Mechanism of hsa-miR-222-3p Targeting Integrin Subunit Beta 3 to Regulate Malignant Behavior of Colorectal Cancer HT29 Cells

被引:0
|
作者
Li, Meng [1 ]
Ni, Qianyang [1 ]
Yu, Suyang [1 ]
机构
[1] Hebei Med Univ, Hosp Affiliated 3, Dept Gastrointestinal Surg, Shijiazhuang 050051, Peoples R China
关键词
by Ingenta Colorectal Cancer; miR-222-3p; Proliferation; Migration; Invasion; ITGB3; POTENTIAL BIOMARKERS; METASTASIS; CARCINOMA;
D O I
10.1166/sam.2023.4534
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Colorectal cancer (CRC) is a prevalent malignancy worldwide, and microRNAs (miRNAs) have been recognized for their significant role in CRC progression and potential as therapeutic targets. This study aimed to investi-gate the impact of miR-222-3p on CRC cell proliferation, migration, and invasion, along with its target genes. HT29 cells were transfected with mimic-negative control (mimic-NC) or mimic-miR-222-3p, while the control group remained untreated. Cell proliferation, migration, and invasion were assessed using CCK-8 and Tran-swell assays. qRT-PCR and Western blotting were employed to measure gene mRNA and protein expression, respectively. A luciferase reporter assay verified the binding between miR-222-3p and its downstream target gene ITGB3. The results revealed that enhanced miR-222-3p expression significantly increased HT29 cell pro-liferation, migration, and invasion. qRT-PCR and Western blotting indicated reduced expression of ITGB3 and E-cadherin, and upregulation of Vimentin and a-SMA by miR-222-3p. The luciferase reporter assay confirmed ITGB3 as a direct target of miR-22-p.In conclusion, miR-222-3p promotes CRC progression by regulating IP: 203.8.109.10 On: Tue, 31 Oct 2023 09:29:27 ITGB3 expression, suggesting its potential as a cruial biomarker and terapeutic target for colorectal cancer. Copyright: American Scientific Publishers
引用
收藏
页码:1401 / 1408
页数:8
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