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Immunomodulatory effects of trastuzumab deruxtecan through the cGAS-STING pathway in gastric cancer cells

Kyoung-Seok Oh, Ah‐Rong Nam, Ju‐Hee Bang, Yoojin Jeong, Sea Young Choo, Hyo Jung Kim, Su In Lee, Jae‐Min Kim, Jeesun Yoon, Tae-Yong Kim, Do‐Youn Oh

2024Cell Communication and Signaling19 citationsDOIOpen Access PDF

Abstract

Abstract Although the efficacy of trastuzumab deruxtecan (T-DXd) against HER2-positive gastric cancers (GCs) has driven its clinical application, the precise mechanisms governing its immunomodulatory role remain unclear. In this study, we examined the immune-related mechanisms of action of T-DXd in GC cells. T-DXd exhibited potent antitumor effects in GC cells across diverse HER2 expression levels by inducing DNA damage and apoptosis. Activation of the DNA damage response by T-DXd led to increased PD-L1 expression. RNA-Seq analysis revealed that T-DXd modulated immune-related pathways, resulting in the upregulation of genes associated with inflammation and IFN signaling. Importantly, T-DXd activated the cGAS-STING pathway, inducing an IFN-I response in HER2-positive GC cells. Furthermore, T-DXd activated dendritic cells via the cancer cell-intrinsic cGAS-STING-IFN axis and enhanced PBMC-mediated tumor cell killing by activating CD8 + T cells. These findings provide valuable insights into the role of the cytosolic DNA sensing pathway in the action of T-DXd and offer a compelling rationale for combining T-DXd with immune checkpoint blockade therapies in GC treatment.

Topics & Concepts

Immune systemCancer researchDownregulation and upregulationMedicineT cellSignal transductionBlockadeApoptosisCancerImmune checkpointImmunotherapyImmunologyReceptorBiologyCell biologyGeneInternal medicineBiochemistryinterferon and immune responsesImmune Cell Function and InteractionCancer-related molecular mechanisms research
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