• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

激活肺癌免疫敏感性的研究。

ALKing the flames of lung cancer immunosensitivity.

机构信息

School of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, UK.

Department of Experimental Immunotherapy, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

出版信息

Mol Oncol. 2023 Nov;17(11):2218-2220. doi: 10.1002/1878-0261.13533. Epub 2023 Oct 12.

DOI:10.1002/1878-0261.13533
PMID:37795653
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10620113/
Abstract

Immune checkpoint inhibitors (ICIs) are utilised in treating non-small cell lung cancer (NSCLC) by enhancing the immune response against cancer cells. However, they are not effective against cancers with certain genetic alterations. A recent study by Mota et al. focussed on understanding why ALK+ NSCLC cancers are immune cold and making them more receptive to ICIs using a vaccine-based approach. The study highlighted cell-specific differences in the presentation of immunogenic peptides and the location of tumours as factors in the poor immune response. Vaccines based on ALK peptides improved immune response, and when combined with ICIs, this led to a striking improvement in survival in a mouse model of ALK+ NSCLC.

摘要

免疫检查点抑制剂(ICIs)通过增强针对癌细胞的免疫反应,被用于治疗非小细胞肺癌(NSCLC)。然而,它们对某些具有特定遗传改变的癌症并不有效。最近由 Mota 等人进行的一项研究集中于了解为什么 ALK+ NSCLC 癌症是免疫冷肿瘤,并通过基于疫苗的方法使它们对 ICI 更敏感。该研究强调了免疫原性肽的呈现和肿瘤位置的细胞特异性差异是免疫反应不佳的因素。基于 ALK 肽的疫苗改善了免疫反应,当与 ICI 联合使用时,这导致 ALK+ NSCLC 的小鼠模型中的生存显著改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ad7/10620113/d511850fbbcd/MOL2-17-2218-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ad7/10620113/d511850fbbcd/MOL2-17-2218-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ad7/10620113/d511850fbbcd/MOL2-17-2218-g001.jpg

相似文献

1
ALKing the flames of lung cancer immunosensitivity.激活肺癌免疫敏感性的研究。
Mol Oncol. 2023 Nov;17(11):2218-2220. doi: 10.1002/1878-0261.13533. Epub 2023 Oct 12.
2
ALK peptide vaccination restores the immunogenicity of ALK-rearranged non-small cell lung cancer.ALK 肽疫苗接种恢复了 ALK 重排的非小细胞肺癌的免疫原性。
Nat Cancer. 2023 Jul;4(7):1016-1035. doi: 10.1038/s43018-023-00591-2. Epub 2023 Jul 10.
3
Integration of comprehensive genomic profiling, tumor mutational burden, and PD-L1 expression to identify novel biomarkers of immunotherapy in non-small cell lung cancer.综合基因组分析、肿瘤突变负担和 PD-L1 表达的整合,以鉴定非小细胞肺癌免疫治疗的新型生物标志物。
Cancer Med. 2021 Apr;10(7):2216-2231. doi: 10.1002/cam4.3649. Epub 2021 Mar 2.
4
Efficacy of a Cancer Vaccine against ALK-Rearranged Lung Tumors.一种癌症疫苗对ALK重排肺肿瘤的疗效。
Cancer Immunol Res. 2015 Dec;3(12):1333-1343. doi: 10.1158/2326-6066.CIR-15-0089. Epub 2015 Sep 29.
5
The efficacy of immune checkpoint inhibitors in anaplastic lymphoma kinase-positive non-small cell lung cancer.免疫检查点抑制剂在间变性淋巴瘤激酶阳性非小细胞肺癌中的疗效。
Thorac Cancer. 2019 Nov;10(11):2117-2123. doi: 10.1111/1759-7714.13195. Epub 2019 Sep 11.
6
KRAS-G12D mutation drives immune suppression and the primary resistance of anti-PD-1/PD-L1 immunotherapy in non-small cell lung cancer.KRAS-G12D 突变驱动免疫抑制和抗 PD-1/PD-L1 免疫疗法在非小细胞肺癌中的原发性耐药。
Cancer Commun (Lond). 2022 Sep;42(9):828-847. doi: 10.1002/cac2.12327. Epub 2022 Jul 11.
7
ILT4 inhibition prevents TAM- and dysfunctional T cell-mediated immunosuppression and enhances the efficacy of anti-PD-L1 therapy in NSCLC with EGFR activation.ILT4 抑制可预防 TAM 和功能失调 T 细胞介导的免疫抑制,并增强 EGFR 激活的 NSCLC 中抗 PD-L1 治疗的疗效。
Theranostics. 2021 Jan 19;11(7):3392-3416. doi: 10.7150/thno.52435. eCollection 2021.
8
The prognostic role of PD-1, PD-L1, ALK, and ROS1 proteins expression in non-small cell lung carcinoma patients from Egypt.埃及非小细胞肺癌患者中 PD-1、PD-L1、ALK 和 ROS1 蛋白表达的预后作用。
J Egypt Natl Canc Inst. 2022 May 30;34(1):23. doi: 10.1186/s43046-022-00121-8.
9
Characteristics of the immune microenvironment and their clinical significance in non-small cell lung cancer patients with ALK-rearranged mutation.具有 ALK 重排突变的非小细胞肺癌患者的免疫微环境特征及其临床意义。
Front Immunol. 2022 Sep 8;13:974581. doi: 10.3389/fimmu.2022.974581. eCollection 2022.
10
Epidermal Growth Factor Receptor (EGFR) Pathway, Yes-Associated Protein (YAP) and the Regulation of Programmed Death-Ligand 1 (PD-L1) in Non-Small Cell Lung Cancer (NSCLC).表皮生长因子受体(EGFR)通路、Yes 相关蛋白(YAP)与非小细胞肺癌(NSCLC)中程序性死亡配体 1(PD-L1)的调控。
Int J Mol Sci. 2019 Aug 5;20(15):3821. doi: 10.3390/ijms20153821.

本文引用的文献

1
ALK peptide vaccination restores the immunogenicity of ALK-rearranged non-small cell lung cancer.ALK 肽疫苗接种恢复了 ALK 重排的非小细胞肺癌的免疫原性。
Nat Cancer. 2023 Jul;4(7):1016-1035. doi: 10.1038/s43018-023-00591-2. Epub 2023 Jul 10.
2
EML4-ALK biology and drug resistance in non-small cell lung cancer: a new phase of discoveries.EML4-ALK 生物学与非小细胞肺癌的药物耐药性:新发现阶段。
Mol Oncol. 2023 Jun;17(6):950-963. doi: 10.1002/1878-0261.13446. Epub 2023 May 15.
3
Adaptive resistance to lorlatinib via EGFR signaling in ALK-rearranged lung cancer.
在ALK重排肺癌中,通过EGFR信号通路对劳拉替尼产生适应性耐药。
NPJ Precis Oncol. 2023 Jan 26;7(1):12. doi: 10.1038/s41698-023-00350-7.
4
Immunotherapy in non-small cell lung cancer: Past, present, and future directions.非小细胞肺癌的免疫疗法:过去、现在及未来方向
Front Oncol. 2022 Aug 2;12:877594. doi: 10.3389/fonc.2022.877594. eCollection 2022.
5
Lack of CD8 T cell effector differentiation during priming mediates checkpoint blockade resistance in non-small cell lung cancer.在非小细胞肺癌中,初始阶段缺乏 CD8 T 细胞效应分化可导致检查点阻断耐药。
Sci Immunol. 2021 Oct 29;6(64):eabi8800. doi: 10.1126/sciimmunol.abi8800.
6
An atlas of the protein-coding genes in the human, pig, and mouse brain.人类、猪和鼠脑的蛋白质编码基因图谱。
Science. 2020 Mar 6;367(6482). doi: 10.1126/science.aay5947.
7
Clinical Management of Adverse Events Associated with Lorlatinib.洛拉替尼不良反应的临床管理。
Oncologist. 2019 Aug;24(8):1103-1110. doi: 10.1634/theoncologist.2018-0380. Epub 2019 Mar 19.
8
Identification of a highly lethal V3 TP53 subset in ALK lung adenocarcinoma.鉴定出 ALK 肺腺癌中高度致死的 V3 TP53 亚群。
Int J Cancer. 2019 Jan 1;144(1):190-199. doi: 10.1002/ijc.31893. Epub 2018 Oct 30.
9
Epitope mapping of spontaneous autoantibodies to anaplastic lymphoma kinase (ALK) in non-small cell lung cancer.非小细胞肺癌中针对间变性淋巴瘤激酶(ALK)的自发性自身抗体的表位作图
Oncotarget. 2017 Sep 23;8(54):92265-92274. doi: 10.18632/oncotarget.21182. eCollection 2017 Nov 3.
10
Anti-ALK Antibodies in Patients with ALK-Positive Malignancies Not Expressing NPM-ALK.不表达NPM-ALK的ALK阳性恶性肿瘤患者中的抗ALK抗体
J Cancer. 2016 Jun 30;7(11):1383-7. doi: 10.7150/jca.15238. eCollection 2016.