Mirra Davida, Esposito Renata, Spaziano Giuseppe, La Torre Chiara, Vocca Cristina, Tallarico Martina, Cione Erika, Gallelli Luca, D'Agostino Bruno
Department of Environmental Biological and Pharmaceutical Sciences and Technologies, University of Campania "Luigi Vanvitelli", 81100 Caserta, Italy.
Department of Pharmacy, Health and Nutritional Sciences-Department of Excellence 2018-2022, University of Calabria, 87036 Rende, Italy.
Biomedicines. 2023 Feb 28;11(3):736. doi: 10.3390/biomedicines11030736.
Non-small cell lung cancer (NSCLC) is one of the deadliest diseases worldwide and represents an impending burden on the healthcare system. Despite increasing attention, the mechanisms underlying tumorigenesis in cancer-related diseases such as COPD remain unclear, making novel biomarkers necessary to improve lung cancer early diagnosis. MicroRNAs (miRNAs) are short non-coding RNA that interfere with several pathways and can act as oncogenes or tumor suppressors. This study aimed to compare miRNA lung expression between subjects with NSCLC and COPD and healthy controls to obtain the miRNA expression profile by analyzing shared pathways. Lung specimens were collected from a prospective cohort of 21 sex-matched subjects to determine the tissue miRNA expression of hsa-miR-34a-5p, 33a-5p, 149-3p, 197-3p, 199-5p, and 320a-3p by RT-PCR. In addition, an in silico prediction of miRNA target genes linked to cancer was performed. We found a specific trend for has-miR-149-3p, 197-3p, and 34a-5p in NSCLC, suggesting their possible role as an index of the tumor microenvironment. Moreover, we identified novel miRNA targets, such as the Cyclin-Dependent Kinase (CDK) family, linked to carcinogenesis by in silico analysis. In conclusion. this study identified lung miRNA signatures related to the tumorigenic microenvironment, suggesting their possible role in improving the evaluation of lung cancer onset.
非小细胞肺癌(NSCLC)是全球最致命的疾病之一,对医疗系统构成了迫在眉睫的负担。尽管受到越来越多的关注,但慢性阻塞性肺疾病(COPD)等癌症相关疾病的肿瘤发生机制仍不清楚,因此需要新的生物标志物来改善肺癌的早期诊断。微小RNA(miRNA)是短链非编码RNA,可干扰多种信号通路,可作为癌基因或肿瘤抑制因子发挥作用。本研究旨在比较非小细胞肺癌、慢性阻塞性肺疾病患者与健康对照者肺部miRNA的表达情况,通过分析共同信号通路来获得miRNA表达谱。从21名性别匹配的前瞻性队列受试者中收集肺组织标本,通过逆转录-聚合酶链反应(RT-PCR)测定hsa-miR-34a-5p、33a-5p、149-3p、197-3p、199-5p和320a-3p的组织miRNA表达。此外,还对与癌症相关的miRNA靶基因进行了计算机预测。我们发现非小细胞肺癌中has-miR-149-3p、197-3p和34a-5p呈现出特定趋势,表明它们可能作为肿瘤微环境的指标。此外,通过计算机分析,我们确定了新的miRNA靶点,如细胞周期蛋白依赖性激酶(CDK)家族,与致癌作用有关。总之,本研究确定了与致瘤微环境相关的肺miRNA特征,表明它们在改善肺癌发病评估方面可能发挥的作用。