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Published on: August 12, 2015
Inhibiting malignant phenotypes of the bladder cancer cells by silencing long noncoding RNA SChLAP1
Jianjun Zhang1, Zhenfeng Shi1, Yukui Nan1
1Department of Urology Surgery Center, The People's Hospital of Xinjiang Uyghur Autonomous Region, Urumqi, 830002, Xinjiang, People's Republic of China.
Background And Objectives:
Long noncoding RNAs (lncRNAs) play key roles in process of cancer cell growth and apoptosis and have received increasing attention. SChLAP1 is a novel lncRNA that is required for development and progression of prostate cancer. We hypothesized that SChLAP1 also has important biological functions in human bladder cancer which is another type of urological cancer.
Methods:
The expression of SChLAP1 in bladder cancer was determined using real-time qPCR. Bladder cancer T24 and 5637 cells were transfected with SChLAP1 siRNA or negative control siRNA. Cell proliferation, apoptosis and migration were determined using CCK-8 assay, flow cytometry analysis and wound healing assay, respectively.
Results:
SChLAP1 was overexpressed in bladder cancer tissues compared to paired normal bladder tissues. Cell growth arrest, apoptosis induction and migration inhibition were also observed in bladder cancer T24 and 5637 cells after transfection with SChLAP1 siRNA.
Conclusions:
Our data suggest that SChLAP1 plays oncogenic roles and can be used as a therapeutic target for treating human bladder cancer.
Insights
Long noncoding RNA SChLAP1 promotes bladder cancer progression. Inhibiting SChLAP1 in bladder cancer cells reduced proliferation and migration, suggesting it as a therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Long noncoding RNAs (lncRNAs) are increasingly recognized for their roles in cancer development.
- SChLAP1, a lncRNA, is crucial for prostate cancer progression.
- The role of SChLAP1 in other urological cancers, like bladder cancer, remains largely unexplored.
Purpose of the Study:
- To investigate the expression and function of SChLAP1 in human bladder cancer.
- To determine if SChLAP1 plays a role in bladder cancer cell growth, apoptosis, and migration.
Main Methods:
- Real-time quantitative PCR (qPCR) was used to measure SChLAP1 expression in bladder cancer tissues and cell lines.
- Bladder cancer cell lines (T24 and 5637) were transfected with SChLAP1 siRNA to inhibit its expression.
- Cell proliferation, apoptosis, and migration were assessed using CCK-8 assay, flow cytometry, and wound healing assays, respectively.
Main Results:
- SChLAP1 was significantly overexpressed in bladder cancer tissues compared to normal adjacent tissues.
- Inhibition of SChLAP1 using siRNA led to cell growth arrest in bladder cancer cells.
- SChLAP1 knockdown induced apoptosis and inhibited migration in T24 and 5637 bladder cancer cells.
Conclusions:
- SChLAP1 exhibits oncogenic properties in human bladder cancer.
- SChLAP1 represents a potential therapeutic target for bladder cancer treatment.
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