在 MYC 表达的 KRAS 突变癌症中,通过对 SUMOylation 和 MEK 的双重抑制,促进全面的抗肿瘤免疫反应。

IF 9.4 1区 医学 Q1 HEMATOLOGY
Hiroshi Kotani, Tomoyoshi Yamano, Justin C Boucher, Shigeki Sato, Hiroyuki Sakaguchi, Koji Fukuda, Akihiro Nishiyama, Kaname Yamashita, Koushiro Ohtsubo, Shinji Takeuchi, Takumi Nishiuchi, Hiroko Oshima, Masanobu Oshima, Marco L Davila, Seiji Yano
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引用次数: 0

摘要

精准医疗极大地改变了癌症治疗策略,包括几十年来一直无法治愈的 KRAS 突变癌症。虽然许多病例的内在或获得性耐药性仍未得到解决,但表观基因组靶向疗法可能是克服耐药性的一种选择。我们最近发现,在表达 MYC 的 KRAS 突变癌细胞中,使用可抑制 SUMOylation 的 SUMO 激活酶 E 抑制剂 TAK-981,可有效阻断小泛素样修饰物(SUMO)信号级联(SUMOylation)。有趣的是,TAK-981 通过泛素-蛋白酶体系统促进了 MYC 的降解。此外,TAK-981与MEK抑制剂曲美替尼联合治疗可通过累积DNA损伤和诱导细胞凋亡,显著消退异种移植的KRAS突变肿瘤。我们最近的研究显示了免疫依赖性抗肿瘤疗效,而本研究则评估了癌细胞和免疫细胞的免疫反应。我们发现,TAK-981诱导的MYC下调促进了STING的激活,其次是Stat1和MHC I类在KRAS突变癌细胞中的激活。经 TAK-981 处理的树突状细胞或 T 细胞的活化也通过树突状细胞活化标志物的上调或 T 细胞向效应样表型的倾斜得到了验证。此外,TAK-981和曲美替尼联合疗法增强的免疫依赖性抗肿瘤疗效还通过免疫细胞对肿瘤组织的浸润以及在合成免疫功能正常的小鼠模型中使用免疫耗竭抗体进行免疫耗竭试验得到了证实。结合我们最近的研究和本文的研究,这些研究结果支持联合抑制 SUMOylation 和 MEK 可通过免疫依赖性和免疫非依赖性抗肿瘤反应全面征服表达 MYC 的 KRAS 突变癌症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comprehensive antitumor immune response boosted by dual inhibition of SUMOylation and MEK in MYC-expressing KRAS-mutant cancers.

Precision medicine has drastically changed cancer treatment strategies including KRAS-mutant cancers which have been undruggable for decades. While intrinsic or acquired treatment resistance remains unresolved in many cases, epigenome-targeted therapy may be an option to overcome. We recently discovered the effectiveness of blocking small ubiquitin-like modifier (SUMO) signaling cascade (SUMOylation) in MYC-expressing KRAS-mutant cancer cells using a SUMO-activating enzyme E inhibitor TAK-981 that results in SUMOylation inhibition. Interestingly, TAK-981 promoted the degradation of MYC via the ubiquitin-proteasome system. Moreover, combination therapy with TAK-981 and MEK inhibitor trametinib remarkably regressed xenografted KRAS-mutant tumors by accumulating DNA damage and inducing apoptosis. Whereas our recent study revealed immune-independent antitumor efficacy, we evaluated the immune responses of cancer cells and immune cells in this study. We found that TAK-981-induced MYC downregulation promoted the activation of STING followed by Stat1 and MHC class I in KRAS-mutant cancer cells. Activation of dendritic cells or T cells treated with TAK-981 was also verified by upregulated activation markers in dendritic cells or skew-toward effector-like phenotypes in T cells. Furthermore, the enhanced immune-dependent antitumor efficacy of the combination therapy with TAK-981 and trametinib was confirmed by infiltration of immune cells into tumor tissues and immunodepleting-test using immunodepleting antibodies in syngeneic immunocompetent mouse models. Together with our recent study and here, the findings support that combination inhibition of SUMOylation and MEK comprehensively conquers MYC-expressing KRAS-mutant cancers by both immune-dependent and immune-independent antitumor responses.

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来源期刊
CiteScore
12.60
自引率
7.30%
发文量
97
审稿时长
6 weeks
期刊介绍: Experimental Hematology & Oncology is an open access journal that encompasses all aspects of hematology and oncology with an emphasis on preclinical, basic, patient-oriented and translational research. The journal acts as an international platform for sharing laboratory findings in these areas and makes a deliberate effort to publish clinical trials with 'negative' results and basic science studies with provocative findings. Experimental Hematology & Oncology publishes original work, hypothesis, commentaries and timely reviews. With open access and rapid turnaround time from submission to publication, the journal strives to be a hub for disseminating new knowledge and discussing controversial topics for both basic scientists and busy clinicians in the closely related fields of hematology and oncology.
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