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Pin1作为致癌信号传导的核心节点:机制洞察与临床前景(综述)

Pin1 as a central node in oncogenic signaling: Mechanistic insights and clinical prospects (Review).

作者信息

Lei Shuning, Luo Min, Wang Yuxue

机构信息

Department of Laboratory Medicine, Hubei University of Chinese Medicine, Wuhan, Hubei 430065, P.R. China.

出版信息

Mol Med Rep. 2025 Mar;31(3). doi: 10.3892/mmr.2025.13445. Epub 2025 Jan 31.

DOI:10.3892/mmr.2025.13445
PMID:39886975
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11795255/
Abstract

Peptidyl‑prolyl cis‑trans isomerase NIMA-interacting 1 (Pin1) is a specific phosphorylated serine/threonine-proline cis-trans isomerase, which is involved in the regulation of a variety of physiological and pathological processes, including cell cycle progression, proliferation and apoptosis. Pin1 plays a key role in tumorigenesis and tumor development and it promotes the proliferation and metastasis of cancer cells by regulating the cell cycle, signaling pathways and the function of tumor suppressors. Upregulated expression of Pin1 is closely associated with a poor prognosis in several types of cancers. Thus, Pin1 is may have potential as a novel potential biomarker for tumor diagnosis and prognosis, as well as a promising anticancer target. The aim of the present review was to discuss the mechanism of Pin1 in tumors and recent research progress in this field.

摘要

肽基脯氨酰顺反异构酶NIMA相互作用蛋白1(Pin1)是一种特异性磷酸化的丝氨酸/苏氨酸-脯氨酸顺反异构酶,参与多种生理和病理过程的调控,包括细胞周期进程、增殖和凋亡。Pin1在肿瘤发生和发展中起关键作用,它通过调节细胞周期、信号通路和肿瘤抑制因子的功能来促进癌细胞的增殖和转移。Pin1的表达上调与多种癌症的不良预后密切相关。因此,Pin1可能具有作为肿瘤诊断和预后的新型潜在生物标志物以及有前景的抗癌靶点的潜力。本综述的目的是探讨Pin1在肿瘤中的作用机制以及该领域的最新研究进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9df8/11795255/c998567eb120/mmr-31-03-13445-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9df8/11795255/6d5b7d0e6f6c/mmr-31-03-13445-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9df8/11795255/b3575f1ea274/mmr-31-03-13445-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9df8/11795255/0b78885899e9/mmr-31-03-13445-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9df8/11795255/c998567eb120/mmr-31-03-13445-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9df8/11795255/6d5b7d0e6f6c/mmr-31-03-13445-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9df8/11795255/b3575f1ea274/mmr-31-03-13445-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9df8/11795255/0b78885899e9/mmr-31-03-13445-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9df8/11795255/c998567eb120/mmr-31-03-13445-g03.jpg

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本文引用的文献

1
The mechanisms of Pin1 as targets for cancer therapy.Pin1作为癌症治疗靶点的作用机制。
Front Immunol. 2024 Nov 18;15:1482088. doi: 10.3389/fimmu.2024.1482088. eCollection 2024.
2
Pin1: Advances in pancreatic cancer therapeutic potential and inhibitors research.Pin1:胰腺癌治疗潜力与抑制剂研究进展
Bioorg Chem. 2024 Dec;153:107869. doi: 10.1016/j.bioorg.2024.107869. Epub 2024 Oct 11.
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The role of the master cancer regulator Pin1 in the development and treatment of cancer.主要癌症调控因子Pin1在癌症发生发展及治疗中的作用。
Front Cell Dev Biol. 2024 Apr 30;12:1343938. doi: 10.3389/fcell.2024.1343938. eCollection 2024.
4
Pin1-Catalyzed Conformation Changes Regulate Protein Ubiquitination and Degradation.Pin1 催化的构象变化调节蛋白质泛素化和降解。
Cells. 2024 Apr 23;13(9):731. doi: 10.3390/cells13090731.
5
Potential of CDC25 phosphatases in cancer research and treatment: key to precision medicine.CDC25磷酸酶在癌症研究与治疗中的潜力:精准医学的关键
Front Pharmacol. 2024 Jan 19;15:1324001. doi: 10.3389/fphar.2024.1324001. eCollection 2024.
6
Prolyl isomerase Pin1 sculpts the immune microenvironment of colorectal cancer.脯氨酰异构酶 Pin1 塑造结直肠癌的免疫微环境。
Cell Signal. 2024 Mar;115:111041. doi: 10.1016/j.cellsig.2024.111041. Epub 2024 Jan 8.
7
Expanding Roles of the E2F-RB-p53 Pathway in Tumor Suppression.E2F-RB-p53通路在肿瘤抑制中的作用扩展
Biology (Basel). 2023 Dec 11;12(12):1511. doi: 10.3390/biology12121511.
8
pH-sensitive niosomes for ATRA delivery: A promising approach to inhibit Pin1 in high-grade serous ovarian cancer.用于 ATRA 递送的 pH 敏感的脂囊泡:一种抑制高级别浆液性卵巢癌中 Pin1 的有前途的方法。
Int J Pharm. 2024 Jan 5;649:123672. doi: 10.1016/j.ijpharm.2023.123672. Epub 2023 Dec 3.
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Cell Rep. 2023 Nov 28;42(11):113198. doi: 10.1016/j.celrep.2023.113198. Epub 2023 Oct 21.
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