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作 者:Sangyeop Hyun Youngmin Han Jae Yun Moon Young-Ah Suh Won-Gun Yun Wooil Kwon Jong-Eun Lee Daeun Kim Ja-Lok Ku Jin-Young Jang Daechan Park
机构地区:[1]Department of Molecular Science and Technology,Ajou University,Suwon,Republic of Korea [2]Department of Surgery and Cancer Research Institute,Seoul National University College of Medicine,Seoul,Republic of Korea [3]Molecular Science and Technology Research Center,Ajou University,Suwon,Republic of Korea [4]DNA Link Inc.,Seoul,Republic of Korea [5]Korean Cell Line Bank,Laboratory of Cell Biology,Cancer Research Institute,Seoul National University College of Medicine,Seoul,Republic of Korea
出 处:《Cancer Communications》2024年第8期915-920,共6页癌症通讯(英文)
基 金:supported by Global-Learning&Academic research institution for Master’s PhD students,Postdocs(G-LAMP)Program through the National Research Foundation of Korea(NRF)funded by the Ministry of Education(RS-2023-00285390 to Daechan Park);the NRF grant funded by the Ministry of Science and ICT(RS-2024-00341899 to Daechan 2022R1A2C2011122 to Jin-Young Jang);supported by DNA Link,Inc.,and there is no conflict of interest.
摘 要:Patient-derived xenograft(PDX)models have been used to explore therapeutic opportunities for pancreatic ductal adenocarcinoma(PDAC)[1].Although original tumor characteristics are altered by cancer-stromal interactions in a PDX-specific manner[2],the implications of clonal evolution from PDAC tumors to PDX are largely unknown.
关 键 词:ADENOCARCINOMA DUCTAL XENOGRAFT
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