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CYR61 作为癌症预后和治疗中的潜在生物标志物与靶点

英文原题:CYR61 as a Potential Biomarker and Target in Cancer Prognosis and Therapies.

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CYR61 as a Potential Biomarker and Target in Cancer Prognosis and Therapies.

PubMed 2025/05/22(内容时间) Cells Q2 · IF 6(JCR 2025)

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中文摘要

富含半胱氨酸蛋白61(CYR61)是CCN家族的一种基质细胞蛋白,参与细胞黏附、迁移、增殖和血管生成。CYR61与整合素α6β1、αvβ3、αvβ5及αIIbβ3相互作用,可调节肿瘤进展和转移,同时改变肿瘤微环境。CYR61在癌症中的作用依赖具体情境,既可能促进肿瘤,也可能抑制肿瘤。CYR61表达升高与细胞外基质重塑、免疫调节和整合素介导信号有关,因此可能成为预后生物标志物和治疗靶点。新兴研究凸显CYR61在液体活检癌症检测和监测中的用途。包括阻断CYR61抗体和CAR-T 策略在内的整合素靶向疗法提供了新的治疗方法,但这些策略仍面临治疗诱导毒性和耐药等挑战。进一步阐明CYR61分子机制,可能有助于加强靶向干预并改善患者结局。

展开英文摘要原文

Cysteine-rich protein 61 (CYR61) is a matricellular protein in the CCN family that is involved in cellular adhesion, migration, proliferation, and angiogenesis. CYR61 interacts with integrins 6 1, v 3, v 5, and IIb 3 to modulate tumor progression and metastasis while modifying the tumor microenvironment. CYR61 exhibits context-dependent roles in cancer, acting as both a tumor promoter and suppressor.

Increased CYR61 expression is linked to extracellular matrix remodeling, immune modulation, and integrin-mediated signaling, making it a potential prognostic biomarker and therapeutic target. Emerging research highlights the utility of CYR61 in liquid biopsies for cancer detection and monitoring. Integrin-targeted therapies, including CYR61-blocking antibodies and CAR-T approaches, offer novel treatment strategies.

However, therapy-induced toxicity and resistance remain challenges with these strategies. The further elucidation of the molecular mechanisms of CYR61 may enhance targeted therapeutic interventions and improve patient outcomes.

论文信息

作者
Schenker AJ、Ortiz-Hernández GL
第一作者单位
Department of Medical Sciences, College of Health Sciences, Western University of Health Sciences, Pomona, CA 91766, USA.United States
通讯作者单位
Division of Biomarkers of Early Detection and Prevention, Department of Population Sciences, City of Hope Comprehensive Cancer Center, Duarte, CA 91010, USA.United States
文献类型
综述 · 美国 NIH 资助研究 · 非美国政府资助研究
期刊
Cells2025 May 22
原文标识
PubMed 40497940 · DOI 10.3390/cells14110761