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Published on: March 30, 2019
Long Noncoding MAGI2-AS3 Suppresses Several Cellular Processes of Lung Squamous Cell Carcinoma Cells by Regulating
Jia He1,2, Xiaoyun Zhou1,2, Li Li1,2
1Department of Thoracic Surgery, Peking Union Medical College Hospital, Beijing 100730, People's Republic of China.
Background:
Lung squamous cell carcinoma (LUSC) accounts for approximately 30% of all lung cancers that possesses the highest occurrence and mortality in all cancer types. Long noncoding RNAs have been reported to modulate tumor development for several decades.
Aim Of The Study:
This research aims to investigate the role of MAGI2-AS3 in LUSC.
Methods:
RT-qPCR tested genes (including MAGI2-AS3, miR-374a/b-5p and CADM2) expression. Cell proliferation was detected by colony formation and EdU assays. Cell migration and invasion were evaluated by transwell assay. Flow cytometry analysis of apoptotic cells and Western blot analysis on apoptosis-related genes were applied to measure cell apoptosis. Nuclear-cytoplasmic fractionation and FISH assay positioned MAGI2-AS3. The combination between miR-374a/b-5p and MAGI2-AS3 (or CADM2) was determined by luciferase reporter assay and RIP assay.
Results:
MAGI2-AS3 inhibited the proliferative, migratory and invasive capability of LUSC cells with upregulated expression. Additionally, MAGI2-AS3 overexpression promoted cell apoptosis. We discovered that MAGI2-AS3 was located in the cytoplasm. Hereafter, we found out that MAGI2-AS3 targeted miR-374a/b-5p. CADM2 was targeted by miR-374a/b-5p. Finally, rescue assays indicated that the promoting effects of miR-374a/b-5p amplification on biological activities were restored by CADM2 addition.
Conclusion:
In conclusion, lncRNA MAGI2-AS3 suppressed LUSC by regulating miR-374a/b-5p/CADM2 axis, which might potentially serve as a therapeutic marker for LUSC patients.
Insights
Long noncoding RNA MAGI2-AS3 inhibits lung squamous cell carcinoma (LUSC) progression by targeting the miR-374a/b-5p/CADM2 pathway. This finding suggests MAGI2-AS3 as a potential therapeutic marker for LUSC.
Area of Science:
- Oncology
- Molecular Biology
- Gene Regulation
Background:
- Lung squamous cell carcinoma (LUSC) is a major cause of cancer mortality.
- Long noncoding RNAs (lncRNAs) are increasingly recognized for their roles in cancer development.
Purpose of the Study:
- To investigate the function of MAGI2-AS3 in LUSC.
- To elucidate the molecular mechanism of MAGI2-AS3 in LUSC progression.
Main Methods:
- Gene expression analysis (RT-qPCR) for MAGI2-AS3, miR-374a/b-5p, and CADM2.
- Cellular assays including proliferation (colony formation, EdU), migration, invasion (Transwell), and apoptosis (flow cytometry, Western blot).
- Molecular assays (nuclear-cytoplasmic fractionation, FISH, luciferase reporter, RIP) to determine MAGI2-AS3 localization and interactions.
Main Results:
- MAGI2-AS3 expression was upregulated and inhibited LUSC cell proliferation, migration, and invasion.
- MAGI2-AS3 overexpression promoted apoptosis in LUSC cells.
- MAGI2-AS3 acts as a sponge for miR-374a/b-5p, which targets CADM2, revealing the MAGI2-AS3/miR-374a/b-5p/CADM2 regulatory axis.
Conclusions:
- lncRNA MAGI2-AS3 suppresses LUSC progression through the miR-374a/b-5p/CADM2 pathway.
- MAGI2-AS3 holds potential as a therapeutic target or biomarker for LUSC.
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