Abstract 5639: A potent aminosteroid (RM-581) that inhibits orally in mice the tumor growth in an orthotopic xenograft pancreatic cancer model

Abstract Pancreatic cancer has a very poor prognosis, with a 5-year survival rate of only 10%, making it imperative to develop effective small molecules as new drugs. The aim of this study was to validate the in vitro and in vivo efficacy of a promising endoplasmic reticulum-stress aggravator, the synthetic aminosteroid RM-581, that induces apoptosis, as a potential treatment for pancreatic cancer. When tested on a panel of human (PANC-1, MIACaPa2, L3.6, CAPAN-1, BxPC3) and murine (Pan02) pancreatic cancer cells, RM-581 strongly reduced their proliferation (IC50 = 0.83, 0.45, 2.10, 0.78, 5.75 and 1.77 μM, respectively), which justified its evaluation in a PANC-1-Luc cell-derived orthotopic xenograft model in nu/nu mice. After 5 weeks of oral treatment with RM-581 by gavage (po) daily, in vivo fluorescence imaging (IVIS) imaging showed inhibited tumor growth of 11, 54 and 76% at 10, 40 and 80 mg/kg, respectively, compared to the untreated control group. Compared with a cholesterol biosynthesis inhibitor pravastatin (4 mg/kg/subcutaneous (sc)), the effect of RM-581 was similar at 40 mg/kg/po and greater at 80 mg/kg/po. Inhibitions obtained with RM-581 and pravastatin were also confirmed by tumor weight measurement at necropsy. A comparison with antineoplastic drug docetaxel (4 mg/kg/intraperitoneal/2 x weekly) was however not possible, since several toxicities were found after 2 weeks of treatment, forcing euthanasia of the mice. From histological evaluation (hematoxylin and eosin staining), no differences were found in the liver, kidney and spleen in all groups, which is consistent with the clinical observation of no signs of toxicities and no differences in body weight for RM-581 treatments. In summary, RM-581 is therefore a promising candidate for a possible oral treatment of pancreatic cancer. Citation Format: Donald Poirier, Qi Chen, René Maltais, Jenny Roy, Forkan Ahamed, Shannon Arnold. A potent aminosteroid (RM-581) that inhibits orally in mice the tumor growth in an orthotopic xenograft pancreatic cancer model [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1):Abstract nr 5639.

Authors

Institutions

Publication Details

Journal
Cancer Research
Published
2025-04-21
DOI
https://doi.org/10.1158/1538-7445.am2025-5639
Primary Topic
Cancer Research and Treatments
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract 5639: A potent aminosteroid (RM-581) that inhibits orally in mice the tumor growth in an orthotopic xenograft pancreatic cancer model

Donald Poirier, René Maltais, Forkan Ahamed, Shannon Arnold et al.
Cancer Research
Cancer Research and Treatments
article

Abstract 5639: A potent aminosteroid (RM-581) that inhibits orally in mice the tumor growth in an orthotopic xenograft pancreatic cancer model

Donald Poirier, René Maltais, Forkan Ahamed, Shannon Arnold, Qi Chen, Jenny Roy
article en

Abstract

Abstract Pancreatic cancer has a very poor prognosis, with a 5-year survival rate of only 10%, making it imperative to develop effective small molecules as new drugs. The aim of this study was to validate the in vitro and in vivo efficacy of a promising endoplasmic reticulum-stress aggravator, the synthetic aminosteroid RM-581, that induces apoptosis, as a potential treatment for pancreatic cancer. When tested on a panel of human (PANC-1, MIACaPa2, L3.6, CAPAN-1, BxPC3) and murine (Pan02) pancreatic cancer cells, RM-581 strongly reduced their proliferation (IC50 = 0.83, 0.45, 2.10, 0.78, 5.75 and 1.77 μM, respectively), which justified its evaluation in a PANC-1-Luc cell-derived orthotopic xenograft model in nu/nu mice. After 5 weeks of oral treatment with RM-581 by gavage (po) daily, in vivo fluorescence imaging (IVIS) imaging showed inhibited tumor growth of 11, 54 and 76% at 10, 40 and 80 mg/kg, respectively, compared to the untreated control group. Compared with a cholesterol biosynthesis inhibitor pravastatin (4 mg/kg/subcutaneous (sc)), the effect of RM-581 was similar at 40 mg/kg/po and greater at 80 mg/kg/po. Inhibitions obtained with RM-581 and pravastatin were also confirmed by tumor weight measurement at necropsy. A comparison with antineoplastic drug docetaxel (4 mg/kg/intraperitoneal/2 x weekly) was however not possible, since several toxicities were found after 2 weeks of treatment, forcing euthanasia of the mice. From histological evaluation (hematoxylin and eosin staining), no differences were found in the liver, kidney and spleen in all groups, which is consistent with the clinical observation of no signs of toxicities and no differences in body weight for RM-581 treatments. In summary, RM-581 is therefore a promising candidate for a possible oral treatment of pancreatic cancer. Citation Format: Donald Poirier, Qi Chen, René Maltais, Jenny Roy, Forkan Ahamed, Shannon Arnold. A potent aminosteroid (RM-581) that inhibits orally in mice the tumor growth in an orthotopic xenograft pancreatic cancer model [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1):Abstract nr 5639.

Cancer ResearchVol. 85(8_Supplement_1)
University of Kansas Medical Center (US), Université Laval (CA)
Openalex Percentile: Top 91%
Cancer Research and Treatments
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.