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外泌体非编码 RNA 在泌尿生殖系统肿瘤肿瘤微环境中的作用。

Role of Exosomal Non-Coding RNA in the Tumour Microenvironment of Genitourinary System Tumours.

机构信息

Basic Medical College, Department of Pathology, Guangdong Medical University, Dongguan, Guangdong, China.

Professor in Basic Medical College, Department of Pathology, Guangdong Medical University, Dongguan, Guangdong, China.

出版信息

Technol Cancer Res Treat. 2023 Jan-Dec;22:15330338231198348. doi: 10.1177/15330338231198348.

DOI:10.1177/15330338231198348
PMID:37981789
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10664451/
Abstract

In recent years, genitourinary system tumors are common in people of all ages, seriously affecting the quality of life of patients, the pathogenesis and treatment of these diseases are constantly being updated and improved. Exosomes, with a lipid bilayer that enable delivery of their contents into body fluids or other cells. Exosomes can regulate the tumor microenvironment, and play an important role in tumor development. In turn, cellular and non-cellular components of tumor microenvironment also affect the occurrence, progression, invasion and metastasis of tumor. Non-coding RNAs have been shown to be able to be ingested and released by exosomes, and are seen as a potential tool in cancer diagnosis and treatment. Here, we summarize the effect of non-coding RNAs of exosome contents on the tumor microenvironment of genitourinary system tumor, expound the significance of non-coding RNAs of exosome in the occurrence, development, diagnosis and treatment of cancers.

摘要

近年来,泌尿系统肿瘤在各年龄段人群中均较为常见,严重影响患者的生活质量,其发病机制和治疗方法也在不断更新和完善。外泌体具有双层脂膜,可将其内容物递送至体液或其他细胞中。外泌体可以调节肿瘤微环境,在肿瘤发生发展中发挥重要作用。反过来,肿瘤微环境中的细胞和非细胞成分也会影响肿瘤的发生、进展、侵袭和转移。现已证实,非编码 RNA 能够被外泌体摄取和释放,并被视为癌症诊断和治疗的潜在工具。在这里,我们总结了外泌体内容物中非编码 RNA 对泌尿系统肿瘤肿瘤微环境的影响,阐述了外泌体中非编码 RNA 在癌症发生、发展、诊断和治疗中的意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e0c/10664451/7f5eb747f606/10.1177_15330338231198348-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e0c/10664451/2da2779c3b22/10.1177_15330338231198348-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e0c/10664451/7f5eb747f606/10.1177_15330338231198348-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e0c/10664451/2da2779c3b22/10.1177_15330338231198348-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e0c/10664451/7f5eb747f606/10.1177_15330338231198348-fig2.jpg

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本文引用的文献

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Urinary MicroRNAs as Biomarkers of Urological Cancers: A Systematic Review.尿 MicroRNAs 作为泌尿系统癌症的生物标志物:系统评价。
Int J Mol Sci. 2023 Jun 29;24(13):10846. doi: 10.3390/ijms241310846.
2
Cellular and Molecular Players in the Tumor Microenvironment of Renal Cell Carcinoma.肾细胞癌肿瘤微环境中的细胞与分子参与者
J Clin Med. 2023 Jun 7;12(12):3888. doi: 10.3390/jcm12123888.
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Immune Checkpoint Inhibitors in Renal Cell Carcinoma: Molecular Basis and Rationale for Their Use in Clinical Practice.肾细胞癌中的免疫检查点抑制剂:其在临床实践中应用的分子基础和原理
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MUC1 Expression Affects the Immunoflogosis in Renal Cell Carcinoma Microenvironment through Complement System Activation and Immune Infiltrate Modulation.MUC1 表达通过补体系统激活和免疫浸润调节影响肾细胞癌微环境中的免疫炎症反应。
Int J Mol Sci. 2023 Mar 2;24(5):4814. doi: 10.3390/ijms24054814.
5
Effect of Exosomal lncRNA MALAT1/miR-370-3p/STAT3 Positive Feedback Loop on PI3K/Akt Pathway Mediating Cisplatin Resistance in Cervical Cancer Cells.外泌体长链非编码RNA MALAT1/miR-370-3p/STAT3正反馈环对PI3K/Akt通路介导宫颈癌细胞顺铂耐药的影响
J Oncol. 2023 Feb 6;2023:6341011. doi: 10.1155/2023/6341011. eCollection 2023.
6
Tumor Cell-Derived Exosomal circ-PRKCI Promotes Proliferation of Renal Cell Carcinoma via Regulating miR-545-3p/CCND1 Axis.肿瘤细胞来源的外泌体环状PRKCI通过调控miR-545-3p/CCND1轴促进肾细胞癌增殖。
Cancers (Basel). 2022 Dec 25;15(1):123. doi: 10.3390/cancers15010123.
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Cancer-derived exosomal miR-375 targets DIP2C and promotes osteoblastic metastasis and prostate cancer progression by regulating the Wnt signaling pathway.癌症来源的外泌体miR-375靶向DIP2C,并通过调节Wnt信号通路促进成骨细胞转移和前列腺癌进展。
Cancer Gene Ther. 2023 Mar;30(3):437-449. doi: 10.1038/s41417-022-00563-1. Epub 2022 Nov 25.
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Cancer-associated fibroblasts promote the stemness and progression of renal cell carcinoma via exosomal miR-181d-5p.癌症相关成纤维细胞通过外泌体miR-181d-5p促进肾细胞癌的干性维持和进展。
Cell Death Discov. 2022 Nov 1;8(1):439. doi: 10.1038/s41420-022-01219-7.
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