miR-10a-3p 在非小细胞肺癌患者中的预后价值

IF 2.7 4区 医学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY OncoTargets and therapy Pub Date : 2024-11-14 eCollection Date: 2024-01-01 DOI:10.2147/OTT.S475644
Julija Simiene, Linas Kunigenas, Rimvile Prokarenkaite, Daiva Dabkeviciene, Egle Strainiene, Vaidotas Stankevicius, Saulius Cicenas, Kestutis Suziedelis
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引用次数: 0

摘要

目的:肺癌患者的预后和生存率不佳,需要发现新的生物标记物,以便对非小细胞肺癌(NSCLC)的进展进行特异性、显著性和微创检测。本研究旨在利用一种临床前细胞培养装置,在三维细胞培养的非小细胞肺癌细胞中筛选 miRNA,研究 miRNA 表达作为非小细胞肺癌生物标志物的潜力:研究使用了不同侵袭性水平的肺癌细胞系:NCI-H1299、A549、Calu-1和NCI-H23,以及在三维细胞培养中生长的非癌支气管上皮细胞系HBEC3。提取所有细胞系的总 RNA,制备小 RNA 文库,并使用 Illumina NGS 平台进行测序。在 89 个配对的 NSCLC 患者组织标本和血浆样本中,进一步验证了 8 个差异表达 miRNA 的表达。研究人员进行了统计分析,以确定NSCLC患者的miRNA表达和临床病理特征是否可被视为显著影响PFS或OS的独立因素:结果:在具有不同侵袭性的NSCLC细胞系中,通过新一代测序鉴定出了不同表达的miRNA,包括let-7d-3p、miR-10a-3p、miR-28-3p、miR-28-5p、miR-100-3p、miR-182-5p、miR-190a-5p和miR-340-5p。对包括肿瘤和血浆标本在内的患者样本进行验证后发现,在所研究的8个miRNA中,只有血浆中的miR-10a-3p出现了显著增加,这与无进展生存期(PFS)的显著延长有关(p=0.009)。此外,血浆中的miR-10a-3p是NSCLC患者无进展生存期的一个具有统计学意义的预后变量(HR:0.5,95% CI:0.3-0.9,p=0.029):我们在三维细胞培养的NSCLC细胞中筛选miRNA表达模式的结果表明,循环miR-10a-3p的表达水平有可能成为反映NSCLC患者短期预后的新型非侵入性生物标志物。
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Prognostic Value of miR-10a-3p in Non-Small Cell Lung Cancer Patients.

Purpose: Poor lung cancer patients' outcomes and survival rates demand the discovery of new biomarkers for the specific, significant, and less invasive detection of non-small cell lung cancer (NSCLC) progression. The present study aimed to investigate the potential of miRNA expression as biomarkers in NSCLC utilizing a preclinical cell culture setup based on screening of miRNAs in NSCLC cells grown in 3D cell culture.

Patients and methods: The study was performed using lung cancer cell lines, varying in different levels of aggressiveness: NCI-H1299, A549, Calu-1, and NCI-H23, as well as noncancerous bronchial epithelial cell line HBEC3, which were grown in 3D cell culture. Total RNA from all cell lines was extracted and small RNA libraries were prepared and sequenced using the Illumina NGS platform. The expression of 8 differentially expressed miRNAs was further validated in 89 paired tissue specimens and plasma samples obtained from NSCLC patients. Statistical analysis was performed to determine whether miRNA expression and clinicopathological characteristics of NSCLC patients could be considered as independent factors significantly influencing PFS or OS.

Results: Differentially expressed miRNAs, including let-7d-3p, miR-10a-3p, miR-28-3p, miR-28-5p, miR-100-3p, miR-182-5p, miR-190a-5p, and miR-340-5p, were identified through next-generation sequencing in NSCLC cell lines with varying levels of aggressiveness. Validation of patient samples, including tumor and plasma specimens, revealed that out of the 8 investigated miRNAs, only plasma miR-10a-3p showed a significant increase, which was associated with significantly extended progression-free survival (PFS) (p=0.009). Furthermore, miR-10a-3p in plasma emerged as a statistically significant prognostic variable for NSCLC patients' PFS (HR: 0.5, 95% CI: 0.3-0.9, p=0.029).

Conclusion: Our findings of screening miRNA expression patterns in NSCLC cells grown in 3D cell culture indicated that the expression level of circulating miR-10a-3p has the potential as a novel non-invasive biomarker to reflect the short-term prognosis of NSCLC patients.

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来源期刊
OncoTargets and therapy
OncoTargets and therapy BIOTECHNOLOGY & APPLIED MICROBIOLOGY-ONCOLOGY
CiteScore
9.70
自引率
0.00%
发文量
221
审稿时长
1 months
期刊介绍: OncoTargets and Therapy is an international, peer-reviewed journal focusing on molecular aspects of cancer research, that is, the molecular diagnosis of and targeted molecular or precision therapy for all types of cancer. The journal is characterized by the rapid reporting of high-quality original research, basic science, reviews and evaluations, expert opinion and commentary that shed novel insight on a cancer or cancer subtype. Specific topics covered by the journal include: -Novel therapeutic targets and innovative agents -Novel therapeutic regimens for improved benefit and/or decreased side effects -Early stage clinical trials Further considerations when submitting to OncoTargets and Therapy: -Studies containing in vivo animal model data will be considered favorably. -Tissue microarray analyses will not be considered except in cases where they are supported by comprehensive biological studies involving multiple cell lines. -Biomarker association studies will be considered only when validated by comprehensive in vitro data and analysis of human tissue samples. -Studies utilizing publicly available data (e.g. GWAS/TCGA/GEO etc.) should add to the body of knowledge about a specific disease or relevant phenotype and must be validated using the authors’ own data through replication in an independent sample set and functional follow-up. -Bioinformatics studies must be validated using the authors’ own data through replication in an independent sample set and functional follow-up. -Single nucleotide polymorphism (SNP) studies will not be considered.
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