Abstract | OBJECTIVE: METHODS: The levels of lncRNA FGF14-AS2, miR-96-5p, and Adherens junction-associated protein-1 (AJAP1) in prostate carcinoma were tested by Western blot and qRT-PCR. How these two genes interacted was confirmed by RNA immunoprecipitation and dualluciferase gene methods. The effect of FGF14-AS2/miR-96-5p/AJAP1 axis in prostate carcinoma progression was determined by MTT, Transwell, and nude mice tumor model. RESULTS: FGF14-AS2 was a downregulated lncRNA in prostate carcinoma tissue and cells. FGF14-AS2 could restrain miR-96-5p expression while miR-96-5p hampered AJAP1. FGF14-AS2 could effectively decrease the biological behaviors of prostate carcinoma cells, while knock-down of FGF14-AS2 triggered opposite results. Moreover, miR-96-5p mimic presented a cancer promoter role in prostate carcinoma cells. AJAP1 expression level could affect levels of proteins related to epithelial-mesenchymal transition. In vivo experiment suggested that overexpressing FGF14-AS2 could reverse the promotion of silenced AJAP1 on prostate carcinoma cell metastasis, thus to inhibit tumor growth. CONCLUSION:
lncRNA FGF14-AS2 was a downregulated lncRNA in prostate carcinoma and influenced cell proliferation and metastasis. The influence relied on modulating miR-96-5p and its target gene AJAP1.
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Authors | Rubing Li, Yingcong Chen, Jingwei Wu, Xiaobo Cui, Sinian Zheng, Huaqing Yan, Yiming Wu, Feng Wang |
Journal | Journal of clinical laboratory analysis
(J Clin Lab Anal)
Vol. 35
Issue 11
Pg. e24012
(Nov 2021)
ISSN: 1098-2825 [Electronic] United States |
PMID | 34655124
(Publication Type: Journal Article)
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Copyright | © 2021 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. |
Chemical References |
- AJAP1 protein, human
- Cell Adhesion Molecules
- MIRN96 microRNA, human
- MicroRNAs
- RNA, Long Noncoding
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Topics |
- Animals
- Cell Adhesion Molecules
(genetics, metabolism)
- Disease Progression
- Humans
- Male
- Mice
- Mice, Nude
- MicroRNAs
(genetics, metabolism)
- Prostate
(metabolism)
- Prostatic Neoplasms
(genetics, metabolism, pathology)
- RNA, Long Noncoding
(genetics, metabolism)
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