دورية أكاديمية

Extracellular vesicle miRNAs for predicting the efficacy of late-line treatment with anlotinib in patients with lung adenocarcinoma

التفاصيل البيبلوغرافية
العنوان: Extracellular vesicle miRNAs for predicting the efficacy of late-line treatment with anlotinib in patients with lung adenocarcinoma
المؤلفون: Aimi Huang, Fuchuang Zhang, Jiyang Zhang, Xiaoya Xu, Zhikuan Li, Sheng Chen, Baoning Nian, Dadong Zhang, Baohui Han, Aiqin Gu, Weimin Wang
المصدر: Cancer Nanotechnology, Vol 15, Iss 1, Pp 1-13 (2024)
بيانات النشر: BMC, 2024.
سنة النشر: 2024
المجموعة: LCC:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
مصطلحات موضوعية: sEVs, miRNA, Anlotinib, NSCLC, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
الوصف: Abstract Background Anlotinib is a targeted therapy indicated for some malignancies, including advanced non-small cell lung cancer (NSCLC). However, noninvasive biomarkers for identifying patients who will benefit from this disease remain lacking. Methods Here, we investigated the potential of small extracellular vesicle (sEV) microRNAs (miRNAs) as predictive biomarkers for anlotinib efficacy. A total of 20 advanced NSCLC patients were enrolled. Patients were classified as having stable disease (SD) or progressive disease (PD) after the initial efficacy assessment. Results Seven differentially expressed miRNAs (DEMs) were identified. Among them, miR-941 was significantly upregulated in the PD group, while the others were downregulated. Furthermore, these six downregulated miRNAs (miR-30a-3p, miR-150-5p, miR-122-5p, miR-10b-5p, miR-92a-3p, and miR-150-3p) were more pronounced in nonsmoking patients. Conclusions It was found that sEV miRNAs have the potential to predict the benefit of anlotinib.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1868-6958
1868-6966
Relation: https://doaj.org/toc/1868-6958; https://doaj.org/toc/1868-6966
DOI: 10.1186/s12645-024-00273-3
URL الوصول: https://doaj.org/article/c33f84d83b864a669b908d652c95d6bd
رقم الأكسشن: edsdoj.33f84d83b864a669b908d652c95d6bd
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:18686958
18686966
DOI:10.1186/s12645-024-00273-3