Mostaghel Elahe A, Martin Paul S, Mongovin Stephen, Frayo Shani, Zhang Ailin, Edlefsen Kerstin L, Press Oliver W, Gopal Ajay K
Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA; Division of Medical Oncology, Department of Medicine, University of Washington, Seattle, WA, USA.
Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Exp Hematol. 2017 May;49:34-38.e2. doi: 10.1016/j.exphem.2017.01.001. Epub 2017 Jan 21.
Mantle cell lymphoma (MCL) affects approximately 4500 patients/year in the US and demonstrates a male to female ratio of approximately 4:1. While the pathobiology underlying this ratio is unknown, the hematopoietic system is characterized by sex-related differences in androgen receptor (AR) expression, leading us to hypothesize that the male-biased incidence of MCL may reflect sex-related differences in AR signaling during MCL lymphomagenesis. To explore the AR axis in MCL, we evaluated AR expression in MCL cell lines and human tumors, and tested the impact of androgen pathway inhibition on MCL proliferation. AR transcript levels ranged up to ~2 fold higher in MCL lines vs non-MCL NHL lines (p = 0.006) and were correlated with expression of the canonical AR-regulated gene, prostate-specific antigen (PSA; r = 0.715, p = 0.001), consistent with functional AR activity. Patient-derived MCL samples demonstrated a range of AR expression. Treatment of four different MCL lines with the potent AR antagonist enzalutamide demonstrated suppression of proliferation across both male and female-derived cell lines. These data suggest androgen-axis blockade may represent a novel therapeutic modality in MCL. This novel treatment approach is currently under investigation in a phase II clinical trial of AR inhibition in patients with relapsed/refractory MCL.
在美国,每年约有4500例患者受套细胞淋巴瘤(MCL)影响,男女比例约为4:1。虽然该比例背后的病理生物学机制尚不清楚,但造血系统存在雄激素受体(AR)表达的性别差异,这使我们推测,MCL男性发病率偏高可能反映了MCL淋巴瘤发生过程中AR信号传导的性别差异。为了探究MCL中的AR轴,我们评估了MCL细胞系和人类肿瘤中的AR表达,并测试了雄激素途径抑制对MCL增殖的影响。与非MCL非霍奇金淋巴瘤(NHL)细胞系相比,MCL细胞系中的AR转录水平高出约2倍(p = 0.006),且与典型AR调控基因前列腺特异性抗原(PSA)的表达相关(r = 0.715,p = 0.001),这与功能性AR活性一致。患者来源的MCL样本显示出不同程度的AR表达。用强效AR拮抗剂恩杂鲁胺处理四种不同的MCL细胞系,结果显示男性和女性来源的细胞系增殖均受到抑制。这些数据表明,雄激素轴阻断可能是MCL的一种新治疗方式。目前,这种新的治疗方法正在一项针对复发/难治性MCL患者的AR抑制II期临床试验中进行研究。