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通过PI3K/AKT/mTOR信号通路探索非编码RNA在前列腺癌中的作用。

Exploring the roles of ncRNAs in prostate cancer via the PI3K/AKT/mTOR signaling pathway.

作者信息

Guo Rongwang, Shi Liji, Chen Yonghui, Lin Canling, Yin Weihua

机构信息

Nanchang University, 999 University Avenue, Honggutan District, Nanchang, China.

School of Chemical and Biological Engineering, Yichun College, Yichun, China.

出版信息

Front Immunol. 2025 Mar 18;16:1525741. doi: 10.3389/fimmu.2025.1525741. eCollection 2025.

DOI:10.3389/fimmu.2025.1525741
PMID:40170845
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11959002/
Abstract

Although various treatment options are available for prostate cancer (PCa), including androgen deprivation therapy (ADT) and chemotherapy, these approaches have not achieved the desired results clinically, especially in the treatment of advanced chemotherapy-resistant PCa. The PI3K/AKT/mTOR (PAM) signaling pathway is a classical pathway that is aberrantly activated in cancer cells and promotes the tumorigenesis, metastasis, resistance to castration therapy, chemoresistance, and recurrence of PCa. Noncoding RNAs (ncRNAs) are a class of RNAs that do not encode proteins. However, some ncRNAs have recently been shown to be differentially expressed in tumor tissues compared with noncancerous tissues and play important roles at the transcription and posttranscription levels. Among the types of ncRNAs, long noncoding RNAs (lncRNAs), microRNAs (miRNAs), circular RNAs (circRNAs), and Piwi-interacting RNAs (piRNAs) can participate in the PAM pathway to regulate PCa growth, metastasis, angiogenesis, and tumor stemness. Therefore, ncRNA therapy that targets the PAM signaling pathway is expected to be a novel and effective approach for treating PCa. In this paper, we summarize the types of ncRNAs that are associated with the PAM pathway in PCa cells as well as the functions and clinical roles of these ncRNAs in PCa. We hope to provide novel and effective strategies for the clinical diagnosis and treatment of PCa.

摘要

尽管前列腺癌(PCa)有多种治疗选择,包括雄激素剥夺疗法(ADT)和化疗,但这些方法在临床上并未取得理想效果,尤其是在治疗晚期化疗耐药性PCa方面。PI3K/AKT/mTOR(PAM)信号通路是一条经典通路,在癌细胞中异常激活,促进PCa的肿瘤发生、转移、去势治疗耐药性、化疗耐药性及复发。非编码RNA(ncRNAs)是一类不编码蛋白质的RNA。然而,最近有研究表明,与非癌组织相比,一些ncRNAs在肿瘤组织中存在差异表达,并在转录和转录后水平发挥重要作用。在ncRNAs类型中,长链非编码RNA(lncRNAs)、微小RNA(miRNAs)、环状RNA(circRNAs)和Piwi相互作用RNA(piRNAs)可参与PAM通路,调节PCa的生长、转移、血管生成和肿瘤干性。因此,靶向PAM信号通路的ncRNA疗法有望成为治疗PCa的一种新型有效方法。在本文中,我们总结了与PCa细胞中PAM通路相关的ncRNAs类型,以及这些ncRNAs在PCa中的功能和临床作用。我们希望为PCa的临床诊断和治疗提供新颖有效的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6ef/11959002/45b7edf19527/fimmu-16-1525741-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6ef/11959002/911f742afbe6/fimmu-16-1525741-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6ef/11959002/eed665600c1a/fimmu-16-1525741-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6ef/11959002/9b1a45397b8f/fimmu-16-1525741-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6ef/11959002/bc9273402810/fimmu-16-1525741-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6ef/11959002/f917b29620bc/fimmu-16-1525741-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6ef/11959002/7a958d4fa57b/fimmu-16-1525741-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6ef/11959002/45b7edf19527/fimmu-16-1525741-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6ef/11959002/911f742afbe6/fimmu-16-1525741-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6ef/11959002/eed665600c1a/fimmu-16-1525741-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6ef/11959002/9b1a45397b8f/fimmu-16-1525741-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6ef/11959002/bc9273402810/fimmu-16-1525741-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6ef/11959002/f917b29620bc/fimmu-16-1525741-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6ef/11959002/7a958d4fa57b/fimmu-16-1525741-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6ef/11959002/45b7edf19527/fimmu-16-1525741-g007.jpg

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本文引用的文献

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Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.2022 年全球癌症统计数据:全球 185 个国家和地区 36 种癌症的发病率和死亡率全球估计数。
CA Cancer J Clin. 2024 May-Jun;74(3):229-263. doi: 10.3322/caac.21834. Epub 2024 Apr 4.
2
Chinese herbal medicines for prostate cancer therapy: From experimental research to clinical practice.用于前列腺癌治疗的中草药:从实验研究到临床实践
Chin Herb Med. 2023 Sep 4;15(4):485-495. doi: 10.1016/j.chmed.2023.05.003. eCollection 2023 Oct.
3
IL-6 Enhances the Viability and Invasion Ability of Prostate Cancer Cells.
白细胞介素-6 增强前列腺癌细胞的活力和侵袭能力。
Stud Health Technol Inform. 2023 Nov 23;308:521-526. doi: 10.3233/SHTI230879.
4
PI3K/AKT/mTOR signaling transduction pathway and targeted therapies in cancer.PI3K/AKT/mTOR 信号转导通路与癌症的靶向治疗。
Mol Cancer. 2023 Aug 18;22(1):138. doi: 10.1186/s12943-023-01827-6.
5
LINC01088/miR-22/CDC6 Axis Regulates Prostate Cancer Progression by Activating the PI3K/AKT Pathway.LINC01088/miR-22/CDC6 轴通过激活 PI3K/AKT 通路调节前列腺癌的进展。
Mediators Inflamm. 2023 Jul 19;2023:9207148. doi: 10.1155/2023/9207148. eCollection 2023.
6
Long non-coding RNA AC245100.4 activates the PI3K/AKT pathway to promote PCa cell proliferation by elevating PAR2.长链非编码RNA AC245100.4通过上调蛋白酶激活受体2(PAR2)激活PI3K/AKT信号通路,促进前列腺癌细胞增殖。
Heliyon. 2023 Jun 3;9(6):e16870. doi: 10.1016/j.heliyon.2023.e16870. eCollection 2023 Jun.
7
Analyzing roles of small nucleolar RNA host gene 25 from clinical, molecular target and tumor formation in prostate cancer.分析小核仁 RNA 宿主基因 25 在前列腺癌中的临床、分子靶点和肿瘤形成中的作用。
Exp Cell Res. 2023 Aug 15;429(2):113686. doi: 10.1016/j.yexcr.2023.113686. Epub 2023 Jun 10.
8
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9
The function and mechanisms of action of circular RNAs in Urologic Cancer.环状 RNA 在泌尿系统癌症中的功能和作用机制。
Mol Cancer. 2023 Mar 25;22(1):61. doi: 10.1186/s12943-023-01766-2.
10
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Oncol Lett. 2023 Feb 17;25(4):138. doi: 10.3892/ol.2023.13724. eCollection 2023 Apr.