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成釉细胞瘤型颅咽管瘤的炎症环境及其对治疗的影响

The Inflammatory Milieu of Adamantinomatous Craniopharyngioma and Its Implications for Treatment.

作者信息

Whelan Ros, Prince Eric, Gilani Ahmed, Hankinson Todd

机构信息

Department of Neurosurgery, University of Colorado Hospital, Aurora, Colorado 80045, USA.

Department of Pediatric neurosurgery, Children's Hospital Colorado, University of Colorado, Aurora, Colorado 80045, USA.

出版信息

J Clin Med. 2020 Feb 14;9(2):519. doi: 10.3390/jcm9020519.

DOI:10.3390/jcm9020519
PMID:32075140
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7074265/
Abstract

Pediatric Adamantinomatous Craniopharyngiomas (ACPs) are histologically benign brain tumors that often follow an aggressive clinical course. Their suprasellar location leaves them in close proximity to critical neurological and vascular structures and often results in significant neuroendocrine morbidity. Current treatment paradigms, involving surgical resection and radiotherapy, confer significant morbidity to patients and there is an obvious need to discover effective and safe alternative treatments. Recent years have witnessed significant efforts to fully detail the genomic, transcriptomic and proteomic make-up of these tumors, in an attempt to identify potential therapeutic targets. These studies have resulted in ever mounting evidence that inflammatory processes and the immune response play a critical role in the pathogenesis of both the solid and cystic portion of ACPs. Several inflammatory and immune markers have been identified in both the cyst fluid and solid tumor tissue of ACP. Due to the existence of effective agents that target them, IL-6 and immune checkpoint inhibitors seem to present the most likely immediate candidates for clinical trials of targeted immune-related therapy in ACP. If effective, such agents may result in a paradigm shift in treatment that ultimately reduces morbidity and results in better outcomes for our patients.

摘要

小儿成釉细胞瘤型颅咽管瘤(ACPs)是组织学上为良性的脑肿瘤,但临床过程往往具有侵袭性。它们位于鞍上区域,与关键的神经和血管结构相邻,常导致显著的神经内分泌功能障碍。目前的治疗模式包括手术切除和放疗,会给患者带来显著的并发症,因此显然需要发现有效且安全的替代治疗方法。近年来,人们付出了巨大努力来全面详细地了解这些肿瘤的基因组、转录组和蛋白质组构成,试图确定潜在的治疗靶点。这些研究不断提供越来越多的证据表明,炎症过程和免疫反应在ACPs实性和囊性部分的发病机制中起着关键作用。在ACPs的囊液和实体瘤组织中都发现了几种炎症和免疫标志物。由于存在针对它们的有效药物,白细胞介素-6(IL-6)和免疫检查点抑制剂似乎是ACPs靶向免疫相关治疗临床试验最有可能的直接候选药物。如果有效,此类药物可能会导致治疗模式的转变,最终降低并发症发生率,为我们的患者带来更好的治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/382a/7074265/7ce564e1b4a0/jcm-09-00519-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/382a/7074265/fc6dd87e8243/jcm-09-00519-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/382a/7074265/5190f8cc7017/jcm-09-00519-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/382a/7074265/7ce564e1b4a0/jcm-09-00519-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/382a/7074265/fc6dd87e8243/jcm-09-00519-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/382a/7074265/5190f8cc7017/jcm-09-00519-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/382a/7074265/7ce564e1b4a0/jcm-09-00519-g003.jpg

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