Abstract 292: AOH1996, a cancer-associated PCNA inhibitor, restores platinum sensitivity in urothelial carcinoma: <i>In vitro</i> and <i>in vivo</i> study.

Abstract Urothelial carcinoma (UC) frequently develops resistance to platinum-based chemotherapy, resulting in limited treatment efficacy and dismal clinical outcomes. Proliferating cell nuclear antigen (PCNA) is a key regulator of DNA replication and repair, and cancer-associated PCNA (caPCNA), a structurally altered form selectively expressed in malignant cells, has emerged as a promising therapeutic target. AOH1996 is a first-in-class small-molecule inhibitor that selectively binds caPCNA and disrupts PCNA-dependent survival pathways. In this study, we investigated the antitumor activity of AOH1996 in UC and its ability to overcome resistance to cisplatin-based chemotherapy. Cisplatin-sensitive (T24, BFTC905) and cisplatin-resistant (T24/R) UC cell lines were treated with AOH1996 alone or in combination with cisplatin or gemcitabine. AOH1996 significantly reduced cell viability and clonogenic survival in both sensitive and resistant cells, induced apoptosis as evidenced by increased Annexin V-positive fractions and cleavage of caspase-3 and PARP, and caused cell-cycle arrest with accumulation of cells in the S/G2 phase. Mechanistically, AOH1996 downregulated PCNA-dependent DNA repair signaling and enhanced DNA damage, as shown by increased γH2AX expression. Combination index analysis demonstrated synergistic interactions between AOH1996 and cisplatin or gemcitabine, particularly in cisplatin-resistant T24/R cells. In a xenograft mouse model of UC, AOH1996 significantly inhibited tumor growth and further potentiated the antitumor effect of cisplatin without causing overt systemic toxicity or significant body weight loss. Together, these findings provide preclinical evidence that targeting caPCNA with AOH1996 exerts robust antitumor activity and restores chemosensitivity in UC, supporting caPCNA inhibition as a promising therapeutic strategy for patients with platinum-resistant disease. Citation Format: Kuan-Lin Kuo, Kuo-How Huang, Yi Ju (Ellen) Kao, Chen-Hsun Hsu. AOH1996, a cancer-associated PCNA inhibitor, restores platinum sensitivity in urothelial carcinoma: In vitro and in vivo study [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 292.

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Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-292
Primary Topic
Nuclear Structure and Function
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article
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article

Abstract 292: AOH1996, a cancer-associated PCNA inhibitor, restores platinum sensitivity in urothelial carcinoma: In vitro and in vivo study.

Chen-Hsun Hsu, Kuan-Lin Kuo, Y. H. Kao, Kuo‐How Huang
Cancer Research
Nuclear Structure and Function
article

Abstract 292: AOH1996, a cancer-associated PCNA inhibitor, restores platinum sensitivity in urothelial carcinoma: In vitro and in vivo study.

Chen-Hsun Hsu, Kuan-Lin Kuo, Y. H. Kao, Kuo‐How Huang
article en

Abstract

Abstract Urothelial carcinoma (UC) frequently develops resistance to platinum-based chemotherapy, resulting in limited treatment efficacy and dismal clinical outcomes. Proliferating cell nuclear antigen (PCNA) is a key regulator of DNA replication and repair, and cancer-associated PCNA (caPCNA), a structurally altered form selectively expressed in malignant cells, has emerged as a promising therapeutic target. AOH1996 is a first-in-class small-molecule inhibitor that selectively binds caPCNA and disrupts PCNA-dependent survival pathways. In this study, we investigated the antitumor activity of AOH1996 in UC and its ability to overcome resistance to cisplatin-based chemotherapy. Cisplatin-sensitive (T24, BFTC905) and cisplatin-resistant (T24/R) UC cell lines were treated with AOH1996 alone or in combination with cisplatin or gemcitabine. AOH1996 significantly reduced cell viability and clonogenic survival in both sensitive and resistant cells, induced apoptosis as evidenced by increased Annexin V-positive fractions and cleavage of caspase-3 and PARP, and caused cell-cycle arrest with accumulation of cells in the S/G2 phase. Mechanistically, AOH1996 downregulated PCNA-dependent DNA repair signaling and enhanced DNA damage, as shown by increased γH2AX expression. Combination index analysis demonstrated synergistic interactions between AOH1996 and cisplatin or gemcitabine, particularly in cisplatin-resistant T24/R cells. In a xenograft mouse model of UC, AOH1996 significantly inhibited tumor growth and further potentiated the antitumor effect of cisplatin without causing overt systemic toxicity or significant body weight loss. Together, these findings provide preclinical evidence that targeting caPCNA with AOH1996 exerts robust antitumor activity and restores chemosensitivity in UC, supporting caPCNA inhibition as a promising therapeutic strategy for patients with platinum-resistant disease. Citation Format: Kuan-Lin Kuo, Kuo-How Huang, Yi Ju (Ellen) Kao, Chen-Hsun Hsu. AOH1996, a cancer-associated PCNA inhibitor, restores platinum sensitivity in urothelial carcinoma: In vitro and in vivo study [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 292.

Cancer ResearchVol. 86(7_Supplement)
National Taiwan University Hospital (TW)
Good health and well-being
Openalex Percentile: Top 7%
Nuclear Structure and Function
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