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细胞外基质分子与免疫检查点抑制剂在癌症中的相互作用:文献系统综述。

The entanglement of extracellular matrix molecules and immune checkpoint inhibitors in cancer: a systematic review of the literature.

机构信息

Department of Biochemistry, Faculty of Medical Sciences, UBT-Higher Education Institute, Prishtina, Kosovo.

Department of Research and Diagnosis, Division of Molecular Oncology, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, Aviano, Italy.

出版信息

Front Immunol. 2023 Oct 3;14:1270981. doi: 10.3389/fimmu.2023.1270981. eCollection 2023.


DOI:10.3389/fimmu.2023.1270981
PMID:37854588
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10579931/
Abstract

INTRODUCTION: Immune-checkpoint inhibitors (ICIs) have emerged as a core pillar of cancer therapy as single agents or in combination regimens both in adults and children. Unfortunately, ICIs provide a long-lasting therapeutic effect in only one third of the patients. Thus, the search for predictive biomarkers of responsiveness to ICIs remains an urgent clinical need. The efficacy of ICIs treatments is strongly affected not only by the specific characteristics of cancer cells and the levels of immune checkpoint ligands, but also by other components of the tumor microenvironment, among which the extracellular matrix (ECM) is emerging as key player. With the aim to comprehensively describe the relation between ECM and ICIs' efficacy in cancer patients, the present review systematically evaluated the current literature regarding ECM remodeling in association with immunotherapeutic approaches. METHODS: This review followed the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines and was registered at the International Prospective Register of Systematic Reviews (PROSPERO, CRD42022351180). PubMed, Web of Science, and Scopus databases were comprehensively searched from inception to January 2023. Titles, abstracts and full text screening was performed to exclude non eligible articles. The risk of bias was assessed using the QUADAS-2 tool. RESULTS: After employing relevant MeSH and key terms, we identified a total of 5070 studies. Among them, 2540 duplicates, 1521 reviews or commentaries were found and excluded. Following title and abstract screening, the full text was analyzed, and 47 studies meeting the eligibility criteria were retained. The studies included in this systematic review comprehensively recapitulate the latest observations associating changes of the ECM composition following remodeling with the traits of the tumor immune cell infiltration. The present study provides for the first time a broad view of the tight association between ECM molecules and ICIs efficacy in different tumor types, highlighting the importance of ECM-derived proteolytic products as promising liquid biopsy-based biomarkers to predict the efficacy of ICIs. CONCLUSION: ECM remodeling has an important impact on the immune traits of different tumor types. Increasing evidence pinpoint at ECM-derived molecules as putative biomarkers to identify the patients that would most likely benefit from ICIs treatments. SYSTEMATIC REVIEW REGISTRATION: https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42022351180, identifier CRD42022351180.

摘要

简介:免疫检查点抑制剂 (ICI) 已成为癌症治疗的核心支柱,无论是在成人还是儿童中,作为单一药物或联合治疗方案均有应用。不幸的是,ICI 在三分之一的患者中仅提供持久的治疗效果。因此,寻找对 ICI 反应的预测性生物标志物仍然是迫切的临床需求。ICI 治疗的疗效不仅受到癌细胞的特定特征和免疫检查点配体水平的强烈影响,还受到肿瘤微环境的其他成分的影响,其中细胞外基质 (ECM) 正成为关键因素。为了全面描述 ECM 与癌症患者 ICI 疗效之间的关系,本综述系统评估了关于 ECM 重塑与免疫治疗方法相关的当前文献。

方法:本综述遵循系统评价和荟萃分析的首选报告项目 (PRISMA) 指南,并在国际前瞻性系统评价登记处 (PROSPERO,CRD42022351180) 进行了注册。从创建到 2023 年 1 月,全面检索了 PubMed、Web of Science 和 Scopus 数据库。通过标题、摘要和全文筛选排除不符合条件的文章。使用 QUADAS-2 工具评估偏倚风险。

结果:通过使用相关的 MeSH 和关键词,我们共确定了 5070 项研究。其中,有 2540 项重复,1521 项是综述或评论,均被排除。经过标题和摘要筛选后,分析了全文,并保留了符合纳入标准的 47 项研究。本综述中纳入的研究全面总结了 ECM 组成的改变与肿瘤免疫细胞浸润特征之间的最新关联。本研究首次提供了 ECM 分子与不同肿瘤类型的 ICI 疗效之间紧密关联的广泛视角,突出了 ECM 衍生的蛋白水解产物作为有前途的液体活检生物标志物来预测 ICI 疗效的重要性。

结论:ECM 重塑对不同肿瘤类型的免疫特征有重要影响。越来越多的证据表明 ECM 衍生分子是潜在的生物标志物,可以识别最有可能从 ICI 治疗中获益的患者。

系统评价注册:https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42022351180,标识符 CRD42022351180。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c7c/10579931/428aabf09b11/fimmu-14-1270981-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c7c/10579931/e13cd794aaa0/fimmu-14-1270981-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c7c/10579931/8ab26680b004/fimmu-14-1270981-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c7c/10579931/428aabf09b11/fimmu-14-1270981-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c7c/10579931/e13cd794aaa0/fimmu-14-1270981-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c7c/10579931/8ab26680b004/fimmu-14-1270981-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c7c/10579931/428aabf09b11/fimmu-14-1270981-g003.jpg

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本文引用的文献

[1]
A fibroblast-associated signature predicts prognosis and immunotherapy in esophageal squamous cell cancer.

Front Immunol. 2023

[2]
Clinical benefits of PD-1 inhibitors in specific subgroups of patients with advanced esophageal squamous cell carcinoma: a systematic review and meta-analysis of phase 3 randomized clinical trials.

Front Immunol. 2023

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Role of Some microRNA/ADAM Proteins Axes in Gastrointestinal Cancers as a Novel Biomarkers and Potential Therapeutic Targets-A Review.

Curr Issues Mol Biol. 2023-4-3

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Predictive biomarkers of immunotherapy response with pharmacological applications in solid tumors.

Acta Pharmacol Sin. 2023-9

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The integrated single-cell analysis developed a lactate metabolism-driven signature to improve outcomes and immunotherapy in lung adenocarcinoma.

Front Endocrinol (Lausanne). 2023

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Prognostic value of extracellular matrix gene mutations and expression in multiple myeloma.

Blood Cancer J. 2023-3-23

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Pharmaceutics. 2023-1-19

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The Intracellular and Secreted Sides of Osteopontin and Their Putative Physiopathological Roles.

Int J Mol Sci. 2023-2-2

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Roles of cancer-associated fibroblasts (CAFs) in anti- PD-1/PD-L1 immunotherapy for solid cancers.

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Front Genet. 2023-1-19

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