دورية أكاديمية

Nuclear respiratory factor 1 drives hepatocellular carcinoma progression by activating LPCAT1-ERK1/2-CREB axis

التفاصيل البيبلوغرافية
العنوان: Nuclear respiratory factor 1 drives hepatocellular carcinoma progression by activating LPCAT1-ERK1/2-CREB axis
المؤلفون: Ran Liu, Chuanzheng Yin, Peng Zhao, Bing Guo, Wenbo Ke, Xichuan Zheng, Dawei Xie, Yaofeng Wang, Gengqiao Wang, Yinzhao Jia, Yang Gao, Wenjun Hu, Gang Logan Liu, Zifang Song
المصدر: Biology Direct, Vol 18, Iss 1, Pp 1-20 (2023)
بيانات النشر: BMC, 2023.
سنة النشر: 2023
المجموعة: LCC:Biology (General)
مصطلحات موضوعية: NRF1, LPCAT1, Hepatocellular carcinoma, Progression, Positive feedback loop, Biology (General), QH301-705.5
الوصف: Abstract Background Nuclear respiratory factor 1 (NRF1) is a transcription factor that participates in several kinds of tumor, but its role in hepatocellular carcinoma (HCC) remains elusive. This study aims to explore the role of NRF1 in HCC progression and investigate the underlying mechanisms. Results NRF1 was overexpressed and hyperactive in HCC tissue and cell lines and high expression of NRF1 indicated unfavorable prognosis of HCC patients. NRF1 promoted proliferation, migration and invasion of HCC cells both in vitro and in vivo. Mechanistically, NRF1 activated ERK1/2-CREB signaling pathway by transactivating lysophosphatidylcholine acyltransferase 1 (LPCAT1), thus promoting cell cycle progression and epithelial mesenchymal transition (EMT) of HCC cells. Meanwhile, LPCAT1 upregulated the expression of NRF1 by activating ERK1/2-CREB signaling pathway, forming a positive feedback loop. Conclusions NRF1 is overexpressed in HCC and promotes HCC progression by activating LPCAT1-ERK1/2-CREB axis. NRF1 is a promising therapeutic target for HCC patients.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1745-6150
Relation: https://doaj.org/toc/1745-6150
DOI: 10.1186/s13062-023-00428-z
URL الوصول: https://doaj.org/article/e635c01c6d284aeb851bb10e8042d600
رقم الأكسشن: edsdoj.635c01c6d284aeb851bb10e8042d600
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:17456150
DOI:10.1186/s13062-023-00428-z