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Updated: Jun 12, 2025

In Silico Identification and Characterization of circRNAs During Host-Pathogen Interactions
Published on: October 21, 2022
Circular RNA hsa_circRNA_101996 modulates gastric cancer cell proliferation and apoptosis through the miR-577/HMGN5
Xiao-Lei Wang1, Lin Zhang2, Qing Shang3
1Department of General Surgery, Xinxiang Central Hospital, Xinxiang 453000, Henan Province, China. wangxl305@163.com.
Background:
Circular RNAs (circRNAs) are critical regulators in tumorigenesis, functioning as microRNA sponges or protein decoys. Although numerous circRNAs have been implicated in gastric cancer progression, the role of hsa_circRNA_101996 remains unclear. This study hypothesizes that hsa_circRNA_101996 promotes gastric cancer cell proliferation and apoptosis via the microRNA-577 (miR-577)/high mobility group nucleosome binding domain 5 (HMGN5) axis.
Aim:
To investigate the role of hsa_circRNA_101996 in gastric cancer proliferation and apoptosis through the miR-577/HMGN5 axis.
Methods:
Forty-one paired gastric cancer tissues and adjacent non-cancerous tissues were analyzed. Differential circRNA expression was identified using GSE83521 and GSE89143 datasets. miR-577 and HMGN5 were predicted via CircInteractome and TargetScan. Functional experiments (MTT, colony formation, Western blot) and dual-luciferase reporter assays were performed in gastric cancer cell lines (OCUM-1, HSC-39). In vivo tumorigenesis was validated in nude mice. Statistical analysis included Student's t-test and one-way ANOVA (P < 0.05).
Results:
Hsa_circRNA_101996 was significantly upregulated in gastric cancer tissues and cell lines compared to adjacent non-cancerous tissues (P < 0.05). Dual-luciferase reporter assays validated the interactions among hsa_circRNA_101996, miR-577, and HMGN5. In vitro, gastric cancer cells overexpressing hsa_circRNA_101996 showed significantly increased proliferation and decreased apoptosis compared to controls (P < 0.05). Cells transfected with miR-577 mimics exhibited reduced proliferation and increased apoptosis (P < 0.05). Co-transfection with hsa_circRNA_101996 or HMGN5 reversed the effects of miR-577 mimics. In vivo, hsa_circRNA_101996-overexpressing tumors showed increased volume and HMGN5 expression (P < 0.05).
Conclusion:
Hsa_circRNA_101996 promotes gastric cancer progression by sponging miR-577 to upregulate HMGN5, suggesting a novel therapeutic target for gastric cancer.
Insights
Circular RNAs (circRNAs) promote gastric cancer by upregulating HMGN5 via sponging miR-577. This study identifies hsa_circRNA_101996 as a potential therapeutic target for gastric cancer treatment.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Circular RNAs (circRNAs) are key regulators in cancer development.
- While many circRNAs are linked to gastric cancer, the function of hsa_circRNA_101996 is not well understood.
- This study investigates hsa_circRNA_101996's role in gastric cancer.
Purpose of the Study:
- To determine the role of hsa_circRNA_101996 in gastric cancer cell proliferation and apoptosis.
- To elucidate the mechanism involving microRNA-577 (miR-577) and high mobility group nucleosome binding domain 5 (HMGN5).
Main Methods:
- Analysis of 41 paired gastric cancer tissues and adjacent non-cancerous tissues.
- Utilized bioinformatics datasets (GSE83521, GSE89143) for differential circRNA expression analysis.
- Performed in vitro experiments (MTT, colony formation, Western blot, dual-luciferase reporter assays) and in vivo tumorigenesis studies in nude mice.
Main Results:
- Hsa_circRNA_101996 was significantly upregulated in gastric cancer tissues and cell lines.
- Validated interactions between hsa_circRNA_101996, miR-577, and HMGN5.
- Overexpression of hsa_circRNA_101996 increased proliferation and decreased apoptosis in vitro, while miR-577 mimics had opposite effects. In vivo studies confirmed increased tumor volume and HMGN5 expression.
Conclusions:
- Hsa_circRNA_101996 promotes gastric cancer progression by acting as a sponge for miR-577, leading to increased HMGN5 expression.
- This circRNA-miRNA-mRNA axis represents a potential novel therapeutic target for gastric cancer.
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