Literature DB >> 8993799

Naturally occurring selenium compounds in cancer chemoprevention trials: a workshop summary.

B H Patterson1, O A Levander.   

Abstract

Evidence from epidemiological studies and a human intervention trial indicates that selenium (Se) may have chemopreventive activity in humans. This report summarizes a workshop held by the National Cancer Institute to address the use of naturally occurring Se compounds in future cancer chemoprevention trials. Differences in the metabolism of inorganic and organic Se compounds can be seen both in the biochemical handling of these forms and in their kinetics in humans. Long-term supplementation could result in greater increases in muscle stores for organic rather than inorganic forms. Because of long half-lives, trials may have to be of long duration to assess efficacy and safety. The optimal size of dose for supplementation is controversial with respect to both efficacy and safety. In China, selenosis was observed in some individuals with a sustained intake of at least 750 micrograms/day but was not observed among others with intakes exceeding 1 mg. These levels exceed the reference dose, a measure of the maximal safe intake, which is 350 micrograms/day. A large-scale Se human intervention trial in the United States suggests no harm due to long-term Se intake of more than 200 micrograms/day. Se deficiency has been shown to have deleterious effects on the immune system, allowing, for example, a benign form of the Coxsackievirus to become virulent in mice. These recent results may provide an explanation of earlier findings showing a protective effect of elevated Se intakes against a mouse mammary tumor virus. Additional studies on the use of Se as a chemopreventive agent in man seem warranted.

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Year:  1997        PMID: 8993799

Source DB:  PubMed          Journal:  Cancer Epidemiol Biomarkers Prev        ISSN: 1055-9965            Impact factor:   4.254


  7 in total

1.  Serum selenium levels in relation to markers of neoplastic progression among persons with Barrett's esophagus.

Authors:  Rebecca E Rudolph; Thomas L Vaughan; Alan R Kristal; Patricia L Blount; Douglas S Levine; Patricia C Galipeau; Laura J Prevo; Carissa A Sanchez; Peter S Rabinovitch; Brian J Reid
Journal:  J Natl Cancer Inst       Date:  2003-05-21       Impact factor: 13.506

2.  Regulation of the extracellular antioxidant selenoprotein plasma glutathione peroxidase (GPx-3) in mammalian cells.

Authors:  Filomena G Ottaviano; Shiow-Shih Tang; Diane E Handy; Joseph Loscalzo
Journal:  Mol Cell Biochem       Date:  2009-02-15       Impact factor: 3.396

Review 3.  [Potential of selenium in gynecologic oncology].

Authors:  A M Funke
Journal:  Med Klin (Munich)       Date:  1999-10-15

Review 4.  Selenium supplementation in thyroid associated ophthalmopathy: an update.

Authors:  Aruna Dharmasena
Journal:  Int J Ophthalmol       Date:  2014-04-18       Impact factor: 1.779

5.  Multilevel modeling and value of information in clinical trial decision support.

Authors:  Yuanyuan Cui; Brendan Murphy; Anastasia Gentilcore; Yugal Sharma; Lori M Minasian; Barnett S Kramer; Paul M Coates; John K Gohagan; Juergen Klenk; Bruce Tidor
Journal:  BMC Syst Biol       Date:  2014-12-24

6.  Phosphorylated IκBα predicts poor prognosis in activated B-cell lymphoma and its inhibition with thymoquinone induces apoptosis via ROS release.

Authors:  Azhar R Hussain; Shahab Uddin; Maqbool Ahmed; Fouad Al-Dayel; Prashant P Bavi; Khawla S Al-Kuraya
Journal:  PLoS One       Date:  2013-03-28       Impact factor: 3.240

7.  A novel chemopreventive mechanism of selenomethionine: enhancement of APE1 enzyme activity via a Gadd45a, PCNA and APE1 protein complex that regulates p53-mediated base excision repair.

Authors:  Hwa Jin Jung; Hye Lim Kim; Yeo Jin Kim; Jong-Il Weon; Young Rok Seo
Journal:  Oncol Rep       Date:  2013-07-11       Impact factor: 3.906

  7 in total

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