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一种呼出气体冷凝物/血浆微小RNA特征可区分肺腺癌与胸膜间皮瘤及健康对照。

An EBC/Plasma miRNA Signature Discriminates Lung Adenocarcinomas From Pleural Mesothelioma and Healthy Controls.

作者信息

Faversani Alice, Favero Chiara, Dioni Laura, Pesatori Angela Cecilia, Bollati Valentina, Montoli Matteo, Musso Valeria, Terrasi Andrea, Fusco Nicola, Nosotti Mario, Vaira Valentina, Palleschi Alessandro

机构信息

Division of Pathology, Fondazione IRCCS Ca' Granda-Ospedale Maggiore Policlinico, Milan, Italy.

EPIGET Lab, Department of Clinical Sciences and Community Health, University of Milan, Milan, Italy.

出版信息

Front Oncol. 2021 Jun 15;11:643280. doi: 10.3389/fonc.2021.643280. eCollection 2021.

Abstract

BACKGROUND

Despite significant improvement in screening programs for cancers of the respiratory district, especially in at-risk subjects, early disease detection is still a major issue. In this scenario, new molecular and non-invasive biomarkers are needed to improve early disease diagnosis.

METHODS

We profiled the miRNome in exhaled breath condensate (EBC) and plasma samples from fourteen patients affected by lung AdCa, nine healthy subjects. miRNA signatures were then analyzed in another neoplasia of the respiratory district, i.e. pleural mesothelioma (n = 23) and subjects previously exposed to asbestos were used as controls for this cohort (n = 19). Selected miRNAs were analyzed in purified pulmonary neoplastic or normal epithelial and stromal cell subpopulation from AdCa patients. Finally, the plasmatic miRNA signature was analyzed in a publicly available cohort of NSCLC patients for data validation and analysis was performed with predicted miRNA targets using the multiMiR tool and STRING database.

RESULTS

miR-597-5p and miR-1260a are significantly over-expressed in EBC from lung AdCa and are associated with AdCa. Similarly, miR-1260a is also up-regulated in the plasma of AdCa patients together with miR-518f-3p and correlates with presence of lung cancer, whereas let-7f-5p is under-expressed. Analysis of these circulating miRNAs in pleural mesothelioma cases confirmed that up-regulation of miR-518f-3p, -597-5p and -1260a, is specific for lung AdCa. Lastly, quantification of the miRNAs in laser-assisted microdissected lung tissues revealed that miR-518f-3p, 597-5p and miR-1260a are predominantly expressed in tumor epithelial cells. Validation analysis confirmed miR-518f-3p as a possible circulating biomarker of NSCLC. analysis of the potentially modulated biological processes by these three miRNAs, shows that tumor bioenergetics are the most affected pathways.

CONCLUSIONS

Overall, our data suggest a 3-miRNAs signature as a non-invasive and accurate biomarker of lung AdCa. This approach could supplement the current screening approaches for early lung cancer diagnosis.

摘要

背景

尽管呼吸道癌症筛查项目有了显著改善,尤其是在高危人群中,但疾病的早期检测仍然是一个主要问题。在这种情况下,需要新的分子和非侵入性生物标志物来改善疾病的早期诊断。

方法

我们分析了14例肺腺癌患者、9例健康受试者的呼出气冷凝物(EBC)和血浆样本中的微小RNA组。然后在另一种呼吸道肿瘤即胸膜间皮瘤(n = 23)中分析微小RNA特征,并将曾接触石棉的受试者作为该队列的对照(n = 19)。在来自肺腺癌患者的纯化肺肿瘤或正常上皮及基质细胞亚群中分析选定的微小RNA。最后,在一个公开的非小细胞肺癌患者队列中分析血浆微小RNA特征以进行数据验证,并使用multiMiR工具和STRING数据库对预测的微小RNA靶标进行分析。

结果

miR - 597 - 5p和miR - 1260a在肺腺癌患者的EBC中显著过表达,并与肺腺癌相关。同样,miR - 1260a在肺腺癌患者血浆中与miR - 518f - 3p一起上调,且与肺癌的存在相关,而let - 7f - 5p表达不足。在胸膜间皮瘤病例中对这些循环微小RNA的分析证实,miR - 518f - 3p、- 597 - 5p和- 1260a的上调是肺腺癌特有的。最后,对激光辅助显微切割的肺组织中微小RNA的定量分析显示,miR - 518f - 3p、597 - 5p和miR - 1260a主要在肿瘤上皮细胞中表达。验证分析证实miR - 518f - 3p可能是非小细胞肺癌的循环生物标志物。对这三种微小RNA可能调节的生物学过程的分析表明,肿瘤生物能量学是受影响最大的途径。

结论

总体而言,我们的数据表明一个由三种微小RNA组成的特征可作为肺腺癌的非侵入性准确生物标志物。这种方法可以补充当前用于早期肺癌诊断的筛查方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/528c/8239300/544dbce7b385/fonc-11-643280-g001.jpg

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