Silencing of long noncoding RNA MIAT inhibits the viability and proliferation of breast cancer cells by promoting miR-378a-5p expression

被引:4
|
作者
Yan, Chao [1 ,2 ]
Jin, Yue [3 ,4 ]
机构
[1] Xuzhou Med Univ, Med Lab, Affiliated Huaian Hosp, Huaian 223003, Jiangsu, Peoples R China
[2] Second Peoples Hosp Huaian, Huaian 223003, Jiangsu, Peoples R China
[3] Xuzhou Med Univ, Med Lab, Affiliated Huaian Hosp, 62, Huaihai South Rd, Huaian 223003, Jiangsu, Peoples R China
[4] Second Peoples Hosp Huaian, 62, Huaihai South Rd, Huaian 223003, Jiangsu, Peoples R China
来源
OPEN MEDICINE | 2023年 / 18卷 / 01期
关键词
breast cancer; MIAT; miR-378a-5p; viability; proliferation; APOPTOSIS; MIGRATION; IDENTIFICATION; INVASION; TARGETS; GENES; RISK;
D O I
10.1515/med-2023-0676
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Myocardial infarction-associated transcript (MIAT) is a long noncoding RNA that plays a critical role in a variety of diseases. Accordingly, this study probed into the possible interaction mechanism between MIAT and miR-378a-5p in breast cancer. Concretely, MIAT and miR-378a-5p expressions in breast cancer tissues and cells were measured. After transfection with siMIAT and miR-378a-5p inhibitor, the viability and proliferation of breast cancer cells were examined by cell counting kit-8 and colony formation assays. The expressions of apoptosis-related proteins were detected. According to the results, MIAT was highly expressed in breast cancer tissues and cells. MIAT silencing could decrease Bcl-2 expression, viability, and proliferation of breast cancer cells and increase the expressions of cleaved caspase-3 and Bax. MIAT and miR-378a-5p could directly bind to each other, and MIAT silencing promoted the expression of miR-378a-5p. miR-378a-5p expression was low in breast cancer tissues. The miR-378a-5p inhibitor enhanced the viability and proliferation of breast cancer cells and partially reversed the effects of MIAT silencing on the breast cancer cells. In conclusion, MIAT silencing inhibits the viability and proliferation of breast cancer cells by promoting miR-378a-5p, indicating the potential of MIAT as a new target for the treatment of breast cancer.
引用
收藏
页数:12
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