Cited by 40Pancreatic and Hepatic Oncology ResearchPancreatitis Pathology and TreatmentCancer, Lipids, and Metabolism

Drug Repurposing, an Attractive Strategy in Pancreatic Cancer Treatment: Preclinical and Clinical Updates

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De Lellis, Laura, Veschi, Serena, Tinari, Nicola, Mokini, Zhirajr, Carradori, Simone, Brocco, Davide, Florio, Rosalba, Grassadonia, Antonino +1 more·2021·Cancers

Abstract

Pancreatic cancer (PC) is one of the deadliest malignancies worldwide, since patients rarely display symptoms until an advanced and unresectable stage of the disease. Current chemotherapy options are unsatisfactory and there is an urgent need for more effective and less toxic drugs to improve the dismal PC therapy. Repurposing of non-oncology drugs in PC treatment represents a very promising therapeutic option and different compounds are currently being considered as candidates for repurposing in the treatment of this tumor. In this review, we provide an update on some of the most promising FDA-approved, non-oncology, repurposed drug candidates that show prominent clinical and preclinical data in pancreatic cancer. We also focus on proposed mechanisms of action and known molecular targets that they modulate in PC. Furthermore, we provide an explorative bioinformatic analysis, which suggests that some of the PC repurposed drug candidates have additional, unexplored, oncology-relevant targets. Finally, we discuss recent developments regarding the immunomodulatory role displayed by some of these drugs, which may expand their potential application in synergy with approved anticancer immunomodulatory agents that are mostly ineffective as single agents in PC.

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  • Candidate repurposed drugs have well-documented pharmacokinetic, pharmacodynamic, dosing and toxicity profiles that accelerate their clinical development.

    “The rationale for this is that the candidate drugs have well‐documented and established pharmacokinetic, pharmacodynamic, dosing and toxicity profiles that accelerate their clinical development [6].”

    From Pyrvinium Pamoate Alone and With Gemcitabine Exhibits Anti‐Pancreatic Cancer Activity in <scp>2D</scp> and <scp>3D</scp> Cell Culture Models (2024) · cites this paper as [6]

    The Introduction states that repurposing candidates have established pharmacokinetic, pharmacodynamic, dosing and toxicity profiles. It says these profiles *may* accelerate clinical development, whereas the citing sentence presents acceleration as certain. (LLM, conf=0.86)

    Experimental — accuracy not yet measured

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Authors
De Lellis, L., Veschi, S., Tinari, N., Mokini, Z., Carradori, S., Brocco, D., Florio, R., Grassadonia, A., & Cama, A.
Affiliations
  • Department of Pharmacy, G. d’Annunzio University of Chieti-Pescara, 66100 Chieti, Italy
  • University of Chieti-Pescara (IT)
  • European Society of Anaesthesiology (BE)
Corresponding author
Cama, Alessandro
Venue
Cancers
Publisher
MDPI AG
Published
2021-08-05
Volume
13
Issue
16
Pages
3946
ISSN
2072-6694 (ISSN-L)
OpenAlex
W3188296940
Cited by
40
References
18
Citations by year
2026: 6 · 2025: 12 · 2024: 7 · 2023: 7 · 2022: 8
FWCI
0.67
Type
journal article
Language
en
Open access
Locations
  • Cancers (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
Ministry of Education, University and Research (MIUR), Progetti di Ricerca di Interesse Nazionale (PRIN) (2017EKMFTN_005)
Topics
  • Health Sciences › Medicine › Oncology › Pancreatic and Hepatic Oncology Research
  • Health Sciences › Medicine › Surgery › Pancreatitis Pathology and Treatment
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Lipids, and Metabolism
Keywords
drug repurposing, pancreatic cancer, FDA-approved drugs, mechanism of action, molecular targets, bioinformatics analysis, immunomodulation, combination therapy

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