Abstract 1891: Minnelide enhances the antitumor activity of pan-KRAS inhibitor RMC-6236 in preclinical models for pancreatic cancer.

Abstract Triptolide, a natural compound from Thunder God Vine, and its water-soluble prodrug Minnelide have shown potent antitumor activity, including promising single-agent efficacy in patients with pancreatic cancer. We previously demonstrated that triptolide suppresses super-enhancer activity in pancreatic cancer and stromal cells by inhibiting the XPB subunit of TFIIH, leading to downregulation of c-Myc and transcriptional effectors of mutant KRAS signaling. In this study, we assessed whether triptolide/Minnelide can enhance the antitumor activity of RMC-6236, a pan-KRAS inhibitor in clinical development for KRAS mutant cancers. We first evaluated the synergistic effects of triptolide and RMC-6236 on pancreatic cancer cell growth across multiple KRAS-mutant lines, including HPAC (KRASG12D), Capan-1 (KRASG12V), Hs766T (KRASQ61H), and BxPC3 (KRASwt). The combination demonstrated strong synergy across a range of concentrations in HPAC and Capan-1 cells and additive effects in BxPC3 and Hs766T. To validate these findings in vivo, we assessed Minnelide in combination with RMC-6236 using an HPAC xenograft model (3 × 106 cells, subcutaneous implantation). Mice received oral Minnelide (0.10 or 0.15 mg/kg, QDx21) with or without a low dose of oral RMC-6236 (15 mg/kg, QDx21; n = 10/group). While Minnelide alone showed modest tumor inhibition, both doses of Minnelide significantly enhanced the antitumor efficacy of low dose RMC-6236 after 21 days (p < 0.01, two-way ANOVA). No weight loss or other toxicities were observed in the single agent or combination groups. Taken together, these results demonstrate that triptolide/Minnelide augments the activity of RMC-6236 in vitro and in vivo, supporting further preclinical and potentially clinical evaluation. (This work was supported by Minneamrita Therapeutics, Purple Pansies, and the Pancreas National Advisory Council) Citation Format: Edgar Banuelos, Jaeger Moore, Mohana Velagapudi, Ashok Saluja, Daniel D. Von Hoff, Haiyong Han. Minnelide enhances the antitumor activity of pan-KRAS inhibitor RMC-6236 in preclinical models for pancreatic cancer [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 1891.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-1891
Primary Topic
Natural Compounds in Disease Treatment
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article
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article

Abstract 1891: Minnelide enhances the antitumor activity of pan-KRAS inhibitor RMC-6236 in preclinical models for pancreatic cancer.

Mohana Velagapudi, Haiyong Han, Daniel D. Von Hoff, Jaeger Moore et al.
Cancer Research
Natural Compounds in Disease Treatment
article

Abstract 1891: Minnelide enhances the antitumor activity of pan-KRAS inhibitor RMC-6236 in preclinical models for pancreatic cancer.

Mohana Velagapudi, Haiyong Han, Daniel D. Von Hoff, Jaeger Moore, Ashok Saluja, Edgar Banuelos
article en

Abstract

Abstract Triptolide, a natural compound from Thunder God Vine, and its water-soluble prodrug Minnelide have shown potent antitumor activity, including promising single-agent efficacy in patients with pancreatic cancer. We previously demonstrated that triptolide suppresses super-enhancer activity in pancreatic cancer and stromal cells by inhibiting the XPB subunit of TFIIH, leading to downregulation of c-Myc and transcriptional effectors of mutant KRAS signaling. In this study, we assessed whether triptolide/Minnelide can enhance the antitumor activity of RMC-6236, a pan-KRAS inhibitor in clinical development for KRAS mutant cancers. We first evaluated the synergistic effects of triptolide and RMC-6236 on pancreatic cancer cell growth across multiple KRAS-mutant lines, including HPAC (KRASG12D), Capan-1 (KRASG12V), Hs766T (KRASQ61H), and BxPC3 (KRASwt). The combination demonstrated strong synergy across a range of concentrations in HPAC and Capan-1 cells and additive effects in BxPC3 and Hs766T. To validate these findings in vivo, we assessed Minnelide in combination with RMC-6236 using an HPAC xenograft model (3 × 106 cells, subcutaneous implantation). Mice received oral Minnelide (0.10 or 0.15 mg/kg, QDx21) with or without a low dose of oral RMC-6236 (15 mg/kg, QDx21; n = 10/group). While Minnelide alone showed modest tumor inhibition, both doses of Minnelide significantly enhanced the antitumor efficacy of low dose RMC-6236 after 21 days (p < 0.01, two-way ANOVA). No weight loss or other toxicities were observed in the single agent or combination groups. Taken together, these results demonstrate that triptolide/Minnelide augments the activity of RMC-6236 in vitro and in vivo, supporting further preclinical and potentially clinical evaluation. (This work was supported by Minneamrita Therapeutics, Purple Pansies, and the Pancreas National Advisory Council) Citation Format: Edgar Banuelos, Jaeger Moore, Mohana Velagapudi, Ashok Saluja, Daniel D. Von Hoff, Haiyong Han. Minnelide enhances the antitumor activity of pan-KRAS inhibitor RMC-6236 in preclinical models for pancreatic cancer [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 1891.

Cancer ResearchVol. 86(7_Supplement)
Translational Genomics Research Institute (US), Saneron CCEL Therapeutics (United States) (US)
Openalex Percentile: Top 4%
Natural Compounds in Disease Treatment
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