Department of Oncology, University Hospital of Udine, Italy; School of Medical Oncology, Department of Medicine, University of Udine, Italy.
Department of Oncology, University Hospital of Udine, Italy; School of Medical Oncology, Department of Medicine, University of Udine, Italy.
Cancer Treat Rev. 2017 Dec;61:15-22. doi: 10.1016/j.ctrv.2017.09.006. Epub 2017 Oct 6.
In recent years, new therapeutic approaches have reshaped the overall strategy of breast cancer (BC) treatment and have markedly improved patient survival. This is, in part, due to novel therapies for estrogen receptor (ER)-positive BC. Unfortunately, many patients present de novo resistance to these therapies or develop an acquired resistance over time. Therefore, research is now focused on discovering new molecular targets to overcome these resistances. Interestingly, preclinical and clinical studies have shown a critical role for the cross-talk between androgen receptor (AR) and ER in luminal-like BC. AR is expressed in >60% of BC and in up to 90% of ERα-positive tumors. Multiple studies suggest that AR is associated with a favorable prognosis. However, AR overexpression and, in particular, the high AR:ER ratio, seem to be involved in resistance to hormonal treatment. In this setting, a group of BCs could benefit from AR-inhibitors; nevertheless, some ER-positive BC patients do not seem to benefit from this strategy. Therefore, it is crucial to identify biomarkers that would enable the selection of patients who might benefit from combination treatment with ER and AR inhibitors.
近年来,新的治疗方法改变了乳腺癌 (BC) 治疗的整体策略,并显著提高了患者的生存率。这在一定程度上要归功于针对雌激素受体 (ER) 阳性 BC 的新型疗法。不幸的是,许多患者最初对这些疗法产生耐药性,或者随着时间的推移产生获得性耐药性。因此,目前的研究重点是发现新的分子靶点来克服这些耐药性。有趣的是,临床前和临床研究表明,雄激素受体 (AR) 和 ER 之间的串扰在腔细胞样 BC 中起着关键作用。AR 在超过 60%的 BC 中表达,在高达 90%的 ERα 阳性肿瘤中表达。多项研究表明,AR 与预后良好相关。然而,AR 的过表达,特别是 AR:ER 比值高,似乎与对激素治疗的耐药性有关。在这种情况下,一组 BC 可能受益于 AR 抑制剂;然而,一些 ER 阳性 BC 患者似乎并未从该策略中获益。因此,确定能够选择可能受益于 ER 和 AR 抑制剂联合治疗的患者的生物标志物至关重要。