Abstract

Simple SummaryNew treatments are urgently needed for pancreatic ductal adenocarcinoma because it is one of the most aggressive and lethal cancers, detected too late and resistant to conventional chemotherapy. Tumors in most patients feature a similar set of core mutations but so far it has not been possible to design a one-fits-all treatment strategy. Instead, efforts are underway to personalize the therapies. To find the treatments that might work the best for each patient, entirely new experimental platforms based on living miniature tumors, organoids, have been developed. We review here the latest international findings in designing personalized treatments pancreatic cancer patients using organoids as testing beds. Our own work adds important clues about how such testing could, and perhaps should, be conducted.Pancreatic ductal adenocarcinoma (PDAC) is a silent killer, often diagnosed late. However, it is also dishearteningly resistant to nearly all forms of treatment. New therapies are urgently needed, and with the advent of organoid culture for pancreatic cancer, an increasing number of innovative approaches are being tested. Organoids can be derived within a short enough time window to allow testing of several anticancer agents, which opens up the possibility for functional precision medicine for pancreatic cancer. At the same time, organoid model systems are being refined to better mimic the cancer, for example, by incorporation of components of the tumor microenvironment. We review some of the latest developments in pancreatic cancer organoid research and in novel treatment design. We also summarize our own current experiences with pancreatic cancer organoid drug sensitivity and resistance testing (DSRT) in 14 organoids from 11 PDAC patients. Our data show that it may be necessary to include a cell death read-out in ex vivo DSRT assays, as metabolic viability quantitation does not capture actual organoid killing. We also successfully adapted the organoid platform for drug combination synergy discovery. Lastly, live organoid culture 3D confocal microscopy can help identify individual surviving tumor cells escaping cell death even during harsh combination treatments. Taken together, the organoid technology allows the development of novel precision medicine approaches for PDAC, which paves the way for clinical trials and much needed new treatment options for pancreatic cancer patients.

Highlights

  • Pancreatic ductal adenocarcinoma (PDAC) is an aggressive malignancy with an overall 5-year survival rate of 9% [1]

  • The organoid technology allows the development of novel precision medicine approaches for PDAC, which paves the way for clinical trials and much needed new treatment options for pancreatic cancer patients

  • patient-derived organoid (PDO) serve as platforms for drug sensitivity and resistance testing (DSRT), which aids in the discovery of novel effective treatments for PDAC patients and can provide new potential diagnostic biomarkers for the disease

Read more

Summary

Introduction

Pancreatic ductal adenocarcinoma (PDAC) is an aggressive malignancy with an overall 5-year survival rate of 9% [1]. Only 4–7% of patients with BRCA1/2-mutated tumors have a marked response to treatment with platinum-based chemotherapy [8,11]. PDOs serve as platforms for drug sensitivity and resistance testing (DSRT), which aids in the discovery of novel effective treatments for PDAC patients and can provide new potential diagnostic biomarkers for the disease. Cancers 2022, 14, 525 resistance testing (DSRT), which aids in the discovery of novel effective treatments for PDAC patients and can provide new potential diagnostic biomarkers for the disease. Cell lines become poor representations of the original tumor specimen This problem is compounded by the fact that normal pancreatic ductal cells are difficult to culture, further hampering comparison between healthy and malignant tissue samples. As with any cell line-based model, spheroids reflect only a fraction of the molecular diversity found in real tumors

Patient-Derived Xenografts
Genetically Engineered Mouse Models
Organoid Culture Conditions and Success Rates
Neoplasia Modeling
Co-Cultures
Organoid Biobanks
A Single-Institute Experience
G2 G2 G2 G2 G2
Organoid Viability Responses Show Both Individual and Shared Patterns
Findings
Conclusions and Future Directions
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call