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Published on: January 2, 2018
Interfering Expression of Chimeric Transcript SEPT7P2-PSPH Promotes Cell Proliferation in Patients with
Jing Wang1,2, Guo-Feng Xie1,2, Yuan He1,2
1State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Sun Yat-sen University Cancer Center, No. 651 Dongfeng East Road, Guangzhou 510060, China.
A novel chimeric transcript, SEPT7P2-PSPH, arises from trans-splicing in nasopharyngeal carcinoma (NPC). Low expression of this transcript promotes NPC cell growth and metastasis, suggesting it may act as a tumor suppressor.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Nasopharyngeal carcinoma (NPC) is a head and neck cancer prevalent in Southern China, characterized by genetic alterations.
- The role of fusion chimeric transcripts in NPC development is not well understood.
- Genetic changes, including chromosomal translocations, are implicated in NPC pathogenesis.
Purpose of the Study:
- To investigate the presence and function of fusion chimeric transcripts in NPC.
- To identify novel molecular mechanisms contributing to NPC development.
- To explore the potential of fusion transcripts as therapeutic targets or biomarkers.
Main Methods:
- RNA sequencing was employed to detect fusion genes in ten NPC tissue samples.
- Sanger sequencing and quantitative RT-PCR were utilized to quantify the fusion chimeric transcript levels.
- In vitro functional assays (CCK8, colony formation, migration/invasion) were performed to assess the transcript's role.
Main Results:
- The chimeric transcript SEPT7P2-PSPH was identified, formed by trans-splicing of adjacent genes without chromosomal rearrangement.
- This transcript was detected in both NPC patients and cell lines.
- Low expression of SEPT7P2-PSPH correlated with increased PSPH protein levels, promoting cell proliferation, invasion, and transformation in vitro.
Conclusions:
- The SEPT7P2-PSPH chimeric transcript is a product of adjacent gene trans-splicing in NPC.
- Its low expression appears to promote malignant phenotypes in NPC cells.
- SEPT7P2-PSPH may function as a tumor suppressor gene with potential anticancer activity.
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