Pressurized intraperitoneal aerosol chemotherapy enhances cisplatin efficacy in colorectal cancer organoids

Pressurized Intraperitoneal Aerosol Chemotherapy (PIPAC) is an emerging method that delivers chemotherapeutic agents as aerosols directly into the peritoneal cavity to overcome poor tissue penetration. Although early clinical outcomes are promising, challenges remain, such as variable patient responses and the lack of appropriate preclinical models. In this study, we investigated the efficacy of PIPAC combined with three cytotoxic agents (Cisplatin, Oxaliplatin, and Paclitaxel) using patient-derived colorectal cancer organoid models. Our results demonstrates that PIPAC, especially when combined with Cisplatin, significantly enhances the cytotoxicity against colorectal cancer organoids and modulates key cancer-related pathways. Transcriptomic analysis revealed significant alterations in gene expression patterns under PIPAC conditions, with notable impacts on cancer-related pathways such as epithelial-mesenchymal-transition and KRAS signaling. Pathway analysis further elucidated the modulation of cell-cycle related and oncogenic pathways by PIPAC, providing insights into its mechanism of action. These key findings suggest that PIPAC, particularly with Cisplatin, can enhance chemotherapeutic efficacy via transcriptomic modulation, supporting its potential clinical application in treating peritoneal carcinomatosis.

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Publication Details

Journal
Scientific Reports
Published
2025-12-19
DOI
https://doi.org/10.1038/s41598-025-27866-1
Citations
1
Primary Topic
Intraperitoneal and Appendiceal Malignancies
Type
article
Field-Weighted Citation Impact
2.01

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article

Pressurized intraperitoneal aerosol chemotherapy enhances cisplatin efficacy in colorectal cancer organoids

Seung‐Yong Jeong, Hee Seung Kim, Soon‐Chan Kim, Ji Won Park et al.
1 citations
Scientific Reports
Intraperitoneal and Appendiceal Malignancies
2.01
article

Pressurized intraperitoneal aerosol chemotherapy enhances cisplatin efficacy in colorectal cancer organoids

Seung‐Yong Jeong, Hee Seung Kim, Soon‐Chan Kim, Ji Won Park, Min Jung Kim, Young-Kyoung Shin, Shin Ae Lee, Ja-Lok Ku
article en
1 citations

Abstract

Pressurized Intraperitoneal Aerosol Chemotherapy (PIPAC) is an emerging method that delivers chemotherapeutic agents as aerosols directly into the peritoneal cavity to overcome poor tissue penetration. Although early clinical outcomes are promising, challenges remain, such as variable patient responses and the lack of appropriate preclinical models. In this study, we investigated the efficacy of PIPAC combined with three cytotoxic agents (Cisplatin, Oxaliplatin, and Paclitaxel) using patient-derived colorectal cancer organoid models. Our results demonstrates that PIPAC, especially when combined with Cisplatin, significantly enhances the cytotoxicity against colorectal cancer organoids and modulates key cancer-related pathways. Transcriptomic analysis revealed significant alterations in gene expression patterns under PIPAC conditions, with notable impacts on cancer-related pathways such as epithelial-mesenchymal-transition and KRAS signaling. Pathway analysis further elucidated the modulation of cell-cycle related and oncogenic pathways by PIPAC, providing insights into its mechanism of action. These key findings suggest that PIPAC, particularly with Cisplatin, can enhance chemotherapeutic efficacy via transcriptomic modulation, supporting its potential clinical application in treating peritoneal carcinomatosis.

Scientific ReportsVol. 15(1)
Seoul National University (KR), University of Suwon (KR), Cancer Research Institute (US), New Generation University College (ET), Seoul National University Hospital (KR), National University College (PR)
National Research Foundation, National Research Foundation of Korea
Openalex Percentile: Top 10%
Intraperitoneal and Appendiceal Malignancies
2.01
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