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AFAP1-AS1: a rising star among oncogenic long non-coding RNAs
Authors:Xiong  Fang  Zhu  Kunjie  Deng  Su  Huang  Hongbin  Yang  Liting  Gong  Zhaojian  Shi  Lei  He  Yi  Tang  Yanyan  Liao  Qianjin  Yu  Jianjun  Li  Xiaoling  Li  Yong  Li  Guiyuan  Zeng  Zhaoyang  Xiong  Wei  Zhang  Shanshan  Guo  Can
Institution:1.Science and Technology on Information System Engineering Laboratory, National University of Defense Technology, Changsha, 410000, China
;2.Department of Periodontology, Center of Stomatology, Xiangya Hospital, Central South University, Changsha, 410078, China
;3.NHC Key Laboratory of Carcinogenesis and Key Laboratory of Carcinogenesis and Cancer Invasion of Ministry of Education of China, Cancer Research Institute, Central South University, Changsha, 410078, China
;4.Hunan Key Laboratory of Cancer Metabolism, Hunan Cancer Hospital and the Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, 410013, China
;5.Department of Oral and Maxillofacial Surgery, The Second Xiangya Hospital Central South University, Changsha, 410011, China
;6.Department of Medicine, Dan L Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, Texas, USA
;
Abstract:Long non-coding RNAs(lnc RNAs) have become a hotspot in biomedical research. This interest reflects their extensive involvement in the regulation of the expression of other genes, and their influence on the occurrence and development of a variety of human diseases. Actin filament associated protein 1-Antisense RNA 1(AFAP1-AS1) is a recently discovered oncogenic lnc RNA. It is highly expressed in a variety of solid tumors, and regulates the expression of downstream genes and signaling pathways through adsorption and competing micro RNAs, or by the direct binding to other proteins. Ultimately, AFAP1-AS1 promotes proliferation, chemotherapy resistance, and resistance to apoptosis, maintains stemness, and enhances invasion and migration of tumor cells. This paper summarizes the research concerning AFAP1-AS1 in malignant tumors, including the clinical application prospects of AFAP1-AS1 as a potential molecular marker and therapeutic target of malignant tumors. We also discuss the limitations in the knowledge of AFAP1-AS1 and directions of further research. AFAP1-AS1 is expected to provide an example for studies of other lnc RNA molecules.
Keywords:
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