Pancreatic Cancer Organoids: An Emerging Platform for Precision Medicine? DOI Creative Commons
Evangelia Sereti, Irida Papapostolou, Konstantinos Dimas

et al.

Biomedicines, Journal Year: 2023, Volume and Issue: 11(3), P. 890 - 890

Published: March 14, 2023

Despite recent therapeutic advances, pancreatic ductal adenocarcinoma (PDAC) remains one of the most aggressive malignancies, with remarkable resistance to treatment, poor prognosis, and clinical outcome. More efficient approaches are urgently needed improve patients’ survival. Recently, development organoid culture systems has gained substantial attention as an emerging preclinical research model. PDAC organoids have been developed study cancer biology, progression, treatment response, filling translational gap between in vitro vivo models. Here, we review rapidly evolving field their potential powerful tools that could pave way towards precision medicine for cancer.

Language: Английский

Versican Associates with Tumor Immune Phenotype and Limits T-cell Trafficking via Chondroitin Sulfate DOI Creative Commons
Priyanka Hirani, Jacqueline McDermott, Vinothini Rajeeve

et al.

Cancer Research Communications, Journal Year: 2024, Volume and Issue: 4(4), P. 970 - 985

Published: March 22, 2024

Abstract Immunotherapies for cancers of epithelial origin have limited efficacy, and a growing body evidence links the composition extracellular matrix (ECM) with likelihood favorable response to treatment. The ECM may be considered an immunologic barrier, restricting localization cytotoxic immune cells stromal areas inhibiting their contact tumor cells. Identifying components this barrier could provide targets that whether degraded in situ support antitumor immunity improve immunotherapy response. Using library primary triple-negative breast cancer tissues, we correlated CD8+ T-cell identified proteoglycan, versican (VCAN), as putative member barrier. Our analysis reveals associates location VCAN expression, specific glycovariant [defined through pattern posttranslational attachments glycosaminoglycans (GAG)], cell types produce variant. In functional studies, isomers chondroitin sulfate presented on opposing roles being either supportive or trafficking, removal GAGs ameliorates these effects trafficking. Overall, conclude can inhibit trafficking within microenvironment depending present, is major component defines type immunotherapy. Significance: has been poor toward solid tumors despite infiltrating into tumor. associated impacting infiltration article its structural modification, having key role invasion.

Language: Английский

Citations

7

Reconstitution of human PDAC using primary cells reveals oncogenic transcriptomic features at tumor onset DOI Creative Commons

Yi Xu,

Michael H. Nipper,

A. Domínguez

et al.

Nature Communications, Journal Year: 2024, Volume and Issue: 15(1)

Published: Jan. 27, 2024

Animal studies have demonstrated the ability of pancreatic acinar cells to transform into ductal adenocarcinoma (PDAC). However, tumorigenic potential human remains under debate. To address this gap in knowledge, we expand sorted as 3D organoids and genetically modify them through introduction common PDAC mutations. The undergo dramatic transcriptional alterations but maintain a recognizable DNA methylation signature. transcriptomes are similar those disease-specific cell populations. Oncogenic KRAS alone do not organoids. can form vivo after acquiring four most driver mutations disease. Similarly, carrying these genetic also PDAC, thus experimentally proving that PDACs originate from both cells. RNA-seq analysis reveal shift normal towards with enhanced proliferation, metabolic rewiring, down-regulation MHC molecules, coagulation complement cascade. By comparing PDAC-like pancreas samples, identify group genes elevated expression during early transformation which represent diagnostic biomarkers.

Language: Английский

Citations

6

Patient‐Derived Organoids as Therapy Screening Platforms in Cancer Patients DOI
Danial Khorsandi, Jiawei Yang, Samuel Foster

et al.

Advanced Healthcare Materials, Journal Year: 2024, Volume and Issue: 13(21)

Published: Feb. 15, 2024

Patient-derived organoids (PDOs) developed ex vivo and in vitro are increasingly used for therapeutic screening. They provide a more physiologically relevant model drug discovery development compared to traditional cell lines. However, several challenges remain be addressed fully realize the potential of PDOs This paper summarizes recent advancements PDO enhancement culture models. is achieved by leveraging materials engineering microfabrication technologies, including organs-on-a-chip droplet microfluidics. Additionally, this work discusses application therapy screening meet diverse requirements overcome bottlenecks cancer treatment. Furthermore, introduces tools data processing analysis organoids, along with their microenvironment. These aim achieve enhanced readouts. Finally, explores future perspectives using personalized patients.

Language: Английский

Citations

6

Therapeutic potential of indole alkaloids in respiratory diseases: A comprehensive review DOI
Saikat Mitra,

Shajuthi Rahman Prova,

Sifat Ara Sultana

et al.

Phytomedicine, Journal Year: 2021, Volume and Issue: 90, P. 153649 - 153649

Published: July 15, 2021

Language: Английский

Citations

36

Pancreatic Cancer Organoids: An Emerging Platform for Precision Medicine? DOI Creative Commons
Evangelia Sereti, Irida Papapostolou, Konstantinos Dimas

et al.

Biomedicines, Journal Year: 2023, Volume and Issue: 11(3), P. 890 - 890

Published: March 14, 2023

Despite recent therapeutic advances, pancreatic ductal adenocarcinoma (PDAC) remains one of the most aggressive malignancies, with remarkable resistance to treatment, poor prognosis, and clinical outcome. More efficient approaches are urgently needed improve patients’ survival. Recently, development organoid culture systems has gained substantial attention as an emerging preclinical research model. PDAC organoids have been developed study cancer biology, progression, treatment response, filling translational gap between in vitro vivo models. Here, we review rapidly evolving field their potential powerful tools that could pave way towards precision medicine for cancer.

Language: Английский

Citations

15