RETRACTED: MiR-320d suppresses the progression of breast cancer via lncRNA HNF1A-AS1 regulation and SOX4 inhibition (Retracted article. See vol. 12, pg. 26639, 2022)

被引:7
|
作者
Shi, Shuai [1 ]
Hu, Xiaoling [2 ]
Xu, Jianpo [3 ]
Liu, Hong [1 ]
Zou, Libo [1 ,4 ]
机构
[1] Zhejiang Normal Univ, Jinhua Peoples Hosp, Reprod Med Ctr, Biomed Res Ctr, Jinhua 321000, Peoples R China
[2] Zhejiang Univ, Dept Reprod Endocrinol, Sch Med, Affiliated Obstet & Gynecol Hosp, Hangzhou 310006, Zhejiang, Peoples R China
[3] Zhejiang Univ, Life Sci Inst, Hangzhou 310058, Zhejiang, Peoples R China
[4] 228 Xinhua Rd, Jinhua 321000, Zhejiang, Peoples R China
关键词
LONG NONCODING RNA; PROMOTES CELL-PROLIFERATION; HEPATOCELLULAR-CARCINOMA; MESENCHYMAL TRANSITION; COLORECTAL-CANCER; UP-REGULATION; MIGRATION; INVASION; METASTASIS; MICRORNA;
D O I
10.1039/c8ra01200h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
MicroRNA-320d (miR-320d) is a novel cancer-related miRNA and functions as a tumor suppressor in human cancers. However, the expression pattern and function of miR-320d in breast cancer remain largely unknown. In the present study, we found that the expression level of miR-320d in breast cancer tissues and cells was significantly lower than in non-tumor tissues and MCF-10A cells. Decreased miR-320d was associated with poor overall survival in patients with breast cancer. Overexpression of miR-320d inhibited proliferation, migration, and invasion and promoted apoptosis of breast cancer cells. In addition, the long non-coding RNA, HNF1A antisense RNA 1 (HNF1A-AS1) was up-regulated in both breast cancer tissues and cell lines. HNF1A-AS1 suppressed the expression and function of miR-320d. Moreover, SRY-related HMG-box 4 (SOX4) was speculated and confirmed as a target of miR-320d. We also demonstrated that HNF1A-AS1 may function as a sponge competitive endogenous RNA for miR-320d, and thus regulate the expression of SOX4. Taken together, our study has identified a novel signaling pathway through which miR-320d exerts its anti-carcinogenic roles and suggested that the HNF1A-AS1/miR-320d/SOX4 may be a potential target for the therapy of breast cancer.
引用
收藏
页码:19196 / 19207
页数:12
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