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LncRNA SNHG7 Functions as an Oncogene in Cervical Cancer by Sponging miR-485-5p to Modulate JUND Expression
Danyang Zhao1, Hui Zhang2, Jianxiong Long3
1Department of Reproductive Center, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Province, People's Republic of China.
Background:
Long non-coding RNA (LncRNA) SNHG7 is involved in the development of multiple cancers. However, its role in cervical cancer (CC) has not been elucidated. This study aimed to explore the function of SNHG7 in CC progression and the underlying mechanisms.
Materials And Methods:
The expression levels of SNHG7 and miR-485-5p in CC tissues and cell lines were measured by qPCR. Functional experiments including CCK-8 assay, wound healing assay, transwell assay, flow cytometry, Western blot, luciferases reporter assay and immunoprecipitation (RIP) were performed to explore the SNHG7/miR-485-5p/JUND pathway. Additionally, in vivo study was carried out by establishing tumor xenograft models.
Results:
We found that SNHG7 was markedly enhanced in CC tissues and cell lines, and associated with poor clinical characteristics. In vitro, knockdown of SNHG7 inhibited CC cell proliferation, migration and invasion, as well as aggravated cell apoptosis. As to mechanism investigation, rescue experiments revealed that miR-485-5p inhibitor could partially reverse the effects on CC cells induced by SNHG7 knockdown. SNHG7 upregulated JUND expression via miR-485-5p. Moreover, tumor xenograft models were established to confirm the findings in vivo.
Conclusion:
SNHG7 promoted CC progression through miR-485-5p/JUND axis. The SNHG7/miR-485-5p/JUND pathway might provide a novel therapeutic target for CC treatment.
Insights
Long non-coding RNA SNHG7 promotes cervical cancer (CC) progression by upregulating JUND via miR-485-5p. This SNHG7/miR-485-5p/JUND pathway presents a potential therapeutic target for CC treatment.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Long non-coding RNA (LncRNA) SNHG7 is implicated in various cancers.
- The specific role of SNHG7 in cervical cancer (CC) progression remains unclear.
- This study investigates the function and mechanism of SNHG7 in CC.
Purpose of the Study:
- To elucidate the role of SNHG7 in cervical cancer progression.
- To explore the underlying molecular mechanisms involving SNHG7.
- To identify potential therapeutic targets for cervical cancer.
Main Methods:
- Quantitative real-time PCR (qPCR) to measure SNHG7 and miR-485-5p expression.
- In vitro assays (CCK-8, wound healing, Transwell, flow cytometry) to assess cell proliferation, migration, invasion, and apoptosis.
- Luciferase reporter assays, Western blot, and RNA immunoprecipitation (RIP) to investigate the SNHG7/miR-485-5p/JUND pathway.
- In vivo tumor xenograft models to validate findings.
Main Results:
- SNHG7 expression was significantly elevated in CC tissues and cell lines, correlating with poor clinical characteristics.
- Knockdown of SNHG7 suppressed CC cell proliferation, migration, and invasion, while enhancing apoptosis.
- SNHG7 upregulates JUND expression by sponging miR-485-5p, a mechanism confirmed in vitro and in vivo.
- MiR-485-5p inhibition partially reversed the effects of SNHG7 knockdown.
Conclusions:
- SNHG7 promotes cervical cancer progression via the miR-485-5p/JUND axis.
- The identified SNHG7/miR-485-5p/JUND pathway represents a promising novel therapeutic target for cervical cancer treatment.
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