抑制 SUMOylation 可通过对肿瘤微环境的多重影响诱导对胰腺癌的适应性抗肿瘤免疫力

IF 5.3 2区 医学 Q1 ONCOLOGY
Suna Erdem, Hyojae James Lee, Jayanth Surya Narayanan Shankara Narayanan, Mohottige Don Neranjan Tharuka, Jorge De la Torre, Tianchen Ren, Yixuan Kuang, Tharindumala Abeywardana, Kevin Li, Allison J Berger, Andrew M Lowy, Rebekah R White, Yuan Chen
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引用次数: 0

摘要

改善胰腺导管腺癌(PDAC)患者的预后需要探索新的治疗靶点。迄今为止,大多数有关 PDAC 疗法(包括抑制泛素样小修饰(SUMOylation)的疗法)的研究都集中在 PDAC 上皮细胞生物学方面,但 SUMOylation 存在于多种细胞类型中。人们对 SUMOylation 在肿瘤微环境中影响 PDAC 的机制还知之甚少。我们利用与临床相关的正位 PDAC 小鼠模型,使用一种特定的临床阶段化合物 TAK-981 来研究 SUMOylation 抑制的效果。与体外抑制 PDAC 细胞增殖不同的是,TAK-981 在体内带来的生存益处依赖于 T 细胞的存在,这表明诱导适应性抗肿瘤免疫是体内 SUMO 抑制的重要抗肿瘤效应。为了了解这种适应性抗肿瘤免疫是如何促进的,我们研究了体内 SUMO 抑制是如何改变 PDAC 肿瘤微环境中的主要细胞类型/亚型及其交流的,方法是进行单细胞分辨率的转录组分析,从而根据基因表达谱将我们的小鼠正位模型中的细胞映射到人类 PDAC 肿瘤中的细胞。流式细胞术、免疫荧光、IHC、Western 印迹和 qPCR 进一步验证了研究结果。本文提供的单细胞转录组数据集提示了几种增强适应性免疫反应的组合策略,这些策略是 PDAC 患者持久控制疾病所必需的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibition of SUMOylation Induces Adaptive Antitumor Immunity against Pancreatic Cancer through Multiple Effects on the Tumor Microenvironment.

Improvement of outcome in patients with pancreatic ductal adenocarcinoma (PDAC) requires exploration of novel therapeutic targets. Thus far, most studies of PDAC therapies, including those inhibiting small ubiquitin-like modifications (SUMOylation), have focused on PDAC epithelial cell biology, yet SUMOylation occurs in a variety of cell types. The mechanisms by which SUMOylation impacts PDAC in the context of its tumor microenvironment are poorly understood. We used clinically relevant orthotopic PDAC mouse models to investigate the effect of SUMOylation inhibition using a specific, clinical-stage compound, TAK-981. In contrast to its inhibition of PDAC cell proliferation in vitro, the survival benefit conferred by TAK-981 in vivo is dependent on the presence of T cells, suggesting that induction of adaptive antitumor immunity is an important antitumor effect of SUMOylation inhibition in vivo. To understand how this adaptive antitumor immunity is promoted, we investigated how SUMOylation inhibition in vivo alters major cell types/subtypes and their communications in the PDAC tumor microenvironment by performing transcriptomic analyses at single-cell resolution, which allowed mapping of cells in our orthotopic mouse model to cells in human PDAC tumors based on gene expression profiles. Findings are further validated by flow cytometry, immunofluorescence, IHC, western blots, and qPCR. The single-cell transcriptome dataset provided here suggests several combination strategies to augment adaptive immune responses that are necessary for durable disease control in patients with PDAC.

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来源期刊
CiteScore
11.20
自引率
1.80%
发文量
331
审稿时长
3 months
期刊介绍: Molecular Cancer Therapeutics will focus on basic research that has implications for cancer therapeutics in the following areas: Experimental Cancer Therapeutics, Identification of Molecular Targets, Targets for Chemoprevention, New Models, Cancer Chemistry and Drug Discovery, Molecular and Cellular Pharmacology, Molecular Classification of Tumors, and Bioinformatics and Computational Molecular Biology. The journal provides a publication forum for these emerging disciplines that is focused specifically on cancer research. Papers are stringently reviewed and only those that report results of novel, timely, and significant research and meet high standards of scientific merit will be accepted for publication.
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