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Updated: Feb 3, 2026

Overexpressing Long Noncoding RNAs Using Gene-activating CRISPR
Published on: March 1, 2019
Long-noncoding RNA IFNG-AS1 exerts oncogenic properties by interacting with epithelial splicing regulatory protein 2
Guohui Lu1, Jian Duan1, Dongwei Zhou1
1Department of Neurosurgery, The First Affiliated Hospital of Nanchang University, Nanchang 330006, China.
Abstract:
Despite the enormous development of medical technologies in recent decades, pituitary adenoma (PA) remains among the most refractory cancers in the world. Elucidating the molecular mechanisms underlying the pathology of PA is essential to identify new treatments for PA. In the present study, we found that IFNG-AS1 expression was significantly higher in PA tissues than in nontumor tissues via qRT-PCR and RNA fluorescence in situ hybridization (FISH). shRNA-mediated IFNG-AS1 knockdown in HP75 cells significantly inhibited tumor progression, and IFNG-AS1 overexpression remarkably promoted tumor progression. Epithelial splicing regulatory protein 2 (ESRP2) was demonstrated to be a target protein of IFNG-AS1 in PA; knocking down ESRP2 reversed the tumor-inhibitory effects of IFNG-AS1 knockdown, and overexpressing ESRP2 abolished the tumor-promoting effects of IFNG-AS1 overexpression in HP75 cells. In conclusion, our findings suggested that IFNG-AS1 may function as an oncogene in PA by interacting with ESRP2.
Insights
Pituitary adenoma (PA) is a challenging cancer. This study reveals that IFNG-AS1 acts as an oncogene in PA by interacting with ESRP2, suggesting new therapeutic targets for pituitary adenoma.
Area of Science:
- Oncology
- Molecular Biology
- Endocrinology
Background:
- Pituitary adenoma (PA) remains a difficult-to-treat cancer despite medical advancements.
- Understanding the molecular underpinnings of PA is crucial for developing novel therapeutic strategies.
Purpose of the Study:
- To investigate the role of IFNG-AS1 in the molecular mechanisms of pituitary adenoma.
- To identify potential molecular targets for PA treatment.
Main Methods:
- Quantitative real-time PCR (qRT-PCR) and RNA fluorescence in situ hybridization (FISH) were used to assess IFNG-AS1 expression.
- shRNA-mediated knockdown and overexpression techniques were employed in HP75 cells to study the functional impact of IFNG-AS1 and ESRP2.
- Interaction between IFNG-AS1 and Epithelial splicing regulatory protein 2 (ESRP2) was investigated.
Main Results:
- IFNG-AS1 expression was significantly elevated in PA tissues compared to non-tumor tissues.
- Knockdown of IFNG-AS1 inhibited tumor progression, while its overexpression promoted it.
- ESRP2 was identified as a target of IFNG-AS1, with its modulation affecting tumor progression in response to IFNG-AS1 manipulation.
Conclusions:
- IFNG-AS1 functions as an oncogene in pituitary adenoma.
- The oncogenic role of IFNG-AS1 in PA is mediated through its interaction with ESRP2.
- Targeting the IFNG-AS1/ESRP2 pathway may offer a novel therapeutic approach for pituitary adenoma.
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