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Navigating the paradox of senescence and chemoresistance in pancreatic cancer

  • Vrije Universiteit Amsterdam
  • Amsterdam UMC
  • General Hospital of People's Liberation Army
  • University of Pisa
  • University of Palermo
  • University of Parma
  • Cancer Pharmacology Lab, AIRC Start Up Unit, Fondazione Pisana per la Scienza Onlus

Research output: Contribution to journalReview articleAcademicpeer-review

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Abstract

Cellular senescence, described as a mechanism of irreversible cell cycle arrest, has emerged as a complex and multifaceted process with significant implications in cancer biology, particularly in pancreatic ductal adenocarcinoma (PDAC). This literature review aims to explore the intricate role of senescence in PDAC, focusing on its dual nature during tumorigenesis, in addition to therapy resistance, and its potential as a therapeutic target. Senescence escape was found to play a crucial role in PDAC progression, prompting the development of various pro-senescence therapies. However, recent studies have revealed a paradoxical aspect of the senescence-associated secretory phenotype, revealing its pro-tumorigenic effects and contribution to immune evasion in PDAC. By integrating insights from recent molecular studies, this review synthesizes current knowledge on the role of senescence in PDAC tumorigenesis and chemoresistance, with an emphasis on the emerging role of the tumor microenvironment and explores current and promising avenues for future research and potential therapeutic interventions.
Original languageEnglish
Pages (from-to)60-72
Number of pages13
JournalSeminars in cancer biology
Volume114
DOIs
Publication statusPublished - 1 Sept 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Chemoresistance
  • Hypoxia
  • Metabolism
  • Oncogene-induced senescence
  • Pancreatic ductal adenocarcinoma
  • Senescence
  • Senescence-associated secretory phenotype
  • Stroma
  • Therapy-induced senescence
  • Tumor microenvironment

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