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利钠肽受体家族在恶性肿瘤中的作用及临床价值

The role and clinical value of natriuretic peptide receptor family in malignant tumor.

作者信息

Quan Chuqi, Shao Weilin, Yang Yihao, Yao Qian, Yang Zuozhang, Yao Zhihong

机构信息

Cancer Research Institute of Yunnan Province, Peking University Cancer Hospital Yunnan,Yunnan Cancer Hospital, The Third Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China.

Bone and Soft Tissue Tumors Research Centre of Yunnan Province, Department of Orthopaedics, Peking University Cancer Hospital Yunnan,Yunnan Cancer Hospital, The Third Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China.

出版信息

Cell Death Discov. 2025 Aug 28;11(1):412. doi: 10.1038/s41420-025-02656-w.

DOI:10.1038/s41420-025-02656-w
PMID:40877221
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12394403/
Abstract

The natriuretic peptide receptor (NPR) family (NPRA, NPRB, NPRC) regulates diverse physiological and pathological processes. Mounting evidence implicates NPRs as key regulators of oncogenesis, metastasis, and therapy resistance in multiple cancers. This review integrates current understanding of the distinct mechanisms by which NPR members contribute to cancer development and progression, explores their molecular underpinnings, and discusses translational potential and future directions. A central focus is the context-dependent functional duality of NPR signaling, where specific subtypes act as either oncogenic drivers or tumor suppressors depending on the malignancy.

摘要

利钠肽受体(NPR)家族(NPRA、NPRB、NPRC)调节多种生理和病理过程。越来越多的证据表明,NPRs是多种癌症发生、转移和治疗耐药性的关键调节因子。本综述整合了目前对NPR成员促进癌症发展和进展的不同机制的理解,探讨了其分子基础,并讨论了转化潜力和未来方向。一个核心重点是NPR信号的上下文依赖性功能二元性,其中特定亚型根据恶性程度充当致癌驱动因子或肿瘤抑制因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d4/12394403/ea221bf1e0df/41420_2025_2656_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d4/12394403/bda036472c2e/41420_2025_2656_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d4/12394403/ea221bf1e0df/41420_2025_2656_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d4/12394403/bda036472c2e/41420_2025_2656_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d4/12394403/ea221bf1e0df/41420_2025_2656_Fig2_HTML.jpg

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本文引用的文献

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Construction and validation of renal cell carcinoma tumor cell differentiation-related prognostic classification (RCC-TCDC): an integrated bioinformatic analysis and clinical study.肾细胞癌肿瘤细胞分化相关预后分类(RCC-TCDC)的构建与验证:一项综合生物信息学分析和临床研究
Ann Med. 2025 Dec;57(1):2490830. doi: 10.1080/07853890.2025.2490830. Epub 2025 Apr 18.
2
Myocarditis prediction in locally advanced or metastatic lung cancer patients with cardiac parameters abnormalities undergoing immunotherapy: development and validation of a risk assessment model.接受免疫治疗的合并心脏参数异常的局部晚期或转移性肺癌患者的心肌炎预测:风险评估模型的建立与验证
BMC Cancer. 2025 Mar 25;25(1):541. doi: 10.1186/s12885-025-13943-1.
3
Modified C-type natriuretic peptide normalizes tumor vasculature, reinvigorates antitumor immunity, and improves solid tumor therapies.
改性 C 型利钠肽可使肿瘤血管正常化,重振抗肿瘤免疫,并改善实体瘤治疗效果。
Sci Transl Med. 2024 Aug 21;16(761):eadn0904. doi: 10.1126/scitranslmed.adn0904.
4
NT-proBNP as a neuroendocrine tumor biomarker: beyond heart failure.N末端B型利钠肽原作为一种神经内分泌肿瘤生物标志物:超越心力衰竭。
Endocr Connect. 2023 Sep 13;12(10). doi: 10.1530/EC-23-0249. Print 2023 Oct 1.
5
NPRA promotes fatty acid metabolism and proliferation of gastric cancer cells by binding to PPARα.NPRA通过与PPARα结合促进胃癌细胞的脂肪酸代谢和增殖。
Transl Oncol. 2023 Sep;35:101734. doi: 10.1016/j.tranon.2023.101734. Epub 2023 Jul 5.
6
MSC-NPRA loop drives fatty acid oxidation to promote stemness and chemoresistance of gastric cancer.MSC-NPRA 环驱动脂肪酸氧化以促进胃癌的干性和化疗耐药性。
Cancer Lett. 2023 Jul 1;565:216235. doi: 10.1016/j.canlet.2023.216235. Epub 2023 May 18.
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BNP protects against diabetic cardiomyopathy by promoting Opa1-mediated mitochondrial fusion via activating the PKG-STAT3 pathway.脑钠肽通过激活 PKG-STAT3 通路促进 Opa1 介导线粒体融合来保护糖尿病心肌病。
Redox Biol. 2023 Jun;62:102702. doi: 10.1016/j.redox.2023.102702. Epub 2023 Apr 20.
8
Sarcomatoid-associated gene risk index for clear cell renal cell carcinoma.透明细胞肾细胞癌的肉瘤样相关基因风险指数
Front Genet. 2022 Sep 8;13:985641. doi: 10.3389/fgene.2022.985641. eCollection 2022.
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Elife. 2021 Dec 17;10:e71689. doi: 10.7554/eLife.71689.
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