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.

Abstract

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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