Long Non-Coding Ribonucleic Acid Forkhead Box P4-Antisense RNA 1 Targets microRNA-655-3p to Regulate the Proliferation, Transfer, and Invasion of Mammary Cancer Cells

Author:

Hu Zhe1,Wang Peien2,Miao Beibei2,Qu Haijiang3

Affiliation:

1. Department of Surgical Oncology, Taizhou Central Hospital (Taizhou University Affiliated Hospital), Taizhou 318000, Zhejiang, PR China

2. Department of Surgical Oncology, Taizhou Cancer Hospital, Taizhou 317502, Zhejiang, PR China

3. Department of Thyroid and Breast, Shulan (Hangzhou) Hospital Affiliated to Zhejiang Shuren University Shulan International Medical College, Hangzhou 310006, Zhejiang, PR China

Abstract

LncRNA FOXP4-AS1 expresses at a higher level in gastric carcinoma cells and can promote proliferation and other biological behaviors. However, the effect of FOXP4-AS1 on mammary cancer cells has not yet been elucidated. Therefore, this article explores the influence of lncRNA FOXP4-AS1 on the proliferation and other biological processes of mammary cancer MDA-MB-231 cells via its regulation of miRNA-655-3p. Firstly, nanoPCR was used to quantify the expression of FOXP4-AS1 and miRNA-655-3p in mammary cancer tissues and adjacent tissues. Compared to the adjacent tissues, the expression level of FOXP4-AS1 in mammary cancer tissue was significantly increased, while that of miRNA-655-3p was substantially reduced. Then, si-FOXP4-AS1, miRNA-655-3p mimics, si-FOXP4-AS1 + anti-miRNA-655-3p were transfected into human mammary cancer MDA-MB-231 cells. The transfection of si-FOXP4-AS1 or miRNA-655-3p mimics considerably reduced cell viability and the protein levels of Ki-67 and MMPs. The transfection of si-FOXP4-AS1 or miRNA-655-3p mimics could reduce cell migration and invasion. The dual-luciferase reporter assays revealed that FOXP4-AS1 could target miRNA-655-3p. The co-transfection of si-FOXP4-AS1 and anti-miRNA-655-3p increased cell viability, migration, and invasion; the same co-transfection also elevated the protein levels of Ki-67 and MMPs. In conclusion, this study suggests that knocking down FOXP4-AS1’s expression can reduce mammary cancer cells’ ability to proliferate and execute other biological processes by targeting the expression of miRNA-655-3p.

Publisher

American Scientific Publishers

Subject

Biomedical Engineering,Medicine (miscellaneous),Bioengineering,Biotechnology

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