miR‐224‐5p inhibits proliferation, migration, and invasion by targeting PIK3R3/AKT3 in uveal melanoma

• Published in: Journal of cellular biochemistry 2019-08, Vol.120 (8), p.12412-12421
• Main Authors: Li, Jianchang, Liu, Xiuming, Li, Chaopeng, Wang, Wenqi
• Format: Article
• Language: English
• Subjects: 1-Phosphatidylinositol 3-kinase; AKT protein; AKT3; Assaying; Cell migration; Cell proliferation; invasion; Malignancy; Melanoma; migration; miRNA; miR‐224‐5p; Motility; PIK3R3; Polymerase chain reaction; proliferation; uveal melanoma; Wound healing
• ISSN: 0730-2312; 1097-4644
• DOI: 10.1002/jcb.28507

Uveal melanoma (UM) is the most common primary intraocular malignancy in adults. Accumulating investigations have identified the aberrant expression of miRNAs (microRNAs) in UM, such as miR‐181, miR‐20a, miR‐144, miR‐146a. The purpose of this study is to investigate the biological function of miR‐224‐5p in UM. The expression of miR‐224‐5p, PIK3R3, and AKT3 in 30 tumor tissues and paired adjacent noncancerous tissues were analyzed using Western blot analysis and quantitative real‐time polymerase chain reaction (qRT‐PCR) assays. Cell proliferation assay, transwell assay, and wound healing assay were used to measure the effects of miR‐224‐5p on the motility of UM in vitro. Western blot analysis and luciferase assays were used to detect the expression of PIK3R3 and AKT3 as miR‐224‐5p downstream targets. The results of Western blot analysis and qRT‐PCR assays indicated that the expression of miR‐224‐5p was lower in UM tissues compared to normal tissue, while the expression of PIK3R3 and AKT3 were simultaneously increased. Upregulation of miR‐224‐5p significantly inhibited capacities of proliferation, invasion, and migration of OCM‐1A cells and decreased expression of PIK3R3 and AKT3. Luciferase assay demonstrated PIK3R3 and AKT3 as downstream targets of miR‐224‐5p. Moreover, upregulating PIK3R3 and AKT3 restrained miR‐224‐5p‐induced inhibition of the motility of OCM‐1A cells. Thus, our study proved that miR‐224‐5p was involved in proliferation, invasion, and migration of UM cells via regulation the expression of PIK3R3 and AKT3. And the results also established a miR‐224‐5p/PIK3R3/PI3K/AKT axis in the regulation of UM progression, providing an experimental basis for further exploring the miR‐224‐5p as a therapeutic and diagnosis target for patients with UM. 1. Upregulation of miR‐224‐5p significantly inhibited capacities of proliferation, invasion, and migration of OCM‐1A cells. 2. Upregulation of miR‐224‐5p decreased expression of PIK3R3 and AKT3. 3. Established a miR‐224‐5p/PIK3R3/PI3K/AKT axis in the regulation of uveal melanoma progression.