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RNA Pull-down Procedure to Identify RNA Targets of a Long Non-coding RNA
Published on: April 10, 2018
Long Noncoding RNA GUSBP11 Knockdown Alleviates Nasopharyngeal Carcinoma via Regulating miR-1226-3p/TM9SF4 Axis
Xiaofeng Zhang1, Jinzhi Liu2, MengMeng Ji3
1Department of Otolaryngology, Head and Neck Surgery, Weihai Maternal and Child Health Hospital, Affiliated Weihai Hospital of Qingdao University, Weihai, China.
Abstract:
Long noncoding RNAs (lncRNAs) have been confirmed related to the occurrence and progress of multiple cancers, including cervical cancer nasopharyngeal carcinoma (NPC). This study focused on assessing GUSBP11 effects on NPC progression and exploring possible mechanisms. RT-qPCR was conducted for assessing GUSBP11 levels within NPC tissues and cells. CCK-8, colony formation, and Transwell were adopted for examining GUSBP11 impacts on NPC cell proliferation and cell metastasis. RT-qPCR analysis and dual-luciferase reporter assay were conducted for judging the expression interrelation of GUSBP11 and its potential target miR-1226-3p. The same methods were carried out for verifying the inhibiting influences of miR-1226-3p upregulation and its potential target TM9SF4. GUSBP11 levels were upregulated within NPC tissues and cells. GUSBP11 downregulation repressed NPC cell proliferation and cell metastasis. In addition, GUSBP11 targeted and negatively regulated miR-1226-3p. Furthermore, miR-1226-3p targeted TM9SF4 and mediated GUSBP11's impacts on TM9SF4 levels. At last, the authors proved the critical role of the GUSBP11/miR-1226-3p/TM9SF4 axis in regulating NPC progression. These findings indicate that downregulation of GUSBP11 alleviates NPC development by regulating the miR-1226-3p/TM9SF4 axis.
Insights
Downregulating long noncoding RNA GUSBP11 inhibits nasopharyngeal carcinoma (NPC) progression by affecting the miR-1226-3p/TM9SF4 axis. This study reveals a novel therapeutic target for NPC treatment.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Long noncoding RNAs (lncRNAs) are implicated in various cancers, including nasopharyngeal carcinoma (NPC).
- Understanding the role of specific lncRNAs like GUSBP11 in NPC progression is crucial for developing targeted therapies.
Purpose of the Study:
- To investigate the functional role of GUSBP11 in nasopharyngeal carcinoma (NPC) progression.
- To elucidate the underlying molecular mechanisms involving GUSBP11, miR-1226-3p, and TM9SF4 in NPC.
Main Methods:
- Quantitative real-time PCR (RT-qPCR) to assess GUSBP11 expression in NPC tissues and cells.
- Cell proliferation and migration assays (CCK-8, colony formation, Transwell) to evaluate GUSBP11's functional impact.
- Dual-luciferase reporter assays to confirm interactions between GUSBP11, miR-1226-3p, and TM9SF4.
Main Results:
- GUSBP11 expression was significantly upregulated in NPC tissues and cells.
- Downregulation of GUSBP11 suppressed NPC cell proliferation and metastasis.
- GUSBP11 was found to directly target and negatively regulate miR-1226-3p.
- miR-1226-3p was confirmed to target TM9SF4, mediating GUSBP11's effect on TM9SF4 levels.
Conclusions:
- The GUSBP11/miR-1226-3p/TM9SF4 axis plays a critical role in regulating NPC progression.
- Downregulation of GUSBP11 alleviates NPC development by modulating the miR-1226-3p/TM9SF4 pathway.
- Targeting the GUSBP11/miR-1226-3p/TM9SF4 axis presents a potential therapeutic strategy for NPC.
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