Fuqua S A, Russo J, Shackney S E, Stearns M E
Breast Center, Baylor College of Medicine, Houston, USA.
Postgrad Med. 2001 Mar;Spec No:3-10.
Breast cancer is a classic hormone-dependent malignant disease that is influenced by estrogen. However, the molecular links between estrogen and cell proliferation in healthy and malignant breast tissue are complex and as yet not well understood. The selective estrogen receptor modulators (SERMs), which are competitive inhibitors of estrogen binding at estrogen receptors alpha and beta, have become important weapons in the prevention and treatment of breast cancer. These agents also offer opportunities for the elucidation of the multiple molecular mechanisms by which estrogen affects cell proliferation. Each SERM-estrogen receptor complex has a unique structure that influences its activity in different body tissues. Unraveling the links between SERM structure and function not only may shed light on the signaling pathways that connect estrogen to cell proliferation but also may allow the design of new agents specifically targeted to affect certain events along these pathways.
乳腺癌是一种典型的激素依赖性恶性疾病,受雌激素影响。然而,雌激素与健康乳腺组织和恶性乳腺组织中细胞增殖之间的分子联系很复杂,目前尚未完全了解。选择性雌激素受体调节剂(SERM)是雌激素与α和β雌激素受体结合的竞争性抑制剂,已成为预防和治疗乳腺癌的重要武器。这些药物也为阐明雌激素影响细胞增殖的多种分子机制提供了机会。每种SERM-雌激素受体复合物都有独特的结构,影响其在不同身体组织中的活性。阐明SERM结构与功能之间的联系不仅可能揭示将雌激素与细胞增殖联系起来的信号通路,还可能有助于设计专门针对影响这些通路中某些事件的新型药物。