Enhancement of gemcitabine toxicity and specificity through PI3K/Akt/Nrf2 pathway inhibition in pancreatic cancer

BD B10 was identified as a non-toxic drug sensitiser that enhanced gemcitabine efficacy in PDAC cells and improved the therapeutic index by inhibiting key survival and resistance pathways. Specific roles for BD B10 in PDAC were identified and further testing may prove drug sensitisers have a more general application to enhance drug therapies.

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Publication Details

Journal
Frontiers in Pharmacology
Published
2026-02-16
DOI
https://doi.org/10.3389/fphar.2026.1724989
Primary Topic
Pancreatic and Hepatic Oncology Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Enhancement of gemcitabine toxicity and specificity through PI3K/Akt/Nrf2 pathway inhibition in pancreatic cancer

Philip J. Day, Stephen O’Hagan, Yu-Shan Chen
Frontiers in Pharmacology
Pancreatic and Hepatic Oncology Research
article

Enhancement of gemcitabine toxicity and specificity through PI3K/Akt/Nrf2 pathway inhibition in pancreatic cancer

Philip J. Day, Stephen O’Hagan, Yu-Shan Chen
article en

Abstract

BD B10 was identified as a non-toxic drug sensitiser that enhanced gemcitabine efficacy in PDAC cells and improved the therapeutic index by inhibiting key survival and resistance pathways. Specific roles for BD B10 in PDAC were identified and further testing may prove drug sensitisers have a more general application to enhance drug therapies.

Frontiers in PharmacologyVol. 17
University of Cape Town (ZA), University of Manchester (GB), Biology of Infection (FR)
Directorate for Biological Sciences, Biotechnology and Biological Sciences Research Council
Good health and well-being
Openalex Percentile: Top 54%
Pancreatic and Hepatic Oncology Research
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