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E. Lasse-Opsahl

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Sep 2026

Abstract B012: Pan-RAS Inhibition Reprograms T Cell Immunity within the Pancreatic Adaptive Immune Microenvironment

The advent of pan-RAS and allele-specific inhibitors in clinical trials have created an urgent need to understand how RAS inhibition remodels the pancreatic immune microenvironment and alters anti-tumor immunity, to guide rational combinations with immunotherapy. We used a murine model with pancreas-specif...

Rashmi J. Kumar, E. Lasse-Opsahl, Lauren Gerbereux et al. · 0 citations
Sep 2026

Abstract A005: Deciphering the Hierarchy of Notch Signaling in Pancreatic Ductal Adenocarcinoma

Notch is a contact-dependent signaling pathway that plays critical roles in spatiotemporal patterning during embryogenesis. Beyond its role in development, Notch signaling regulates tissue patterning in adult organs in response to tissue injury or cancer. In the context of cancer, the role of Notch signaling has been...

Allison C. Bischoff, Wei Yan, Carlos E. Espinoza et al. · 0 citations
Sep 2026

Abstract B031: Spatial profiling reveals distinct tumor and myeloid ecosystems across lung and liver metastases in pancreatic ductal adenocarcinoma

Pancreatic ductal adenocarcinoma (PDA) exhibits marked organotropism, with the liver and lung representing the most common sites of metastatic recurrence. While PDA most often metastasizes to the liver, patients with only lung metastasis have a better overall prognosis, highlighting a role for both tumor-intrinsic pr...

E. Lasse-Opsahl, Daksh Thakkar, Julie M. Clark et al. · 0 citations
Sep 2026

Abstract B087: Impact of RAS inhibition on T cell maturation in the PDAC microenvironment

It is suggested that pharmacologic and genetic KRAS inhibition differentially remodel the intratumoral T cell compartment, whereas both induce similar T cell changes within the liver premetastatic niche.

Lauren Gerbereux, Rashmi Kumar, E. Lasse-Opsahl et al. · 0 citations
Jul 2026

GSTT1 promotes stemness and FGFR inhibitor sensitivity in pancreatic cancer through regulation of CD133 (PROM1).

A GSTT1HighCD133High stem-like subpopulation in metastatic PDA is identified and an FGFR-dependent signaling axis that sustains this state is identified, representing a potential therapeutic vulnerability.

Delgado Herrera Deborah de la Caridad, Alejandro Arroyo Roman, Riyan N. Campbell et al. · 0 citations

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