Abstract 3421: Bioprinted colorectal cancer organoids as a platform for large-scale therapeutic screening

Abstract Colorectal cancer is the fourth leading cause of cancer-related deaths in the United States. Among patients with metastatic colorectal cancer, approximately 70-75% survive more than 1 year after diagnosis, 30-35% survive more than 3 years, and fewer than 20% survive beyond 5 years. The main treatment options for unresectable metastatic colorectal cancer include cytotoxic chemotherapy, biologics, immunotherapy, and combinations thereof. Therapeutic options for unresectable metastatic disease remain limited, and more predictive preclinical platforms are urgently needed. To address this need, we developed a high-throughput mini-ring screening platform using patient-derived colorectal cancer organoids generated through 3D bioprinting. We generated and screened more than 28,000 bioprinted organoid mini-rings to ensure uniform size, architecture, and reproducibility across models.Screens incorporated standard colorectal cancer agents, including 5-fluorouracil, capecitabine, irinotecan, leucovorin, and oxaliplatin, along with a targeted 100-compound targeted panel spanning diverse pathways. Dose-response profiling enabled robust IC50 determination and revealed distinct sensitivity and resistance patterns across organoid models representing multiple disease stages. Transcriptomic analyses for each model were integrated to contextualize these functional profiles and identify pathway-level features associated with therapeutic vulnerability.This work shows how bioprinted colorectal cancer organoids provide a scalable and biologically relevant platform for high-throughput drug screening to support the development of more precise and effective therapeutic strategies for colorectal cancer. Citation Format: Taehee Kim, Jonathan Levi, Catherine Chen, Lindsay Ng, Alice Soragni. Bioprinted colorectal cancer organoids as a platform for large-scale therapeutic screening [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 3421.

Authors

Institutions

Publication Details

Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-3421
Primary Topic
Cancer Cells and Metastasis
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract 3421: Bioprinted colorectal cancer organoids as a platform for large-scale therapeutic screening

Alice Soragni, Lindsay Ng, Catherine Chen, Jonathan N. Levi et al.
Cancer Research
Cancer Cells and Metastasis
article

Abstract 3421: Bioprinted colorectal cancer organoids as a platform for large-scale therapeutic screening

Alice Soragni, Lindsay Ng, Catherine Chen, Jonathan N. Levi, Taehee Kim
article en

Abstract

Abstract Colorectal cancer is the fourth leading cause of cancer-related deaths in the United States. Among patients with metastatic colorectal cancer, approximately 70-75% survive more than 1 year after diagnosis, 30-35% survive more than 3 years, and fewer than 20% survive beyond 5 years. The main treatment options for unresectable metastatic colorectal cancer include cytotoxic chemotherapy, biologics, immunotherapy, and combinations thereof. Therapeutic options for unresectable metastatic disease remain limited, and more predictive preclinical platforms are urgently needed. To address this need, we developed a high-throughput mini-ring screening platform using patient-derived colorectal cancer organoids generated through 3D bioprinting. We generated and screened more than 28,000 bioprinted organoid mini-rings to ensure uniform size, architecture, and reproducibility across models.Screens incorporated standard colorectal cancer agents, including 5-fluorouracil, capecitabine, irinotecan, leucovorin, and oxaliplatin, along with a targeted 100-compound targeted panel spanning diverse pathways. Dose-response profiling enabled robust IC50 determination and revealed distinct sensitivity and resistance patterns across organoid models representing multiple disease stages. Transcriptomic analyses for each model were integrated to contextualize these functional profiles and identify pathway-level features associated with therapeutic vulnerability.This work shows how bioprinted colorectal cancer organoids provide a scalable and biologically relevant platform for high-throughput drug screening to support the development of more precise and effective therapeutic strategies for colorectal cancer. Citation Format: Taehee Kim, Jonathan Levi, Catherine Chen, Lindsay Ng, Alice Soragni. Bioprinted colorectal cancer organoids as a platform for large-scale therapeutic screening [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 3421.

Cancer ResearchVol. 86(7_Supplement)
University of California, Los Angeles (US)
Good health and well-being
Openalex Percentile: Top 8%
Cancer Cells and Metastasis
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.