Silencing LINC00663 inhibits inflammation and angiogenesis through downregulation of NR2F1 via EBF1 in bladder cancer

Bibliographic Details
Title: Silencing LINC00663 inhibits inflammation and angiogenesis through downregulation of NR2F1 via EBF1 in bladder cancer
Authors: Xiulong Zhong, Lijiang Sun, Junxiang Liu, Xiaokun Yang, Minghui Hou, Xinning Wang, Huifeng Diao
Source: RNA Biology, Vol 21, Iss 1, Pp 673-686 (2024)
Publisher Information: Taylor & Francis Group, 2024.
Publication Year: 2024
Collection: LCC:Genetics
Subject Terms: LINC00663, EBF1, nuclear receptor subfamily 2 group F member 1, bladder cancer, inflammation, angiogenesis, Genetics, QH426-470
More Details: This study is to elucidate the effect of the LINC00663/EBF1/NR2F1 axis on inflammation and angiogenesis in bladder cancer (BC) and related molecular mechanisms. After transfection, functional experiments were conducted to test cell proliferation and invasion, tube formation ability, and content of inflammatory factors, Snail, E-cadherin, and VEGFA. Meanwhile, the relationships among LINC00663, EBF1, and NR2F1 were predicted and verified. In addition, xenograft experiments in nude mice were performed to observe the oncogenicity of 5637 BC cells in vivo. In BC tissues and cells, LINC00663 and NR2F1 were upregulated. Silencing NR2F1 or LINC00663 repressed cell proliferation and invasion, weakened vascular mimicry in vitro, decreased inflammatory factor, Snail, and VEGFA levels, and increased expression of E-cadherin. LINC00663 positively regulated NR2F1 expression through EBF1. Additionally, in vivo experiments showed that NR2F1 upregulation reversed the suppression effects of LINC00663 silencing on tumour growth, inflammation, and angiogenesis. Silencing LINC00663 decreased NR2F1 expression by mediating EBF1, thereby inhibiting BC inflammation and angiogenesis.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 15476286
1555-8584
1547-6286
Relation: https://doaj.org/toc/1547-6286; https://doaj.org/toc/1555-8584
DOI: 10.1080/15476286.2024.2368304
Access URL: https://doaj.org/article/ea161a9f31ee454aad8d52b5d91e39ea
Accession Number: edsdoj.161a9f31ee454aad8d52b5d91e39ea
Database: Directory of Open Access Journals
More Details
ISSN:15476286
15558584
DOI:10.1080/15476286.2024.2368304
Published in:RNA Biology
Language:English