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2
SNORD6 promotes cervical cancer progression by accelerating E6-mediated p53 degradation.小分子核仁RNA SNORD6通过加速E6介导的p53降解促进宫颈癌进展。
Cell Death Discov. 2023 Jun 27;9(1):192. doi: 10.1038/s41420-023-01488-w.
3
Plasma SNORD42B and SNORD111 as potential biomarkers for early diagnosis of non-small cell lung cancer.血浆 SNORD42B 和 SNORD111 作为非小细胞肺癌早期诊断的潜在生物标志物。
J Clin Lab Anal. 2022 Nov;36(11):e24740. doi: 10.1002/jcla.24740. Epub 2022 Oct 25.
4
SNORA70E promotes the occurrence and development of ovarian cancer through pseudouridylation modification of RAP1B and alternative splicing of PARPBP.SNORA70E 通过 RAP1B 的假尿嘧啶化修饰和 PARPBP 的可变剪接促进卵巢癌的发生发展。
J Cell Mol Med. 2022 Oct;26(20):5150-5164. doi: 10.1111/jcmm.17540. Epub 2022 Sep 3.
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Box C/D snoRNA SNORD89 influences the occurrence and development of endometrial cancer through 2'-O-methylation modification of Bim.C/D 盒小核仁RNA SNORD89通过对Bim进行2'-O-甲基化修饰影响子宫内膜癌的发生发展。
Cell Death Discov. 2022 Jul 5;8(1):309. doi: 10.1038/s41420-022-01102-5.
6
SNORD15B and SNORA5C: Novel Diagnostic and Prognostic Biomarkers for Colorectal Cancer.SNORD15B 和 SNORA5C:结直肠癌的新型诊断和预后生物标志物。
Biomed Res Int. 2022 May 9;2022:8260800. doi: 10.1155/2022/8260800. eCollection 2022.
7
Targeting SNORA38B attenuates tumorigenesis and sensitizes immune checkpoint blockade in non-small cell lung cancer by remodeling the tumor microenvironment via regulation of GAB2/AKT/mTOR signaling pathway.靶向 SNORA38B 通过调控 GAB2/AKT/mTOR 信号通路重塑肿瘤微环境,抑制非小细胞肺癌的肿瘤发生并增强免疫检查点阻断作用。
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8
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Mol Oncol. 2022 May;16(9):1947-1965. doi: 10.1002/1878-0261.13186. Epub 2022 Mar 30.
9
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10
Bacteriophages as Solid Tumor Theragnostic Agents.噬菌体作为实体瘤治疗诊断试剂。
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实体瘤中的小核仁 RNA:对这些潜在生物标志物的文献综述。

Small Nucleolar RNAs in Solid Tumors: A Brief Review of the Literature on These Potential Biomarkers.

机构信息

State University of Maranhão, Zé Doca, MA, Brazil.

Oncology Research Center, Federal University of Pará, Belém, Pará, Brazil.

出版信息

Asian Pac J Cancer Prev. 2024 Aug 1;25(8):2585-2591. doi: 10.31557/APJCP.2024.25.8.2585.

DOI:10.31557/APJCP.2024.25.8.2585
PMID:39205555
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11495440/
Abstract

OBJECTIVE

The objective of this study was to conduct an integrative review, addressing the key findings, biological functions, and clinical significance of these biomolecules in solid tumors.

METHODS

This document analyzes the main data on the involvement of snoRNAs in solid tumors. For this, Pubmed and Science direct were used, with keywords. Additionally, a search for the host gene was conducted using the snoDB tool, and its chromosomal location was identified using the Hugo Gene Nomenclature Committee (HGNC).

RESULTS

According to research conducted in the literature, the majority of snoRNAs were found to be overexpressed and described as regulators of processes such as invasion, cellular proliferation, apoptosis, and migration. They are associated with clinical prognostic factors such as metastasis and worse survival.

CONCLUSION

Therefore, it is essential to expand the investigation of snoRNAs in oncology across different types of tumors. The utilization of these biomolecules may pave the way for innovative clinical applications, such as their use in the early detection of neoplasms in non-invasive samples and as therapeutic targets. Broadening research on snoRNAs across various tumor types is crucial.

摘要

目的

本研究旨在进行综合回顾,探讨这些生物分子在实体瘤中的主要发现、生物学功能和临床意义。

方法

本文件分析了 snoRNAs 参与实体瘤的主要数据。为此,使用了 Pubmed 和 Science direct,并使用了关键词。此外,使用 snoDB 工具进行了宿主基因的搜索,并使用人类基因命名委员会 (HGNC) 确定了其染色体位置。

结果

根据文献中的研究,大多数 snoRNAs 被发现过度表达,并被描述为调节侵袭、细胞增殖、凋亡和迁移等过程的调节剂。它们与转移和生存预后不良等临床预后因素相关。

结论

因此,有必要在不同类型的肿瘤中扩大 snoRNAs 在肿瘤学中的研究。这些生物分子的利用可能为创新的临床应用铺平道路,例如在非侵入性样本中早期检测肿瘤以及作为治疗靶点的应用。扩大对各种肿瘤类型 snoRNAs 的研究至关重要。