Endocrine Surgery Section, Surgical Oncology Program, Center for Cancer Research, NCI, NIH, Bethesda, Maryland.
UAB Heersink School of Medicine, Birmingham, Alabama.
Mol Cancer Ther. 2023 Sep 5;22(9):1052-1062. doi: 10.1158/1535-7163.MCT-22-0798.
Pancreatic neuroendocrine tumors (PNET) express high levels of somatostatin receptor type 2 (SSTR2), a unique target for both tumor imaging and therapy. This surface expression is lost in metastatic high-grade PNETs, making patients ineligible for SSTR2-targeted 177 Lutetium (Lu)-DOTATATE peptide receptor radionuclide therapy (PRRT), and represents an unmet clinical need. Here, we aimed to restore SSTR2 expression through the reversal of inhibitory epigenetic gene silencing to improve tumor responsiveness to PRRT. We first assessed human SSTR2 promoter methylation and expression levels in 96 patient samples. We then used three NET cell lines (QGP-1, BON-1, GOT-1) with variable SSTR2 expression profiles for functional in vitro studies using histone deacetylase inhibitors (HDACi). Finally, the QGP-1 xenograft mouse model, with low basal SSTR2 expression, was used to assess the therapeutic efficacy of combined HDACi and 177Lu-DOTATATE therapies. We confirm that SSTR expression is decreased and correlates with SSTR2 promoter methylation in patients with high-grade NETs. When exposed to HDACis, SSTR2 surface expression is increased in three NET cell lines in vitro. In an in vivo PNET xenograft model with low basal SSTR2 expression, our studies demonstrate significantly higher tumor uptake of SSTR2-targeted 177Lu-DOTATATE in animals pretreated with HDACis compared with controls. For the first time, we show that this higher tumor uptake results in significant antitumor response when compared with standard PRRT alone. These preclinical results provide a rationale for utilizing HDACi pretreatment to improve targeted radionuclide therapy in patients with SSTR2-negative, metastatic PNETs.
胰腺神经内分泌肿瘤 (PNET) 表达高水平的生长抑素受体 2 (SSTR2),这是肿瘤成像和治疗的独特靶点。这种表面表达在转移性高级别 PNET 中丢失,使患者不符合 SSTR2 靶向的 177 镥 (Lu)-DOTATATE 肽受体放射性核素治疗 (PRRT) 的条件,这代表了未满足的临床需求。在这里,我们旨在通过逆转抑制性表观遗传基因沉默来恢复 SSTR2 表达,从而提高肿瘤对 PRRT 的反应性。我们首先评估了 96 个患者样本中的人 SSTR2 启动子甲基化和表达水平。然后,我们使用三种具有不同 SSTR2 表达谱的神经内分泌肿瘤细胞系 (QGP-1、BON-1、GOT-1) 进行功能体外研究,使用组蛋白去乙酰化酶抑制剂 (HDACi)。最后,我们使用 QGP-1 异种移植小鼠模型,该模型具有低基础 SSTR2 表达,用于评估联合 HDACi 和 177Lu-DOTATATE 治疗的疗效。我们证实,SSTR 表达降低与高级别 NET 患者的 SSTR2 启动子甲基化相关。当暴露于 HDACi 时,SSTR2 表面表达在三种 NET 细胞系中增加。在具有低基础 SSTR2 表达的 PNET 异种移植小鼠模型中,我们的研究表明,与对照组相比,预先用 HDACi 处理的动物中 SSTR2 靶向的 177Lu-DOTATATE 摄取明显更高。我们首次表明,与单独的标准 PRRT 相比,这种更高的肿瘤摄取导致显著的抗肿瘤反应。这些临床前结果为利用 HDACi 预处理来改善 SSTR2 阴性、转移性 PNET 患者的靶向放射性核素治疗提供了依据。