Literature DB >> 10625935

Suppression of lung and liver carcinogenesis in mice by oral administration of myo-inositol.

H Nishino1, M Murakoshi, M Masuda, H Tokuda, Y Satomi, M Onozuka, S Yamaguchi, P Bu, A Tsuruta, K Nosaka, M Baba, N Takasuka.   

Abstract

It has been reported that myo-inositol can inhibit carcinogenesis in various organs, such as the mammary gland, colon and lung. In the present study, at first, inhibitory effects of myo-inositol on lung carcinogenesis were confirmed. Then, the influence of myo-inositol on liver carcinogenesis in mice was investigated. In C3H/He male mice, the rate of spontaneous liver carcinogenesis is known to be high. Using this experimental model, the effects of oral administration of myo-inositol (added into the drinking water at the concentration of 1%) were assessed. Significant suppression of liver carcinogenesis was observed in mice treated with myo-inositol for 40 weeks. In the control group without myo-inositol administration, 88% of the animals developed liver tumors, whereas in the myo-inositol-supplemented group, the incidence of liver tumors was 38% (p < 0.05). The average number of liver tumors per mouse was also decreased significantly by myo-inositol treatment; from 7.8 in the control group to 0.8 in the myo-inositol-supplemented group (p < 0.01). Thus, myo-inositol may be useful for cancer chemoprevention in the liver, as well as the lung.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10625935

Source DB:  PubMed          Journal:  Anticancer Res        ISSN: 0250-7005            Impact factor:   2.480


  3 in total

1.  Transcriptional changes associated with reduced spontaneous liver tumor incidence in mice chronically exposed to high dose arsenic.

Authors:  Gail M Nelson; Gene J Ahlborn; James W Allen; Hongzu Ren; J Christopher Corton; Michael P Waalkes; Kirk T Kitchin; Bhalchandra A Diwan; Geremy Knapp; Don A Delker
Journal:  Toxicology       Date:  2009-10-12       Impact factor: 4.221

Review 2.  Myo-Inositol and Its Derivatives: Their Emerging Role in the Treatment of Human Diseases.

Authors:  Dhani Raj Chhetri
Journal:  Front Pharmacol       Date:  2019-10-11       Impact factor: 5.810

3.  Glycerophosphodiester phosphodiesterase 1 (GDE1) acts as a potential tumor suppressor and is a novel therapeutic target for non-mucin-producing colon adenocarcinoma.

Authors:  Qiu Shen; Chao Lu; Hua Yang; Ming-Xia Ge; Wang-Xiao Xia; Qing-Peng Kong; Gong-Hua Li; Yan-Hong Gu
Journal:  PeerJ       Date:  2020-02-11       Impact factor: 2.984

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.