| Literature DB >> 31331909 |
Zi-Qi Zheng1, Zhi-Xuan Li1, Guan-Qun Zhou1, Li Lin1, Lu-Lu Zhang1, Jia-Wei Lv1, Xiao-Dan Huang1, Rui-Qi Liu1, FoPing Chen1, Xiao-Jun He1, Jia Kou1, Jian Zhang1,2, Xin Wen1, Ying-Qin Li1, Jun Ma1, Na Liu3, Ying Sun3.
Abstract
Long noncoding RNAs (lncRNA) play important roles in the tumorigenesis and progression of cancers. However, the clinical significance of lncRNAs and their regulatory mechanisms in nasopharyngeal carcinogenesis (NPC) are largely unknown. Here, based on a microarray analysis, we identified 384 dysregulated lncRNAs, of which, FAM225A was one of the most upregulated lncRNAs in NPC. FAM225A significantly associated with poor survival in NPC. N(6)-Methyladenosine (m6A) was highly enriched within FAM225A and enhanced its RNA stability. FAM225A functioned as an oncogenic lncRNA that promoted NPC cell proliferation, migration, invasion, tumor growth, and metastasis. Mechanistically, FAM225A functioned as a competing endogenous RNA (ceRNA) for sponging miR-590-3p and miR-1275, leading to the upregulation of their target integrin β3 (ITGB3), and the activation of FAK/PI3K/Akt signaling to promote NPC cell proliferation and invasion. In summary, our study reveals a potential ceRNA regulatory pathway in which FAM225A modulates ITGB3 expression by binding to miR-590-3p and miR-1275, ultimately promoting tumorigenesis and metastasis in NPC. SIGNIFICANCE: These findings demonstrate the clinical significance of the lncRNA FAM225A in nasopharyngeal carcinoma (NPC) and the regulatory mechanism involved in NPC development and progression, providing a novel prognostic indicator and promising therapeutic target. ©2019 American Association for Cancer Research.Entities:
Mesh:
Substances:
Year: 2019 PMID: 31331909 DOI: 10.1158/0008-5472.CAN-19-0799
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701