The Molecular Mechanism of LncRNA HOTAIR Regulating the Proliferation, Invasion and Migration of Lymphoma Cells through Target Gene miR-20a-5p.
10.19746/j.cnki.issn.1009-2137.2023.01.014
- Author:
A-Ming LEI
1
;
Ping-An ZHU
1
;
Li-Mei FU
1
;
Xin LIAO
2
;
Gu-Li AZI
3
;
Ping ZHU
4
,
5
Author Information
1. Department of Hematology, The First People's Hospital of Chenzhou City, Chenzhou 423000, Hunan Province, China.
2. Department of Hematology, The First People's Hospital of Chenzhou City, Chenzhou 423000, Hunan Province, China.E-mail: 2449902032@qq.com.
3. Department of Hematology, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi 830001, Xinjiang Uygur Autonomous Region, China.
4. Department of Hematology, The First People's Hospital of Chenzhou City, Chenzhou 423000, Hunan Province, China.E-mail: zhupingno1@
5. com.
- Publication Type:Journal Article
- Keywords:
HOTAIR;
invasion;
lymphoma;
miR-20a-5p;
migration;
proliferation
- MeSH:
Humans;
Cell Line, Tumor;
Cell Movement/genetics*;
Cell Proliferation;
Gene Expression Regulation, Neoplastic;
Lymphoma;
MicroRNAs/genetics*;
RNA, Long Noncoding/genetics*;
RNA, Small Interfering
- From:
Journal of Experimental Hematology
2023;31(1):89-95
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To investigate the effects of lncRNA HOTAIR on the proliferation, invasion and migration of lymphoma cells through target gene miR-20a-5p and its molecular mechanism.
METHODS:After synthesizing HOTAIR siRNA and siRNA NC plasmids, they were transfected into lymphoma Raji cells, respectively. The expression of HOTAIR mRNA was detected by RT-qPCR. The proliferation, invasion and migration of lymphoma Raji cells were detected by CCK-8 assay, Transwell assay and cell scratch healing assay, respectively. The target gene of lncRNA HOTAIR was predicted by miRcode software, and the relationship between HOTAIR and target gene was analyzed by dual luciferase assay. After synthesis of miR-20a-5p inhibitor and inhibitor NC, Raji cells were transiently transfected. The expression of miR-20a-5p was detected by RT-qPCR, and the effects of down-regulation of miR-20a-5p on the proliferation, invasion and migration of Raji cells were analyzed. The overexpression plasmid of lncRNA HOTAIR and miR-20a-5p mimics were transfected into Raji cells simultaneously to analyze the proliferation, invasion and migration ability of Raji cells. After overexpression or down-regulation of miR-20a-5p, the expression of JAK/STAT3 signaling pathway related proteins was analyzed.
RESULTS:HOTAIR expression in Raji cells was decreased after transfection of HOTAIR siRNA (P<0.01), and miR-20a-5p expression was also decreased after transfection of miR-20a-5p inhibitor (P<0.01). HOTAIR had a targeting and negative regulation relationship with miR-20a-5p (r=-0.826). Silencing HOTAIR promoted the expression of miR-20a-5p and inhibited the proliferation, invasion and migration of Raji cells. Down-regulation of miR-20a-5p expression promoted the proliferation, invasion and migration of Raji cells. Effect of HOTAIR overexpression on the proliferation, invasion and migration of Raji cells could be reversed by up-regulation of miR-20a-5p. Down-regulation of miR-20a-5p expression activated the intracellular JAK/STAT3 signaling pathway.
CONCLUSION:HOTAIR affects the proliferation, invasion and migration of lymphoma cells by targeting miR-20a-5p, and its mechanism may be related to the activation of JAK/STAT3 signaling pathway.
