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Published on: November 29, 2016
LncRNA SOX2OT affects cervical cancer cell growth, migration and invasion by regulating SOX2
Xiaohan Chang1, Huijie Zhang1, Qing Yang1
1Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University , Shenyang, People's Republic of China.
Abstract:
Long non-coding RNA (lncRNA) SOX2 overlapping transcript (SOX2OT) has been shown to play an oncogenic role in diverse cancers, generating eight transcript variants. SOX2 is located in the third intron of SOX2OT. However, the biological function of SOX2OT in cervical cancer and implication with SOX2 remain to be further explored. In this study, we screened the expression pattern of different SOX2OT transcript variants in cervical cancer cells. Interestingly, both high-expression levels of SOX2OT transcript 7 (SOX2OT-7) and SOX2 were detected in C-33A (HPV-) and SiHa (HPV16+) cells. Thus, C-33A and SiHa cells were conducted to investigate the effects of SOX2OT on cell growth, migration and invasion. Finally, rescue experiments were performed to confirm the role of SOX2 in SOX2OT-mediated regulation of cervical cancer progression. The results showed that knockdown of SOX2OT suppressed cell viability, arrested cell cycle and ameliorated migration and invasion ability of C-33A and SiHa cells. Ectopic expression of SOX2OT-7 exacerbated cervical cancer cell proliferation, migration and invasion. In addition, we found that the expression levels and protein stability of SOX2 were positively regulated by SOX2OT. Inhibition of SOX2 could block the malignant phenotypes of C-33A and SiHa cells by SOX2OT-7. In conclusion, these findings indicate that lncRNA SOX2OT contributes to the growth, migration and invasion of cervical cancer cells by modulating SOX2. Importantly, we demonstrate that the transcript SOX2OT-7 may be a novel and promising biomarker for both HPV- and HPV16+ cervical cancer.
Insights
Long non-coding RNA SOX2 overlapping transcript (SOX2OT), specifically SOX2OT-7, promotes cervical cancer growth and spread by regulating SOX2. This lncRNA is a potential biomarker for both HPV-negative and HPV-positive cervical cancers.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Long non-coding RNAs (lncRNAs) are increasingly recognized for their roles in cancer.
- SOX2 overlapping transcript (SOX2OT) is implicated in various cancers, but its function in cervical cancer is unclear.
- SOX2OT harbors the SOX2 gene, suggesting a potential regulatory relationship.
Purpose of the Study:
- To investigate the expression patterns of SOX2OT variants in cervical cancer.
- To elucidate the biological function of SOX2OT in cervical cancer progression.
- To determine the relationship between SOX2OT and SOX2 in cervical cancer.
Main Methods:
- Screening of SOX2OT transcript variants in cervical cancer cell lines (C-33A and SiHa).
- Functional assays including cell viability, cell cycle, migration, and invasion assays after SOX2OT manipulation.
- Rescue experiments to confirm SOX2's role in SOX2OT-mediated effects.
- Analysis of SOX2 expression levels and protein stability.
Main Results:
- SOX2OT transcript 7 (SOX2OT-7) and SOX2 were highly expressed in both HPV-negative (C-33A) and HPV16-positive (SiHa) cervical cancer cells.
- Knockdown of SOX2OT suppressed cell viability, arrested cell cycle, and reduced migration and invasion.
- Overexpression of SOX2OT-7 enhanced proliferation, migration, and invasion.
- SOX2OT positively regulated SOX2 expression and protein stability.
- Inhibition of SOX2 counteracted the malignant phenotypes induced by SOX2OT-7.
Conclusions:
- lncRNA SOX2OT promotes cervical cancer cell growth, migration, and invasion by modulating SOX2.
- SOX2OT-7 is identified as a potential diagnostic biomarker for both HPV-negative and HPV16-positive cervical cancers.
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