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环状 RNA 在前列腺癌中的作用。

Role of Circular RNAs in Prostate Cancer.

机构信息

The First Clinical Medical College of Lanzhou University, No. 119, Donggang Road West, Chengguan District, Lanzhou, 730000, Gansu Province, China.

Department of Urology, Gansu Provincial Hospital, No. 204, Donggang Road West, Chengguan District, Lanzhou, 730000, Gansu Province, China.

出版信息

Curr Med Chem. 2024;31(29):4640-4656. doi: 10.2174/0929867330666230531095850.

DOI:10.2174/0929867330666230531095850
PMID:37259936
Abstract

OBJECTIVES

This study aims to summarize the current literature to demonstrate the importance of circular RNAs (circRNAs) in multiple aspects of prostate cancer (PCa) occurrence, progression, and treatment resistance and explore the potential role in therapeutic strategies aimed at targeting this molecule in PCa.

METHODS

The relevant literature from PubMed and Medline databases is reviewed in this article.

RESULTS

Non-coding RNA has been proven to play a vital role in regulating tumor progression. Among them, circular RNA plays a more unique role due to its nonlinear structure. Lots of circRNAs were found to be differentially expressed in PCa and regulate cell signaling pathways by regulating particular gene expressions. Recent studies have demonstrated that circRNAs are associated with the chemoresistance of urinary tumors, suggesting that circRNAs might be a novel therapeutic target and a marker for therapeutic response and prognosis assessment.

CONCLUSION

The potential crosstalk of circRNAs modifications in PCa development, therapy, and regulation of tumor metabolism is portrayed in this review. However, more preclinical and clinical trials of this targeted strategy are necessary for the treatment of urinary tumors.

摘要

目的

本研究旨在总结目前的文献,以证明环状 RNA(circRNA)在前列腺癌(PCa)发生、进展和治疗耐药性的多个方面的重要性,并探讨其在针对 PCa 中该分子的治疗策略中的潜在作用。

方法

本文综述了来自 PubMed 和 Medline 数据库的相关文献。

结果

非编码 RNA 已被证明在调节肿瘤进展中发挥重要作用。其中,环状 RNA 由于其非线性结构而发挥更独特的作用。大量 circRNAs 在 PCa 中差异表达,并通过调节特定基因的表达来调节细胞信号通路。最近的研究表明,circRNAs 与尿肿瘤的化疗耐药性相关,提示 circRNAs 可能是一种新的治疗靶点,以及治疗反应和预后评估的标志物。

结论

本综述描绘了 circRNAs 修饰在 PCa 发展、治疗和肿瘤代谢调控中的潜在串扰。然而,针对该靶向策略的更多临床前和临床试验对于治疗尿肿瘤是必要的。

相似文献

1
Role of Circular RNAs in Prostate Cancer.环状 RNA 在前列腺癌中的作用。
Curr Med Chem. 2024;31(29):4640-4656. doi: 10.2174/0929867330666230531095850.
2
Functions of circular RNAs in bladder, prostate and renal cell cancer (Review).环状 RNA 在膀胱癌、前列腺癌和肾细胞癌中的功能(综述)。
Mol Med Rep. 2021 May;23(5). doi: 10.3892/mmr.2021.11946. Epub 2021 Mar 2.
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Circular RNAs in Prostate Cancer: Is it Time to Further Explore Liquid Biopsies?环状 RNA 与前列腺癌:是否到了进一步探索液体活检的时候?
Mini Rev Med Chem. 2023;23(18):1772-1779. doi: 10.2174/1389557523666230209152948.
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Int J Biochem Cell Biol. 2021 May;134:105968. doi: 10.1016/j.biocel.2021.105968. Epub 2021 Mar 14.
5
Circular RNAs and Their Linear Transcripts as Diagnostic and Prognostic Tissue Biomarkers in Prostate Cancer after Prostatectomy in Combination with Clinicopathological Factors.环状 RNA 及其线性转录物作为前列腺癌根治术后结合临床病理因素的诊断和预后组织生物标志物。
Int J Mol Sci. 2020 Oct 22;21(21):7812. doi: 10.3390/ijms21217812.
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Hsa_circ_0004296 inhibits metastasis of prostate cancer by interacting with EIF4A3 to prevent nuclear export of ETS1 mRNA.hsa_circ_0004296 通过与 EIF4A3 相互作用抑制前列腺癌的转移,从而阻止 ETS1 mRNA 的核输出。
J Exp Clin Cancer Res. 2021 Oct 25;40(1):336. doi: 10.1186/s13046-021-02138-8.
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Circular RNA circHIPK3 modulates prostate cancer progression via targeting miR-448/MTDH signaling.环状RNA circHIPK3通过靶向miR-448/MTDH信号通路调节前列腺癌进展。
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Circular RNAs are differentially expressed in prostate cancer and are potentially associated with resistance to enzalutamide.环状 RNA 在前列腺癌中表达差异,并可能与恩杂鲁胺耐药相关。
Sci Rep. 2019 Jul 24;9(1):10739. doi: 10.1038/s41598-019-47189-2.
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Cell Mol Life Sci. 2021 Sep;78(17-18):6201-6213. doi: 10.1007/s00018-021-03908-5. Epub 2021 Aug 3.

本文引用的文献

1
Circular RNA LPAR3 targets JPT1 via microRNA-513b-5p to facilitate glycolytic activation but repress prostate cancer radiosensitivity.环状RNA LPAR3通过微小RNA-513b-5p靶向JPT1,以促进糖酵解激活但抑制前列腺癌放射敏感性。
Acta Biochim Pol. 2023 Mar 17;70(1):153-162. doi: 10.18388/abp.2020_6379.
2
CircDHRS3 inhibits prostate cancer cell proliferation and metastasis through the circDHRS3/miR-421/MEIS2 axis.环状 RNA 结构特异性解旋酶 3 通过环状 RNA 结构特异性解旋酶 3/miR-421/MEIS2 轴抑制前列腺癌细胞增殖和转移。
Epigenetics. 2023 Dec;18(1):2178802. doi: 10.1080/15592294.2023.2178802.
3
Circ-ABCC4 contributes to prostate cancer progression and radioresistance by mediating miR-1253/SOX4 cascade.
环状 RNA-ABCC4 通过调控 miR-1253/SOX4 级联促进前列腺癌的进展和放射抵抗。
Anticancer Drugs. 2023 Jan 1;34(1):155-165. doi: 10.1097/CAD.0000000000001361. Epub 2022 Nov 15.
4
circPHF16 suppresses prostate cancer metastasis via modulating miR-581/RNF128/Wnt/β-catenin pathway.circPHF16 通过调控 miR-581/RNF128/Wnt/β-catenin 通路抑制前列腺癌转移。
Cell Signal. 2023 Feb;102:110557. doi: 10.1016/j.cellsig.2022.110557. Epub 2022 Dec 9.
5
Circular RNAs: emerging players in brain aging and neurodegenerative diseases.环状RNA:脑衰老和神经退行性疾病中的新兴角色。
J Pathol. 2023 Jan;259(1):1-9. doi: 10.1002/path.6021. Epub 2022 Nov 24.
6
CircRNAs: Key molecules in the prevention and treatment of ischemic stroke.环状 RNA:预防和治疗缺血性脑卒中的关键分子。
Biomed Pharmacother. 2022 Dec;156:113845. doi: 10.1016/j.biopha.2022.113845. Epub 2022 Oct 13.
7
Circular RNA-regulated autophagy is involved in cancer progression.环状RNA调控的自噬参与癌症进展。
Front Cell Dev Biol. 2022 Sep 14;10:961983. doi: 10.3389/fcell.2022.961983. eCollection 2022.
8
Circular RNAs: New Players in Cardiomyopathy.环状 RNA:心肌病的新角色。
Genes (Basel). 2022 Aug 26;13(9):1537. doi: 10.3390/genes13091537.
9
Exosomal circRNA Scm-like with four malignant brain tumor domains 2 (circ-SFMBT2) enhances the docetaxel resistance of prostate cancer via the microRNA-136-5p/tribbles homolog 1 pathway.外泌体环状 RNA Scm 样结构域蛋白 2(circ-SFMBT2)通过 microRNA-136-5p/ 三叶因子同源物 1 途径增强前列腺癌对多西他赛的耐药性。
Anticancer Drugs. 2022 Oct 1;33(9):871-882. doi: 10.1097/CAD.0000000000001365. Epub 2022 Sep 14.
10
CircSMARCC1 facilitates tumor progression by disrupting the crosstalk between prostate cancer cells and tumor-associated macrophages via miR-1322/CCL20/CCR6 signaling.环状 RNA SMARCC1 通过 miR-1322/CCL20/CCR6 信号通路干扰前列腺癌细胞与肿瘤相关巨噬细胞之间的串扰促进肿瘤进展。
Mol Cancer. 2022 Sep 1;21(1):173. doi: 10.1186/s12943-022-01630-9.