Cyclosporine A Decreased Paclitaxel Resistance in Prostate Cancer Cells by Inhibiting MTDH Expression

Am J Mens Health. 2025 Jan-Feb;19(1):15579883241310834. doi: 10.1177/15579883241310834.

Abstract

This study aims to investigate the effect and mechanism of cyclosporine A (CsA) on paclitaxel-resistant prostate cancer cells. Paclitaxel-resistant prostate cancer cell lines were established by gradual increment method. The proliferation of cells was tested using MTT and colony formation assay. Western blot was used to detect protein expression. Expression levels of gene mRNA were detected using real-time polymerase chain reaction (RT-PCR). Xenografts in nude mice were used to validate the conclusion in vitro. The results showed that CsA could increase the sensitivity of prostate cancer cells to paclitaxel. Treatment of paclitaxel-resistant prostate cancer cell lines with CsA gradients decreased metadherin (MTDH) protein expression. RT-PCR showed that CsA could decrease the mRNA level of MTDH. Overexpression of MTDH in prostate cancer cells increases paclitaxel resistance in prostate cancer cells. Conversely, knockdown of MTDH reduced paclitaxel resistance in prostate cancer cells. Treating cells with CsA failed to reduce paclitaxel resistance in prostate cancer cells when MTDH was overexpressed. Xenografts in nude mice yielded consistent conclusions with the in vitro results. In conclusion, CsA can reduce the resistance of prostate cancer cells to paclitaxel. In vitro and in vivo experiments have shown that CsA can reduce paclitaxel resistance in prostate cancer cells by decreasing MTDH expression. In clinical practice, CsA can be used in combination with paclitaxel to improve the therapeutic effect on prostate cancer. MTDH may serve as a novel target for treating paclitaxel resistance in prostate cancer.

Keywords: MTDH; cyclosporine A; drug resistance; paclitaxel; prostate cancer.

MeSH terms

  • Animals
  • Antineoplastic Agents, Phytogenic / pharmacology
  • Cell Adhesion Molecules* / genetics
  • Cell Adhesion Molecules* / metabolism
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cyclosporine* / pharmacology
  • Drug Resistance, Neoplasm* / genetics
  • Humans
  • Male
  • Membrane Proteins* / genetics
  • Membrane Proteins* / metabolism
  • Mice
  • Mice, Nude*
  • Paclitaxel* / pharmacology
  • Prostatic Neoplasms* / drug therapy
  • Prostatic Neoplasms* / pathology
  • RNA-Binding Proteins* / genetics
  • RNA-Binding Proteins* / metabolism
  • Xenograft Model Antitumor Assays

Substances

  • Paclitaxel
  • Cyclosporine
  • Membrane Proteins
  • RNA-Binding Proteins
  • MTDH protein, human
  • Cell Adhesion Molecules
  • Antineoplastic Agents, Phytogenic