• 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

了解食管腺癌的免疫生物学:迈向改善治疗方法。

Understanding the immuno-biology of oesophageal adenocarcinoma: Towards improved therapeutic approaches.

机构信息

The University of Queensland Diamantina Institute, Translational Research Institute, Brisbane, Queensland, Australia.

The University of Queensland Diamantina Institute, Translational Research Institute, Brisbane, Queensland, Australia; Princess Alexandra Hospital, Brisbane, Queensland, Australia.

出版信息

Cancer Treat Rev. 2021 Jul;98:102219. doi: 10.1016/j.ctrv.2021.102219. Epub 2021 May 7.

DOI:10.1016/j.ctrv.2021.102219
PMID:33993033
Abstract

With an incidence that is constantly rising, oesophageal adenocarcinoma (OAC) is becoming an increasing health burden worldwide. Although significant advances in treatment regimens have improved patient outcomes, survival rates for this deadly cancer remain unsatisfactory. This highlights the need to improve current therapeutic approaches and develop novel therapeutic strategies for treating OAC patients. The advent of immunotherapy has revolutionised treatment across a range of malignancies, however outcomes in OAC show modest results. The inherent resistance of OAC to treatment reflects the complex genomic landscape of this cancer, which displays a lack of ubiquitous driver mutations and large-scale genomic alterations along with high tumour and immune heterogeneity. Research into the immune landscape of OAC is limited, and elucidation of the mechanisms surrounding the immune responses to this complex cancer will result in improved therapeutic approaches. This review explores what is known about the immuno-biology of OAC and explores promising therapeutic avenues that may improve responses to immunotherapeutic regimens.

摘要

食管腺癌(OAC)的发病率不断上升,正在成为全球日益严重的健康负担。尽管治疗方案的显著进展改善了患者的预后,但这种致命癌症的生存率仍不尽如人意。这凸显了需要改进当前的治疗方法并为 OAC 患者开发新的治疗策略的必要性。免疫疗法的出现已经彻底改变了一系列恶性肿瘤的治疗方法,然而 OAC 的治疗结果却并不理想。OAC 对治疗的固有耐药性反映了这种癌症复杂的基因组景观,其缺乏普遍存在的驱动突变和大规模的基因组改变,同时具有高肿瘤和免疫异质性。对 OAC 免疫景观的研究有限,阐明围绕这种复杂癌症的免疫反应的机制将导致改善治疗方法。这篇综述探讨了 OAC 的免疫生物学的已知内容,并探讨了可能改善对免疫治疗方案反应的有前途的治疗途径。

相似文献

1
Understanding the immuno-biology of oesophageal adenocarcinoma: Towards improved therapeutic approaches.了解食管腺癌的免疫生物学:迈向改善治疗方法。
Cancer Treat Rev. 2021 Jul;98:102219. doi: 10.1016/j.ctrv.2021.102219. Epub 2021 May 7.
2
Expression pattern of immune suppressive cytokines and growth factors in oesophageal adenocarcinoma reveal a tumour immune escape-promoting microenvironment.食管腺癌中免疫抑制细胞因子和生长因子的表达模式揭示了一种促进肿瘤免疫逃逸的微环境。
Scand J Immunol. 2008 Dec;68(6):616-23. doi: 10.1111/j.1365-3083.2008.02183.x.
3
GRB7 is an oncogenic driver and potential therapeutic target in oesophageal adenocarcinoma.GRB7 是食管腺癌中的致癌驱动因子和潜在治疗靶点。
J Pathol. 2020 Nov;252(3):317-329. doi: 10.1002/path.5528. Epub 2020 Sep 15.
4
Tumour microenvironment influences response to treatment in oesophageal adenocarcinoma.肿瘤微环境影响食管腺癌的治疗反应。
Front Immunol. 2023 Dec 13;14:1330635. doi: 10.3389/fimmu.2023.1330635. eCollection 2023.
5
Real-time metabolic profiling of oesophageal tumours reveals an altered metabolic phenotype to different oxygen tensions and to treatment with Pyrazinib.实时代谢组学分析食管肿瘤显示,不同氧张力和吡唑尼布治疗会导致代谢表型改变。
Sci Rep. 2020 Jul 21;10(1):12105. doi: 10.1038/s41598-020-68777-7.
6
Identification of plasma proteins associated with oesophageal cancer chemotherapeutic treatment outcomes using SWATH-MS.应用 SWATH-MS 鉴定与食管癌化疗治疗结果相关的血浆蛋白。
J Proteomics. 2022 Aug 30;266:104684. doi: 10.1016/j.jprot.2022.104684. Epub 2022 Jul 14.
7
Novel therapeutic strategies for treating esophageal adenocarcinoma: the potential of dendritic cell immunotherapy and combinatorial regimens.治疗食管腺癌的新型治疗策略:树突状细胞免疫疗法及联合治疗方案的潜力
Hum Immunol. 2008 Oct;69(10):614-24. doi: 10.1016/j.humimm.2008.07.006. Epub 2008 Aug 12.
8
Impact of radiotherapy on the immune landscape in oesophageal adenocarcinoma.放疗对食管腺癌免疫图谱的影响。
World J Gastroenterol. 2022 Jun 7;28(21):2302-2319. doi: 10.3748/wjg.v28.i21.2302.
9
The intra-class heterogeneity of immunophenotyping and immune landscape in oesophageal cancer and clinical implications.食管癌免疫表型和免疫图谱的组内异质性及其临床意义。
Ann Med. 2021 Dec;53(1):626-638. doi: 10.1080/07853890.2021.1912385.
10
Preclinical models of esophageal adenocarcinoma for drug development.用于药物研发的食管腺癌临床前模型。
Discov Med. 2016 Dec;22(123):371-379.

引用本文的文献

1
Prognostic immune markers in esophageal cancer patients managed with trimodal therapy.接受三联疗法治疗的食管癌患者的预后免疫标志物。
Cancer Immunol Immunother. 2025 Jan 3;74(2):57. doi: 10.1007/s00262-024-03891-3.
2
Spatial intra-tumour heterogeneity and treatment-induced genomic evolution in oesophageal adenocarcinoma: implications for prognosis and therapy.食管腺癌中的肿瘤内空间异质性和治疗诱导的基因组进化:对预后和治疗的影响。
Genome Med. 2024 Jul 17;16(1):90. doi: 10.1186/s13073-024-01362-z.
3
Tumour microenvironment influences response to treatment in oesophageal adenocarcinoma.
肿瘤微环境影响食管腺癌的治疗反应。
Front Immunol. 2023 Dec 13;14:1330635. doi: 10.3389/fimmu.2023.1330635. eCollection 2023.
4
The oesophageal adenocarcinoma tumour immune microenvironment dictates outcomes with different modalities of neoadjuvant therapy - results from the AGITG DOCTOR trial and the cancer evolution biobank.食管腺癌肿瘤免疫微环境决定了新辅助治疗不同模式的结局 - 来自 AGITG DOCTOR 试验和癌症进化生物库的结果。
Front Immunol. 2023 Oct 12;14:1220129. doi: 10.3389/fimmu.2023.1220129. eCollection 2023.
5
Tumor-Infiltrating Neutrophils after Neoadjuvant Therapy are Associated with Poor Prognosis in Esophageal Cancer.新辅助治疗后肿瘤浸润中性粒细胞与食管癌预后不良相关。
Ann Surg Oncol. 2023 Mar;30(3):1614-1625. doi: 10.1245/s10434-022-12562-5. Epub 2022 Oct 2.
6
Comprehensive Analysis of YTHDF1 Immune Infiltrates and ceRNA in Human Esophageal Carcinoma.YTHDF1免疫浸润与ceRNA在人食管癌中的综合分析
Front Genet. 2022 Mar 23;13:835265. doi: 10.3389/fgene.2022.835265. eCollection 2022.