دورية أكاديمية

Hsa_circ_0006571 promotes spinal metastasis through sponging microRNA-138 to regulate sirtuin 1 expression in lung adenocarcinoma

التفاصيل البيبلوغرافية
العنوان: Hsa_circ_0006571 promotes spinal metastasis through sponging microRNA-138 to regulate sirtuin 1 expression in lung adenocarcinoma
المؤلفون: Wang, Hou-Lei, Wang, Hui-Ren, Liang, Yun, Hu, An-Nan, Enguita, Francisco J., Zhou, Xiao-Gang, Dong, Jian
المساهمون: Repositório da Universidade de Lisboa
بيانات النشر: AME Publishing Company, 2020.
سنة النشر: 2020
مصطلحات موضوعية: RNA circular, Lung adenocarcinoma, Metastasis, miR-138-5p, Spine
الوصف: Copyright © 2009 - 2021 AME Publishing Company. All rights reserved. Open Access Statement:This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0Test
الوصف (مترجم): Background: Circular RNAs (circRNAs) are known to participate in lung cancer. However, their role in spinal metastasis (SM) of lung adenocarcinoma remains elusive. In this study, we determined that hsa_circ_0006571 serves as a sponge for miR-138, which targets sirtuin 1 (Sirt1) in the development of SM. Methods: A human circRNA microarray was performed to compare SM and lung adenocarcinoma samples. The expression of hsa_circ_0006571 and miR-138 was determined using quantitative polymerase chain reaction (qPCR) in vitro and in vivo. Cell proliferation was performed by Cell Counting Kit-8 (CCK-8) and apoptosis was analyzed by Annexin V/PI staining. RNA-pulldown and RNA immunoprecipitation (RIP) were used to analyze the interaction between hsa_circ_0006571. Tumor metastasis was determined through a xenograft experiment in vivo. Results: Hsa_circ_0006571 was observed to be significantly upregulated in SM tissues through circRNA microarray and qPCR. We detected a lower expression of miR-138 in SM tissues compared with lung adenocarcinoma. Hsa_circ_0006571 silencing suppressed lung cancer cell proliferation and migration while promoting apoptosis. Hsa_circ_0006571 interacted with miR-138 to promote expression of Sirt1, leading to activation of epithelial-mesenchymal transition (EMT). Xenograft experiments showed that downregulation of hsa_circ_0006571 delayed the SM of lung adenocarcinoma cells via the miR-138-Sirt1 axis. Conclusions: Hsa_circ_0006571 promoted tumor cell migration and invasion via the miR-138/Sirt1 pathway. Our observations indicate that circRNAs are possible novel therapeutic targets for SM of lung adenocarcinoma.
This work was supported by the National Natural Science Foundation of China (81572629, 81772855 and 81701370).
نوع الوثيقة: journal article
وصف الملف: application/pdf
اللغة: English
العلاقة: Transl Lung Cancer Res. 2020 Dec;9(6):2411-2427; 2218-6751; 2226-4477
DOI: 10.21037/tlcr-20-1250
الإتاحة: http://hdl.handle.net/10451/47248Test
حقوق: open access
رقم الانضمام: rcaap.com.ul.repositorio.ul.pt.10451.47248
قاعدة البيانات: RCAAP