B023: SP/ nk1r复合物抑制剂阿瑞吡坦在肝胰腺恶性肿瘤中的应用

IF 16.6 1区 医学 Q1 ONCOLOGY
Matthias Ilmer, Maximilian Viessmann, Bernhard Renz, Frank Braun, Jens Werner
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引用次数: 0

摘要

背景:由P物质(SP)激活的神经激肽-1受体(NK1R)复合物已成为一个有希望的靶点。SP促进细胞生长,而其拮抗剂Aprepitant (AP),临床上用于化疗引起的恶心,已显示出抗肿瘤活性。然而,需要进一步了解复合物拮抗靶向后的抗肿瘤机制。方法:对公开的和自己的RNAseq数据进行生物信息学分析。检测细胞增殖和细胞活力(MTT、划痕实验、菌落形成)以及细胞凋亡和自噬。通过海马分析、ROS、NAD+/NADH和MitoTracker检测代谢变化。结果:AP治疗后,患者来源的类器官培养显示球体形成减少和形态改变,而SP增强球体形成。SP通过rho激酶依赖机制促进增殖,激活ERK信号通路,AP轻微降低pERK水平。进一步的分析表明,AP诱导细胞凋亡信号,而不会导致DNA断裂。Annexin V/PI染色提示24h后凋亡诱导,而subG1分析提示凋亡级联阻滞。长时间暴露于AP导致坏死,与n -乙酰半胱氨酸共同治疗可减轻坏死。Western blot分析证实caspase-9和-3活化,但未显示PARP裂解,可能是由于凋亡蛋白(IAPs)抑制剂(如XIAP)的高表达。结论:综上所述,AP在胰腺肿瘤细胞中表现出抗增殖和细胞毒性作用,可能破坏自分泌/旁分泌SP-NK1R反馈回路并改变代谢弹性。未来的研究应该探索代谢应激反应,并研究共处理是否可以克服不完全的细胞凋亡激活。引文格式:Matthias Ilmer, Maximilian Viessmann, Bernhard Renz, Frank Braun, Jens Werner。SP/ nk1r复合物抑制剂阿瑞吡坦在肝胰腺恶性肿瘤中的应用[摘要]。摘自:AACR癌症研究特别会议论文集:胰腺癌研究进展-新兴科学驱动变革解决方案;波士顿;2025年9月28日至10月1日;波士顿,MA。费城(PA): AACR;癌症研究2025;85(18_Suppl_3): nr B023。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract B023: Repurposing of the SP/NK1R-complex inhibitor aprepitant in hepatopancreatic malignancies
Background: The neurokinin-1 receptor (NK1R) complex, activated by Substance P (SP), has emerged as a promising target. SP promotes cell growth, whereas its antagonist, Aprepitant (AP), used clinically for chemotherapy-induced nausea, has demonstrated anti-tumor activity. However, further insight on the anti-tumoral mechanisms after antagonistic targeting of the complex are required. Methods: We conducted bioinformatical analysis of public as well as own RNAseq data. Assays to assess cell proliferation and cell viability (MTT, scratch assays, colony formation) as well as apoptosis and autophagy were carried out. Metabolic changes were detected by SeaHorse analysis, ROS, NAD+/NADH, and MitoTracker. Results: Patient-derived organoid cultures showed reduced spheroid formation and altered morphology following AP treatment, while SP enhanced spheroid formation. SP promoted proliferation via Rho-kinase-dependent mechanisms and activated the ERK signaling pathway, with AP slightly reducing pERK levels. Further analyses revealed that AP induces apoptosis signaling without subsequent DNA fragmentation. Annexin V/PI staining indicated apoptosis induction after 24 hours, while subG1 analysis suggested a blockade in the apoptosis cascade. Prolonged AP exposure led to necrosis, which was mitigated by co-treatment with N-acetylcysteine. Western blot analysis confirmed caspase-9 and -3 activation but showed no PARP cleavage, likely due to high expression of inhibitors of apoptosis proteins (IAPs), such as XIAP. Conclusion: In conclusion, AP exhibits antiproliferative and cytotoxic effects in pancreatic tumor cells, potentially disrupting an autocrine/paracrine SP-NK1R feedback loop and altering metabolic resilience. Future studies should explore metabolic stress responses and investigate whether co-treatment could overcome incomplete apoptosis activation. Citation Format: Matthias Ilmer, Maximilian Viessmann, Bernhard Renz, Frank Braun, Jens Werner. Repurposing of the SP/NK1R-complex inhibitor aprepitant in hepatopancreatic malignancies [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Advances in Pancreatic Cancer Research—Emerging Science Driving Transformative Solutions; Boston, MA; 2025 Sep 28-Oct 1; Boston, MA. Philadelphia (PA): AACR; Cancer Res 2025;85(18_Suppl_3): nr B023.
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来源期刊
Cancer research
Cancer research 医学-肿瘤学
CiteScore
16.10
自引率
0.90%
发文量
7677
审稿时长
2.5 months
期刊介绍: Cancer Research, published by the American Association for Cancer Research (AACR), is a journal that focuses on impactful original studies, reviews, and opinion pieces relevant to the broad cancer research community. Manuscripts that present conceptual or technological advances leading to insights into cancer biology are particularly sought after. The journal also places emphasis on convergence science, which involves bridging multiple distinct areas of cancer research. With primary subsections including Cancer Biology, Cancer Immunology, Cancer Metabolism and Molecular Mechanisms, Translational Cancer Biology, Cancer Landscapes, and Convergence Science, Cancer Research has a comprehensive scope. It is published twice a month and has one volume per year, with a print ISSN of 0008-5472 and an online ISSN of 1538-7445. Cancer Research is abstracted and/or indexed in various databases and platforms, including BIOSIS Previews (R) Database, MEDLINE, Current Contents/Life Sciences, Current Contents/Clinical Medicine, Science Citation Index, Scopus, and Web of Science.
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