Sadozai Hassan
MBS Biomedical Sciences, University of Guelph, Guelph, Ontario.
J Pak Med Assoc. 2013 Apr;63(4):509-15.
Manipulation of the hormone oestrogen has been used for decades to treat hormone-dependent breast cancer. Currently, aromatase inhibitors (AIs) are used as first-line therapy against early and metastatic breast cancer in post-menopausal women. Despite these advances, several patients eventually experience a relapse of breast cancer and declined clinical response to treatment. As per recent findings, steroid sulfatase (STS) has emerged as a novel therapy target. This review aims at summarising the emerging field of STS inhibitor development and highlighting current findings from pre-clinical and clinical trials. The recently-developed dual-targeting compounds, such as dual aromatase-sulfatase inhibitors (DASI), have shown encouraging preclinical results and represent important new treatments for hormone-dependent breast cancer.
几十年来,人们一直通过调控雌激素来治疗激素依赖性乳腺癌。目前,芳香化酶抑制剂(AIs)被用作绝经后女性早期和转移性乳腺癌的一线治疗药物。尽管取得了这些进展,但仍有一些患者最终出现乳腺癌复发,对治疗的临床反应也有所下降。根据最近的研究结果,类固醇硫酸酯酶(STS)已成为一个新的治疗靶点。本综述旨在总结STS抑制剂开发这一新兴领域,并突出临床前和临床试验的当前研究结果。最近开发的双靶点化合物,如双芳香化酶-硫酸酯酶抑制剂(DASI),已显示出令人鼓舞的临床前结果,是激素依赖性乳腺癌重要的新治疗方法。