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Drug screening on digital microfluidics for cancer precision medicine.
Zhai, Jiao; Liu, Yingying; Ji, Weiqing; Huang, Xinru; Wang, Ping; Li, Yunyi; Li, Haoran; Wong, Ada Hang-Heng; Zhou, Xiong; Chen, Ping; Wang, Lianhong; Yang, Ning; Chen, Chi; Chen, Haitian; Mak, Pui-In; Deng, Chu-Xia; Martins, Rui; Yang, Mengsu; Ho, Tsung-Yi; Yi, Shuhong; Yao, Hailong; Jia, Yanwei.
  • Zhai J; State Key Laboratory of Analog and Mixed-Signal VLSI, Institute of Microelectronics, University of Macau, Macau SAR, China.
  • Liu Y; Department of Biomedical Sciences, and Tung Biomedical Sciences Centre, City University of Hong Kong, Hong Kong SAR, China.
  • Ji W; State Key Laboratory of Analog and Mixed-Signal VLSI, Institute of Microelectronics, University of Macau, Macau SAR, China.
  • Huang X; Faculty of Science and Technology, University of Macau, Macau SAR, China.
  • Wang P; School of Computer and Communication Engineering, University of Science and Technology Beijing, Beijing, China.
  • Li Y; Liver Transplantation Center, The Third Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China.
  • Li H; Department of Hepatobiliary Surgery, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
  • Wong AH; State Key Laboratory of Analog and Mixed-Signal VLSI, Institute of Microelectronics, University of Macau, Macau SAR, China.
  • Zhou X; State Key Laboratory of Analog and Mixed-Signal VLSI, Institute of Microelectronics, University of Macau, Macau SAR, China.
  • Chen P; Faculty of Science and Technology, University of Macau, Macau SAR, China.
  • Wang L; MoE Frontiers Science Center for Precision Oncology, University of Macau, Macau SAR, China.
  • Yang N; State Key Laboratory of Analog and Mixed-Signal VLSI, Institute of Microelectronics, University of Macau, Macau SAR, China.
  • Chen C; College of electrical and information engineering, Hunan University, Changsha, China.
  • Chen H; Cancer Center, Faculty of Health Sciences, University of Macau, Macau SAR, China.
  • Mak PI; College of electrical and information engineering, Hunan University, Changsha, China.
  • Deng CX; State Key Laboratory of Analog and Mixed-Signal VLSI, Institute of Microelectronics, University of Macau, Macau SAR, China.
  • Martins R; Department of Electronic Information Engineering, Jiangsu University, Zhenjiang, China.
  • Yang M; Liver Transplantation Center, The Third Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China.
  • Ho TY; Liver Transplantation Center, The Third Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China.
  • Yi S; State Key Laboratory of Analog and Mixed-Signal VLSI, Institute of Microelectronics, University of Macau, Macau SAR, China.
  • Yao H; Faculty of Science and Technology, University of Macau, Macau SAR, China.
  • Jia Y; Cancer Center, Faculty of Health Sciences, University of Macau, Macau SAR, China.
Nat Commun ; 15(1): 4363, 2024 May 22.
Article en En | MEDLINE | ID: mdl-38778087
ABSTRACT
Drug screening based on in-vitro primary tumor cell culture has demonstrated potential in personalized cancer diagnosis. However, the limited number of tumor cells, especially from patients with early stage cancer, has hindered the widespread application of this technique. Hence, we developed a digital microfluidic system for drug screening using primary tumor cells and established a working protocol for precision medicine. Smart control logic was developed to increase the throughput of the system and decrease its footprint to parallelly screen three drugs on a 4 × 4 cm2 chip in a device measuring 23 × 16 × 3.5 cm3. We validated this method in an MDA-MB-231 breast cancer xenograft mouse model and liver cancer specimens from patients, demonstrating tumor suppression in mice/patients treated with drugs that were screened to be effective on individual primary tumor cells. Mice treated with drugs screened on-chip as ineffective exhibited similar results to those in the control groups. The effective drug identified through on-chip screening demonstrated consistency with the absence of mutations in their related genes determined via exome sequencing of individual tumors, further validating this protocol. Therefore, this technique and system may promote advances in precision medicine for cancer treatment and, eventually, for any disease.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Ensayos Antitumor por Modelo de Xenoinjerto / Microfluídica / Medicina de Precisión Límite: Animals / Female / Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Ensayos Antitumor por Modelo de Xenoinjerto / Microfluídica / Medicina de Precisión Límite: Animals / Female / Humans Idioma: En Año: 2024 Tipo del documento: Article