Manouchehri Jasmine M, Turner Katherine A, Kalafatis Michael
Department of Chemistry, Cleveland State University, Cleveland, OH, USA.
Center for Gene Regulation in Health and Disease (GRHD), Cleveland State University, Cleveland, OH, USA.
Breast Cancer (Auckl). 2018 Jan 15;12:1178223417749855. doi: 10.1177/1178223417749855. eCollection 2018.
Breast cancer is the most commonly diagnosed cancer in women. There is a continued interest for the development of more efficacious treatment regimens for breast carcinoma. Recombinant human tumor necrosis factor-related apoptosis-inducing ligand (rhTRAIL) shows potential as a potent anticancer therapeutic for the treatment of breast cancer, whereas displaying minimal toxicity to normal cells. However, the promise of rhTRAIL for the treatment of breast cancer is dismissed by the resistance to rhTRAIL-induced apoptosis exhibited by many breast cancers. Thus, a cotreatment strategy was examined by applying the natural compound quercetin (Q) as a sensitizing agent for rhTRAIL-resistant breast cancer BT-20 and MCF-7 cells. Quercetin was able to sensitize rhTRAIL-resistant breast cancers to rhTRAIL-induced apoptosis as detected by Western blotting through the proteasome-mediated degradation of c-FLIP and through the upregulation of DR5 expression transcriptionally. Overall, these in vitro findings establish that Q is an effective sensitizing agent for rhTRAIL-resistant breast cancers.
乳腺癌是女性中最常被诊断出的癌症。人们一直对开发更有效的乳腺癌治疗方案有着浓厚兴趣。重组人肿瘤坏死因子相关凋亡诱导配体(rhTRAIL)显示出作为一种有效的抗癌治疗药物治疗乳腺癌的潜力,同时对正常细胞的毒性极小。然而,许多乳腺癌对rhTRAIL诱导的凋亡具有抗性,这使得rhTRAIL治疗乳腺癌的前景受到质疑。因此,研究了一种联合治疗策略,即应用天然化合物槲皮素(Q)作为对rhTRAIL耐药的乳腺癌BT-20和MCF-7细胞的致敏剂。通过蛋白质印迹法检测发现,槲皮素能够使rhTRAIL耐药的乳腺癌对rhTRAIL诱导的凋亡敏感,其机制是通过蛋白酶体介导的c-FLIP降解以及转录水平上DR5表达的上调。总体而言,这些体外研究结果表明,Q是一种对rhTRAIL耐药乳腺癌有效的致敏剂。