Effects of Organic Selenium Against Colon Cancer

有机硒对结肠癌的作用

• 批准号: 6542194
• 负责人: Mark Anthony Nelson
• 金额: $ 26.28万
• 依托单位: UNIVERSITY OF ARIZONA
• 依托单位国家: 美国
• 财政年份: 2002
• 资助国家: 美国
• 起止时间: 2002-08-01 至 2007-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6542194
• 关键词: cell cycle proteins; cell growth regulation; chemoprevention; clinical research; colon neoplasms; cyclins; dietary supplements; dietary trace element; enzyme activity; enzyme inhibitors; gene environment interaction; gene expression; human tissue; immunocytochemistry; neoplastic cell; nutrition related tag; patient oriented research; phosphorylation; prostaglandin E; prostaglandin endoperoxide synthase; prostaglandin receptor; protein kinase; selenium; selenomethionine; yeasts

DESCRIPTION (provided by applicant): Colorectal cancer is the third leading cause of cancer death in both males and females in the U.S. Thus, the development of dietary and novel chemopreventive approaches for this segment of the population could provide a practical approach for significantly reducing colon cancer occurrence. Recent studies indicate that supplemental Se (in the form of high selenium containing yeast) reduces cancer risk in humans. However, the mechanism by which organic selenium exerts its anticancer effects remains to be identified. Selenomethionine is the predominant form of selenium in the yeast. We have developed evidence indicating that selenomethionine, inhibits Cox 2 protein expression in colon cancer cells. Thus, the first hypothesis to be tested is that the anticancer effects of dietary selenium (in the form of Se-yeast or selenomethionine) are mediated, in part, by inhibition of cyclooxygenase 2 (COX-2) activity. We also have evidence for a COX-2 independent mechanism. We can demonstrate alterations in cyclin A, cyclin B, and p34 cdc2 phosphorylation in selenomethionine treated colon cancer cells. These observations lead to the second hypothesis of the proposed studies that selenomethionine causes growth arrest by inappropriate expression of cyclins A and cyclins B as well increased phosphorylation of p34cdc2. To test our two main hypotheses, the three specific aims are performed 1) To determine the molecular basis of the effects of selenomethionine on COX-2 protein expression. 2: To investigate the role prostanoid receptors play in mediating the downstream effects of PGE2 in selenomethionine-induced growth inhibition. 3: To identify the mechanism for the COX-2 independent anti-cancer effects of selenium. We have a unique opportunity to translate our basic science experimental findings to clinical intervention trials. The data from these studies will identify the key mechanisms involved in the anticancer effects of selenium and increase understanding of eicosinoids in the biology of colorectal cancer. The greatest impact is realized by the provision of new molecular markers for the efficacy of selenium compounds for clinical intervention trials and the development of novel molecular targets for therapeutic intervention strategies.

描述（由申请人提供）：结直肠癌是美国男性和女性癌症死亡的第三大原因。因此，为这部分人群开发饮食和新的化学预防方法可以为显著降低结肠癌发生率提供实用方法。最近的研究表明，补充硒（以高硒酵母的形式）可以降低人类患癌症的风险。然而，有机硒发挥其抗癌作用的机制仍有待确定。硒代蛋氨酸是酵母中硒的主要形式。我们已经发现了硒代蛋氨酸抑制结肠癌细胞中考克斯2蛋白表达的证据。因此，要检验的第一个假设是，膳食硒（以硒酵母或硒代蛋氨酸的形式）的抗癌作用部分是通过抑制环加氧酶2（考克斯-2）活性来介导的。我们也有考克斯-2独立机制的证据。我们可以证明硒代蛋氨酸处理的结肠癌细胞中细胞周期蛋白A、细胞周期蛋白B和p34 cdc 2磷酸化的改变。这些观察结果导致了所提出的研究的第二个假设，即硒代蛋氨酸通过细胞周期蛋白A和细胞周期蛋白B的不适当表达以及p34 cdc 2的磷酸化增加而引起生长停滞。 为了验证我们的两个主要假设，我们进行了三个具体的目标：1）确定硒代蛋氨酸对考克斯-2蛋白表达影响的分子基础。2.研究前列腺素受体在硒代蛋氨酸抑制前列腺增生中的作用。3.探讨硒非考克斯-2依赖性抗癌作用的机制。我们有一个独特的机会将我们的基础科学实验结果转化为临床干预试验。这些研究的数据将确定硒抗癌作用的关键机制，并增加对大肠癌生物学中类花生酸的理解。最大的影响是通过为临床干预试验提供硒化合物功效的新分子标志物和为治疗干预策略开发新的分子靶点来实现的。