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• W2111292073 abstract "The aim of this study wsa to evaluate the additive effect of valproic acid (VPA) to γδ T-cell cytotoxicity against bladder cancer cells. Materials and Methods: Human bladder cancer cell lines TCCSUP and 253J were treated with VPA and mRNA expression of natural killer group 2D (NKG2D) ligands was determined. The antitumour effect of expanded γδ T-cells against zoledronic acid (ZOL) and VPA pre-treated cancer cells was subsequently determined. Results: VPA increased mRNA expression of NKG2D ligands on both cancer cell types. A blocking study revealed that 253J cells were recognised through NKG2D, while TCCSUP cells were mainly recognised through γδ T-cell receptor. VPA pre- treatment increased sensitivity to cytolysis by γδ T-cells for both cancer cell types, whereas ZOL pre-treatment was only effective against TCCSUP. Conclusion: Induction of NKG2D ligands by VPA increased the susceptibility of cancer cells that are recognised by NKG2D to cytolysis by γδ T-cells. Superficial bladder carcinomas represent 70% of all bladder carcinomas and are managed with transurethral surgical treatment followed by intravesical instillation of chemotherapeutic agents or Bacillus Calmette-Guerin (BCG) treatment (1). BCG, which exerts antitumour effects through the local immune response, is considered the most effective agent, particularly in carcinoma in situ (2). Other immunotherapeutic approaches, including vaccine therapy," @default.
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• W2111292073 date "2010-11-01" @default.
• W2111292073 modified "2023-10-02" @default.
• W2111292073 title "The antitumour effect of {gamma}{delta} T-cells is enhanced by valproic acid-induced up-regulation of NKG2D ligands." @default.
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