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April 5, 2026Cancer Research0 citations

Abstract 2946: RQ43: A quinoline derivative that inhibits pancreatic cancer cell EMT and migration.

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SDSreyoshi DasQCQi Chen

Key Points

  • The study aims to evaluate the cytotoxic and anti-migratory effects of RQ-43 on pancreatic cancer cells and explore underlying mechanisms.
  • Treatment of human (PANC1) and murine (PAN02) PDAC cell lines with RQ-43 for 48 hours.
  • Assessment of cell viability using MTT assay.
  • Evaluation of migration and invasion using wound-healing and Boyden chamber assays.
  • Analysis of EMT-related genes and transcription factors through qPCR.
  • Utilization of an orthotopic PDAC mouse model for in vivo effects.
  • RQ-43 reduced PDAC cell viability in a dose-dependent manner (IC50 of 3.61 µM for PANC1, 8.24 µM for PAN02).
  • Significant inhibition of migration observed, with a 27.5% reduction in PANC1 and 78% in PAN02 (p < 0.05).
  • Invasion through Matrigel significantly suppressed in both cell lines (p < 0.01).
  • Downregulation of Snail and B-catenin transcription factors (p < 0.05).
  • In vivo treatment decreased tumor weight by 62.95% and reduced metastasis from 80% to 25%.

Abstract

Abstract Background: Pancreatic ductal adenocarcinoma (PDAC) is one of the deadliest cancers due to early metastasis and therapeutic resistance. The epithelial-to-mesenchymal transition (EMT) drives PDAC invasiveness and poor prognosis. RQ-43, a novel quinoline derivative, has shown antiproliferative activity in other cancer models previously with unclear mechanisms. This study investigated its cytotoxic, anti-migratory/invasive effects, and mechanisms of action in PDAC. Methods: Human (PANC1) and murine (PAN02) PDAC cell lines were treated with RQ-43 (0.625-20 µM) for 48 h, and cell viability measured by MTT assay. Migration and invasion were assessed using wound-healing and Boyden chamber assays at sub-cytotoxic drug concentrations. EMT-related genes and transcription factors were assessed by qPCR. A syngeneic orthotopic PDAC mouse model was used to assess the in vivo effects of RQ-43 in C57/BL/6 mice. Results: RQ-43 selectively decreased PDAC cell viability in a dose-dependent manner with IC50 values of 3.61 µM (PANC1) and 8.24 µM (PAN02). At concentrations of 2.5 µM for PANC1 and 5-20 µM for PAN02, RQ-43 significantly inhibited migration, reducing wound closure by 27.5% in PANC1 and 78% in PAN02 (p 0.05 compared to controls). Invasion through Matrigel-coated Boyden chamber was also significantly suppressed in both cell lines (p 0.01). EMT-related transcription factors Snail and B-catenin were downregulated (p 0.05). In the orthotopic model, RQ-43 treatment (80 mg/kg, daily IP) significantly reduced tumour weight by 62.95% compared with controls. Metastasis rate was 80% in the control group and 25% in the treated group. Conclusions: RQ-43 demonstrates cytotoxic, anti-migratory/invasive effects in vitro and effectively reduces tumour growth and metastasis in vivo. EMT-related transcription factors were downregulated. Further efficacy and mechanistic evaluation are warranted. Citation Format: Sreyoshi Das, Qi Chen. RQ43: A quinoline derivative that inhibits pancreatic cancer cell EMT and migration 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 2946.

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Cite This Study

Das et al. (2026) studied this question.

synapsesocial.com/papers/69d1fcc0a79560c99a0a261dhttps://doi.org/10.1158/1538-7445.am2026-2946
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Isoquinolinequinone N-Oxides as Promising Antitumor Compounds in Pancreatic Cancer Cell Lines2026
  2. 2Abstract 576: The pan-quadruplex drug QN-302 selectively down-regulates key pathway targets in pancreatic cancer cells that are up-regulated in human pancreatic cancer2024
  3. 3Abstract 3350: The pan-quadruplex drug QN-302 targets up-regulated genes in pancreatic cancer and in other cancer types and correlate with poor patient prognosis2024
  4. 4Abstract 4525: Potential of Rac and Cdc42 inhibitors as pancreatic cancer therapeutics.2026
  5. 5Abstract 3652: Thymoquinone blocks pancreatic ductal adenocarcinoma growth by altering novel circRNAs and miRNAs2026