Related Experiment Video
Updated: Nov 24, 2025

CRISPR Gene Editing Tool for MicroRNA Cluster Network Analysis
Published on: April 25, 2022
Long noncoding RNA small nucleolar RNA host gene 15 deteriorates liver cancer via microRNA-18b-5p/LIM-only 4 axis
Wei Chen1, Li Huang2, Junhua Liang1
1Department of Gastroenterology, Xiangyang No.1 People's Hospital, Hubei University of Medicine, Xiangyang, China.
Abstract:
Extensive studies have explored the involvements of long noncoding RNAs (lncRNAs) in liver cancer. Limitedly, the concrete function of lncRNA small nucleolar RNA host gene 15 (SNHG15) is still elusive. Therefore, the work was initiated to unearth SNHG15-oriented mechanism in liver cancer. Liver cancer tissues were resected. The connection between SNHG15 expression with prognosis and clinicopathological traits of liver cancer patients was evaluated. Liver cancer cells SMMC-7721 were transfected with restored microRNA (miR)-18b-5p or depleted SNHG15 to discover their effects on the proliferation, migration, invasion, cycle arrest, and apoptosis of SMMC-7721 cells. The transfected SMMC-7721 cells were injected into nude mice for further investigation. SNHG15, miR-18b-5p, and LIM-only 4 (LMO4) expressions in tissues and cells were tested. The regulatory connections among SNHG15, miR-18b-5p, and LMO4 were detected. SNHG15 and LMO4 were overexpressed while miR-18b-5p was downregulated in liver cancer tissues and cells. Up-regulated SNHG15 was connected with inferior prognosis and aggressive behaviors of liver cancer patients. SNHG15 knockdown or miR-18b-5p restoration depressed SMMC-7721 cell growth in vivo and in vitro. SNHG15 bound to miR-18b-5p and miR-18b-5p targeted LMO4. The work has illuminated that silencing SNHG15 represses liver cancer progression by modulating miR-18b-5p and LMO4, indicating the therapeutic potency of SNHG15/miR-18b-5p/LMO4 axis in liver cancer.
Insights
This study reveals that long noncoding RNA SNHG15 promotes liver cancer by interacting with microRNA 18b-5p and LIM-only 4. Silencing SNHG15 inhibits liver cancer progression, suggesting a potential therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Long noncoding RNAs (lncRNAs) play roles in liver cancer, but the function of small nucleolar RNA host gene 15 (SNHG15) remains unclear.
- Understanding lncRNA mechanisms is crucial for developing novel liver cancer therapies.
Purpose of the Study:
- To investigate the role and mechanism of SNHG15 in liver cancer.
- To explore the regulatory network involving SNHG15, microRNA-18b-5p (miR-18b-5p), and LIM-only 4 (LMO4) in liver cancer progression.
Main Methods:
- Analysis of SNHG15 expression in liver cancer tissues and correlation with patient prognosis and clinicopathological features.
- In vitro and in vivo experiments using SMMC-7721 liver cancer cells with SNHG15 knockdown or miR-18b-5p restoration.
- Detection of SNHG15, miR-18b-5p, and LMO4 expression and investigation of their regulatory interactions.
Main Results:
- SNHG15 and LMO4 were upregulated, while miR-18b-5p was downregulated in liver cancer tissues and cells.
- High SNHG15 expression correlated with poor prognosis and aggressive tumor behavior.
- SNHG15 knockdown or miR-18b-5p restoration suppressed liver cancer cell proliferation, migration, and invasion.
- SNHG15 directly binds to miR-18b-5p, and miR-18b-5p targets LMO4.
Conclusions:
- Silencing SNHG15 inhibits liver cancer progression by modulating the miR-18b-5p/LMO4 axis.
- The SNHG15/miR-18b-5p/LMO4 pathway represents a potential therapeutic target for liver cancer treatment.
Related Concept Videos
MicroRNAs
MicroRNAs
lncRNA - Long Non-coding RNAs
lncRNA - Long Non-coding RNAs
siRNA - Small Interfering RNAs
In the cytoplasm, siRNA is processed from a double-stranded RNA, which comes from either endogenous DNA transcription or exogenous sources like a virus. This double-stranded RNA is then cleaved by the...
Types of RNA
RNA Performs Diverse...
