中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Malignant ascites-derived organoid (MADO) cultures for gastric cancer in vitro modelling and drug screening

文献类型:期刊论文

作者Li, Jie4; Xu, Huawei4; Song, Lele4; Feng, Dan4; Peng, Xiaobo4; Wu, Meihong4; Wang, Bin4; Zhan, Xianbao4; Zhang, Lixing5; Zou, Yang1
刊名JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY
出版日期2019
卷号145期号:11页码:2637-2647
关键词Gastric cancer Malignant ascites Organoid Drug screening Personalised medicine
ISSN号0171-5216
DOI10.1007/s00432-019-03004-z
文献子类Article
英文摘要Purpose Malignant ascites (MA) is a common manifestation in advanced gastric cancer with peritoneal carcinomatosis and usually indicates a poor prognosis. However, lack of in vitro models that can faithfully recapitulate the characteristics of tumour cells in ascites hinders related researches. Tumour organoids have emerged as a robust in vitro model for tumour research and drug screening. Hence, we aimed to generate a 3-D in vitro organoid cultures from malignant ascites of gastric cancer for disease modelling and drug screening. Methods Eleven MADOs were generated from the MA tumour cells of gastric cancer patients. We made comparisons between MADOs and original MA tumour cells in histopathology by immunohistochemistry and genomics by whole-exome sequencing. In order to evaluate MADOs as functional in vitro disease models, we tested whether MADOs could be used for drug sensitivity screens. Results Eleven MADO cultures from human gastric cancer were established. MADOs demonstrated divergent growth characteristics and morphologies. MADO cultures preserve the histological architecture, genomic landscape of the corresponding MA tumour cells. MADOs exhibited heterogeneous responses to standard-of-care chemotherapeutics. Conclusions We generated MADOs modelling characteristics and mutated genes of MA tumour cells. A broad range of intrinsic MADO response to conventional chemotherapeutics suggests MADOs are amenable to drug screening.
学科主题Biochemistry & Molecular Biology ; Biotechnology & Applied Microbiology ; Genetics & Heredity
WOS关键词OVARIAN-CANCER ; CELL ; MUTATIONS ; CHEMOTHERAPY ; MANAGEMENT ; ADHESION ; BIOBANK
语种英语
CSCD记录号CSCD:31598791
WOS记录号WOS:000489287300001
出版者SPRINGER
版本出版稿
源URL[http://202.127.25.144/handle/331004/770]  
专题中国科学院上海生命科学研究院营养科学研究所
作者单位1.East China Normal Univ, Sch Life Sci, Inst Biomed Sci, Shanghai Key Lab Regulatory Biol, Shanghai 200241, Peoples R China;
2.Fudan Univ, Shanghai Canc Ctr, Shanghai 230032, Peoples R China,
3.Fudan Univ, Inst Radiat Med, Shanghai 230032, Peoples R China;
4.Second Mil Med Univ, Changhai Hosp, Dept Oncol, Shanghai 200433, Peoples R China;
5.Shanghai 121Biomed Inc, Res & Early Dev, Shanghai 200235, Peoples R China;
6.Univ Chinese Acad Sci, CAS Key Lab Nutr Metab & Food Safety, Shanghai Inst Nutr & Hlth, Shanghai Inst Biol Sci,Chinese Acad Sci, Shanghai 200031, Peoples R China;
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GB/T 7714
Li, Jie,Xu, Huawei,Song, Lele,et al. Malignant ascites-derived organoid (MADO) cultures for gastric cancer in vitro modelling and drug screening[J]. JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY,2019,145(11):2637-2647.
APA Li, Jie.,Xu, Huawei.,Song, Lele.,Feng, Dan.,Peng, Xiaobo.,...&,.(2019).Malignant ascites-derived organoid (MADO) cultures for gastric cancer in vitro modelling and drug screening.JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY,145(11),2637-2647.
MLA Li, Jie,et al."Malignant ascites-derived organoid (MADO) cultures for gastric cancer in vitro modelling and drug screening".JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY 145.11(2019):2637-2647.

入库方式: OAI收割

来源:上海营养与健康研究所

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