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In vivo Imaging and Therapeutic Treatments in an Orthotopic Mouse Model of Ovarian Cancer
Published on: August 17, 2010
CLDN6 Expression Plasticity in Ovarian Cancer: Insights into Therapeutic Optimization for CLDN6-Targeted
Naoki Kimura1, Kenji Taniguchi1, Shinichi Onishi1
1Research Division, Chugai Pharmaceutical, Yokohama, Japan.
Abstract:
Epithelial ovarian cancer (EOC) represents the most lethal gynecologic malignancy, characterized by extensive tumor heterogeneity that contributes to treatment resistance and high recurrence rates. Recently, we developed SAIL66, a CLDN6-targeting T-cell engager currently in clinical evaluation for CLDN6-positive solid cancers, including EOC. Whereas CLDN6 is considered an attractive target for cancer therapy due to its cancer specificity, its biology remains poorly understood. In this study, we investigated the biological characteristics of CLDN6-positive EOC to identify its significance as a therapeutic target for ovarian cancer treatment. We demonstrated heterogeneous CLDN6 expression in xenograft and clinical tumors. In vitro-cultured ovarian cancer cell lines showed reversible changes in CLDN6 expression depending on cell density, accompanied by alterations in epithelial-mesenchymal transition (EMT)-related and stemness-related genes. Spatial transcriptomic analysis of clinical specimens revealed that CLDN6-positive areas formed both solid regions and dispersed small clusters within the same tumors, with differential expression of EMT-related and cell matrix remodeling genes between these areas, consistent with our in vitro observations at varying cell densities. Furthermore, carboplatin treatment increased CLDN6 expression, accompanied by changes in EMT-related genes. Leveraging these biological characteristics of CLDN6, we discovered that significant tumor regression was observed in mice treated with SAIL66 following carboplatin pretreatment. Post-carboplatin analysis revealed increased CLDN6 expression, EMT-related gene changes, and enhanced T-cell infiltration, which were associated with the synergistic effect of SAIL66. Our study provides insights into the biology and plasticity of CLDN6-positive cells in EOC heterogeneity and highlights the clinical significance of CLDN6-targeting therapies for ovarian cancer treatment.
Significance:
CLDN6-positive ovarian cancer cells exhibit remarkable plasticity influenced by microenvironmental factors and chemotherapy, providing critical insights for understanding the biology of ovarian cancer progression and optimizing CLDN6-targeting therapy.
Insights
This study reveals that CLDN6 expression in ovarian cancer (OC) changes with cell density and chemotherapy. Targeting CLDN6 with SAIL66 after carboplatin significantly enhances tumor regression by increasing CLDN6 and T-cell infiltration.
Area of Science:
- Oncology
- Molecular Biology
- Immunotherapy
Background:
- Epithelial ovarian cancer (EOC) is a lethal malignancy with high recurrence rates due to tumor heterogeneity and treatment resistance.
- CLDN6 is a potential therapeutic target in CLDN6-positive solid tumors, including EOC, but its biology in this context is not well understood.
Purpose of the Study:
- To investigate the biological characteristics of CLDN6-positive EOC and assess its significance as a therapeutic target.
- To understand the plasticity of CLDN6 expression in response to microenvironmental cues and chemotherapy.
Main Methods:
- Analysis of CLDN6 expression in xenograft and clinical EOC samples.
- In vitro studies using OC cell lines to assess CLDN6 expression changes with cell density.
- Spatial transcriptomic analysis of clinical specimens.
- Evaluation of SAIL66 efficacy in combination with carboplatin in preclinical models.
Main Results:
- CLDN6 expression is heterogeneous in EOC and dynamically changes with cell density, affecting EMT and stemness markers.
- Spatial transcriptomics revealed distinct molecular profiles in CLDN6-positive areas.
- Carboplatin treatment upregulates CLDN6 and alters EMT-related genes, enhancing sensitivity to SAIL66.
- Combination therapy with carboplatin and SAIL66 resulted in significant tumor regression and increased T-cell infiltration.
Conclusions:
- CLDN6 expression in EOC exhibits plasticity influenced by cell density and chemotherapy.
- CLDN6-targeting therapy (SAIL66) shows synergistic effects with carboplatin, offering a promising therapeutic strategy for ovarian cancer.
- Understanding CLDN6 biology is crucial for developing effective immunotherapies for ovarian cancer.
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