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The establishment of kidney cancer organoid line in drug testing

Authors :
Ryan Tsz‐Hei Tse
Christine Yim‐Ping Wong
Xiaofan Ding
Carol Ka‐Lo Cheng
Chit Chow
Ronald Cheong‐Kin Chan
Joshua Hoi‐Yan Ng
Victor Wai‐Lun Tang
Peter Ka‐Fung Chiu
Jeremy Yuen‐Chun Teoh
Nathalie Wong
Ka‐Fai To
Chi‐Fai Ng
Source :
Cancer Medicine, Vol 13, Iss 12, Pp n/a-n/a (2024)
Publication Year :
2024
Publisher :
Wiley, 2024.

Abstract

Abstract Introduction Kidney cancer is a common urological malignancy worldwide with an increasing incidence in recent years. Among all subtypes, renal cell carcinoma (RCC) represents the most predominant malignancy in kidney. Clinicians faced a major challenge to select the most effective and suitable treatment regime for patients from a wide range of modalities, despite improved understanding and diagnosis of RCC. Objective Recently, organoid culture gained more interest as the 3D model is shown to be highly patient specific which is hypothetically beneficial to the investigation of precision medicine. Nonetheless, the development and application of organotypic culture in RCC is still immature, therefore, the primary objective of this study was to establish an organoid model for RCC. Materials and Methods Patients diagnosed with renal tumor and underwent surgical intervention were recruited. RCC specimen was collected and derived into organoids. Derived organoids were validated by histological examminations, sequencing and xenograft. Drug response of organoids were compared with resistance cell line and patients' clinical outcomes. Results Our results demonstrated that organoids could be successfully derived from renal tumor and they exhibited high concordance in terms of immunoexpressional patterns. Sequencing results also depicted concordant mutations of driver genes in both organoids and parental tumor tissues. Critical and novel growth factors were discovered during the establishment of organoid model. Besides, organoids derived from renal tumor exhibited tumorigenic properties in vivo. In addition, organoids recapitulated patient's in vivo drug resistance and served as a platform to predict responsiveness of other therapeutic agents. Conclusion Our RCC organoid model recaptiluated histological and genetic features observed in primary tumors. It also served as a potential platform in drug screening for RCC patients, though future studies are necessary before translating the outcomes into clinical practices.

Details

Language :
English
ISSN :
20457634
Volume :
13
Issue :
12
Database :
Directory of Open Access Journals
Journal :
Cancer Medicine
Publication Type :
Academic Journal
Accession number :
edsdoj.8568ecb3f89e4e14bb1fd30b5680afa0
Document Type :
article
Full Text :
https://doi.org/10.1002/cam4.7432