor Suppressor Protein p53
  • Methylnitrosourea
  • Nicotine
Topics
  • Animals
  • Carcinogens
  • Carcinoma, Transitional Cell (chemically induced, genetics)
  • Female
  • Methylnitrosourea
  • Mutation
  • Nicotine (adverse effects)
  • Rats
  • Rats, Wistar
  • Tumor Suppressor Protein p53 (genetics, metabolism)
  • Urinary Bladder Neoplasms (chemically induced, genetics)

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