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Improved Drug-Response Prediction Model of APC Mutant Colon Cancer Patient-Derived Organoids for Precision Medicine.
Shin, Yong Jae; Jo, Eun Hae; Oh, Yunjeong; Kim, Da Som; Hyun, Seungyoon; Yu, Ahran; Hong, Hye Kyung; Cho, Yong Beom.
Afiliación
  • Shin YJ; Innovative Institute for Precision Medicine, Samsung Medical Center, Seoul 06351, Republic of Korea.
  • Jo EH; Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 06351, Republic of Korea.
  • Oh Y; Innovative Institute for Precision Medicine, Samsung Medical Center, Seoul 06351, Republic of Korea.
  • Kim DS; Innovative Institute for Precision Medicine, Samsung Medical Center, Seoul 06351, Republic of Korea.
  • Hyun S; Innovative Institute for Precision Medicine, Samsung Medical Center, Seoul 06351, Republic of Korea.
  • Yu A; Department of Health Sciences and Technology, Samsung Advanced Institute for Health Science & Technology (SAIHST), Sungkyunkwan University, Seoul 06351, Republic of Korea.
  • Hong HK; Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 06351, Republic of Korea.
  • Cho YB; Innovative Institute for Precision Medicine, Samsung Medical Center, Seoul 06351, Republic of Korea.
Cancers (Basel) ; 15(23)2023 Nov 22.
Article en En | MEDLINE | ID: mdl-38067236
ABSTRACT
Colorectal cancer is the third most common cancer in the world, with an annual incidence of 2 million cases. The success of first-line chemotherapy plays a crucial role in determining the disease outcome. Therefore, there is an increasing demand for precision medicine to predict drug responses and optimize chemotherapy in order to increase patient survival and reduce the related side effects. Patient-derived organoids have become a popular in vitro screening model for drug-response prediction for precision medicine. However, there is no established correlation between oxaliplatin and drug-response prediction. Here, we suggest that organoid culture conditions can increase resistance to oxaliplatin during drug screening, and we developed a modified medium condition to address this issue. Notably, while previous studies have shown that survivin is a mechanism for drug resistance, our study observed consistent survivin expression irrespective of the culture conditions and oxaliplatin treatment. However, clusterin induced apoptosis inhibition and cell survival, demonstrating a significant correlation with drug resistance. This study's findings are expected to contribute to increasing the accuracy of drug-response prediction in patient-derived APC mutant colorectal cancer organoids, thereby providing reliable precision medicine and improving patient survival rates.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cancers (Basel) Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cancers (Basel) Año: 2023 Tipo del documento: Article