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Published on: March 30, 2019
The lncRNA UBE2R2-AS1 suppresses cervical cancer cell growth in vitro
Chunyan Liu1, Huajun Li1, Qinan Yin2
1Department of Obstetrics and Gynaecology, China-Japan Friendship Hospital, Beijing, 100029, China.
Purpose:
This study explores the effects and mechanisms of the long noncoding RNA (lncRNA) UBE2R2-AS1 activity in the cervical cancer development.
Methods:
Thirty-four pairs of normal adjacent and cancer tissues were collected from cervical cancer patients. Pathology was evaluated by HE staining, and UBE2R2-AS1 expression was evaluated by in situ hybridization assays. HeLa and SiHa cells were respectively divided into negative control, pcDNA 3.1 vehicle control and lncRNA-expressing groups. Cell proliferation and apoptosis were measured by CCK8 expression and flow cytometry. The number of invading cells and the wound healing rate were measured by transwell and wound healing assays, respectively. Relative protein levels (caspase-3, caspase-8, MMP-2 and MMP-9) were measured by Western blot.
Results:
Compared with adjacent normal tissues, UBE2R2-AS1 expression was significantly suppressed in cancer tissues correlated with the increasing stage. UBE2R2-AS1 suppressed cell proliferation and enhanced apoptosis, as well as decreased cell invasion and wound healing in cervical cancer cell lines. UBE2R2-AS1 overexpression significantly upregulated caspase-3 and caspase-8 protein expressions and significantly downregulated MMP-2 and MMP-9 protein expressions by Western blot.
Conclusion:
UBE2R2-AS1 suppressed cervical cancer cell biological activities and might represent an antitumor factor in cervical cancer.
Insights
The long noncoding RNA UBE2R2-AS1 acts as a tumor suppressor in cervical cancer. Its reduced expression in tumors correlates with advanced stages, and restoring it inhibits cancer cell growth and invasion.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Cervical cancer remains a significant global health challenge.
- Long noncoding RNAs (lncRNAs) are increasingly recognized for their roles in cancer development.
- The specific function of lncRNA UBE2R2-AS1 in cervical cancer is not well understood.
Purpose of the Study:
- To investigate the role and underlying mechanisms of lncRNA UBE2R2-AS1 in cervical cancer progression.
- To determine the expression levels of UBE2R2-AS1 in cervical cancer tissues and cell lines.
- To evaluate the impact of UBE2R2-AS1 on cervical cancer cell proliferation, apoptosis, and invasion.
Main Methods:
- Analysis of UBE2R2-AS1 expression in 34 pairs of cervical cancer and adjacent normal tissues using in situ hybridization.
- Cellular assays including CCK8, flow cytometry, Transwell, and wound healing to assess proliferation, apoptosis, and invasion.
- Western blot analysis to measure protein expression levels of apoptosis-related (caspase-3, caspase-8) and invasion-related (MMP-2, MMP-9) markers.
Main Results:
- UBE2R2-AS1 expression was significantly lower in cervical cancer tissues compared to normal tissues, inversely correlated with cancer stage.
- Overexpression of UBE2R2-AS1 in HeLa and SiHa cells suppressed cell proliferation and invasion while promoting apoptosis.
- UBE2R2-AS1 overexpression led to increased levels of caspase-3 and caspase-8, and decreased levels of MMP-2 and MMP-9.
Conclusions:
- UBE2R2-AS1 functions as a suppressor of cervical cancer cell biological activities.
- UBE2R2-AS1 exhibits potential as an antitumor factor for cervical cancer therapy.
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