Increased complexity in carcinomas: Analyzing and modeling the interaction of human cancer cells with their microenvironment

被引:48
作者
Stadler, Mira [1 ]
Walter, Stefanie [1 ]
Walzl, Angelika [1 ]
Kramer, Nina [1 ]
Unger, Christine [1 ]
Scherzer, Martin [1 ]
Unterleuthner, Daniela [1 ]
Hengstschlaeger, Markus [1 ]
Krupitza, Georg [2 ]
Dolznig, Helmut [1 ]
机构
[1] Med Univ Vienna, Inst Med Genet, Wahringer Str 10, A-1090 Vienna, Austria
[2] Med Univ Vienna, Inst Pathol, A-1090 Vienna, Austria
关键词
Cancer heterogeneity; Tumor stroma; 3D; Spheroid; Drug development; LASER-CAPTURE MICRODISSECTION; MULTICELLULAR TUMOR SPHEROIDS; IMAGING MASS-SPECTROMETRY; EPITHELIAL-MESENCHYMAL TRANSITIONS; STEM-CELLS; IN-VITRO; COLORECTAL-CANCER; GENE-EXPRESSION; STROMAL FIBROBLASTS; DRUG-RESISTANCE;
D O I
10.1016/j.semcancer.2015.08.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Solid cancers are not simple accumulations of malignant tumor cells but rather represent complex organ-like structures. Despite a more chaotic general appearance as compared to the highly organized setup of healthy tissues, cancers still show highly differentiated structures and a close interaction with and dependency on the interwoven connective tissue. This complexity within cancers is not known in detail at the molecular level so far. The first part of this article will shortly describe the technology and strategies to quantify and dissect the heterogeneity in human solid cancers. Moreover, there is urgent need to better understand human cancer biology since the development of novel anti-cancer drugs is far from being efficient, predominantly due to the scarcity of predictive preclinical models. Hence, in vivo and in vitro models were developed, which better recapitulate the complexity of human cancers, by their intrinsic three-dimensional nature and the cellular heterogeneity and allow functional intervention for hypothesis testing. Therefore, in the second part 3D in vitro cancer models are presented that analyze and depict the heterogeneity in human cancers. Advantages and drawbacks of each model are highlighted and their suitability to preclinical drug testing is discussed. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:107 / 124
页数:18
相关论文
共 248 条
[1]  
Aaberg-Jessen C, 2013, INT J CLIN EXP PATHO, V6, P546
[2]   Continuous microcarrier-based cell culture in a benchtop microfluidic bioreactor [J].
Abeille, F. ;
Mittler, F. ;
Obeid, P. ;
Huet, M. ;
Kermarrec, F. ;
Dolega, M. E. ;
Navarro, F. ;
Pouteau, P. ;
Icard, B. ;
Gidrol, X. ;
Agache, V. ;
Picollet-D'hahan, N. .
LAB ON A CHIP, 2014, 14 (18) :3510-3518
[3]   MALDI Imaging mass spectrometry: current frontiers and perspectives in pathology research and practice [J].
Aichler, Michaela ;
Walch, Axel .
LABORATORY INVESTIGATION, 2015, 95 (04) :422-431
[4]  
Andersen T, 2014, TISSUE ENG PT A, V20, P600, DOI 10.1089/ten.TEA.2013.0223
[5]   Phase II and Phase III attrition rates 2011-2012 [J].
Arrowsmith, John ;
Miller, Philip .
NATURE REVIEWS DRUG DISCOVERY, 2013, 12 (08) :568-568
[6]   A 3-D organoid kidney culture model engineered for high-throughput nephrotoxicity assays [J].
Astashkina, Anna I. ;
Mann, Brenda K. ;
Prestwich, Glenn D. ;
Grainger, David W. .
BIOMATERIALS, 2012, 33 (18) :4700-4711
[7]   De novo discovery of phenotypic intratumour heterogeneity using imaging mass spectrometry [J].
Balluff, Benjamin ;
Frese, Christian K. ;
Maier, Stefan K. ;
Schoene, Cedrik ;
Kuster, Bernhard ;
Schmitt, Manfred ;
Aubele, Michaela ;
Hoefler, Heinz ;
Deelder, Andre M. ;
Heck, Albert J. R. ;
Hogendoorn, Pancras C. W. ;
Morreau, Johannes ;
Altelaar, A. F. Maarten ;
Walch, Axel ;
McDonnell, Liam A. .
JOURNAL OF PATHOLOGY, 2015, 235 (01) :3-13
[8]   Vorinostat Eliminates Multicellular Resistance of Mesothelioma 3D Spheroids via Restoration of Noxa Expression [J].
Barbone, Dario ;
Cheung, Priscilla ;
Battula, Sailaja ;
Busacca, Sara ;
Gray, Steven G. ;
Longley, Daniel B. ;
Bueno, Raphael ;
Sugarbaker, David J. ;
Fennell, Dean A. ;
Broaddus, V. Courtney .
PLOS ONE, 2012, 7 (12)
[9]   Identification of stem cells in small intestine and colon by marker gene Lgr5 [J].
Barker, Nick ;
van Es, Johan H. ;
Kuipers, Jeroen ;
Kujala, Pekka ;
van den Born, Maaike ;
Cozijnsen, Miranda ;
Haegebarth, Andrea ;
Korving, Jeroen ;
Begthel, Harry ;
Peters, Peter J. ;
Clevers, Hans .
NATURE, 2007, 449 (7165) :1003-U1
[10]   Lgr5+ve Stem Cells Drive Self-Renewal in the Stomach and Build Long-Lived Gastric Units In Vitro [J].
Barker, Nick ;
Huch, Meritxell ;
Kujala, Pekka ;
van de Wetering, Marc ;
Snippert, Hugo J. ;
van Es, Johan H. ;
Sato, Toshiro ;
Stange, Daniel E. ;
Begthel, Harry ;
van den Born, Maaike ;
Danenberg, Esther ;
van den Brink, Stieneke ;
Korving, Jeroen ;
Abo, Arie ;
Peters, Peter J. ;
Wright, Nick ;
Poulsom, Richard ;
Clevers, Hans .
CELL STEM CELL, 2010, 6 (01) :25-36