Harnessing preclinical models for the interrogation of ovarian cancer

被引:17
作者
Qin, Tianyu [1 ,2 ]
Fan, Junpeng [1 ,2 ]
Lu, Funian [1 ,2 ]
Zhang, Li [1 ,2 ]
Liu, Chen [1 ,2 ,3 ]
Xiong, Qiyue [1 ,2 ]
Zhao, Yang [4 ]
Chen, Gang [1 ,2 ]
Sun, Chaoyang [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Obstet & Gynecol, Res Bldg,2 Jiankang Ave,Caidian St, Wuhan 430030, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Canc Biol Res Ctr, Wuhan 430030, Peoples R China
[3] Shanghai Gen Hosp, Dept Obstet & Gynecol, Shanghai 200000, Peoples R China
[4] Hubei Univ Med, Taihe Hosp, Dept Plast Cosmet & Burn Surg, Shiyan 442008, Peoples R China
关键词
Ovarian cancer; Preclinical models; Patient-derived xenograft; Patient-derived organoids; Genetically engineered mouse models; Personalised medicine; ENGINEERED MOUSE MODELS; CELL-LINES REVEALS; IN-VIVO MODELS; FALLOPIAN-TUBE; XENOGRAFT MODELS; ORGANOID MODELS; MOLECULAR CHARACTERIZATION; SURFACE EPITHELIUM; DRUG-SENSITIVITY; TUMOR XENOGRAFTS;
D O I
10.1186/s13046-022-02486-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ovarian cancer (OC) is a heterogeneous malignancy with various etiology, histopathology, and biological feature. Despite accumulating understanding of OC in the post-genomic era, the preclinical knowledge still undergoes limited translation from bench to beside, and the prognosis of ovarian cancer has remained dismal over the past 30 years. Henceforth, reliable preclinical model systems are warranted to bridge the gap between laboratory experiments and clinical practice. In this review, we discuss the status quo of ovarian cancer preclinical models which includes conventional cell line models, patient-derived xenografts (PDXs), patient-derived organoids (PDOs), patient-derived explants (PDEs), and genetically engineered mouse models (GEMMs). Each model has its own strengths and drawbacks. We focus on the potentials and challenges of using these valuable tools, either alone or in combination, to interrogate critical issues with OC.
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页数:27
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共 184 条
[1]   The Exomes of the NCI-60 Panel: A Genomic Resource for Cancer Biology and Systems Pharmacology [J].
Abaan, Ogan D. ;
Polley, Eric C. ;
Davis, Sean R. ;
Zhu, Yuelin J. ;
Bilke, Sven ;
Walker, Robert L. ;
Pineda, Marbin ;
Gindin, Yevgeniy ;
Jiang, Yuan ;
Reinhold, William C. ;
Holbeck, Susan L. ;
Simon, Richard M. ;
Doroshow, James H. ;
Pommier, Yves ;
Meltzer, Paul S. .
CANCER RESEARCH, 2013, 73 (14) :4372-4382
[2]   Patient-derived ovarian cancer explants: preserved viability and histopathological features in long-term agitation-based cultures [J].
Abreu, Sofia ;
Silva, Fernanda ;
Mendes, Rita ;
Mendes, Teresa F. ;
Teixeira, Marta ;
Santo, Vitor E. ;
Boghaert, Erwin R. ;
Felix, Ana ;
Brito, Catarina .
SCIENTIFIC REPORTS, 2020, 10 (01)
[3]   SV40 large T antigen targets multiple cellular pathways to elicit cellular transformation [J].
Ahuja, D ;
Sáenz-Robles, MT ;
Pipas, JM .
ONCOGENE, 2005, 24 (52) :7729-7745
[4]   Establishment and characterization of a new malignant peritoneal mesothelioma cell line, KOG-1, from the ascitic fluid of a patient with pemetrexed chemotherapy resistance [J].
Akahane, Tomoko ;
Hirasawa, Akira ;
Imoto, Issei ;
Okubo, Aki ;
Itoh, Manabu ;
Nanki, Yoshiko ;
Yoshihama, Tomoko ;
Tominaga, Eichiro ;
Aoki, Daisuke .
HUMAN CELL, 2020, 33 (01) :272-282
[5]   Biobanking of patient and patient-derived xenograft ovarian tumour tissue: efficient preservation with low and high fetal calf serum based methods [J].
Alkema, Nicolette G. ;
Tomar, Tushar ;
Duiker, Evelien W. ;
Meersma, Gert Jan ;
Klip, Harry ;
van der Zee, Ate G. J. ;
Wisman, G. Bea A. ;
de Jong, Steven .
SCIENTIFIC REPORTS, 2015, 5
[6]   Be open about drug failures to speed up research [J].
Alteri, Enrica ;
Guizzaro, Lorenzo .
NATURE, 2018, 563 (7731) :317-319
[7]  
Anglesio MS, 2013, PLOS ONE, V8, DOI [10.1371/annotation/ffcaf179-872f-470b-8bb6-f06d8ba6d03a, 10.1371/journal.pone.0072162]
[8]  
[Anonymous], LIST NCI 60 HUMAN TU
[9]   Distinct transcriptional programs stratify ovarian cancer cell lines into the five major histological subtypes [J].
Barnes, Bethany M. ;
Nelson, Louisa ;
Tighe, Anthony ;
Burghel, George J. ;
Lin, I-Hsuan ;
Desai, Sudha ;
McGrail, Joanne C. ;
Morgan, Robert D. ;
Taylor, Stephen S. .
GENOME MEDICINE, 2021, 13 (01)
[10]   The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity [J].
Barretina, Jordi ;
Caponigro, Giordano ;
Stransky, Nicolas ;
Venkatesan, Kavitha ;
Margolin, Adam A. ;
Kim, Sungjoon ;
Wilson, Christopher J. ;
Lehar, Joseph ;
Kryukov, Gregory V. ;
Sonkin, Dmitriy ;
Reddy, Anupama ;
Liu, Manway ;
Murray, Lauren ;
Berger, Michael F. ;
Monahan, John E. ;
Morais, Paula ;
Meltzer, Jodi ;
Korejwa, Adam ;
Jane-Valbuena, Judit ;
Mapa, Felipa A. ;
Thibault, Joseph ;
Bric-Furlong, Eva ;
Raman, Pichai ;
Shipway, Aaron ;
Engels, Ingo H. ;
Cheng, Jill ;
Yu, Guoying K. ;
Yu, Jianjun ;
Aspesi, Peter, Jr. ;
de Silva, Melanie ;
Jagtap, Kalpana ;
Jones, Michael D. ;
Wang, Li ;
Hatton, Charles ;
Palescandolo, Emanuele ;
Gupta, Supriya ;
Mahan, Scott ;
Sougnez, Carrie ;
Onofrio, Robert C. ;
Liefeld, Ted ;
MacConaill, Laura ;
Winckler, Wendy ;
Reich, Michael ;
Li, Nanxin ;
Mesirov, Jill P. ;
Gabriel, Stacey B. ;
Getz, Gad ;
Ardlie, Kristin ;
Chan, Vivien ;
Myer, Vic E. .
NATURE, 2012, 483 (7391) :603-607