Simiene Julija, Kunigenas Linas, Prokarenkaite Rimvile, Dabkeviciene Daiva, Strainiene Egle, Stankevicius Vaidotas, Cicenas Saulius, Suziedelis Kestutis
Laboratory of Molecular Oncology, National Cancer Institute, Vilnius, LT-08406, Lithuania.
Institute of Biosciences, Life Sciences Center, Vilnius University, Vilnius, LT-10223, Lithuania.
Onco Targets Ther. 2024 Nov 14;17:1017-1032. doi: 10.2147/OTT.S475644. eCollection 2024.
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.
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.
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).
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.
肺癌患者较差的治疗结果和生存率促使人们去发现新的生物标志物,用于非小细胞肺癌(NSCLC)进展的特异性、显著性及微创检测。本研究旨在利用基于三维细胞培养中NSCLC细胞miRNA筛选的临床前细胞培养设置,探讨miRNA表达作为NSCLC生物标志物的潜力。
本研究使用了侵袭性水平不同的肺癌细胞系:NCI-H1299、A549、Calu-1和NCI-H23,以及非癌性支气管上皮细胞系HBEC3,这些细胞系在三维细胞培养中生长。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。在从NSCLC患者获得的89对组织标本和血浆样本中进一步验证了8种差异表达miRNA的表达。进行统计分析以确定NSCLC患者的miRNA表达和临床病理特征是否可被视为显著影响无进展生存期(PFS)或总生存期(OS)的独立因素。
通过下一代测序在侵袭性水平不同的NSCLC细胞系中鉴定出差异表达的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。对患者样本(包括肿瘤和血浆标本)的验证显示,在8种研究的miRNA中,只有血浆miR-10a-3p显示出显著增加,这与无进展生存期(PFS)显著延长相关(p=0.009)。此外,血浆中的miR-10a-3p成为NSCLC患者PFS的统计学显著预后变量(HR:0.5,95%CI:0.3-0.9,p=0.029)。
我们在三维细胞培养中生长的NSCLC细胞中筛选miRNA表达模式的研究结果表明,循环miR-10a-3p的表达水平有潜力作为一种新型非侵入性生物标志物来反映NSCLC患者的短期预后。