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结直肠癌肝转移:机制与临床治疗(综述)

Liver metastasis of colorectal cancer: Mechanism and clinical therapy (Review).

作者信息

Yang Changjiang, Zhao Long, Wang Caihong, Ye Yingjiang, Shen Zhanlong

机构信息

Department of Gastroenterological Surgery, Peking University People's Hospital, Beijing 100044, P.R. China.

出版信息

Oncol Rep. 2025 Oct;54(4). doi: 10.3892/or.2025.8963. Epub 2025 Aug 8.

DOI:10.3892/or.2025.8963
PMID:40776741
Abstract

Liver metastasis is a common complication in colorectal cancer (CRC), with its presence and progression significantly shortening patient survival. Therefore, a deeper understanding of the underlying mechanisms driving liver metastasis in CRC is essential to identify more effective and actionable therapeutic targets and improve prognosis. Liver metastasis in CRC is a multifaceted and dynamic process. Tumor cells with invasive properties communicate with the surrounding microenvironment through mechanisms such as immune checkpoint molecules and cytokines, thereby establishing a supportive niche for their colonization and proliferation. Moreover, suppressive immune cells may enhance the invasiveness of tumor cells. The interplay between tumor cells and the microenvironment is an interdependent process. Targeting these interactions offers promising potential for novel therapeutic strategies. The present review outlined mechanisms of colorectal cancer liver metastasis, emphasizing the immune microenvironment's role, current treatment approaches, and future development prospects.

摘要

肝转移是结直肠癌(CRC)常见的并发症,其出现和进展会显著缩短患者生存期。因此,深入了解CRC肝转移的潜在机制对于确定更有效且可实施的治疗靶点及改善预后至关重要。CRC肝转移是一个多方面的动态过程。具有侵袭性的肿瘤细胞通过免疫检查点分子和细胞因子等机制与周围微环境相互作用,从而为其定植和增殖建立支持性微环境。此外,抑制性免疫细胞可能增强肿瘤细胞的侵袭性。肿瘤细胞与微环境之间的相互作用是一个相互依存的过程。针对这些相互作用为新型治疗策略提供了有前景的潜力。本综述概述了结直肠癌肝转移的机制,强调了免疫微环境的作用、当前的治疗方法以及未来的发展前景。

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Liver metastasis of colorectal cancer: Mechanism and clinical therapy (Review).结直肠癌肝转移:机制与临床治疗(综述)
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本文引用的文献

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New Frontiers of Biomarkers in Metastatic Colorectal Cancer: Potential and Critical Issues.转移性结直肠癌生物标志物的新前沿:潜力与关键问题
Int J Mol Sci. 2025 May 30;26(11):5268. doi: 10.3390/ijms26115268.
2
Oncolytic Viruses as a Novel Therapeutic Approach for Colorectal Cancer: Mechanisms, Current Advances, and Future Directions.溶瘤病毒作为一种治疗结直肠癌的新型方法:作用机制、当前进展及未来方向
Cancers (Basel). 2025 May 31;17(11):1854. doi: 10.3390/cancers17111854.
3
Mechanisms of CD8 T cell exhaustion and its clinical significance in prognosis of anti-tumor therapies: A review.
CD8 T细胞耗竭机制及其在抗肿瘤治疗预后中的临床意义:综述
Int Immunopharmacol. 2025 Jun 26;159:114843. doi: 10.1016/j.intimp.2025.114843. Epub 2025 May 19.
4
Advancing Cancer Treatment: A Review of Immune Checkpoint Inhibitors and Combination Strategies.推进癌症治疗:免疫检查点抑制剂及联合策略综述
Cancers (Basel). 2025 Apr 23;17(9):1408. doi: 10.3390/cancers17091408.
5
mA-modified MIR670HG suppresses tumor liver metastasis through enhancing Kupffer cell phagocytosis.mA修饰的MIR670HG通过增强库普弗细胞吞噬作用抑制肿瘤肝转移。
Cell Mol Life Sci. 2025 Apr 28;82(1):185. doi: 10.1007/s00018-025-05700-1.
6
Hepatic iNKT cells facilitate colorectal cancer metastasis by inducing a fibrotic niche in the liver.肝脏不变自然杀伤T细胞通过在肝脏中诱导纤维化微环境促进结直肠癌转移。
iScience. 2025 Apr 6;28(5):112364. doi: 10.1016/j.isci.2025.112364. eCollection 2025 May 16.
7
The E3 Ligase NEDD4L Prevents Colorectal Cancer Liver Metastasis via Degradation of PRMT5 to Inhibit the AKT/mTOR Signaling Pathway.E3 泛素连接酶 NEDD4L 通过降解 PRMT5 抑制 AKT/mTOR 信号通路来预防结直肠癌肝转移。
Adv Sci (Weinh). 2025 Jul;12(26):e2504704. doi: 10.1002/advs.202504704. Epub 2025 Apr 25.
8
Promising immunotherapeutic treatments for colon cancer.结肠癌有前景的免疫治疗方法。
Med Oncol. 2025 Apr 23;42(5):175. doi: 10.1007/s12032-025-02724-2.
9
Reprogramming liver metastasis-associated macrophages toward an anti-tumoral phenotype through enforced miR-342 expression.通过强制表达miR-342将肝转移相关巨噬细胞重编程为抗肿瘤表型。
Cell Rep. 2025 May 27;44(5):115592. doi: 10.1016/j.celrep.2025.115592. Epub 2025 Apr 19.
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PRIM1 enhances colorectal cancer liver metastasis via promoting neutrophil recruitment and formation of neutrophil extracellular trap.PRIM1通过促进中性粒细胞募集和中性粒细胞胞外诱捕网的形成来增强结直肠癌肝转移。
Cell Signal. 2025 Aug;132:111822. doi: 10.1016/j.cellsig.2025.111822. Epub 2025 Apr 16.