Song Xianzhou, Zhang Chengwei, Zhao Mingkun, Chen Hui, Liu Xing, Chen Jianwei, Lonard David M, Qin Li, Xu Jianming, Wang Xiaosong, Li Feng, O'Malley Bert W, Wang Jin
Department of Pharmacology, Baylor College of Medicine, Houston, Texas, United States of America.
Department of Pharmacology, Baylor College of Medicine, Houston, Texas, United States of America; Integrative Molecular and Biomedical Sciences Graduate Program, Baylor College of Medicine, Houston, Texas, United States of America.
PLoS One. 2015 Oct 2;10(10):e0140011. doi: 10.1371/journal.pone.0140011. eCollection 2015.
Triple negative breast cancer (TNBC) has the poorest prognosis of all types of breast cancer and currently lacks efficient targeted therapy. Chemotherapy is the traditional standard-of-care for TNBC, but is frequently accompanied by severe side effects. Despite the fact that high expression of steroid receptor coactivator 3 (SRC-3) is correlated with poor survival in estrogen receptor positive breast cancer patients, its role in TNBC has not been extensively investigated. Here, we show that high expression of SRC-3 correlates with both poor overall survival and post progression survival in TNBC patients, suggesting that SRC-3 can serve as a prognostic marker for TNBC. Furthermore, we demonstrated that bufalin, a SRC-3 small molecule inhibitor, when introduced even at nM concentrations, can significantly reduce TNBC cell viability and motility. However, because bufalin has minimal water solubility, its in vivo application is limited. Therefore, we developed a water soluble prodrug, 3-phospho-bufalin, to facilitate its in vivo administration. In addition, we demonstrated that 3-phospho-bufalin can effectively inhibit tumor growth in an orthotopic TNBC mouse model, suggesting its potential application as a targeted therapy for TNBC treatment.
三阴性乳腺癌(TNBC)在所有类型的乳腺癌中预后最差,目前缺乏有效的靶向治疗方法。化疗是TNBC的传统标准治疗方法,但常常伴有严重的副作用。尽管类固醇受体辅激活因子3(SRC-3)的高表达与雌激素受体阳性乳腺癌患者的不良生存相关,但其在TNBC中的作用尚未得到广泛研究。在此,我们表明SRC-3的高表达与TNBC患者的总生存期和进展后生存期较差均相关,这表明SRC-3可作为TNBC的预后标志物。此外,我们证明,蟾毒灵,一种SRC-3小分子抑制剂,即使以纳摩尔浓度引入,也能显著降低TNBC细胞的活力和运动能力。然而,由于蟾毒灵的水溶性极低,其体内应用受到限制。因此,我们开发了一种水溶性前药,3-磷酸蟾毒灵,以促进其体内给药。此外,我们证明3-磷酸蟾毒灵可有效抑制原位TNBC小鼠模型中的肿瘤生长,表明其作为TNBC治疗靶向疗法的潜在应用价值。