[Derepression of CXCR7 indicates resistance to enzalutamide in castration resistant prostate cancer]

Zhonghua Yi Xue Za Zhi. 2019 Apr 23;99(16):1237-1240. doi: 10.3760/cma.j.issn.0376-2491.2019.16.009.
[Article in Chinese]

Abstract

Objective: To investigate the effect of the derepression of chemokine receptor-7 (CXCR7) in prostatic tissues from patients with Castration Resistant Prostate Cancer (CRPC) on the resistance to enzalutamide (Enza). Methods: During the period of January 2015 to December 2017 all CRPC cases who underwent radical radiotherapy or androgen deprivation therapy (ADT) were evaluated. After prostatic puncture biopsy, the tissues were treated for immunostaining with CXCR7. Cox proportional hazard modeling and Kaplan-Meier analysis were used to determine PSA Progression-Free Survival (PSAP-FS) and Clinical or Radiographic Progression-Free Survival (CRP-FS) in the cohort. At last, PSA response rates and progression outcomes in CXCR7 negative cases and CXCR7 positive cases were analyzed. Results: Total 39 CRPC patients were enrolled in this study. And 23 cases derepress CXCR7, 16 cases negatively express CXCR7. The median follow-up duration was 12 months (range: 6-18) in the cohort. Chi-square analysis confirmed that PSA response rates after Enza treatment were significantly associated with CXCR7 derepression (χ(2)=22.129, P=0.000 06). Compared with CXCR7 positive expression group, CXCR7 negative expression group displayed improved median PSAP-FS (4.4 mon vs 11.7 mon, P=0.040 8) and CRP-FS (5.2 mon vs 13.1 mon, P=0.036 2) after Enza treatment. Conclusion: Derepression of CXCR7 in CRPC patients may be associated with resistance to enzalutamide. This protein may be novel target for treatment of CRPC.

目的:探讨趋化因子受体7(CXCR7)脱抑制表达与去势抵抗型前列腺癌(CRPC)发生恩杂鲁胺(Enza)治疗耐药之间的临床关联。 方法:将符合条件的2015年1月至2017年12月在北京安贞医院CRPC患者收纳入组,获取前列腺穿刺标本,进行免疫组织化学染色,分析CXCR7表达情况,并随访总结Enza治疗后前列腺特异抗原(PSA)反应、PSA无进展生存率(PSAP-FS)、临床/影像无进展生存率(CRP-FS)。评价CXCR7对Enza治疗结局的预测价值。 结果:本研究共入组39例CRPC患者,CXCR7脱抑制阳性表达23例,阴性表达16例。中位随访时间12(6~18)个月。χ(2)分析证实,恩杂鲁胺治疗后的PSA反应与CXCR7脱抑制阳性表达强度显著相关(χ(2)=22.129,P=0.000 06)。与CXCR7阳性组相比,CXCR7阴性组的中位PSA进展时间延长了7.3个月(4.4个月与11.7个月,P=0.040 8),中位临床/影像进展时间延长了7.9个月(5.2个月与13.1个月,P=0.036 2)。CXCR7阳性组患者则于Enza治疗11个月全部发生PSA进展、13个月后全部临床/影像进展。 结论:CXCR7脱抑制表达与CRPC患者发生Enza耐药密切相关,未来可能成为CRPC治疗的新靶点。.

Keywords: CXCR7; Castration Resistant Prostate Cancer; Enzalutamide; Resistance.

MeSH terms

  • Androgen Antagonists
  • Benzamides
  • Disease-Free Survival
  • Humans
  • Male
  • Nitriles
  • Phenylthiohydantoin / analogs & derivatives
  • Prostate-Specific Antigen
  • Prostatic Neoplasms, Castration-Resistant*
  • Receptors, CXCR / metabolism*

Substances

  • ACKR3 protein, human
  • Androgen Antagonists
  • Benzamides
  • Nitriles
  • Receptors, CXCR
  • Phenylthiohydantoin
  • enzalutamide
  • Prostate-Specific Antigen