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神经母细胞瘤细胞系对遗传毒性药物介导的 NK 细胞激活受体配体的诱导具有抗性。

Neuroblastoma Cell Lines Are Refractory to Genotoxic Drug-Mediated Induction of Ligands for NK Cell-Activating Receptors.

机构信息

Department of Pediatric Hematology and Oncology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.

Laboratorio Cellule Staminali Post Natali e Terapie Cellulari, Istituto Giannina Gaslini, Genova, Italy.

出版信息

J Immunol Res. 2018 Apr 1;2018:4972410. doi: 10.1155/2018/4972410. eCollection 2018.

Abstract

Neuroblastoma (NB), the most common extracranial solid tumor of childhood, causes death in almost 15% of children affected by cancer. Treatment of neuroblastoma is based on the combination of chemotherapy with other therapeutic interventions such as surgery, radiotherapy, use of differentiating agents, and immunotherapy. In particular, adoptive NK cell transfer is a new immune-therapeutic approach whose efficacy may be boosted by several anticancer agents able to induce the expression of ligands for NK cell-activating receptors, thus rendering cancer cells more susceptible to NK cell-mediated lysis. Here, we show that chemotherapeutic drugs commonly used for the treatment of NB such as cisplatin, topotecan, irinotecan, and etoposide are unable to induce the expression of activating ligands in a panel of NB cell lines. Consistently, cisplatin-treated NB cell lines were not more susceptible to NK cells than untreated cells. The refractoriness of NB cell lines to these drugs has been partially associated with the abnormal status of genes for ATM, ATR, Chk1, and Chk2, the major transducers of the DNA damage response (DDR), triggered by several anticancer agents and promoting different antitumor mechanisms including the expression of ligands for NK cell-activating receptors. Moreover, both the impaired production of reactive oxygen species (ROS) in some NB cell lines and the transient p53 stabilization in response to our genotoxic drugs under our experimental conditions could contribute to inefficient induction of activating ligands. These data suggest that further investigations, exploiting molecular strategies aimed to potentiate the NK cell-mediated immunotherapy of NB, are warranted.

摘要

神经母细胞瘤(NB)是儿童期最常见的颅外实体瘤,几乎有 15%的癌症患儿因此死亡。NB 的治疗基于联合化疗与其他治疗干预,如手术、放疗、分化剂的使用和免疫治疗。特别是,过继性 NK 细胞转移是一种新的免疫治疗方法,几种能够诱导 NK 细胞激活受体配体表达的抗癌药物可以增强其疗效,从而使癌细胞更容易被 NK 细胞介导的裂解。在这里,我们表明,用于治疗 NB 的几种常用化疗药物,如顺铂、拓扑替康、伊立替康和依托泊苷,不能在一组 NB 细胞系中诱导激活配体的表达。同样,与未经处理的细胞相比,用顺铂处理的 NB 细胞系对 NK 细胞的敏感性没有增加。NB 细胞系对这些药物的耐药性部分与 ATM、ATR、Chk1 和 Chk2 基因的异常状态有关,这些基因是多种抗癌药物触发的 DNA 损伤反应(DDR)的主要转导因子,可促进包括 NK 细胞激活受体配体表达在内的不同抗肿瘤机制。此外,一些 NB 细胞系中活性氧(ROS)的产生受损,以及我们的遗传毒性药物在实验条件下短暂稳定 p53,这可能导致激活配体的诱导效率低下。这些数据表明,需要进一步研究,利用旨在增强 NB 的 NK 细胞介导免疫治疗的分子策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8625/5901817/136d5e7b0a10/JIR2018-4972410.001.jpg

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