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本文引用的文献

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N Engl J Med. 2020 Dec 3;383(23):2207-2218. doi: 10.1056/NEJMoa2017699.
2
Molecular subtypes and the evolution of treatment management in metastatic colorectal cancer.转移性结直肠癌的分子亚型与治疗管理的演变
Ther Adv Med Oncol. 2020 Jul 24;12:1758835920936089. doi: 10.1177/1758835920936089. eCollection 2020.
3
Localised colon cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up.局限性结肠癌:ESMO 诊断、治疗及随访临床实践指南
Ann Oncol. 2020 Oct;31(10):1291-1305. doi: 10.1016/j.annonc.2020.06.022. Epub 2020 Jul 20.
4
ColoType: a forty gene signature for consensus molecular subtyping of colorectal cancer tumors using whole-genome assay or targeted RNA-sequencing.ColoType:一种使用全基因组检测或靶向 RNA 测序对结直肠癌肿瘤进行共识分子亚型分型的 40 基因特征。
Sci Rep. 2020 Jul 21;10(1):12123. doi: 10.1038/s41598-020-69083-y.
5
Neoadjuvant immunotherapy leads to pathological responses in MMR-proficient and MMR-deficient early-stage colon cancers.新辅助免疫治疗导致 MMR 功能正常和 MMR 缺陷的早期结肠癌发生病理应答。
Nat Med. 2020 Apr;26(4):566-576. doi: 10.1038/s41591-020-0805-8. Epub 2020 Apr 6.
6
Cyclin-dependent kinase 9 expression and its association with CD8 T cell infiltration in microsatellite-stable colorectal cancer.细胞周期蛋白依赖性激酶9在微卫星稳定型结直肠癌中的表达及其与CD8 T细胞浸润的关系
Oncol Lett. 2019 Dec;18(6):6046-6056. doi: 10.3892/ol.2019.10970. Epub 2019 Oct 8.
7
The ProteomeXchange consortium in 2020: enabling 'big data' approaches in proteomics.2020 年蛋白质组交换联盟:在蛋白质组学中启用“大数据”方法。
Nucleic Acids Res. 2020 Jan 8;48(D1):D1145-D1152. doi: 10.1093/nar/gkz984.
8
Review of PD-1/PD-L1 Inhibitors in Metastatic dMMR/MSI-H Colorectal Cancer.转移性错配修复缺陷/微卫星高度不稳定结直肠癌中PD-1/PD-L1抑制剂的综述
Front Oncol. 2019 May 14;9:396. doi: 10.3389/fonc.2019.00396. eCollection 2019.
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Proteogenomic Analysis of Human Colon Cancer Reveals New Therapeutic Opportunities.人类结肠癌的蛋白质基因组分析揭示了新的治疗机会。
Cell. 2019 May 2;177(4):1035-1049.e19. doi: 10.1016/j.cell.2019.03.030. Epub 2019 Apr 25.
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Harnessing the innate immune system and local immunological microenvironment to treat colorectal cancer.利用固有免疫系统和局部免疫微环境治疗结直肠癌。
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微卫星稳定、复发性结直肠癌中蛋白质组变化的映射揭示了显著的免疫系统特征。

Mapping Proteome Changes in Microsatellite Stable, Recurrent Colon Cancer Reveals a Significant Immune System Signature.

机构信息

Department of Clinical Medicine, University of Bergen, Bergen, Norway;

Department of Surgery, Haukeland University Hospital, Bergen, Norway.

出版信息

Cancer Genomics Proteomics. 2022 Mar-Apr;19(2):130-144. doi: 10.21873/cgp.20309.

DOI:10.21873/cgp.20309
PMID:35181583
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8865039/
Abstract

BACKGROUND/AIM: Better stratification of the risk of relapse will help select the right patients for adjuvant treatment and improve targeted therapies for patients with colon cancer.

MATERIALS AND METHODS

To understand why a subset of tumors relapse, we compared the proteome of two groups of patients with colon cancer with similar stage, stratified based on the presence or absence of recurrence.

RESULTS

Using tumor biopsies from the primary operation, we identified dissimilarity between recurrent and nonrecurrent mismatch satellite stable colon cancer and found that signaling related to immune activation and inflammation was associated with relapse.

CONCLUSION

Immune modulation may have an effect on mismatch satellite stable colon cancer. At present, immune therapy is offered primarily to microsatellite instable colon cancer. Hopefully, immune therapy in mismatch satellite stable colon cancer beyond PD-1 and PD-L1 inhibitors can be implemented.

摘要

背景/目的:更好地对复发风险进行分层,将有助于为辅助治疗选择合适的患者,并为结肠癌患者提供靶向治疗。

材料与方法

为了了解为什么一部分肿瘤会复发,我们比较了两组具有相似分期的结肠癌患者的蛋白质组学,这些患者根据是否存在复发进行了分层。

结果

使用原发性手术中的肿瘤活检,我们发现复发和非复发错配卫星稳定结肠癌之间存在差异,并且发现与免疫激活和炎症相关的信号与复发有关。

结论

免疫调节可能对错配卫星稳定结肠癌有影响。目前,免疫疗法主要用于微卫星不稳定结肠癌。希望可以在错配卫星稳定结肠癌中实施 PD-1 和 PD-L1 抑制剂以外的免疫治疗。