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微小RNA表达影响阻塞性睡眠呼吸暂停和转移性结直肠癌患者的生存。

MiRNA expression affects survival in patients with obstructive sleep apnea and metastatic colorectal cancer.

作者信息

Soccio Piera, Moriondo Giorgia, Scioscia Giulia, Tondo Pasquale, Bruno Giuseppina, Giordano Guido, Sabato Roberto, Foschino Barbaro Maria Pia, Landriscina Matteo, Lacedonia Donato

机构信息

Respiratory Diseases Unit, Department of Medical and Surgical Sciences, University of Foggia, Italy.

Institute of Respiratory Diseases, Policlinico of Foggia, Italy.

出版信息

Noncoding RNA Res. 2024 Sep 13;10:91-97. doi: 10.1016/j.ncrna.2024.09.008. eCollection 2025 Feb.

Abstract

INTRODUCTION

The relationship between obstructive sleep apnea (OSA) and cancer has been recognized for some time now. However, little is known about the mechanisms by which sleep apnea promotes tumorigenesis and the impact of OSA on survival after cancer diagnosis. In the last few years, research has focused on the exploration of different biomarkers to understand the mechanisms underlying this relationship and miRNAs, non-coding single strands of about 22 nucleotides that post-transcriptionally regulate gene expression, have emerged as possible actors of this process.The aim of the study was to evaluate the impact of OSA on survival of metastatic colorectal cancer (mCRC) patients based on the expression of specific miRNAs.

METHODS

The expression of 6 miRNAs, respectively miR-21, miR-23b, miR-26a, miR-27b, miR-145 and miR-210, was analyzed by qRT-PCR in patients' sera. Response to first-line therapy, Kaplan-Meier curves of overall and progression-free survival were used to evaluate survival in mCRC patients with and without OSA stratified for the expression of miRNAs.

RESULTS

The expression of miR-21, miR-23b, miR-26a and miR-210 was significantly upregulated in mCRCs with OSA compared to no OSA. In mCRC patients with OSA and increasing expression of miR-21, miR-23b, miR-26a and miR-210 risk of progression after first-line therapy was higher and both overall and progression-free survival were significantly worst. Conversely, as miR-27b and miR-145 expression increased, the life expectancy of patients diagnosed with OSA and mCRC improved markedly.

CONCLUSIONS

This study highlights the relevance of specific miRNAs on OSA in mCRCs and their significance as non-invasive biomarkers in predicting the prognosis in patients with mCRC and OSA.

摘要

引言

阻塞性睡眠呼吸暂停(OSA)与癌症之间的关系已被认识一段时间了。然而,对于睡眠呼吸暂停促进肿瘤发生的机制以及OSA对癌症诊断后生存率的影响知之甚少。在过去几年中,研究集中在探索不同的生物标志物以了解这种关系背后的机制,而微小RNA(miRNA),即约22个核苷酸的非编码单链,可在转录后调节基因表达,已成为这一过程中可能的作用因素。本研究的目的是基于特定miRNA的表达评估OSA对转移性结直肠癌(mCRC)患者生存率的影响。

方法

通过qRT-PCR分析患者血清中6种miRNA(分别为miR-21、miR-23b、miR-26a、miR-27b、miR-145和miR-210)的表达。采用一线治疗反应、总生存和无进展生存的Kaplan-Meier曲线来评估有或无OSA且根据miRNA表达分层的mCRC患者的生存情况。

结果

与无OSA的mCRC相比,有OSA的mCRC中miR-21、miR-23b、miR-26a和miR-210的表达显著上调。在有OSA且miR-21、miR-23b、miR-26a和miR-210表达增加的mCRC患者中,一线治疗后的进展风险更高,总生存和无进展生存均显著更差。相反,随着miR-27b和miR-145表达增加,诊断为OSA和mCRC的患者的预期寿命显著改善。

结论

本研究强调了特定miRNA在mCRC的OSA中的相关性及其作为非侵入性生物标志物在预测mCRC和OSA患者预后方面的意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52da/11419774/9040c84131c4/gr1.jpg

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