# Patient-derived d-MMR/MSI phenotype urachal cancer organoids for personalized drug screening

## TL;DR

Researchers created organoid models of urachal cancer that mimic the original tumors and can be used for personalized drug testing.

## Contribution

The study introduces patient-derived organoids with d-MMR/MSI phenotype for modeling rare urachal cancer and drug screening.

## Key findings

- UrC organoids accurately reflect the genomic and transcriptomic profiles of original tumors, including heterogeneity.
- Drug response profiles in organoids align with molecular features like RAS/MAPK and PI3K/AKT/mTOR pathways and PD-L1 expression.
- Organoids offer a platform for studying treatment responses and resistance mechanisms in rare cancers.

## Abstract

Urachal cancer (UrC) is a rare, aggressive malignancy typically diagnosed at advanced stages, where systemic treatment becomes necessary. However, cytotoxic chemotherapy offers limited efficacy, and prospective clinical trials are exceedingly difficult due to the rarity of the disease. Thus, robust in vitro models are urgently needed to support precision medicine approaches for UrC.

Fresh UrC tumor samples were collected from patients undergoing en bloc resection and cultured to generate PDOs. These organoids were subjected to drug screening using standard chemotherapeutic agents. Whole-exome sequencing (WES) and RNA sequencing (RNA-seq) were conducted to compare the molecular profiles of the PDOs with their corresponding parental tumors. Associations between drug responses and genomic/transcriptomic features were analyzed. Student’s t-test was used for statistical assessment.

The established d-MMR/MSI phenotype UrC PDOs faithfully reproduced the genomic and transcriptomic landscapes of the original tumors, including intratumoral heterogeneity, and demonstrated consistent drug response profiles. Molecular characterization further revealed actionable targets within the RAS/MAPK and PI3K/AKT/mTOR pathways, as well as immune-related targets such as PD-L1. These findings highlight the utility of PDOs in modeling rare cancers and guiding personalized therapeutic strategies.

d-MMR/MSI phenotype UrC PDOs recapitulate the phenotypic and molecular features of their parental tumors, capturing critical heterogeneity. As such, they represent a valuable platform for reflecting treatment responses, investigating resistance mechanisms, and developing individualized therapeutic regimens.