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靶向胃肠道恶性肿瘤血管生成和肿瘤微环境的新兴策略:综述

Emerging Strategies for Targeting Angiogenesis and the Tumor Microenvironment in Gastrointestinal Malignancies: A Comprehensive Review.

作者信息

Nghiem Emily, Friedman Briana, Srivastava Nityanand, Takchi Andrew, Mohammadi Mahshid, Dedushi Dior, Edelmann Winfried, Kuang Chaoyuan, Bteich Fernand

机构信息

Department of Surgery, Montefiore Einstein, Bronx, NY 10461, USA.

Department of Medicine, Montefiore Einstein, Bronx, NY 10461, USA.

出版信息

Pharmaceuticals (Basel). 2025 Aug 5;18(8):1160. doi: 10.3390/ph18081160.


DOI:10.3390/ph18081160
PMID:40872551
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12389621/
Abstract

Gastrointestinal (GI) cancers represent a significant global health burden, with high morbidity and mortality often linked to late-stage detection and metastatic disease. The progression of these malignancies is critically driven by angiogenesis, the formation of new blood vessels, and the surrounding dynamic tumor microenvironment (TME), a complex ecosystem comprising various cell types and non-cellular components. This comprehensive review, based on a systematic search of the PubMed database, synthesizes the existing literature to define the intertwined roles of angiogenesis and the TME in GI tumorigenesis. The TME's influence creates conditions favorable for tumor growth, invasion, and metastasis, but sometimes induces resistance to current therapies. Available therapeutic strategies for inhibiting angiogenesis involve antibodies and oral tyrosine kinase inhibitors, while immune modulation within the tumor microenvironment is mainly achieved through checkpoint inhibitor antibodies and chemotherapy. Creative emerging strategies encompassing cellular therapies, bispecific antibodies, and new targets such as CD40, DLL4, and Ang2, amongst others, are focused on inhibiting proangiogenic pathways more profoundly, reversing resistance to prior drugs, and modulating the TME to enhance therapeutic efficacy. A deeper understanding of the complex interactions between components of the TME is crucial for addressing the unmet need for novel and effective therapeutic interventions against aggressive GI cancers.

摘要

胃肠道(GI)癌症是一项重大的全球健康负担,其高发病率和死亡率往往与晚期检测和转移性疾病有关。这些恶性肿瘤的进展主要由血管生成(即新血管的形成)以及周围动态的肿瘤微环境(TME)驱动,肿瘤微环境是一个由各种细胞类型和非细胞成分组成的复杂生态系统。本综述基于对PubMed数据库的系统检索,综合现有文献,以明确血管生成和肿瘤微环境在胃肠道肿瘤发生过程中的相互交织作用。肿瘤微环境的影响为肿瘤生长、侵袭和转移创造了有利条件,但有时也会导致对当前治疗产生耐药性。现有的抑制血管生成的治疗策略包括抗体和口服酪氨酸激酶抑制剂,而肿瘤微环境内的免疫调节主要通过检查点抑制剂抗体和化疗来实现。包括细胞疗法、双特异性抗体以及CD40、DLL4和血管生成素2等新靶点在内的新兴创新策略,致力于更深入地抑制促血管生成途径、逆转对先前药物的耐药性以及调节肿瘤微环境以提高治疗效果。深入了解肿瘤微环境各成分之间的复杂相互作用,对于满足针对侵袭性胃肠道癌症的新型有效治疗干预措施的未满足需求至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/945f/12389621/61b9dd6c176b/pharmaceuticals-18-01160-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/945f/12389621/ad1ff2313dd2/pharmaceuticals-18-01160-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/945f/12389621/61b9dd6c176b/pharmaceuticals-18-01160-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/945f/12389621/ad1ff2313dd2/pharmaceuticals-18-01160-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/945f/12389621/61b9dd6c176b/pharmaceuticals-18-01160-g002.jpg

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本文引用的文献

[1]
Bispecific Antibodies in Solid Tumors: Advances and Challenges.

Int J Mol Sci. 2025-6-18

[2]
Claudin-18 isoform 2-specific CAR T-cell therapy (satri-cel) versus treatment of physician's choice for previously treated advanced gastric or gastro-oesophageal junction cancer (CT041-ST-01): a randomised, open-label, phase 2 trial.

Lancet. 2025-6-7

[3]
The IL-22-oncostatin M axis promotes intestinal inflammation and tumorigenesis.

Nat Immunol. 2025-6

[4]
Targeting angiogenesis in gastrointestinal tumors: strategies from vascular disruption to vascular normalization and promotion strategies angiogenesis strategies in GI tumor therapy.

Front Immunol. 2025-4-22

[5]
Neoantigen-specific tumor-infiltrating lymphocytes in gastrointestinal cancers: a phase 2 trial.

Nat Med. 2025-4-1

[6]
Efficacy and safety of KN026, a bispecific anti-HER2 antibody, in combination with KN046, an anti-CTLA4/PD-L1 antibody, in patients with advanced HER2-positive nonbreast cancer: a combined analysis of a phase Ib and a phase II study.

Signal Transduct Target Ther. 2025-3-19

[7]
Combining Apatinib and Oxaliplatin Remodels the Immunosuppressive Tumor Microenvironment and Sensitizes Desert-Type Gastric Cancer to Immunotherapy.

Cancer Res. 2025-6-2

[8]
Regulatory role of non-coding RNAs in 5-Fluorouracil resistance in gastrointestinal cancers.

Cancer Drug Resist. 2025-1-16

[9]
Differential response to immunotherapy in different lesions of MSI-H double primary colorectal cancer: a case report and literature review.

AME Case Rep. 2024-11-25

[10]
First-line cadonilimab plus chemotherapy in HER2-negative advanced gastric or gastroesophageal junction adenocarcinoma: a randomized, double-blind, phase 3 trial.

Nat Med. 2025-4

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