Dowsett Mitch, Martin Lesley-Ann, Smith Ian, Johnston Stephen
Academic Department of Biochemistry, Royal Marsden Hospital, London SW3 6JJ, UK.
J Steroid Biochem Mol Biol. 2005 May;95(1-5):167-72. doi: 10.1016/j.jsbmb.2005.04.022.
Aromatase inhibitors are rapidly becoming the first choice for hormonal treatment of steroid receptor positive breast cancer in postmenopausal women. An understanding of the resistance mechanisms to these agents is, therefore, important for the appropriate delivery of treatment to responsive patients and the rational development of new agents targeted at the resistance pathways. De novo resistance appears to be a quantitative rather than qualitative phenomenon with virtually all oestrogen receptor positive tumours showing an anti-proliferative response to the aromatase inhibitor anastrozole. While the expression of type 1 growth factor receptors reduces response to tamoxifen this appears to have little detrimental effect on response to aromatase inhibitors. Studies of acquired resistance in vitro have indicated that acquisition of hypersensitivity to oestrogenic stimulation is a key mechanism that is dependent on enhanced cross-talk of growth factor and oestrogen signaling pathways. Collection of resistant biopsy tissues from patients is important to determine if this mechanism is clinically relevant.
芳香化酶抑制剂正迅速成为绝经后女性激素受体阳性乳腺癌激素治疗的首选药物。因此,了解这些药物的耐药机制对于为反应性患者提供适当的治疗以及合理开发针对耐药途径的新药物至关重要。原发性耐药似乎是一种定量而非定性现象,几乎所有雌激素受体阳性肿瘤对芳香化酶抑制剂阿那曲唑均表现出抗增殖反应。虽然1型生长因子受体的表达会降低对他莫昔芬的反应,但这似乎对芳香化酶抑制剂的反应几乎没有不利影响。体外获得性耐药研究表明,对雌激素刺激的超敏反应的获得是一种关键机制,这依赖于生长因子和雌激素信号通路之间增强的相互作用。从患者身上收集耐药活检组织对于确定该机制是否具有临床相关性很重要。