[S100A4, a potential therapeutic target on bladder cancer stem cells]

Chun-Yan Wang1, Qing-Wen Nie, Xuan Zhou

  • 1Department of Neurology, Integrated Hospital of Traditional Chinese Medicine, Southern Medical University, Guangzhou 510315, China.E-mail: 362142518@qq.com.

Abstract

Insights

Small interfering RNA (siRNA) targeting S100A4 gene effectively inhibited bladder cancer stem cell (CSC) proliferation and tumor formation. S100A4 silencing presents a potential therapeutic strategy for bladder cancer treatment.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Context:

  • Bladder cancer is a significant health concern, often characterized by recurrence and metastasis.
  • Cancer stem cells (CSCs) play a crucial role in tumor initiation, progression, and therapeutic resistance.
  • S100A4, a calcium-binding protein, has been implicated in various cancers, but its role in bladder CSCs requires further elucidation.

Purpose:

  • To investigate the effect of S100A4 gene silencing using small interfering RNA (siRNA) on the proliferation and xenograft tumor formation of bladder cancer stem cells (CSCs).

Summary:

  • S100A4 was identified as a highly differentially expressed protein in MB49 bladder cancer stem cells (MCSCs) using iTRAQ technology.
  • Transfection of MCSCs with S100A4-targeting siRNA significantly reduced S100A4 expression at both mRNA and protein levels.
  • siRNA-mediated S100A4 silencing suppressed MCSC proliferation and attenuated their ability to form xenograft tumors in vivo.

Impact:

  • S100A4 is associated with bladder cancer recurrence and metastasis.
  • Targeting S100A4 in bladder CSCs represents a promising therapeutic strategy for eliminating cancer stem cells and potentially preventing disease progression.