MOLECULAR MECHANISMS OF ESTROGEN INDUCED CELL GROWTH

雌激素诱导细胞生长的分子机制

• 批准号: 2862748
• 负责人: JYOTI J WATTERS
• 金额: $ 3.17万
• 依托单位: UNIVERSITY OF WISCONSIN-MADISON
• 依托单位国家: 美国
• 财政年份: 1999
• 资助国家: 美国
• 起止时间: 1999-11-05 至
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/2862748
• 关键词: BCL2 gene /protein; MCF7 cell; biological signal transduction; breast neoplasms; cell growth regulation; cell proliferation; cyclins; enzyme activity; estrogens; gene induction /repression; hormone regulation /control mechanism; hormone related neoplasm /cancer; hyperplasia; mitogen activated protein kinase; molecular oncology; neoplasm /cancer genetics; northern blottings; p53 gene /protein; phosphorylation; western blottings

The proposed research will investigate the molecular events involved in the proliferative actions of estrogen in breast cancer cells. We will investigate the MAPK signal transduction cascade as a potential pathway utilized by estrogen to cause the hyperplasia of breast cells. This could potentially lead to the identification of molecular targets for the actions of estrogen in breast tissue against which to generate new pharmacotherapies for the treatment or prevention of breast cancer. The physiologic and/or morphologic effects of the estrogen induction of the MAPK pathway has not yet been investigated in any cell type and therefore presents a logical starting point for the investigation of the means by which estrogen induces the proliferation of hyperplasia of breast/breast cancer cells. These studies will be accomplished by utilizing standard proliferative assays (MTS and 3H incorporation) to measure the growth of human breast cancer cells (MCF-7) in response to estrogen treatment. Direct measurements of MAPK or MAPK related enzymatic activities will also be performed. Mutant MAPK enzymes will be transfected into MCF-7 cells to determine if their activity is necessary for the proliferative effects of estrogen. The genes that are turned by initiation of the MAPK cascade such as cyclin D1 will then be evaluated.

本研究将探讨雌激素在乳腺癌细胞中增殖作用的分子机制。我们将研究MAPK信号转导级联作为雌激素引起乳腺细胞增生的潜在途径。这可能会导致识别乳腺组织中雌激素作用的分子靶标，从而产生新的药物治疗或预防乳腺癌。雌激素诱导MAPK通路的生理和/或形态学效应尚未在任何细胞类型中进行研究，因此为研究雌激素诱导乳腺/乳腺癌细胞增生的方式提供了一个合乎逻辑的起点。这些研究将通过使用标准增殖试验（MTS和3H掺入）来测量人乳腺癌细胞（MCF-7）对雌激素治疗的反应来完成。还将进行MAPK或MAPK相关酶活性的直接测量。突变的MAPK酶将被转染到MCF-7细胞中，以确定其活性是否对雌激素的增殖作用是必要的。然后将评估由MAPK级联启动而转变的基因，如细胞周期蛋白D1。